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Greatest Vitamins World

Sick and Tired of Aching Joints?

by Ellen DuBois on 01/05/12

Undenatured Type II Collagen - Chicken Soup for Your Joints

by Karen Lee Richards*
Source:
ProHealth.com

Undenatured chicken collagen, the primary ingredient in OsteoTec™ UC·II®, has been shown in studies and trials to help the body repair and rebuild joint cartilage - reducing joint pain, increasing joint mobility and flexibility, and promoting long-term joint health.

Grandmothers around the world have been treating colds with chicken soup for generations; then a few years ago scientists confirmed that several ingredients in chicken soup do, indeed, affect the immune system. What grandma didn't realize, though, is that one part of the chicken in particular may also help ameliorate the joint pain of arthritis.

Taken from the chicken's sternum cartilage, UC·II is an innovative, patented form of undenatured type II collagen that works with the immune system to reduce inflammation and restore cartilage (unlike glucosamine & chondroitin, which are materials involved in the structure of healthy cartilage). Extensive research and clinical studies have shown UC·II to be both safe and effective in supporting joint health - and clarify how it helps the body derail a destructive process involved in both types of arthritis.

Like Grandma's Cold Remedy, UC·II was Discovered in the Kitchen.

Dr. Eugene Moore, a chemical engineer, had an 8-year-old daughter, Anne Marie, who was diagnosed with rheumatoid arthritis. Her swollen and painful joints continued to worsen until, by the time she was in her late 20's, much of her life was spent in an electric wheelchair.

One day Dr. Moore read about some studies on chicken collagen which showed that a small amount taken orally could have a preventive effect on rheumatoid arthritis. Putting his chemical engineering background to work, he went to the grocery, bought some chickens, and turned his kitchen into a laboratory. What Dr. Moore discovered was that, unlike grandma's chicken soup, if he cooked the chicken collagen, it became ineffective. So he formulated a recipe for an 'undenatured' (also called natural or native; not processed by high heat or chemicals) chicken collagen using the chicken's sternum cartilage.

After his daughter's rheumatoid arthritis began to improve, Dr. Moore shared his preparation with his good friend, Roger, who suffered with osteoarthritis so severe he could no longer function normally. Within a few weeks, Roger, too, began to feel and function much better. Both Anne Marie and Roger described the results as extraordinary - a significantly improved quality of life with no side effects.

Since Dr. Moore's initial discovery, a number of other studies have confirmed the benefits of undenatured type II collagen for joint health in both humans and animals.

Trial Shows UC·II More Than Twice as Effective as Glucosamine and Chondroitin

In a randomized, double-blind study of 52 osteoarthritis patients, one group took 40 mg UC·II and the other a combination of 1500 mg glucosamine and 1200 mg chondroitin. (Double-blind means neither the study subjects nor those tracking the results knew which patients were receiving which doses.) The table below shows the results after 90 days (percentages indicate the reduction in symptomatology):

Symptom UC·II G & C
Stiffness and difficulty in physical function 33.3% less 14.0% less
General level of pain 40.4% less 15.4% less
Effect of pain on daily activities 20.2% less 5.9% less

A small daily dosage of UC·II reduced joint pain and increased joint mobility and flexibility significantly - more than twice as much as the larger dosages of glucosamine and chondroitin.(1)

Additional Human Clinical Trials

  • A pilot study looked at five women who had significant joint pain symptoms. Each took 40 mg of UC·II for 42 days. Four of the five reported significant reductions in pain and stiffness. The average reduction in pain level was 26 percent.(2)

  • Six out of 10 rheumatoid arthritis patients reported significant improvement after taking UC·II for three months. One patient experienced complete remission. No side effects were reported.(3)

  • In a 90-day, double-blind, placebo-controlled study, 60 patients with severe, active rheumatoid arthritis were split into two groups. In the half taking UC·II, 28 showed considerable improvement compared to the placebo group. Four patients recovered completely.(3)

  • Ten children (8 to 14 years old) with active juvenile rheumatoid arthritis were given UC·II for three months. Eight of the 10 experienced a reduction in swollen and tender joints and one experienced a complete remission.(4)


