Go to Part 2
No
longer is involuntary drugging only a concern to
those locked away in an institution. "Laws quietly
passed in 36 US states now allow the government to court
order you to take psychiatric drugs, even though you're
law abiding and living at home, in your own
neighborhood. These court orders are known as
"Involuntary Outpatient Commitment" (IOC). Typically,
you'd be required to report to your community mental
health center every few weeks for a "depot injection" of
a "neuroleptic drug" such as Prolixin or Haldol in your
butt. These drugs are time released [in a base of oil
and injected intramuscularly], so that the
super-powerful impact lasts weeks until your next
injection. The court orders can be routinely
re-approved, so these injections can go on for years."
Disclaimer: Many
of the statements that follow in this report (Namely the
effect that neuroleptic drugs have on the duration of
life span and sense of well being.) have not been
investigated or evaluated by the FDA (so they claim) nor
do they care to. The FDA does not even require animal
studies to determine how these drugs affect the duration
of life span which is shocking considering that the FDA
is supposed to be charged with protecting the American
people. The conclusions in this report are based on
available facts, for which a positive assertion can be
made by putting the information together so that the
true nature of these drugs can be established. This
information is what the FDA, psychiatrists, and the
pharmaceutical companies do NOT WANT YOU TO KNOW. This
information is both shocking and scandalous and reveals
a probable conspiracy so be warned. The common people
that are affected by this are not supposed to be smart
enough to understand and figure it out, but I have.
The purpose of this report is to prove conclusively that
neuroleptic drugs (Also know as antipsychotics or
antipsychotic drugs, tranquilizers, psychotropics or
psychotrophics, or psychotropic drugs or psychotrophic
drugs) shorten life span, destroy sexual function and
fertility, take away sense of well being which can
precipitate suicide and or violent behavior etc. This
will be established in this discussion through a
rudimentary explanation of some facets of biochemistry
and by quoting reputable sources. Also to empower the
people who may be affected by this with knowledge that
they can use to defend their rights and help overturn
these laws as unconstitutional and as basic human rights
violations. Also to help educate people who have friends
and or family members who are affected by this and to
provide understandable information to the general public
who are being denied the facts.
These drugs are not just given to those labeled as
"schizophrenic" or said to be "psychotic" or have
"psychosis" or have "schizophrenia". These drugs are
often given to people with depression, manic depression
or bipolar disorder, mania, Alzheimer’s patients or
those suffering from Alzheimer’s Disease, people with
brain damage or head injuries, retarded children and
adults, many children with Attention Deficit Disorder or
ADD or ADHD and children and teenagers who simply have a
hot temper (which ironically the drugs will make worse)
as well as many other things. If you are unsure whether
a certain drug is a neuroleptic or not then here is a
list of many names for neuroleptic drugs.
List of neuroleptic drug names: Chlorpromazine, (Brand
names are as follows; Chlor-PZ, Klorazine, Promachlor,
Promapar, Sonazine, Thorazine, Chlorprom, Chlor-Promanyl
and Largactil) Fluphenazine, (Brand names are as
follows; Permitil, Prolixin, Modecate, Moditen)
Mesoridazine Besylate, (Brand name is Serentil)
Perphenazine, (Brand names are as follows; Trilafon,
Etrafon, Triavil, Phenazine and Etrafon)
Prochlorperazine, (Brand names are as follows; Compazine
and Stemetil) Promazine Hydrocloride, (Brand name
Sparine) Thioridazine, (Brand names are Mellaril,
Novoridazine and Thioril) Trifuoperazine, (Brand names
are as follows; Stelazine, Clinazine, Novaflurazine,
Pentazine, Terfluzine and Triflurin) Clozapine, (Brand
named Clozaril, in Germany called Leponex) Haloperadol,
(Brand name Haldol) Loxapine, (Brand name Loxitane)
Pimozide (Brand name is Orap) Thiothixene, (Brand name
Navane) Risperidone (Brand name Risperdal), Zyprexa
(Brand name is Olanzapine), Sertindole, Ziprasidone
(Brand name Geodon or Geodone was planned to be named
Zeldox), Amperozide, Remoxipride, Melperone, Zotepine,
Isofloxythepin, Setoperone, Perospirone, Quetiapine
(Brand name Seroquel)Methotrimeprazine (Brand name
Nozinan or Nosinan, called Levomepromazin in Germany),
Zuclopenthixol (Brand name Clopixol), Zuclopenthixol
Acetate (Brand name Clopixol Acuphase), Amisulpride
(Brand name Solian). Also the antidepressant drug
Sertraline (Brand name Zoloft) is molecularly
indistinguishable from that of the neuroleptics and has
even been tried as a neuroleptic. This list contains
generic names and many brand names used in the USA and
Canada. This list is by no means comprehensive. Please
help provide the names used in other countries by
E-mailing me at:
moser@donet.com.
The compulsory administration of neuroleptic drugs by
order of the state is not only a violation of one's
right to liberty but also the right to life and the
pursuit of happiness. The right to life because
neuroleptics shorten life span and the precipitous onset
of degenerative disease that these drugs induce. The
right to the pursuit of happiness because neuroleptics
take away sense of well being. The right to liberty
because of not being able to make ones own decision
regarding the administration of these drugs and the
right to freedom of religious worship when the
administration of these drugs precludes their use when
it violates one's religious values and convictions. For
legitimate religious grounds to refuse these drugs see
Footnote C below.
The compulsory administration of neuroleptics because of
state order is a violation to one's right to life
because the drugs not only shorten life span but also
make the quality of one's life inferior due to the
precipitous onset of degenerative disease that these
drugs induce. This is not a statement unsupported by
fact. Let me now explain.
Dopamine, norepinephrine, and epinephrine all belong to
the class of neurotransmitters called catecholamines.
Catecholamines are synthesized from the amino acids
L-Phenylalanine and L-Tyrosine. This is the complete
step by step synthesis of these substances:
L-Phenylalanine --> L-Tyrosine -- > L-DOPA --> Dopamine
--> Norepinephrine --> Epinephrine. L-Tyrosine is also
converted to the thyroid hormone thyroxine by the
thyroid and dopamine is also converted to the skin
pigment melanin.
Serotonin is a neurotransmitter that is synthesized from
the amino acid L-Tryptophan. Melatonin the
sleep-inducing hormone produced by the pineal gland is
synthesized from Serotonin. Here is the complete step by
step synthesis of these substances. L-Tryptophan -->
5-Hydroxy - L-Tryptophan (5-HTP) --> 5-Hydroxy - L-Tryptomine
(Serotonin) --> Melatonin (O-methyl - N -
Acetylserotonin).
The main function of neuroleptics is blockage of
catecholamines in the brain. They have greatest affinity
for dopamine receptors and to a lesser extent
norepinephrine and epinephrine. (A future report of mine
will prove that these drugs destroy dopaminergic
receptors. See Footnote B for a simplified explanation
of this.) Neuroleptics block dopamine receptors in the
brain with generally greatest affinity for D1 and D2
receptors. Dopamine is a neurotransmitter and a receptor
is the "keyhole" which dopamine like a key, plugs into
for neuronal communication. There are many other
neurotransmitters, all with their respective "key holes"
or receptors. But the analogy of a "keyhole" is
insufficient because there are different receptors that
fit their corresponding neurotransmitter. Different
sides of the neurotransmitters will fit into the
different types of receptors. It is like the fact that a
puzzle piece has different sides with different shapes.
It's the different sides of the neurotransmitter that
fit into their corresponding receptors. Since these
neurotransmitter molecules are three dimensional in
shape, the different sides of its shape fit the
different receptors.
When a dopaminergic neuron fires, it releases dopamine
into the synapse from vesicles within the presynaptic
dendrite. The synapse is a gap or space between
dendrites, which are branches off the neuron and a
presynaptic dendrite is the dendrite that releases the
neurotransmitter. Think of this gap as if it were the
gap of a spark plug in an automobile except it is not
electricity that fires within this gap it is a chemical
messenger; a neurotransmitter. This dopamine then binds
with dopamine receptors on postsynaptic dendrites, which
are the dendrites on the other end of the gap that are
the recipient of the neurotransmitter that branch off
another neuron. The neurotransmitter then floats within
the synapse and through quantum mechanics is drawn to
the postsynaptic receptors on the end of the other
dendrite where they bind activating ion pumps. Ion pumps
are tubular molecular machines made up of amino acid
building blocks, which is a protein. Ion pumps are also
called channels. These receptors surrounding the
circumference of the ion pump cause this ion pump to
dilate when activated by the stimulating
neurotransmitter dopamine which allows electrolytes to
pass through the cell membrane causing an electrical
shift in polarity which causes the neuron to fire an
electrical charge down its axon. When the electrical
charge reaches the other end it causes dopamine to be
released from that neuron’s presynaptic dendrites and
the process continues in a cascade.
The neurotransmitter Serotonin is an inhibiting
neurotransmitter that mediates the ___expression of the
stimulating neurotransmitter Dopamine. There are third
dendrites from neurons of the serotoninergic system
utilizing this inhibiting neurotransmitter serotonin
that act as variable switches at different points within
the dopaminergic system. If serotonin is being released
into a synapse from a third dendrite where dopamine had
just been released, this inhibiting neurotransmitter
then acts as a chemical straight jacket by binding to
serotoninergic receptors on these same ion pumps which
mediates the degree to which dopamine will cause this
neuron to fire its electrical charge. This is the
simplified relationship dopamine has with serotonin.
