Muscle wasting is produced by autoimmune disorders and mitochondrial 
disorders. Both conditions are marked by the reduced production of 
ATP energy, and indeed a few of the autoimmunes are also part of the 
mitochondrial dosirders list. ATP production can be impaired by toxin 

load including drugs, statins specially.

> Muscle wasting?  How in the world would that happen? 
> I think I'll forward this on to my silver list and see what they 
have to
> say.  I'll forward back any comments.      MA
> 

Here's an article I wrote for the newspaper a couple of weeks ago:

_________________________________________________

Autoimmune and mitochondrial disorders linked to energy production

Body Electric
Duncan Crow

  Most of the autoimmune disorders such as diabetes, myasthenia 
gravis, polymyalgia, fibromyalgia, lupus, Crohn’s disease, arthritis, 
myositis, scleroderma, multiple sclerosis, muscular dystrophy and 
several others are characterized by low energy. The energy produced 
in the mitochondria of the cells, called ATP, is depleted while 
dealing with the toxins absorbed through exposure to a wide variety 
of environmental contaminants. Toxin load including infection, 
besides being a physical energy drain can be a trigger for an 
autoimmune disorder, and ATP deficiency increases the pain and other 
disabling symptoms. 

  In the body, ATP: moves substances into and out of the cell; moves 
muscles; opens and closes channels; produces signals that stimulate 
hormones; detoxifies the body; teams up with sulfate to become a 
sulfate donor for renewal and repair. Without it, cellular function 
is impaired or stopped and the cell dies; this is what produces the 
wasting. The body needs ATP to repair and renew the same parts the 
deteriorate and cause pain in autoimmune disorders: chondroitin 
sulfate (cartilage, bone, skin, cornea, arteries); dermatan sulfate 
(skin, blood vessels, heart); heparan sulfate (lungs, arteries, 
basement membranes); heparin (lung, liver, skin, mast cell granules); 
keratan sulfate (cartilage, cornea, vertebral discs).

   About 88 lbs. of ATP per day are required for a resting human. 
Illness robs our bodies of ATP, and the sicker one is, the more 
energy one needs. Mitochondrial disorders (that involve the reduced 
production of ATP) are also serious and because there hasn't even 
been a treatment for these disorders the prognosis is always poor, 
ranging from progressive weakness to death. Using just one example, 
scleroderma is characterized by excessive deposits of collagen. 
Progressive systemic scleroderma, the serious type of the disease, 
can be fatal. In an article (published in Scleroderma Voice, 2003 #3) 
titled Fatigue and Weakness in Scleroderma Patients by Jane H. Park, 
Ph.D., from Vanderbilt University School of Medicine, Dr. Park 
reports, "Our studies showed that the thigh muscles of scleroderma 
patients at rest had an average reduction of 35% in concentrations of 
both ATP (adenosine triphosphate) and PCr (phosphocreatine) compared 
to normal muscles. These decreases were present in patients with both 
diffuse or limited scleroderma."

  Mitochondrial and autoimmune disorders are now sometimes treated 
with supplements that increase ATP recycling. These common 
supplements include coenzyme Q10, carnitine, vitamins C and K, and 
various components of the vitamin B complex, especially riboflavin. 
Lecithin, which contains the needed phosphate for ATP and PCr 
production, should be an asset. Ginseng and Rhea extract take the 
more direct approach; they actually contain ATP. Magnesium is also an 
important supplement because it is required by all the muscle enzymes 
involved in energy production. Magnesium and ATP always tightly bind 
together, and ATP is only active in the presence of proper 
concentrations of magnesium. Magnesium levels are low in the muscles 
of patients with either diffuse or localized disease. During the 
stress of exercise,  magnesium deficit in the muscle is actually 
increased, and this is probably why wasting disorders are usually 
made worse rather than better when a person exercises.

  Salvatore DiMauro and Eric Schon, both of the Neurology Department 
at New York's Columbia University, reported in the January 1998 issue 
of The Neuroscientist, that even a little help can mean a lot in 
mitochondrial disorders, says DiMauro, a published neurologist. 
"Patients can be sick when they have 85 percent mutant mitochondria 
in a given tissue, but if they have 80 percent, they may be much, 
much better and may not show symptoms. So, if you can change the 
proportions even slightly, you may do the patient a lot of good." But 
ATP increase is useful not only to people with 'mutant mitchondria'. 
In an open label clinical study, people with allergies and autoimmune 
disorders who were given a commercial Rhea extract called ATP Boost 
in 1998 reported the following results of symptom remission: 
allergies 73 percent; pain, 77 percent; range of motion improvement, 
76 percent. And 73 percent noted an increased energy level.

  If a tiny ATP boost from an external source can produce these 
results, a supplement that helps the mitochondria to function better 
may do much more than increase energy, it may help people with 
mitochondrial disorders, autoimmune diseases, and cancer. The work of 
Dr. William Koch and others who investigated this avenue showed that 
when ATP is elevated the cells become more aerobic and cancer often 
goes away. There's a summary article on the approach at 
http://tinyurl.com/5cdkv. Researcher Michel Grise really found 
something big when he discovered Prosoteine (TM), a protein molecule 
that improves mitochondrial health, an option that was previously 
unavailable. 

  Prosoteine's launch promo is 1/3 off wholesale; if you buy 12 
bottles you get them for the price of 9. See corporate here: 
http://eyicom.com/?key=comox  my son's referred page :)

_________________________________________________

Duncan Crow




Duncan Crow (copyright waived)
http://profiles.yahoo.com/duncancrow/

---    live and help live...     --- 


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