Animal Studies

Humans are not the only ones who suffer the pain of arthritis. One in four pet dogs in the U.S. is diagnosed with some form of arthritis, as are millions of horses worldwide. A number of studies have been done using UC·II to treat osteoarthritic dogs and horses, with good results. For example:

  • Osteoarthritic dogs were given either 40 mg of UC·II or a placebo for 120 days. The dogs given the UC·II exhibited significant improvements as measured by detailed observation of pain-related behaviors and responses: 77 percent less evidence of overall pain, 83 percent less evidence of pain after limb manipulation, and 84 percent less pain after exercise. The dogs receiving the placebo exhibited no significant change in observed pain behaviors/responses.(5)

  • Osteoarthritic horses were divided into groups of five or six, receiving either 320 mg of UC·II, 480 mg of UC·II, 640 mg of UC-II, 5,400 mg of glucosamine plus 1,800 mg of chondroitin, or a placebo. The horses who received the 320, 480 or 640 mg of UC·II exhibited significant reductions in arthritic pain. The UC·II dosages of 480 or 640 mg had equal effects - an 88 percent decrease in overall pain and a 78 percent decrease in pain upon limb manipulation. UC·II was found to be more effective than glucosamine plus chondroitin.(6)


How UC·II Works on Rheumatoid Arthritis and Osteoarthritis

Rheumatoid arthritis is an autoimmune disease in which the body's own immune system turns against itself, and killer T-cells begin to attack the joint cartilage, resulting in inflammation and joint destruction.

UC·II contains molecular regions called
epitopes. These are immune system markers that interact with certain antibodies to trigger the deactivation of collagen-specific killer T-cells, and in turn help deactivate the inflammatory process.

Osteoarthritis is characterized by an inflammatory synovial response that leads to joint wear and tear and is usually attributed to aging.

Many of the biochemical markers associated with OA inflammation are also associated with RA inflammation; therefore similar therapies are usually used. Research has shown that UC·II suppresses the T-cell-mediated inflammation in both forms of arthritis.

Denatured vs. Undenatured - Why the Difference Is Important

Denatured (hydrolyzed). As Dr. Moore discovered in his kitchen laboratory, when chicken sternum collagen is heated, it loses its ability to repair and rebuild the joints. Most of the type II chicken collagen found in dietary supplements is denatured or hydrolized, which means that high heat and/or chemicals have been used to process it. These processes fundamentally alter the molecular structure of the protein, rendering the collagen ineffective as an immunomodulator. There are no peer-reviewed scientific studies showing that denatured type II collagen provides any joint health benefits. And in fact one study states, "denatured type II collagen has no observable effect on the incidence and severity of the disease [arthritis]."(7)

Undenatured (native). Undenatured type II collagen is made using little or no heat and very limited processing - just enough to concentrate the collagen and make it soluble. The UC·II manufacturing process ensures that the collagen remains biologically active in its most native, triple helix form, with its immunomodulating ability intact.

The Right Dosage is Essential

Although some people think "if a little is good, more must be better," this definitely does not apply to undenatured type II collagen.

Small amounts have been found to be the most effective in modulating the body's immune response, but too much can produce a negative or opposite result. The daily dosage recommended for maximum effectiveness is 40 mg UC·II (containing 10 mg bioactive undenatured type II collagen).

In addition to the bioactive UC·II undenatured type II collagen,
OsteoTec UC·II contains Aquamin® (mineralized red algae) - a source of calcium plus more than 70 naturally occurring trace minerals absorbed from the sea; clinically proven to improve bone and joint health.(8)

Unique Natural Support for Joint Health & Function

Overall, clinical trials and studies strongly support OsteoTec UC·II's unique ability to work with the immune system naturally, often helping to defuse the destructive inflammatory processes responsible for stiffness and pain in both rheumatoid and osteoarthritis.

You can purchase OsteoTec UC-II at ProHealth.com

Source: ProHealth.com -
"Undenatured Type II Collagen - Chicken Soup for Your Joints"

____
* Karen Lee Richards is the Lead Expert specializing in Fibromyalgia and ME/CFS, for HealthCentral's ChronicPainComnection (
www.chronicpainconnection.com). Karen is co-founder of the National Fibromyalgia Association (NFA) and was Executive Editor of Fibromyalgia AWARE magazine for four years.