There are many other neurotransmitters both stimulatory
and inhibitory that act in many complex ways that have
yet to be understood by science up until this point in
time. (For instance the neurotransmitter GABA
(4-AminoButyric Acid) is another inhibiting
neurotransmitter that has a mediating effect on the
stimulating neurotransmitter Glutamate and also has a
mediating affect on the stimulating neurotransmitter
dopamine in some dopaminergic pathways. The seizure drug
Valproic acid or Valproate (brand name Depakote or
Depakane) is often prescribed for "mania" or "manic
psychosis" and Bi Polar disorder also known as manic
depression. Depakote causes an increase in GABA in the
brain by inhibiting the two enzymes that are involved in
breaking down this neurotransmitter.) Many newer
neuroleptic drugs bind with both dopamine and
serotoninergic receptors. These serotoninergic receptors
are activated continuously by these drugs while at the
same time blocking normal serotoninergic function,
greatly inhibiting dopaminergic ___expression.
Neuroleptic drugs block dopamine receptors in all areas
of the brain for the types of receptors they have
affinity for. Antagonism of a type of receptor is not
neurological pathway specific and antagonizes all
receptors of the type it has affinity for without regard
for the actual function of the neurological pathways
they affect. Most dopaminergic function takes place
within the limbic system of the brain. (See the article
in the magazine called "American Scientist" March-April
1996 Volume 84 called "Reward Deficiency Syndrome" on
pages 134 and 135 for an explanation of the limbic
system and how it relates to the "reward cascade" which
I will discuss later in this report.
Click Here for the Article Online )
The limbic system of the brain contains a structure
called the hypothalamus. This area of the brain called
the hypothalamus is responsible for the regulation of
pituitary hormones by the release of controlling
hormones. The pituitary is a small gland located at the
base of the brain just under the hypothalamus. The
pituitary in turn regulates all other bodily hormones.
See the book "Facts and Comparisons" III W. Port Plaza,
Suite 300 St. Louis MO. USA 63146-3098 (telephone
314-216-2100 or 1-800-223-0554). (Note this book is
currently used by Rite Aid Pharmacies in the USA as a
reference aid and it is a loose bound updatable book.
The updatable section called "Antipsychotic Agents" is
(c) 1990) This book states under "antipsychotic agents"
that "Antipsychotics block postsynaptic dopamine
receptors in the basal ganglia, hypothalamus, limbic
system, brain stem and medulla... The phenothiazines
appear to act at both D1 and D2 receptors, whereas
haloperidol appears to act primarily at D2 receptors."
("D" here stands for dopamine and each different
receptor is numbered.) Also see the book "Drug Info for
the Health Care Professional 17th edition volume I 1997"
by Authority of the United States Pharmacopeial
Convention, Inc. (c) 1997 by The United States
Pharmacopeial Convention Inc. printed by Rand McNally,
Taunton, Massachusetts. Distributed by USPC 12601
Twinbrook Parkway, Rockville, Maryland USA. This book
states on page 2321 in the section on phenothiazines
under the subheading "Mechanism of action/Effect" that
neuroleptics "block postsynaptic mesolimbic dopaminergic
receptors in the brain... and depress the release of
hypothalamic and hypophyseal hormones." Hypophyseal
hormones are pituitary hormones.
One hormone the hypothalamus produces is TRH (thyrotropin
releasing hormone or thyrotrophin releasing hormone).
This hormone when released by the hypothalamus
stimulates the release of the pituitary hormone TSH
(thyroid stimulating hormone also called thyroidea
stimulating hormone, thyreotropic hormone, threotrophin
hormone, TTH, thyrotropin, thyrotrophin). TSH in turn
when released by the pituitary stimulates the production
or release of the thyroid hormone thyroxine which is
abbreviated T4 (four because this is the number of
iodine atoms the hormone contains). Thyroxine is the
hormone that regulates bodily metabolism. Lowering
metabolism by lowering the body's capacity to produce
thyroxine shortens life span. See the book "Handbook of
Vitamins, Minerals and Hormones 2nd Edition" by Roman J.
Kutsky, Ph.D. published by Van Nostrand Reinhold Company
New York (c)1973. On page 369 in this book under
"Essentially for Life" it states "Deficiency" of
thyroxine "in adult shortens life span". Also on page
367 of this book in paragraph three it states that the
capacity to produce this hormone is associated with
aging. And on page 371 under "Deficiency Symptoms" where
it states among other things that deficiency of
thyroxine causes "Decreased BMR" (BMR is the
abbreviation of Basal Metabolic Rate), "Increase in
blood lipid and cholesterol" (lipid is fat). Also see
the book "Fats that Heal Fats that Kill" (c) 1986,1993
by Udo Erasmus Ph.D. and published by Alive Books,
Fraser Park Drive, Burnaby BC Canada V5J 5B9. On page 37
of this book at the top of the page it states that
"Decreased metabolic rate is also involved in aging,
arthritic diseases, cancer, and cardiovascular
disorders, and is another general symptom of
degenerative diseases." Published by Alive Books, 7436
Fraser Park Drive, Burnaby BC Canada V5J 5B9. (c)
1986,1993.
Exposure to cold temperatures will stimulate the
production of TRH by means of dopaminergic neurons
within the hypothalamus which stimulates the production
of TSH by the pituitary which in turn stimulates the
production of T4 by the thyroid which raises metabolism
and body temperature to keep the body warm and to
regulate the burning of fat and carbohydrates as fuel.
The increased body temperature from a good metabolism
stimulates the production of the anabolic hormone
testosterone and anabolism keeps the body rejuvenated
and fights aging. As I have shown interfering with this
process lowers metabolism and shortens life span.
Lowered metabolism causes weight gain and according to
the American Medical Association's own statistics the
more overweight a person is the more likely that person
will suffer a premature death. See the chapter called
"Drugs Used in Obesity" starting on page 2439 of the
book "Drug Evaluations Annual 1995" by the American
Medical Association. Neuroleptic drugs suppress the
production of T4 thereby lowering metabolism by
suppressing the release of the hypothalamic hormone TRH.
Metabolism is the main mechanism that promotes
thermogenesis. Thermogenesis is the production of body
heat from the burning of fatty acids and glucose when
body heat is lost due to exposure to cold temperatures
and simply the continuous normal loss of body heat. It
is T4 in the end that is responsible for helping to
generate body heat that is lost and to keep the bodies
metabolism going which includes both catabolism the
burning of fat and glucose as fuel and anabolism the
building up of the body through the maintenance and
manufacture of replacement biochemical substances and
structure which fights aging. Metabolism is both
catabolic and anabolic. Although T4 technically is a
catabolic hormone catabolism and anabolism are
interconnected in a continues cycle so catabolism
through T4 promotes anabolism. A healthy well nourished
body will not burn protein as fuel.
Because of the neuroleptics or antipsychotics actions on
the hypothalamus suppressing the release of TRH the
pituitary doesn't produce as much TSH and in turn the
Thyroid doesn't produce as much T4. See the book again
"Facts and Comparisons". This book states under
"Antipsychotic Agents" that neuroleptics "depress
various components of the reticular activating system
which is involved in the control of basal metabolic rate
and body temperature, wakefulness, vasomotor tone,
emesis, and hormonal balance." Also see the book "Cecil
Textbook of Medicine 19th edition" edited by James B.
Wyngaarden, MD, Lloyd H. Smith, Jr., MD and J. Claude
Bennett, MD published by W.B. Saunders Company, Harcourt
Brace Jovanovich, Inc. Philadelphia London, Toronto,
Montreal, Sydney, Tokyo. This book states on page 1569
under "The Pathogenesis of Fever" under the subheading
"Initiation of Fever" that "...thermoregulation
originate[s] in the hypothalamus" and "... neuroleptic
drugs are capable of disrupting the hypothalamic
response and may interfere with the development of
fever. Among these, [the neuroleptic] phenothiazines are
the best known for their poikilothermic effect. These
agents are not specifically active in febrile states;
rather, they act to disable thermoregulatory mechanisms
at all times following their administration." Also see
the book called "AHFS 96 Drug Information" published by
American Hospital Formulary Service and "published by
the authority of the board of directors of the American
Hospital Formulary Service. This book states on page
1617 at the bottom right of the page; "Phenothiazines
have a poikilothermic effect, interfering with
temperature regulation in the hypothalamus: depending on
environmental conditions, hypothermia or hyperthermia
can occur." Hypothermia is under heating of the body and
hyperthermia is overheating of the body. Many people
forced to take neuroleptics have died of heatstroke. See
footnote A at the end of this thesis.
Again see the book "Drug Info for the Health Care
Professional 17th edition volume I 1997" on page 2321 in
the section on phenothiazines under the subheading
"Mechanism of action/Effect" that neuroleptics "block
postsynaptic mesolimbic dopaminergic receptors in the
brain... and depress the release of hypothalamic and
hypophyseal hormones." These effects are the result of
blockage or destruction of dopamine receptors within the
hypothalamus. Suppression of this hormonal system is one
of the main mechanisms in which neuroleptics shorten
life span.
