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Re: Niacinamide ok if you're on Parkinson's meds? » KaraS

Posted by Larry Hoover on December 30, 2004, at 12:48:37

In reply to Re: Niacinamide ok if you're on Parkinson's meds? » Larry Hoover, posted by KaraS on December 29, 2004, at 17:38:18

> A friend of mine has Parkinson's. She is looking for something to help her sleep. I suggested B3 but I wanted to make sure that it's not contraindicated with any of her other medications. She takes Requipt, L-Dopa and selegiline. She used to take Benedryl but then read about it not being good for you to take long-term - esp. if you have Parkinson's. Can you shed any light here?
>
> Thanks,
> K

Actually, I would think Benadryl might have adverse effects...

Anyway, I am pleased to report that niacinamide may even be an effective adjunctive treatment for Parkinson's. Picamilon is supposed to be very helpful, too.

Ann Neurol. 2003;53 Suppl 3:S39-47; discussion S47-8.

Bioenergetic approaches for neuroprotection in Parkinson's disease.

Beal MF.

Department of Neurology and Neuroscience, Weill Medical College of Cornell University, New York Presbyterian Hospital, New York, NY, USA. fbeal@mail.med.cornell.edu

There is considerable evidence suggesting that mitochondrial dysfunction and oxidative damage may play a role in the pathogenesis of Parkinson's disease (PD). This possibility has been strengthened by recent studies in animal models, which have shown that a selective inhibitor of complex I of the electron transport gene can produce an animal model that closely mimics both the biochemical and histopathological findings of PD. Several agents are available that can modulate cellular energy metabolism and that may exert antioxidative effects. There is substantial evidence that mitochondria are a major source of free radicals within the cell. These appear to be produced at both the iron-sulfur clusters of complex I as well as the ubiquinone site. Agents that have shown to be beneficial in animal models of PD include creatine, coenzyme Q(10), Ginkgo biloba, nicotinamide, and acetyl-L-carnitine. Creatine has been shown to be effective in several animal models of neurodegenerative diseases and currently is being evaluated in early stage trials in PD. Similarly, coenzyme Q(10) is also effective in animal models and has shown promising effects both in clinical trials of PD as well as in clinical trials in Huntington's disease and Friedreich's ataxia. Many other agents show good human tolerability. These agents therefore are promising candidates for further study as neuroprotective agents in PD.

Lar

 

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