References:
1. Bagchi M, et al. Beneficial effects of oral administration of undenatured type-II collagen on osteoarthritis: a human clinical trial. Presented at: Journal of the American College of Nutrition 49th Annual Meeting; October 2008; Arlington, Va. Abstract No. 30. (See also Crowley DC, et al.
Safety and efficacy of undenatured type II collagen in the treatment of osteoarthritis of the knee: A clinical trial. International Journal of Medical Sciences, 2009;6:312-321. November 2009)

2. Bagchi D, et al.
Effects of orally administered undenatured type II collagen against arthritic inflammatory diseases: a mechanistic exploration. Int J Clin Pharmacol Res. 22(3-4):101-10, 2002.

3. Trentham D, et al.
Effects of Oral Administration of Type-II Collagen on Rheumatoid Arthritis. Science. 261:1727-1730, 1993.

4. Barnett, et al.
A Pilot Trial of Oral Type-II Collagen in the Treatment of Juvenile Rheumatoid Arthritis. Arthritis & Rheumatism. 39:623-628, 1996.

5. Gupta RC, et al. Pain reduction measured by ground force plate in arthritic dogs treated with type-II collagen. Presented at: Society of Toxicology 48th Annual Meeting; March 2009. (See also: D'Altilio M, et al. Therapeutic efficacy and safety of undenatured type II collagen singly or in combination with glucosamine and chondroitin in arthritic dogs. Toxicol Mech Methods. 17:189-196, 2007; and Deparle LA, et al.
Efficacy and safety of glycosylated undenatured type-II collagen (UC-II) in therapy of arthritic dogs. J Vet Pharmacol Therap. 28:385-390, 2005.)

6. Gupta RC, et al.
Therapeutic efficacy of undenatured type-II collagen (UC-II) in comparison to glucosamine and chondroitin in arthritic horses. J Vet Pharmacol Therap. 32:577-584, 2009.

7. Nagler-Anderson C, et al.
Suppression of type II collagen-induced arthritis by intragastric administration of soluble type II collagen. Proc Natl Acad Sci USA. 83:7443-7446, 1986.

8. Frestedt, JL, et al.
A Natural mineral supplement [Aquamin] provides relief from knee osteoarthritis symptoms: a randomized controlled pilot trial. Nutrition Journal, 7(9), 2008.

___
Note: This information has not been evaluated by the FDA. It is general and is not meant to prevent, diagnose, treat or cure any condition, illness, or disease. It is very important that you make no change in your healthcare plan or health support regimen without researching and discussing it in collaboration with your professional healthcare team.

 

Super Sweet Vitamin Sale!

by Ellen DuBois on 10/23/11

Vitamin World

 

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Running on Empty? Fuel Up with NADH

by Karen Lee Richards*
Source: ProHealth.com

Do you ever feel like a car that has run out of gas? If so, it may be time to add some NADH to your cellular tank. NADH is the fuel our cells need to produce energy and function properly. NADH, a reduced form of nicotinamide adenine dinucleotide, is a naturally occurring coenzyme formed from Niacin (vitamin B3) that plays an essential role in the energy production of every human cell - all 100 trillion of them.

Studies suggest NADH may help:

  • Increase energy and reduce fatigue.

  • Support the immune system with powerful antioxidants and free-radical scavengers.

  • Improve memory, focus and mental clarity.

  • Support the creation of neurotransmitters, like serotonin, dopamine, and norepinephrine.

  • Enhance mood and emotional balance.

How NADH Works

In order to understand how NADH works, it is first necessary to understand mitochondria. Picture the mitochondria as little engines - or energy producers - within each cell of your body. It's the job of your mitochondria to supply energy to your cells in the form of adenosine triphosphate (ATP). But exactly how does that happen?

This is where NADH comes in. NADH sets off a chemical chain reaction by transforming Coenzyme Q10 into its reduced form. Then, in its reduced form, Co-Q10 becomes active and serves as the catalyst that makes it possible for the mitochondria to produce ATP. Every molecule of NADH results in the production of three molecules of ATP energy.