Many of the quotes are obtained from statements
concerning the class of neuroleptics called
phenothiazines but since all neuroleptics block or
destroy dopamine receptors they all produce the same
undesirable symptoms. For instance this quote from the
book "Drug Info for the Health Care Professional" page
1564 under the heading of "haloperidol" a neuroleptic in
a class by its self; "[The] Pharmacological effects of
haloperidol are similar to the effects of...
phenothiazines". All neuroleptics block or destroy
dopamine receptors so therefore all suppress
hypothalamic hormone secretion. Now again see the book
"Fats that Heal Fats that Kill" on page 37 at the top of
the page where it states that "Decreased metabolic rate
is also involved in aging, arthritic diseases, cancer,
and cardiovascular disorders, and is another general
symptom of degenerative disease." On page 191 of the
same book at the top of the page it states; "The
brightness of the fire is the rate at which our body
produces energy our metabolic rate. For continued good
health, it is vital that the fire of life burns
brightly." Decreased metabolic rate not only leads to
obesity but also to degenerative disease. Not only do
neuroleptic drugs shorten life span but also make life
inferior due to inducing the onset of degenerative
disease.
See the book "Facts and Comparisons" again under
"antipsychotic agents" and note that one of the
neuroleptic drugs is sarcastically named "thioridazine"
(Brand names are Mellaril, Novoridazine and Thioril)
denoting the fact that these drugs suppress the
production of the thyroid hormone thyroxine or T4. "Thio"
being a grammatical construct from the beginning of the
word thyroxine and also the beginning of the word
iodine, which is the mineral that this hormone contains,
followed by the word rid in the middle of this construct
denoting the fact that these drugs get rid of or
suppress the release of this hormone. In my opinion this
reveals the utter contempt the designers of these drugs
have for those labeled "mentally ill". Also the question
must be asked, why would a drug be named after a life
span shortening "side effect" unless that was its sole
intended purpose? This also reveals that the designers
of these drugs knew the biological effects of these
drugs even before they were pushed on the public. Also
notice that one of the neuroleptics is called "mesoridazine
besylate" (Brand name is Serentil). Meso means middle
which is where the limbic system is located in the
brain. Since neuroleptic drugs shorten life span, the
compulsory administration of these drugs by court order
of the state is a violation of one's right to life.
Again see the book "Drug Info for the Health Care
Professional 17th edition volume I 1997" on page 2321
which states that neuroleptics "block postsynaptic
mesolimbic dopaminergic receptors in the brain ... [and]
... depress the release of hypothalamic and hypophyseal
hormones." Again hypophyseal hormones are hormones
produced by the pituitary gland. Because hypothalamic
hormones control the release of pituitary hormones this
is the reason pituitary hormones are suppressed. Most
hypothalamic hormones are releasing hormones. One
hypothalamic hormone which is an inhibiting hormone is
prolactin release-inhibiting hormone (abbreviated PRIH
also called PIF, RIH, prolactin inhibiting factor or
prolactin inhibiting hormone, PIH, prolactostatin).
Since neuroleptic drugs suppress the release of this
inhibiting hormone then the pituitary is free to secrete
abnormal amounts of this female hormone that regulates
lactation into the blood stream of both males and
females. Most other bodily hormones are suppressed by
neuroleptics except for prolactin for this reason. Since
phenothiazines were the first neuroleptics used starting
with Thorazine and the fact that phenothiazines have
been used on more people then all other neuroleptics
combined, the affect on hormone production caused by
these drugs has been well established. All the other
neuroleptics have been designed after what has been
learned from the phenothiazines.
The level of hypothalamic hormone production is in
direct correlation with dopaminergic activity or the
ability of the dopaminergic system to function normally
without interference. For this reason all neuroleptics
that block or destroy dopamine receptors or utilize the
serotoninergic system or both will suppress the
production of all hypothalamic hormones which in turn
suppresses pituitary hormone production and in turn all
other bodily hormones.
Serotonin is an inhibiting neurotransmitter that
mediates the function of the dopaminergic system. Excess
serotonin stimulation has the effect of suppressing the
dopaminergic system. One neuroleptic called Molindone
(brand names Lidone and Moban) utilizes this function by
mimicking serotonin. Also this is why antidepressant
drugs that raise levels of serotonin cause sexual
dysfunction. One "antidepressant" drug Sertraline (Brand
name Zoloft) is molecularly indistinguishable from that
of the neuroleptics. In fact Zoloft has even been tried
as a neuroleptic. Perhaps it's labeled as an
antidepressant just for people who insist that their
"problems are just depression". A man I talked to on the
telephone at the FDA told me that Zoloft was so powerful
at destroying sexual function that if just one pill is
taken by someone with premature ejaculation it will slow
him down. But don't take this man's word for it. Even
the PDR says Zoloft causes sexual dysfunction.
Percentage rates of impotence listed in the PDR for
various drugs is misleading as only people who were
sexually active and not embarrassed to speak about it
would even report impotence or sexual dysfunction as a
side effect. Every male I have questioned who has been
on these drugs has confided in me that these drugs have
caused them some type of major sexual problem.
See the book "Biochemistry A Case-Oriented Approach
fifth edition" by the Department of Biochemistry, The
University of Iowa College of Medicine, Iowa City, Iowa.
Montgomery Rex Ph.D., Thomas Conway Ph.D. and Arthur A.
Spector MD (c) 1990 The C.V. Mosby Company. This book
states on page 761 that prolactin secretion is increased
by "serotonin". See the book "Facts and Comparisons"
again under "antipsychotic agents" under
"Carcinogenicity / prolactin secretion:" which states "Neuroleptic
drugs elevate prolactin levels which persist during
chronic administration." This is a reference to all
neuroleptics, not just phenothiazines. Also see the book
again called "Biochemistry A Case-Oriented Approach
fifth edition" on page 761 in the seventh paragraph
where it states that "Some medications, acting as
dopamine antagonist, increase prolactin secretion.
Although many drugs of this type exist, the most common
are the antipsychotic phenothiazines, such as thorazine."
On page 778 of this same book it states in the first
paragraph; "Dopamine is an active compound believed to
inhibit prolactin secretion".
Since neuroleptics block or destroy dopamine receptors
there is no dopaminergic activity to inhibit prolactin
secretion. Going back to page 761 of this same book it
sates in the fifth paragraph under "Disorders associated
with prolactin" that "Prolactin secretion has a dramatic
effect in blocking the pituitary gonadotrophs, and
elevated prolactin levels are associated with sexual
dysfunction. Hyperprolactinemia before puberty blocks
sexual maturation and the pubertal growth spurt. After
puberty, hyperprolactinemia is associated with loss of
libido and impotence in males and amenorrhea in
females." The gonads are testicles in men and ovaries in
women and amenorrea is the abnormal suspension or
suppression of menstruation. Hyperprolactinemia is the
abnormal excessive production of the female hormone
prolactin.
One pituitary gonadotroph is luteinizing hormone
(abbreviated LH and also called luteotrophin or
luteotropin, interstitial cell-stimulating hormone, ICSH,
Prolan B, gonadotrophin II or gonadotropin II,
metakentrin, corpus luteum-ripening hormone). See the
book again "Handbook of Vitamins, Minerals and Hormones"
on page 323 under "Deficiency Diseases, Disorders" where
it states that deficiency of this hormone causes "Hypogonadism".
(Hypogonadism is the inability of the gonads to perform
their function of remaining fertile and producing sex
hormones.) Also on this page it states that this hormone
is necessary for "reproduction". Now reference page 327
of this book under "Mode of Action" where it states that
this hormone "increases synthesis of steroid hormones
(sex hormones) ... estradiol (estrogen) ... [and]
testosterone". Also here it also states that this
hormone "stimulates rupture of follicles in ovary".
(This is so the ova or egg can be released from the
ovary.)
The other pituitary gonadotroph is follicle stimulating
hormone (abbreviated FSH, and also called Follotropin or
Follotrophin, Thylakentrin, Prolan A, gonadotrophin I or
gonadotrophin I, gametogenic hormone, follicle ripening
hormone, gametokinetic hormone). See the book again
"Handbook of Vitamins, Minerals and Hormones" on page
330 where it states that this hormone is required for
"reproduction". Also see page 332 under "Deficiency
Symptoms" where it states that deficiency of this
hormone causes "Decreased gametogenic function and
development (nonfunctional)". (This is just a fancy way
of saying that deficiency of this hormone will cause any
sperm or ova produced to be genetically incapable of
producing offspring or rendering any sperm or ova (eggs)
produced "nonfunctional") Also on this page it states
that deficiency of this hormone also causes "Atrophy of
the gonads" (atrophy means to waste away), "No
maturation of ova, sperm", "Obesity", "Decreased libido,
potency, hair growth" and "decreased blood levels of
estrogen". (Estrogen is the female sex hormone.)
Pituitary gonadotrophs stimulate the production of sex
hormones by the gonads.
The hypothalamic hormone, luteinizing hormone-releasing
hormone regulates these pituitary gonadotrophs.
(Abbreviated LRH also called LRF, LH-releasing factor or
LH-releasing hormone, (LH-RH/FSH-RH), Gonadotropin
releasing hormone (abbreviated Gon-RH or GnRH)) This
hormone is suppressed by neuroleptics so here is another
mechanism by which sex hormone production is inhibited
besides the inhibition due to excessive prolactin
secretion.
