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The Coliseum
Rome Italy Photo by: Marty L. Hinz, MD |
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Contact us or find a caregiver using this
approach. |
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Depression Cause
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Written by:
Marty L. Hinz, MD |
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President
Clinical
Research |
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NeuroResearch
Clinics, Inc |
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Cape Coral,
Florida USA
Research
Office |
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POSTED by J1237 Jan 31, 2009 06:59PM: I have suffered with severe depression and anxiety for about 10 years. I was very, extremely skeptical about the NeuroResearch formulas in treatment after having been on a myriad of antidepressant SSRI's. I thought it was just a money making scheme and I was scared. Let me just say that I'm glad I did my research and I'm glad I tried it because it has made a WORLD OF DIFFERENCE. |
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The bundle damage theory states,
“Neurotransmitter dysfunction
disease symptoms, such as
symptoms of depression, develop
when the electrical flow through
the neuron bundles that regulate
function is compromised by
damage to the individual neurons
or the neuron components
composing the neuron bundle
which conducts electricity to
regulate or control function.
In order to optimally restore
neuron bundle regulatory
function, synaptic
neurotransmitter levels of the
remaining viable neurons must be
increased to levels higher than
is normally found in the system,
which restores adequate
electrical outflow resulting in
relief of symptoms and optimal
regulatory function.” Bundles of
neurons convey electricity that
regulates and/or controls
numerous functions in the body.
If enough of the individual
neurons of a bundle become
damaged the flow of electricity
through the bundle is |
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diminished
leading to the function being controlled
and/or regulated not controlling
properly causing symptoms of disease
develop. Technically synaptic
neurotransmitter levels prior to
treatment in patients with disease due
to neuron bundle damage are in the
normal range for the population.
The
Bundle Damage Theory and The Monoamine
Theory are not mutually exclusive of
each other. Instead these two theories
can be viewed a complimentary in
treatment. They address different mechanisms of
action leading to neurotransmitter
dysfunction and compromised electrical
flow out of the post-synaptic neuron.
The Monoamine Theory addresses low
levels of neurotransmitters in the
synapse as the etiology of impedance of
electrical flow needed to regulate
function and keep disease symptoms under
control. Whereas, The Bundle Damage
Theory addresses damage to the neuron
structures (primarily post-synaptic)
which impede the flow of electricity
needed to regulate function and keep
disease symptoms under control. With the
monoamine theory and the bundle damage
theory the flow of electrical energy
needed to regulate function is not
adequate. Differentiation of the two
theories lies in the etiology of the
dysfunction. Under monoamine theory
returning neurotransmitter levels to
normal will relieve disease symptoms.
Under the bundle damage theory synaptic
neurotransmitter levels need to be
established that are higher than the
reference range of the population.
It is
the mechanical damage to the
post-synaptic neurons as suggested by
the bundle damage theory and not the
synaptic neurotransmitter levels that is
the primary cause of monoamine disease.
This subset is composed of about 88% of
adult patients and 100% of the elderly
patients with depressive symptoms – the
nonresponders from the depression
studies above.
Neurons are intended to function for
life. Loss of a neuron to apoptosis is
permanent, although in limited areas of
the brain neurons may regenerate to
replace the neurons that have undergone
apoptosis.58 As neurons go
into apoptosis in the post-synaptic
neuron becomes completely non-functional
they tend to go through an agonizing
death where the electrical brilliance
with which they function slowly fades
until the electrical flow through the
neuron regulating function decreases and
stops over time.
The
only way to increase neurotransmitter
levels in the central nervous system is
to administer amino acid precursors
which cross the blood brain barrier and
are then synthesized into
neurotransmitters. Increasing
neurotransmitter levels in the synapse
is analogous to increasing the voltage
in an electrical wire, where by turning
up the voltage you get more electricity
out the other end of the wire. Turning
up the voltage increases the electrical
potential (pressure) of the electrons
entering a partially damaged wiring
connection leading to more electrons
(electricity) flowing out the other end.
In the case of neurotransmitter disease
where the neurons of the neuron bundles
are damaged to the point that the
electricity flowing out of the neuron
bundles is diminished disease develops.
Increasing neurotransmitter levels will
effectively increase voltage in the
remaining viable neurons in the bundle
causing electrical flow out of the
damaged neuron bundles to increase to
the point that normal regulation and/or
control is once again observed. In this
state, from a clinical standpoint, the
symptoms of disease are under control.
Its no secret, NeuroResearch Clinics uses the nutrients
5-HTP, tyrosine, levodopa, and
cysteine for treatment of medical
patients in order to get these
results. Proper
use of these simple ingredients in
medical treatment is not simple.
From time to time a patient will
say, "Why do I want to take that, I
can go to a health food store and
buy it?" People off the street
buying in a health food store is
like going to an art store and
buying a bunch of oil paints then
going home and expecting to paint
like a mater artist even though
there was no previous painting
experience. These nutrients have
tremendous potential due to their
chemical properties. This potential
is only fully realized in the hands
of the trained professional using
neurotransmitter testing. Treatment
is not just giving a nutrient pill, it is the whole medical management approach doctors are trained in to insure that that treatment is on track in order to get symptoms under control.
The Peer Reviewed Research
of NeuroResearch Clinics
The neurotransmitter treatment research findings of NeuroResearch Clinics
have not been ignored. The University of
Minnesota Medical School is writing a series of
papers on the neurotransmitter testing research of NeuroResearch Clinics. The first of a series of papers by University of Minnesota Medical School based on the neurotransmitter testing research of NeuroResearch was published in "NeuroPsychiatric Disease and Treatment" May 1, 2009. Ingrid
Kohlstadt, MD of Johns Hopkins in her new
medical text book released February 7, 2009
included a chapter on depression written by
Marty L. Hinz, MD President Clinical
Research NeuroResearch Clinics outlining in
depth the proper use of amino acids and
neurotransmitter testing in treatment of
depression.
Depression Cause
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