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Can benfotiamine cure neuropathy?

Treatment was well tolerated by patients, and no benfotiamine-drug interactions were reported. A study of 20 patients given 400mg daily of benfotiamine showed improvement in neuropathy scores and decrease in pain complaints over a 3-week period.

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What is benfotiamine and what are the effects of it?

Side Effects and Health Benefits of Benfotiamine. Benfotiamine, a lipid-soluble derivative from thiamine, is also known as benfotiamine. Benfotiamine's increased lipid solubility allows it to penetrate nerve cells better. Benfotiamine has a higher bioavailability after oral intake than a comparable dose of water-soluble Thiamine Ram.

Can you use vitamin C and alpha-lipoic acid together?

No interactions were found between alpha-lipoic acid and Vitamin C. Does ALA suppress appetite? Although ALA treatment caused a slight weight loss, it was not statistically significant. Appetite scores were decreased in the diabetes group but it did not cause statistically significant weight loss. There was no significant change in metabolic parameters or adiponectin after the treatment.

Is lipoic acid a vitamin?

Lipoic acid is another B-complex vitamin, whose only known function is to participate in the oxidative decarboxylations of α-ketoacids, principally conversion of pyruvate to acetyl-CoA, and α-ketoglutarate to succi-nyl-CoA, two similar dehydrogenase complexes of the TCA cycle. Is alpha-lipoic acid good for the liver? ► ALA is a powerful antioxidant effects on fatty liver. ► ALA prevents degenerations and induces liver regeneration.

Can turmeric help neuropathy?

Curcumin, a strong antioxidant found within turmeric, is known for its analgesic and anti-inflammatory properties. Curcumin can prevent chronic pain from neuropathy when taken early. It has also been shown that it can reduce inflammation and pain.

What causes lipoic acid deficiency?

People affected by this condition generally experience early-onset lactic acidosis, severe encephalopathy , seizures , poor growth, hypotonia , and developmental delay . It is caused by changes ( mutations ) in the LIAS gene and it is inherited in an autosomal recessive pattern.

By Claiborne

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