Going further on to the sex hormones which neuroleptic
drugs inhibit we will learn more about what these drugs
do to the body. Estradiol also called estrogen (some
other names are female hormone, dihydrotheelin,
dihydrofollicular hormone, dihydrofolliculin) "is
essential for reproduction and female characteristics.
Its chief functions are to maintain and regulate female
sex characteristics and behavior. Its chief importance
is as the major female sex hormone with its command of
female sex development and maintenance of female body
characteristics and behavior. ...Deficiency conditions
include menopause and delayed maturation." As stated in
the book "Hand Book of Vitamins, Minerals and Hormones"
on page 415. (See footnote D) On page 419 of the book
"Handbook of Vitamins, Minerals and Hormones" it states
that deficiency of estrogen will cause "Delayed
maturation", "Female accessory and reproductive organs
recess" (recess means not to function), "Decreased
female behavior pattern", "Senescence" (means Growing
old, aging), and "Menopause". Here is further proof that
neuroleptic drugs program the body to self-destruct,
grow old and die and proof that these drugs prevent
reproduction.
Another female hormone that is stimulated by the
hypothalamic hormone, luteinizing hormone-releasing
hormone through the pituitary hormone luteinizing
hormone is progesterone. So therefore neuroleptics also
inhibit the production of this hormone as well. On page
423 of the book "Handbook of Vitamins, Minerals and
Hormones" it states that progesterone "is indirectly
essential for life, since it is a precursor to
aldosterone and cortisol, which is essential. Its chief
functions are to synergize the actions of estradiol
(estrogen) in the female organs, especially during
pregnancy. Its importance stems from the fact that it is
a precursor to all the steroid hormones and that
estradiol (estrogen) requires its presence for many of
its actions. ...Deficiency conditions [include]...
dysfunctional uterine bleeding." On page 427 under
"Deficiency Symptoms" this book states that deficiency
of progesterone causes "Termination of pregnancy",
"Decreased production of steroids", Decreased
ovulation", "Loss of normal cyclic changes" and
"Decreased development for implantation and gestation".
This is shocking because neuroleptics are routinely
given to pregnant women who commonly have miscarriages
and then the prescribing psychiatrists will deny that
the drugs were the cause!
Now onto the male sex hormone testosterone;
Testosterone's "chief functions are: development and
maintenance of the male organs, male sex
characteristics, and behavior, as well as stimulation of
growth (anabolic), and metabolism of muscles, liver; and
kidney. The chief importance of testosterone lies in its
major command of male sex development, body
characteristics, and behavior. Deficiencies include
eunuchoidism, and male hypogonadism. ...Testosterone is
formed mainly in the testes (interstitial cells) but
also in small amounts in the adrenal cortex and the
ovary[s]." (From page 431 of the book "Handbook of
Vitamins, Minerals and Hormones") On page 433 of this
book it states that testosterone is "essential for
reproduction in all (male) vertebrates". On page 435 of
this book it states that deficiency of testosterone will
cause, "Involution of accessory organs (prostate,
seminal vesicles)", (involution is the progressive
decline or degeneration of normal physiological
functioning occurring as a result of the aging process
and or decrease in size of an organ.) "Decreased male
behavior patterns and libido", "Decreased secondary sex
traits", "Poor muscle development and function".
Neuroleptic drugs will destroy sexual function in men
and produce sterility and will cause musculature to
waste away since this is another hormone that
neuroleptic drugs suppress the production of. See the
web address below that states that risperidone (which is
a neuroleptic in a class by itself) will cause
"testicular atrophy" because of its "antidopaminergic
activity". All neuroleptics though will cause testicular
atrophy due to hormonal suppression. See "Atypical
Antipsychotics: A Practical Review" at:
Risperidone and do a search on the page for
"testicular atrophy". You must first have a user name
and password before accessing this article. It is open
to anyone who wants a password.
I have received this
argument from someone who presented himself as a medical
student. He said that dopamine and Prolactin
Release-Inhibiting Hormone is one and the same. He also
said "of course a drug acting as a dopamine antagonist
is going to affect this hormone". I had to set this man
straight. I told him this: "That is not true. Prolactin
Release Inhibiting-Hormone (also known as PRIH,
Prolactostatin, RIH, Prolactin Inhibiting Factor or
hormone, PIF, PIH, PRIF), which is produced by the
hypothalamus is a chain of amino acids similar in
structure to Luteinizing Hormone-Releasing Hormone. This
can be found in the book "The Handbook of Vitamins
Minerals and Hormones" by Roman J. Kutsky, Ph.D. on page
303, which is a very good biochemistry fact book written
in outline form. At the time of publication of this book
the exact structure of Prolactin Release-Inhibiting
Hormone had not been determined but they knew enough
about it that they knew it was similar in structure to
Luteinizing Hormone-Releasing Hormone which is a chain
of amino acids called a peptide which is a small
protein. Dopamine is a monoamine derived from the amino
acids L-Tyrosine and or L-Phenylalanine. It has been
called "Prolactin Inhibiting Factor" but should never be
called "hormone" since it is a neurotransmitter.
Apparently there is much confusion in the medical field
regarding this. I also told this man this; "I can
understand your confusion because it has been known for
years that Dopamine affected Prolactin, but by the
mechanisms pointed out in this report. Dopamine affects
the release of all hypothalamic hormones not just
Prolactin Release Inhibiting Hormone or Prolactostatin.
Here is the exact amino acid sequence of PRIH; Asp - Ala
- Glu - Asn - Leu - Ile - Asp - Ser - Phe - Gln - Glu -
Ile -Val - Lys - Glu - Val - Gly - Gln - Leu - Ala - Glu
- Thr - Gln - Arg - Phe - Glu - Cys - Thr - Thr - His -
Gln - Pro - Arg - Ser - Pro - Leu - Arg - Asp - Leu -
Lys - Gly - Ala - Leu - Glu - Ser - Leu - Ile - Glu -
Glu - Glu - Thr - Gly - Gln - Lys - Lys - Ile". I also
told him this: "Dopamine is not a hormone but a
neurotransmitter. No doubt there are many independent
neurological pathways that utilize this stimulating
neurotransmitter in the control of the release of these
hypothalamic hormones. That is why the release of these
hormones operate independently of each other and that
dopamine antagonism inhibits all hypothalamic hormone
production because antagonism is not neurological
pathway specific and never will be. Which is why the
drug chemical approach to treating "mental illness" is
fundamentally flawed and will never be the answer.
Go to this web-site where the hypothalamic peptide
prolactostatin or prolactin release-inhibiting hormone
is available for sale for research purposes.
http://www.penlabs.com/biopro/biopeptides3_32.html
It is called Prolactin Release Inhibiting Factor or (PIF)
on this Web-site. Go here to this German language
web-site where it is identified as a hypothalamic
hormone.
http://www-stud.uni-essen.de/~st0184/Infos/eseldiv.htm.
The name Prolactostatin is used on this web-site. There
are three hypothalamic "statins" and they are all
inhibiting peptides. The idea that PRIH is dopamine is
outmoded and erroneous. Dopamine is the controlling
neurotransmitter involved in the release of PRIH. There
have been studies in the past that seemed to suggest
that dopamine acts directly on the pituitary to inhibit
prolactin, but such studies are flawed in that infusing
dopamine into the area of the pituitary to observe the
affect on Prolactin release could very well be effecting
real PRIH release from the hypothalamus simply because
of the close proximity of the pituitary to the
hypothalamus. The pituitary is after all at the base of
the hypothalamus and this dopamine infusion could easily
be crossing over into the hypothalamus and stimulating
the dopaminergic system and therefore releasing real
PRIH which in turn would inhibit prolactin thus giving
the appearance that dopamine was the sole causative
factor acting directly on the pituitary.
As has already been established neuroleptic drugs
inhibit the production of the hormone progesterone and
it is a precursor to the hormone aldosterone, (Precursor
means the body uses one substance to synthesis or to
produce another substance. In simpler words the body
makes the hormone aldosterone from the hormone
progesterone) so therefore aldosterone is also inhibited
by neuroleptic drugs. See the book "Handbook of
Vitamins, Minerals and Hormones" again on page 406 where
many deficiency symptoms are cited which include
"Muscular weakness" and "Stress intolerance". See the
book again on page 401 where it states at the bottom of
the page that aldosterone is "One of the most essential
of all hormones; absence can be fatal in [a] short time
period". Now look at the book "Facts and Comparisons"
again under "antipsychotic agents" under "adverse
reactions" where it states that after the administration
of neuroleptics that "Sudden Death has occasionally been
reported." Could this perhaps at least be partly due to
the inhibition of aldosterone secretion by these
neuroleptic drugs? Aldosterone secretion is partly
governed by the pituitary hormone ACTH (the abbreviation
for adrenocorticotropic hormone or adrenocorticotrophic
hormone and also called adrenocorticotropin or
adrenocorticotrophin, corticotropic hormone or
corticotrophin hormone) which is in turn governed by
release of the hypothalamic hormone corticotropin-releasing
hormone or corticotrophin-releasing hormone.