NADH is a critical component of your body's ability to function. Without NADH, the mitochondria cannot produce energy and the cells will die.

ME/CFS and Fibromyalgia

Fatigue is a key symptom of both ME/CFS and fibromyalgia. Since recurring fatigue is marked by low cellular ATP, which results in low cellular energy production, researchers have studied the use of NADH to increase energy.

  • A pilot study at Georgetown University gave 26 ME/CFS patients either 10 mg of NADH or a placebo daily for four weeks. After a four-week washout period, participants switched to the alternate regimen for four weeks. At the end of the study 31% had a favorable response to the NADH. The scientists concluded that "NADH may be a valuable adjunctive therapy in the management of the chronic fatigue syndrome."(1)

  • In a 2004 study, 31 ME/CFS patients were randomly assigned to receive either NADH or nutritional supplements and psychological therapy for two years. The patients who received NADH had a dramatic and statistically significant reduction of the mean symptom score in the first eight months and they tended to continue improving through the rest of the trial.(2)

Another major complaint of ME/CFS and fibromyalgia patients is cognitive functioning problems, such as memory loss, difficulty concentrating and mental fogginess.

George Birkmayer, MD, PhD, director of the Institute for Parkinson's Therapy in Vienna, and a leader in NADH research for nearly 30 years, explains how NADH can help improve mental clarity.

"One third of all the energy we produce in our body is used up by our brain. Due to this, an energy deficiency is first realized in the brain with symptoms such as lack of concentration and alertness, or mental fog. With more NADH the brain cells function better...

"A further mechanism by which NADH affects cognitive function is by stimulating the production of adrenaline and dopamine. Both of these substances are essential for our cognitive performance and our memory."(3)

NADH is frequently recommended for ME/CFS and fibromyalgia patients by well-known specialists like Drs. Charles Lapp, Jacob Teitelbaum, Dale Guyer, Michael Rosenbaum, and Mark Pellegrino.

Parkinson's Disease

Because NADH is known to help increase levels of the important neurotransmitter dopamine, there have been several studies of NADH as a possible adjunctive treatment for Parkinson's disease (which involves a slow destruction of the nerve cells in the brain that make dopamine).

  • Between 1989 and 1993, Austrian scientists, led by Dr. Birkmayer, conducted a series of open label trials of NADH on more than 2,000 Parkinson's patients. Through these studies, Dr. Birkmayer found that NADH not only alleviated the impairment in motor skills caused by Parkinson's but also effectively treated their cognitive dysfunction.

  • Below is a summary of the results from three of those studies. More than a 30% improvement was considered to be a very good response and up to 30% was rated as a moderate response.


No. of Participants Very Good Response Moderate Response No Response
34 61.7% 38.3% 0%
161 71.4% 17.4% 11.2%
885 19.3% 58.8% 21.8%

  • The researchers found a dose of 25 to 50 mg of NADH per day to be the most effective. They also discovered that younger patients and patients with a shorter duration of disease have a better chance to gain a marked improvement than older patients and patients with a longer duration of the disease.(4-7)

  • In a German study, 15 Parkinson's patients received intravenous infusions of 10 mg NADH for seven days in addition to conventional Parkinsonian pharmacotherapy. The patients all showed a significantly positive response and the scientists found that the application of NADH significantly increased the bioavailability of their plasma levodopa. They concluded that NADH "may be a potent stimulator of endogenous levodopa biosynthesis with clinical benefit for Parkinsonian patients."(8)

Although several of the Parkinson's studies have used intravenous or intramuscular injections of NADH, trials using oral NADH have shown it to be equally effective.(4)

Alzheimer's Disease

In 2004, a randomized, placebo-controlled, matched-pairs, double-blind, clinical study was conducted testing NADH as a treatment for Alzheimer's disease. Twenty-four patients with probable Alzheimer's disease received either 10 mg of oral NADH or a placebo.

