Mercury Amalgams 
A book on how to cure mercury poisoning by Andrew Hall Cutler, PhD, PE
Possible Health Effects and Dental Amalgam-A scientific review from an expert group to the Swedish National Board of Health and Welfare.

by University of Calgary, Faculty of Medicine, Dept. of Physiology & Biophysics. Video that shows neuron degeneration upon exposure to trace amounts of mercury.
Abstract supporting above video.
Transcript:
How Mercury Causes Brain Neuron Degeneration.
F. L. Lorscheider, C. C-W. Leong, N. I. Syed.
University of Calgary, Faculty of Medicine, Dept. of Physiology & Biophysics.
Mercury has long been known to be a potent neurotoxic substance whether
it is inhaled or consumed in the diet as a food contaminant. Over the
past 15 years medical research laboratories have established that
dental amalgam tooth fillings are a major contributor to mercury body
burden.
In 1997, a team of research scientists demonstrated
that mercury vapour inhalation by animals produced a molecular lesion
in brain protein metabolism which was similar to a lesion seen in 80%
of Alzheimer diseased brains.
Recently completed experiments
by scientists at the University of Calgary's Faculty of Medicine now
reveal, with direct visual evidence from brain neuron tissue cultures,
how mercury ions actually alter the cell membrane structure of
developing neurons.
To better understand mercury's effect on the brain, let us first illustrate what brain neurons look like and how they grow.
In this animation, we see three brain neurons growing in a tissue
culture, each with a central cell body and numerous neurite processes.
At the end of each neurite is a growth cone where structural proteins
are assembled to form the cell membrane. Two principal proteins
involved in growth cone function are actin, which is responsible for
the pulsating motions seen here, and tubulin, a major structural
component of the neurite membrane.
During normal cell
growth, tubulin molecules link together, end to end, to form
micro-tubules which surround neurofibrils, another structural component
of the neuronal axon.
Shown here is the neurite of a live
neuron isolated from snail brain tissue displaying linear growth due to
growth cone activity. It is important to note that growth cones in all
animal species, ranging from snails to humans, have identical
structural and behavioural characteristics and use proteins of
virtually identical composition.
In this experiment, neurons
also isolated from snail brain tissue were grown in culture for several
days after which very low concentrations of mercury were added to the
culture medium for 20 minutes. Over the next 30 minutes, the neurite
membrane underwent rapid degeneration leaving behind a denuded
neurofibril seen here.
In contrast, other heavy metals added
to this same concentration such as aluminum, lead, cadmium and
manganese did not produce this effect.
To understand how
mercury causes this degeneration, let us return to our illustration. As
mentioned before, tubulin proteins linked together during normal cell
growth form the microtubules which support the neurite's structure.
When mercury ions are introduced into the culture medium, they
infiltrate the cell and bind themselves to newly synthesized tubulin
molecules.
More specifically, the mercury ions attach
themselves to the binding site reserved for guanosine triphosphate or
GTP, and a beta-subunit of the affected tubulin molecules. Since all?
GTP normally allows????? the energy which allows tubulin molecules to
attach to one another, mercury ions bound to these sites prevent
tubulin proteins from linking together. Consequently, the neurite's
microtubules begin to disassemble into free tubule molecules leaving
the neurite stripped of its supporting structure.
Ultimately, both the developing neurite and it's growth cone collapse
and some denuded neurofibrils from aggregates are tangled, as depicted
here.
Shown here is a neurite growth cone stained
specifically for tubulin and actin before and after mercury exposure.
Note that the mercury has caused disintegration of tubulin's
microtubule structure.
These new findings reveal important
visual evidence as to how mercury causes neuro-degeneration. More
importantly, the study provides the first direct evidence that
low-level mercury exposure is indeed a precipitating factor that can
initiate this neuro-degenerative process within the brain.
The IAOMT is a membership organization for dental, medical and research professionals who seek to promote mercury-free dentistry, and raise the standards of scientific biocompatibility in dental practice.
Smoking Teeth Video and presentation.
Search for dentists in your area:
The diagnostic arena now occupied by autoimmune disorders provides us with terms that could be best described as "alphabet soup." Such problems include RA (rheumatoid arthritis), HT (Hashimoto's thyroiditis), HAD (human adjuvant disease), MS (multiple sclerosis), ALS (amyotrophic lateral sclerosis or, more commonly, Lou Gehrig's disease) and MCTD (mixed connective tissue disease).Should we now add MT (mercury toxicity)?
Accurate modern diagnostics using the Melisa Test detects undesirable health effects from dental metals and metal allergies.

Article by Dr. Zoltan P. Rona MD MSc Vancouver, BC, Canada

Dr. Riina Bray and Dr. Kathleen Kerr. The Environmental Health Committee produced this pamphlet as a tool for patients seeking more information regarding mercury exposure.
Could high Mercury levels be making you sick. There many sources of Mercury Poisoning on our planet. Links to sites covering different sources of mercury poisoning including amalgam fillings.
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