(Abbreviated CRH and also called CRF, cortical-releasing
factor or cortical-releasing hormone,
adrenocorticotropin-releasing factor or
adrenocorticotrophin-releasing factor, corticotropin-releasing
factor or corticotrophin-releasing factor.) See the book
"Handbook of Vitamins Minerals and Hormones" again on
page 342 at the bottom of the page where it states that
ACTH is "one of the most essential hormones-Absence
causes notable shortening of normal life span." Now see
page 344 of this same book where it states that
deficiency of ACTH causes "Decreased weight of adrenal
(atrophy)", "Decreased mobilization of free fatty acids"
(so fat can be burned as fuel). It also states here that
deficiency of ACTH causes "Decreased steroids in blood,
urine (17-hydroxy and 17-keto)" (ketones are produced as
a byproduct of the burning of fat as fuel. Since
deficiency of ACTH decreases ketones it means that fat
is not being utilized as fuel which will lead to weight
gain), "Fasting hypoglycemia" and "Increased insulin
sensitivity" Which explains why it is common for people
on these neuroleptic drugs to be glucose intolerant.
Since neuroleptic drugs inhibit the production of all
these hormones described above, they also cause all the
problems associated with deficiency of these hormones.
Here is unquestionable proof that neuroleptic drugs not
only shorten life span but also destroy sexual function
and fertility or the ability to procreate offspring or
have children.
Aldosterone is not the only hormone that is controlled
by the ACTH, CRH hormonal cascade. ACTH and CRH also
control the release of the adrenal hormone cortisol
(Also called hydrocortisone, Compound F,
17-hydroxycorticosterone. Substance M, glucocorticoid)
(also cortisol is converted into cortisone in the body).
On page 407 of the book "Handbook of Vitamins, Minerals
and Hormones" it states that the "chief functions" of
cortisol "are to maintain stress reactions, capillary
permeability, release of other hormones, liver
anabolism, and extrahepatic catabolism. Its chief
importance is maintenance of stress reactions". ("liver
anabolism" is the rejuvenation of the liver and liver
synthesis of substances that keep the body rejuvenated
and "extrahepatic catabolism" is the burning of fat as
fuel in all parts of the body except for the liver.)
Also on this page it states that "Factors inhibiting the
release" of cortisol "are: high glucocorticoids, low
ACTH, and pituitary hormones." On page 408 of this book
it states at the bottom of the page that "Absence" of
cortisol "causes shortening of life span due to
inability to respond to stress situations." On page 411
of this book it states that deficiency of cortisol
causes decreases in "Kidney function, leading to death",
"Liver glycogen, gluconeogenesis", "Intestinal
absorption, blood sugar" and "Stress response-Ultimately
death". Also on page 411 it states that deficiency of
cortisol will cause increases in "Fat anabolism,
hemoconcentration" (Fat anabolism is the depositing of
new fat tissue), "Muscular weakness" and others. Here is
further proof that neuroleptic drugs shorten life span.
Now on to another hormone which neuroleptic drugs
suppress the release of which is the pituitary hormone
growth hormone. (Abbreviated GH and also called
somatotropin or somatotrophin, phyone, anterior
pituitary growth hormone, adenohypophyseal growth
hormone, somatotrophic hormone, STH) You may think that
this is not a problem because most of the people these
drugs are given to are already adults or in their teens.
(I have been recently discovering that a growing number
of children with ADD or similar "conduct disorder" are
being given these drugs.) But growth hormone has other
functions in adults. See the book again called "Handbook
of Vitamins, Minerals and Hormones" on page 307 where it
states that "Because growth hormone controls the
nitrogen balance of an organism, it is thought to be
involved in the aging process." On page 309 of this same
book it states that absence of growth hormone will
result in a "decrease in normal life span." On page 311
it states that deficiency will result in "Increased fat
deposition." The hypothalamic hormone growth
hormone-releasing hormone (abbreviated GRH and also
called GHRH, GRF, somatotropin-releasing factor or
somatotrophin-releasing factor or somatotropin-releasing
hormone or somatotrophin-releasing hormone, growth
hormone releasing-releasing factor or growth hormone
releasing-releasing hormone, SRF, GHRF) stimulates the
secretion of growth hormone by the pituitary. As we have
already learned neuroleptics suppress the release of
both hypothalamic and pituitary hormones. Here is
further evidence that neuroleptic drugs shorten life
span. Therefore the compulsory administration of
neuroleptic drugs by court order of the state is a
violation of one's right to life.
Neuroleptic drugs also possess "adrenergic blocking
effects". Again reference the book "Facts and
Comparisons" under the section "Antipsychotic agents".
The book states on the first page of this section "In
addition, the drugs exert anticholinergic and
alpha-adrenergic blocking effects." Also see the book
"Drug Info for the Health Care Professional" again on
page 2321 under the section on phenothiazines where it
states under the subheading "Mechanism of action/effect"
that "Phenothiazines also produce an alpha-adrenergic
blocking effect." (Phenothiazines being just one of the
classes of neuroleptic drugs all of which block dopamine
receptors and cause the same effects due to blockage of
these receptors.) This is so because of the chemical
similarity of dopamine to the adrenergic
neurotransmitters, all of which belong to a family of
neurotransmitters called catecholamines. The adrenergic
neurotransmitters are adrenaline and noradrenaline.
(Also called epinephrine and norepinephrine) These two
neurotransmitters are synthesized or created from
dopamine; thus the similarity in their molecular
structure. Both these neurotransmitters double as
hormones. Since neuroleptics block or destroy
alpha-adrenergic postsynaptic receptors this would
simulate a deficiency.
See the book again "Handbook of Vitamins, Minerals and
Hormones" this time under "Epinephrine". This book
states on page 445 concerning epinephrine that "It is
not essential for life, but it is indirectly essential,
since it is involved in stress responses via cortisol,
which is essential". (We have already learned the
importance of cortisol.) On this same page it states
that one of the functions of epinephrine or adrenaline
is increasing metabolic rate in time of need to respond
to stress or emergency. Also see page 447 under the
subheading "Essentiality for Life" where it states that
deficiency of this hormone and neurotransmitter will
cause "possible shortening of life span due to decreased
response to emergencies." So if threatened by a life
threatening situation neuroleptic drugs make one
physically ill equipped to face the threat. Also on page
448 under "Deficiency Symptoms", "Not fatal, but
organism cannot respond to emergency, hard work,
temperature extreme, emotional disturbance". Not fatal
of course unless one fails to respond adequately to an
emergency or dies of heatstroke. Again see the book
"Facts and Comparisons" under "Antipsychotic Agents"
under "Adverse Reactions" where it states that
"Heatstroke/Hyperpyrexia induced by neuroleptics has
occurred. They may act in several ways including
disrupting the hypothalamic thermoregulator center,
alpha-adrenergic blockage and autonomic mechanisms."
(Hyperpyrexia is overheating of the body.) And of course
not being able to respond to emotional disturbance or
stress blocking the stress response making one incapable
of dealing with stress thus precipitating agitation.
This is destructive to the body in it's own right so
here is another way these neuroleptic drugs shorten life
span. Also appetite is controlled in part by
noradrenaline within the hypothalamus. Lowered
metabolism and the compulsion to consume more food due
to increased appetite from the blockage of noradrenaline
receptors within the hypothalamus equals weight gain. It
can not be avoided. See the book again called "Facts and
Comparisons" under "antipsychotic agents" under "Adverse
Reactions" under "Miscellaneous" which states that
neuroleptics will cause "increases in appetite and
weight".
Neuroleptics also have "anticholinergic blocking
effects". Acetylcholine is a neurotransmitter. The brain
produces an enzyme called acetylcholinesterase to break
down excess acetylcholine to prevent it from
accumulating to abnormal levels. This break down of
acetylcholine by this enzyme comprises the
anticholinergic system. Neuroleptic drugs have "anticholinergic
blocking effects" meaning they cause the accumulation of
acetylcholine to abnormal levels. Nerve gas's method of
causing death is by its anticholinergic blocking
activity. Also insecticide kills insects by this same
method causing an abnormal build up of acetylcholine in
the brain and nervous system of the insect.
See the book again called "Facts and Comparisons" under
"antipsychotic agents" at the bottom of the first page
in this section where it states that "In addition, the
drugs exert anticholinergic and alpha-adrenergic
blocking effects." Now see the book called "Brainscapes"
by Richard M. Restak, MD published by NY Herperion (c)
1995. On page 57 of this book it states; "As we have
discussed earlier, after a neurotransmitter and it's
receptor have reacted, the process must be brought to a
halt, which is accomplished either by the destruction of
the neurotransmitter and recycling of it's constituents,
or by a so-called reuptake system, whereby the
neurotransmitter is recaptured and stored once again
within the vesicle. In the case of acetylcholine, the
process involves a breakdown brought about by the enzyme
acetylcholinesterase, which cleaves the neurotransmitter
back to its original chemical building blocks. This
process can be interfered with by compounds responsible
for some of the worst horrors of twentieth-century
warfare. Nerve gases, such as the deadly Sarin released
into the subway system in Tokyo in March 1995, form
irreversible bonds with anticholinesterase [acetylcholinesterase],
thus inhibiting the enzymes' ability to break down
acetylcholine in the synapse." Then on page 121 of this
same book it states; "In the section on
neurotransmitters we mentioned another class of
neurotoxins, inhibitors of the enzyme
acetylcholinesterase, which breaks down the
neurotransmitter acetylcholine. Many pesticides are
designed to attack the nervous system of insects by
altering the breakdown of acetylcholine. Not
surprisingly, these agents also act on our brains and
nervous systems to produce symptoms like weakness,
difficulty in breathing, visual disturbances, and in
some cases explosive violence. With low rates of
exposure the problems are more subtle, a prevailing
sense of tension, disturbed sleep, restlessness, chronic
anxiety, and nervousness when standing in lines."