After six months, participants treated with NADH showed no evidence of progressive cognitive deterioration. They also showed significantly higher performance scores than the placebo group in the areas of verbal fluency and visual-constructional ability as well as a trend to better performance in abstract verbal reasoning. The researchers concluded, "Consistent with earlier studies, the present findings support NADH as a treatment for AD."(9)

Need-to-Know Information

Food Sources - NADH can be found naturally in the muscle tissue of fish, poultry and cattle, and in food products made with yeast. However, it is not known whether the NADH from these food sources is efficiently absorbed or utilized by the body.

Absorption - NADH must be absorbed in the intestinal tract to be effective. Therefore, oral NADH must be formulated for stability and delivered via a coated tablet so it does not dissolve in the stomach, but rather stays intact until it reaches the intestine. ProHealth's Energy NADH is an exclusive formulation that provides improved stability for 100% guaranteed potency. And its unique cellulose matrix coating enhances absorption by ensuring that the NADH reaches the intestine where it is quickly dissolved.

Dosage -The recommended dosage is generally 5 to 10 mg per day taken in the morning on an empty stomach, 30 minutes before a meal. However, studies with Parkinson's disease patients found that 25 to 50 mg per day was the most effective dose.

Side Effects - No significant side effects have been reported. Supplementing with NADH appears to be very safe.

Drug Interactions - There are no reported drug interactions.

In Summary

NADH is a powerful cellular energy producer. Research has demonstrated the ability of supplemental NADH to promote fatigue reduction, enhanced mental clarity, and increased levels of important neurotransmitters like dopamine.

To purchase NADH visit ProHealth.com


Resources:

1. Forsyth LM, et al. "Therapeutic effects of oral NADH on the symptoms of patients with chronic fatigue syndrome." Ann Allergy Asthma Immunol. 1999 Feb;82(2):185-91.

2. Santaella ML, Font I, Disdier OM. "Comparison of oral nicotinamide adenine dinucleotide (NADH) versus conventional therapy for chronic fatigue syndrome." P R Health Sci J. 2004 Jun;23(2):89-93.

3. "Interview: Dr. George Birkmayer on NADH for Energy, Healthy Immune Function and More." ProHealth. January 30, 2006.

4. Birkmayer GJ, Birkmayer W. "Stimulation of endogenous L-dopa biosynthesis - a new principle for the therapy of Parkinson's disease. The clinical effect of nicotinamide adenine dinucleotide (NADH) and nicotinamide adenine dinucleotidephosphate (NADPH)." Acta Neurol Scand Suppl. 1989;126:183-7.

5. Birkmayer JG, et al. "Nicotinamide adenine dinucleotide (NADH) - a new therapeutic approach to Parkinson's disease. Comparison of oral and parenteral application." Acta Neurol Scand Suppl. 1993;146:32-5.

6. Birkmayer W, et al. "The coenzyme nicotinamide adenine dinucleotide (NADH) improves the disability of parkinsonian patients." J Neural Transm Park Dis Dement Sect. 1989;1(4):297-302.

7. Birkmayer W, Birkmayer GJ. "Nicotinamidadenindinucleotide (NADH): the new approach in the therapy of Parkinson's disease." Ann Clin Lab Sci. 1989 Jan-Feb;19(1):38-43. .

8. Kuhn W, et al. "Parenteral application of NADH in Parkinson's disease: clinical improvement partially due to stimulation of endogenous levodopa biosynthesis." J Neural Transm. 1996;103(10):1187-93.

9. Demarin V, Podobnik SS, Storga-Tomic D, Kay G. "Treatment of Alzheimer's disease with stabilized oral nicotinamide adenine dinucleotide: A randomized, double-blind study." Drugs Exp Clin Res. 2004;30(1):27-33.

___

* Supplement research writer Karen Lee Richards is the Lead Expert specializing in Fibromyalgia and ME/CFS, for HealthCentral's ChronicPainConnection. Karen is co-founder of the National Fibromyalgia Association (NFA) and was Executive Editor of Fibromyalgia AWARE magazine for four years.

Note: This information has not been evaluated by the FDA. It is general information and is not intended to diagnose, prevent, treat or cure any illness, condition or disease. It is very important that you make no change in your healthcare plan or health support regimen without researching and discussing it in collaboration with your professional healthcare team.



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