All of these symptoms can be observed in people on
neuroleptics. For instance "visual disturbances", see
the book again "Facts and Comparisons" under "Ocular" in
Adverse Reactions which states that neuroleptics will
cause "Glaucoma; photophobia; blurred vision; miosis;
mydriasis; ptosis; star-shaped lenticular opacities;
epithelial keratopathies; pigmentary retinopathy. Eye
lesions may regress after drug withdrawal." Also as
Richard Restak MD reports insecticide exposure will
cause "restlessness" and or "nervousness when standing
in lines." This has been given a name "Akathisia", see
the book again "Facts and Comparisons" under "Extrapyramidal"
under "akathisia" which states that neuroleptics cause
"a condition of constant motor restlessness [called
akathisia] and may include feelings of muscle quivering,
an inability to sit still and an urge to constantly move
about." Akathisia comes from the Greek word meaning
"can't sit still," and refers to significant physical
and mental agitation. Akathisia is to violence what a
match is to gasoline. Also he reports that insecticide
exposure will cause "difficulty breathing", again see
the book "Facts and Comparisons" in the same section
under "Respiratory" which states that neuroleptics cause
"Laryngospasm; bronchospasm; increased depth of
respiration; dyspnea." (Dyspnea is difficulty breathing
or shortness of breath.) Also he states that insecticide
exposure will cause "weakness", again see the book
"Facts and Comparisons" in the same section under "Other
CNS effects:" that neuroleptic drugs will cause
"Cerebral edema, headache, weakness, tremor, staggering
gait; twitching; tension; jitteriness; akinesia; ataxia;
fatigue; slurring [of speech]; abnormal cerebrospinal
fluid proteins;" etc. Also Richard Restak MD reports
that insecticide exposure will cause "disturbed sleep".
Again see the book "Facts and Comparisons" in the same
section under "Other CNS effects" where it states that
these drugs cause "insomnia" and under "Adverse
behavioral effects:" where it states that neuroleptic
drugs cause "nocturnal confusion" and "bizarre dreams".
Richard Restak MD also reports that insecticide exposure
will cause "a prevailing sense of tension", again see
the book "Facts and Comparisons" under "Other CNS
effects" where it states that neuroleptics cause
"tension". Also he reports that insecticide exposure
will cause "anxiety". Now see the book called "The
Essential Guide to Prescription Drugs Revised Edition"
(c) 1980 by James W. Long MD and published by Harper &
Row on page 344 under haloperadol (a neuroleptic drug)
that this drug can cause "anxiety". Also Richard Restak
MD reports in his book that insecticide exposure causes
"in some cases, explosive violence." Now see the book
"Facts and Comparisons" in the same section under
"Adverse behavioral effects:" where it states that
neuroleptics can cause "hyperactivity" and "agitation".
(See the commentary coming up concerning a Star Trek
Voyager episode entitled "The Chute" where the story
centered on this very effect.)
Of course nerve gas and insecticide are poisons and
neuroleptics have blatantly poisonous properties in that
part of their function is the same as that of nerve gas
and insecticide in causing an abnormal build up of
acetylcholine. In fact the very molecular base of one
class of neuroleptics called phenothiazines is used as
an insecticide! See the book again entitled "AHFS 96
Drug Information American Hospital Formulary Service" in
the second paragraph in the right column, which states
that "Phenothiazine [a class of neuroleptics] is still
used as an anthelmintic in veterinary medicine and as an
insecticide." The very insecticides that Richard Restak
MD is referring to in his book "Brainscapes" are being
given to those labeled mentally ill as a claimed
"beneficial medical treatment"! Here is further evidence
that neuroleptics shorten life span. Again remember that
all neuroleptics interfere with the breakdown of
acetylcholine so don't assume that because the drug
isn't a phenothiazine that it will not have these
effects. Other neuroleptics may even be worse at
interfering with the break down of acetylcholine then
phenothiazine.
Personally every time I have been on neuroleptics I have
been extremely agitated sometimes breaking things. One
time I even assaulted my father because of these drugs.
These drugs can cause extreme feelings of rage. This is
precipitated by the horrible torturous feelings that
these drugs induce. This well-known effect of excess
acetylcholine was even the theme for a Star Trek Voyager
episode called "The Chute" (this is an American science
fiction television show) in which two of the members of
the crew were abducted and placed aboard a space station
prison. In order to keep the prison population down the
prisoners where unknowingly exposed to a chemical that
caused the build up of acetylcholine by interfering with
its breakdown. This caused the prisoners to be violent
and enraged often killing each other. After the crew
members were rescued the "holographic" doctor on Voyager
revealed that it was interference with the breakdown of
acetylcholine that was causing the violence and that the
prison's operators must be using the chemical to keep
the prison’s population down. (Could this be why many
prisoners in the USA are forced or coerced into taking
neuroleptic drugs?) Based on this fact of neuroleptics,
not only is compulsory administration of neuroleptic
drugs by court order of the state a violation of the
right to life but also the pursuit of happiness because
these drugs take away one's sense of well being causing
"agitation". Ironically these drugs are often prescribed
under the pretense that they will prevent violence when
in reality they can actually promote it.
This leads to another problem with neuroleptic drugs and
how they take away sense of well being. Within the
limbic system of the brain is an electrochemical cascade
called the "reward system". This system is responsible
for giving a person their sense of well being.
Disruption of this electrochemical neuronal cascade
results in ones sense of well being, being supplanted
with negative emotions such as anxiety, depression,
anger and generally a very negative outlook on things.
The end result of the reward system's neuronal cascade
is stimulation of dopamine D2 receptors within the
nucleus accumbens and the hippocampus, which are located
within the limbic system of the brain.
See a problem yet? Remember neuroleptic drugs as you
have already learned block or destroy dopamine D2
receptors preventing their stimulation by the
neurotransmitter dopamine. Again see the book "Facts and
Comparisons" under "Antipsychotic Agents" where it
states on the first page of this section; "Antipsychotics
block postsynaptic dopamine receptors in the basal
ganglia, hypothalamus, limbic system, brain stem and
medulla. ...The phenothiazines appear to act at both D1
and D2 receptors, whereas haloperadol appears to act
primarily at D2 receptors."
Neuroleptics do indeed take away one's sense of well
being by utilizing more then one mechanism. This is very
self destructive to the body and will result in a
premature death if one doesn't commit suicide first.
Ironically these drugs are prescribed to people to
prevent suicide when in reality they actually promote
it. Perhaps the designers of these drugs want to give
the person that extra amount to push them over the edge
and actually do it. Personally two times I was on these
drugs for extended periods I attempted suicide because
of them.
So here is further proof that the compulsory
administration of neuroleptic drugs because of court
order of the state is not only a violation of one's
right to life but also one's right to the pursuit of
happiness. This is so since the administration of these
drugs take away sense of well being making it very
difficult to feel happiness.
Read the article entitled "Reward Deficiency Syndrome"
as published in "American Scientist" magazine
March-April 1996 for a detailed and in depth discussion
of this brain function called the "reward cascade".
Click Here for Article Online. This magazine article
states on page 135 under figure 4, "If the activity of
the dopamine D2 receptor is deficient, the activity of
neurons in the nucleus accumbens and the hippocampus is
decreased, and the individual experiences unpleasant
emotions or cravings for substances that can provide
temporary relief by releasing dopamine." On page 132 of
this article it states that disruption of the
stimulation of D2 receptors as part of the "reward
cascade" will "supplant an individual's feeling of well
being with anxiety, anger or a craving for a substance
that can alleviate the negative emotions." In this
magazine article it explains that "reward deficiency
syndrome" is the cause of behavioral disorders such as
attention deficit disorder (with and without
hyperactivity), personality disorder, conduct disorder,
antisocial personality, aggressive behavior, autism
(autism is the abnormal introversion and egocentricity,
acceptance of fantasy rather then reality).
After reading this article I came to understand the
source of many of my own problems and why neuroleptics
were exasperating them. And also why I had an insatiable
craving for alcohol whenever I was on neuroleptics that
even persisted for a long time after they were
discontinued since the damage caused by neuroleptics to
the dopaminergic system is long term. Or I would consume
caffeinated cola flavored soda - craving the caffeine -
until my stomach would become bloated and I would throw
up. Again see the book "Facts and Comparisons" under
"antipsychotic agents" under "Adverse Reactions" under
"Adverse behavioral effects:" where it states that
neuroleptics will cause "...restlessness; hyperactivity;
agitation; ... depression; ... paranoid reactions." And
again see the book "The Essential Guide to Prescription
Drugs Revised Edition" (c) 1980 where it states that
haloperadol (a neuroleptic) causes "anxiety". Also as
reported in this report, since these neuroleptic drugs
cause adrenergic blocking and inhibition of the adrenal
hormone cortisol, these drugs reduce capacity to deal
with stress both emotionally and physically. So here is
irrefutable proof that these drugs not only take away
sense of well being but also shorten life span.
The state does NOT have the right under any
circumstances to order the compulsory administration of
a substance, which shortens life span and takes away
one's sense of well being, a substance with poisonous
properties like that of nerve gas and insecticide! The
constitution of the United States of America guarantees
certain inalienable rights, namely the right to liberty
(making one’s own decision regarding personal matters),
the right to life, and the right to the pursuit of
happiness. When the state orders the compulsory
administration of neuroleptics EVERY ONE of these
inalienable rights is being violated.
Mental health officials will first do their very best to
intimidate and coerce a "patient" or "client" into
"voluntarily" taking neuroleptics before they will
attempt to get a court order that will allow them to
involuntarily drug someone. They will use mind games or
psychology on a person coming back to them repeatedly
telling them such things as "Don’t you want to get
better?". Many times when doing this they will invade
your personal space. Perhaps in an attempt to provoke
you into an act of violence that they will then use as
"evidence" that you "need" these drugs. Many times they
will tell the person that they will not qualify for
social security assistance if they do not take the drugs
or that they will remain locked up in an institution if
they do not take the drugs. Any call to the Social
Security Administration will reveal that it is not
required that someone takes neuroleptics in order to
receive or continue to receive social security. Perhaps
what the psychiatrists are really saying is that they
will not support a disability claim if the person
doesn't take the drugs. In such case this is blackmail.
Don't be tricked by a psychiatrist's attempts to get you
to try a new drug that is supposed to be "safer" then
the older ones. All neuroleptics block or destroy
dopamine receptors even the newer ones. Therefore the
newer so called, "safer" neuroleptics will also cause
what has been described in this report by the very fact
that they also block or destroy dopamine receptors.
Risperidone (Brand name Risperdal) and Zyprexa (Brand
name is Olanzapine) affect higher reasoning centers and
make it almost impossible to form complex thoughts. This
is due to its effects on the neurotransmitter Serotonin.
If I were on either of these two drugs it would have
been impossible for me to do the research and write this
report. I speak form experience because I have
temporarily taken both Zyprexa and Risperidone. On just
two pills of Zyprexa I could not even access my memories
of research on these drugs. On Risperidone I had slurred
speech, word substitutions, difficulty forming complex
thoughts pages of text appeared as blank piece of paper
when previously I could rapidly digest the material.
Resist psychiatric drugging. Use the evidence in this
report to argue in probate court that the involuntary
administration of these drugs is a violation of all your
fundamental constitutional rights, most importantly the
right to life and the pursuit of happiness. They will
not be able to get around these two rights. They take
away liberty from the "mentally ill" under the guise
that they are supposedly not competent to make their own
decisions regarding their own medical care, but they
will not be able to get around these other two rights.
If possible get your own attorney rather then allowing
the court to appoint one for you because it is my
experience that these court appointed attorneys are not
really motivated to defend you and may even be secretly
serving the interest of the mental health officials and
the state. If you do not get a favorable decision in the
probate court then insist on an appeal and remember to
attempt to maintain your determination to follow through
with the appeal realizing that these drugs take away
your will power and ability to resist domination. Use
this knowledge to fight this effect of the drugs. If
necessary appeal these constitutional issues all the way
to the Supreme Court. Only when we as a people fight and
defend our rights will changes be made, not only for our
personal protection but also for that of our loved ones
and our children and our children's children. It is not
just the "mentally ill" that are affected by this.
Routinely these drugs are administered to the retarded
(including children) and the elderly in nursing homes as
well as Alzheimer's patients, people with head injuries
or brain damage etc.
It is very clear that the motivation behind the
administration of antipsychotics, antipsychotic drugs,
neuroleptics, or neuroleptic drugs to the "mentally ill"
and others is eugenic in nature. For those who do not
know what eugenics is, it is idea that the human race
can be improved by preventing "inferior stock" from
reproducing and by inducing an early death. The eugenic
idea got its start with psychiatrists in the USA. Later
Hitler shocked the world with the holocaust of millions
of people, basing his program on eugenics practices that
were already being carried out in the USA. But the first
to be killed in Nazi Germany was the "mentally ill".
Before Hitler did the things he did, the forced
sterilization of the "mentally ill" in the USA was
common practice. But as you are already probably
starting to see after reading the evidence centered on
neuroleptic drugs, the same eugenics program is being
covertly carried out under the guise of a "beneficial
medical treatment". In the 1960s, the Eugenics Society
of England adopted what they called "Crypto-eugenics",
stating in their official reports that they would do
eugenics through means and instruments not labeled as
eugenics. Abortion and the push of birth control is one
of these and as it should be clear from reading this
report on the true nature of neuroleptic drugs that it
is a eugenics conspiracy also.
After World War II so many psychiatrists immigrated to
the USA that some time after the war, one third of all
psychiatrists in the USA were former Nazi's.
The founder or "father"
of psychiatry in the United States was a Freemason named
Benjamin Rush. He was one of the signers of the United
States constitution. Psychiatry was founded as a means
to take care of critics of Freemasonry or the Masonic
Lodge. Also to take care of people who are revealing
"National Security Secrets" and also to take care of
people who "step on the big guys toes" by challenging
their interests or causing them to loose money. Also to
take care of "whistle blowers" and to take care of
people who are attempting to change Satan's demon
inspired "status quo". "Status Quo" means the generally
accepted viewpoint which is often wrong. To take care of
true Christians who are discovering truths from the Holy
Scriptures and revealing them to the people. The Mason
or Freemason named Benjamin Rush invented a restraint
chair with straps on it that he named "the tranquilizer"
which is where this word originated. He also invented
the straight jacket. The electric chair today is a
modification of Benjamin Rushes invention. The Masonic
Lodge is evil to the core. The Catholic Church is no
better because they also run psychiatric wards and
coperate with the government to silence people by
"taking care of them". The Catholic Church has a lot of
stock in the pharmacutical industry which includes
psychiatric drugs. Psychiatry has become for the
Catholic Church their new means of inquisition and their
psychiatric wards in their hospitals are their
inquisition halls were people are tortured chemically.
The following excerpt is taken from the public service
publication entitled "Psychiatry Destroying Religion in
the Name of Salvation" by the Citizens Commission on
Human Rights under the chapter entitled "The Devil's
Doctors - From the Nazi Holocaust to 'Assisted Suicide'"
"While psychiatry has tried to expunge any connection
between itself and the racial genocide of the Nazi
Holocaust, the hard facts is that psychiatry spawned
"eugenics" almost three decades before the Nazi's took
power in 1933. It was psychiatry that turned the Nazis
into the mass murders, not vice versa. And it was their
ideology which fired Hitler's mania to eradicate
religion."
"As early as 1895, German psychiatrist Alfred Ploetz
wrote: "Should it turn out that in spite of it the
new-born is a weakly and ill-bread child, then a gentle
death will be provided for him by the medical board,
which decides over the citizenship papers of the
society, let's say through a small dose of morphine....
[The parents] will not give themselves over to
rebellious feelings for long but will try it fresh and
happily a second time, if they are permitted to do so
and have a certificate granting them the right to the
procedure."" [Dr. Thomas Roder and Volker Kubillus,
Manner hinter Hitler (Malters: p Pi-Verlag fur Politik
und Gesellschaft, 1994) pp. 65-66]
"Within ten years, Ploetz founded the German Society for
Racial Hygiene, joining with another psychiatrist, Ernst
Rudin who would later turn sterilization operations into
one of the Nazi's most prolific death machines.
Declaring racial hygiene a "spiritual movement," Rudin
and his associates worked to disseminate their ideas and
principles to the public. Despite "quietly and gradually
winning over the hearts and minds of our best Germans,"
they could not gain support at upper government levels.
Eventually they found a willing collaborator in Adolf
Hitler. "Only through [the Fuhrer] did our dream of over
thirty years, that of applying racial hygiene to
society, become a reality,"" Rudin said. [Dr. Thomas
Ruder, Volker Kubillus and Anthony Burwell, Psychiatrist
the Men Behind Hitler (Los Angeles: Freedom Publishing,
1995) p. 94.]
"Hitler was also influenced by two psychiatric books:
The Release of the Destruction of Life Devoid of Value
(1920) by Hoche and Binding and The Principles of Human
Heredity and Racial Hygiene (1921) by Bauer, Fischer and
Lentz. Lentz wrote, "I have heard that Hitler had read
the second edition of Bauer-Fischer-Lentz during his
incarceration in Landsberg. Some parts of it are
mirrored in Hitler's phrases. In any case, with great
mental energy, he had made the basic ideas of racial
hygiene and their importance his own, while most of the
academic authorities still look upon these issues rather
unappreciatively." [Roder, Kubillus, and Burwell, op.
Cit., p. 37.]
"According to Hoche and Binding:
1. The suffering of a sick or wounded person who is
about to die can be shortened through the use of a
medical drug.
2. The acceleration of the death process is not an act
of murder but "in truth a pure act of healing."
3. A doctor should be allowed to employ euthanasia on
any unconscious person without legal consequences.
4. There are people who are worthless to society.
Primary among these are the inmates of the "idiot
institutions," who are "not only worthless, but of
absolutely negative value."
5. The incurably dumb who can neither agree to survive
or to be killed should be killed. "Their death will not
be missed in the least except maybe in the hearts of
their mother or guardian.... When we become more
advanced, we will probably be saving those poor humans
from themselves."" [Ibid., p.41.]
"With Hitler providing the public face and vehicle for
implementation, the next few years saw an avalanche of
legislation which legitimized psychiatry's demonic
plans. On July 4, 1933, the Sterilization Act was
enacted, clearing the path for wholesale euthanasia.
July 4, 1933 saw the Law for the Prevention of
Genetically Diseased Children passed."
"By 1936, the first systematic transfers of the mentally
ill from various institutions to the concentration camps
began. In 1937, criminals and repeat offenders were
relocated to the camps, followed by "vagrants,
alcoholics, work dodgers, welfare recipients and even
already-sterilized, feeble minded women." That same
year, the Third Reich embarked upon a cleansing of the
churches and charitable establishments. People were
relocated first into state institutions, then ultimately
to the death camps."
"The number of sterilizations performed in Germany
between 1934 and 1945 is estimated to be as high as
350,000. And while German psychiatric hospitals held
300,000 to 320,000 patients in 1939, only 40,000 were
alive in 1946. The rest had met their deaths at the
hands of psychiatry. [Ibid., p. 48; Fredric Wertham,
M.D., A Sign For Cain: An Exploration of Human Violence
(London: Robert Hale Limited, 1966), p. 158.] In 1941,
the Hadamar psychiatric institution "celebrated the
cremation of the ten thousandth mental patient in a
special ceremony. Psychiatrists, nurses, attendants, and
secretaries all participated. Everybody received a
bottle of beer for the occasion," author Fredric Wertham,
M.D. reported." [Wertham, A Sign For Cain..., op. Cit.,
p. 157.]
End of excerpt from the public service publication
entitled "Psychiatry Destroying Religion in the Name of
Salvation" by the Citizens Commission on Human Rights
under the chapter entitled "The Devil's Doctors - From
the Nazi Holocaust to 'Assisted Suicide.'"
The Citizens Commission on Human Rights is a non-profit
anti-psychiatry organization that works hard to expose
psychiatry for what it is. They offer many public
service publications free of charge. But I recommend a
small donation so they can keep up their very important
work. Their address is: Citizens Commission on Human
Rights International, 6362 Hollywood Boulevard, Suite B,
Los Angeles, CA 90028. Their telephone numbers are
1-800-869-2247 or 213-467-4242. Their web-address is:
http://www.cchr.org
Although this organization is run by the Church of
Scientology their anti-psychiatry public service
literature doesn't teach Scientology. My quote from them
above should not be misconstrued as my endorsement of
Scientology as I am not a Scientologist nor am I
familiar with what they teach.
Also another organization to get in contact with is
Support Coalition International a group calling
themselves "psychiatric survivors" at the web address
http://www.mindfreedom.org See this web-site
on psychiatric drugs:
http://www.antipsychiatry.org/drugs.htm .
Also go here.
http://www.wildestcolts.com Also see
http://home.earthlink.net/~bazillion/psych_news.html .
Discusses electroconvulsive "therapy". This Internet
resource called Psychiatric Tattler contains information
worth reading.
http://www.ect.org/tattler and a links page
to other fine sites here:
http://www.ect.org/tattler/links.html. Also
see these anti-psychiatry links on this web-site:
http://www.psychnet-uk.com/psychiatry/antipsychiatry.htm.
Also see the links at:
http://www.mentalhealthfacts.com/mhresources.html
and
http://www.schizoaffective.org and
http://www.mentalhealthfacts.com
It is very clear that psychiatry kills. The term
psychiatric abuse is an understatement because the whole
purpose of psychiatry is to abuse. The only legitimate
form of psychiatry is that of the talking psychiatrist
who doesn't use mind altering chemicals. This is the
type of psychiatrist Dr. Peter R. Breggin, M.D. author
of Toxic Psychiatry is. God bless Dr. Peter Breggin MD
for his work. If you haven't already, read his book
entitled Toxic Psychiatry for a lot of good info. This
is Dr. Peter Breggin’s web-site address.
http://www.breggin.com Psychiatry kills.
The thesis above concerning the biological ramifications
of the administration of these drugs is new and is not
contained in Dr. Peter Breggin's book but his book does
contain a great deal of useful information not contained
in this report.
Resist psychiatry’s forced drugging. Use the evidence in
this report to argue in probate court that the
involuntary administration of these drugs is a violation
of all your fundamental constitutional rights, most
importantly the right to life and the pursuit of
happiness. They will not be able to get around these two
rights. They take away liberty from the "mentally ill"
under the guise that they are supposedly not competent
to make their own decisions regarding their own medical
care, but they will not be able to get around these
other two rights. If possible get your own attorney
rather then allowing the court to appoint one for you
because it is my experience that these court appointed
attorneys are not really motivated to defend you and may
even be secretly serving the interest of the other side.
If you do not get a favorable decision in the probate
court then insist on an appeal and remember to attempt
to maintain your determination to follow through with
the appeal realizing that these drugs take away your
will power and ability to resist domination. Use this
knowledge to fight this effect of the drugs. If
necessary appeal these constitutional issues all the way
to the Supreme Court. Only when we as a people fight and
defend our rights will changes be made, not only for our
personal protection but also for that of our loved ones
and our children and our children's children.
You can beat psychiatric drugging. If you resist they
will more then likely back down. It costs a lot of money
to house someone in an institution and the county you
live in must pay for it. In Ohio medicaid pays $480 a
day and the state picks up the rest for a total cost of
$800 to $1000 a day. Nine times out of ten they will be
unwilling to do this, so stick by your guns and resist
psychiatric drugging. Don’t show up to get the
injections and make them send a police officer after you
to bring you into the inpatient unit. All this
resistance will pay off because they will more then
likely give up. They will lock you up in isolation for a
few days hoping they will be able to brake your will
power. If you continue to resist and maintain your
resolve they will give up. Believe me, I speak from
experience. If they do send you to an institution then 9
times out of 10 this will be a scare tactic and will
only be temporary so maintain your resolve to resist. Be
sure to never sign anything they want you to sign no
matter what. If they apply a lot of pressure to get you
to sign something just say that you want your lawyer to
read it first. They keep people up to 90 days by court
order in an institution so stick by your guns on the
rare chance that this happens to you. Use the evidence
in this report to fight for your rights in court and
appeal if necessary all the way to the USA Supreme
Court. Also remember to not fight back in any physical
way even under extreme provocation because they will
take this as proof that they are justified in any action
they take against you and will be detrimental in any
defense you may offer to the court. Use passive
resistance. Make them hold you down to give you
injections but do not try to harm the provocateurs.
You can also protect yourself by getting a living will,
which states your wishes should you ever become
"incompetent". If you are currently involved in the
mental health system it will become necessary to have
your lawyer accompany you to see your psychiatrist,
psychologist, counselor, therapist etc. to get them to
sign an affidavit concerning your current competency to
enter into a living will. Don’t tell the mental health
official that you want this affidavit for the purpose of
avoiding involuntary drugging or you will most likely
not get their cooperation. Tell them that you need a
living will so you will not be kept on life support
should you become brain dead etc. so they will be likely
to cooperate. You will need this affidavit as a
technicality so it can not be claimed at a later date
that because you were involved in the mental health
system that at the time you entered into the living will
you were not competent to do so.
It is not just the "mentally ill" that are affected by
this. Routinely these drugs are administered to the
retarded (including children) and the elderly in nursing
homes as well as Alzheimer's patients, people with head
injuries or brain damage etc... These drugs are even
prescribed to teenagers and young children who simply
have a hot temper, which ironically the drugs make
worse.
To biochemist, biologist, nutritionist, physicians, etc.
If you have additional information and or references to
add to the material presented below then please contact
me at one of the E-mail addresses provided or contact
the mailing address provided. It would be greatly
appreciated. Also if any psychiatrists, psychologists,
FDA or pharmaceutical officials or employees etc. that
want to turn whistle blower by adding more information
to what is provided in this report or by providing proof
that a conspiracy is involved concerning these drugs
then please E-mail one of the E-mail addresses or the
mailing address provided below. Words can not express
how much it would be appreciated. Your identity will be
held in the strictest of confidence if you so desire.
IMPORTANT! Save this document while you have it because
it is actively being censored. Please aggressively
disseminate this information. E-mail, fax or mail this
report to senators, congressmen and others involved in
the government and politics. Also give a copy to your
family doctor because many doctors are ignorant of the
facts or have never considered the ramifications.
E-mail, fax or mail this report to probate judges,
appeal judges, and others involved in the government and
politics. E-mail, fax or mail it to lawyers, civil and
human rights organizations. E-mail, fax or mail this
report to the media. Give a copy to local law
enforcement officials. Give copies to neighbors, family,
friends, people at work, and mental health patients and
their family. Post this report on wwwboards and the news
groups all over the Internet, not only in the USA but
also in other countries. Please post it to the web and
get others to link to it. Pass it along by direct E-mail
to others on the Internet. It is very important that
this information be disseminated to everyone. You can
only protect yourself, friends, family and other loved
ones through knowledge and knowledge is power. PLEASE
disseminate this information aggressively so changes can
be made in current law in many states. And please keep
this entire report complete and intact when doing so.
Go to Part 2
