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Home: Papers of the Week
Annotation


Morris MC, Evans DA, Bienias JL, Scherr PA, Tangney CC, Hebert LE, Bennett DA, Wilson RS, Aggarwal N. Dietary niacin and the risk of incident Alzheimer's disease and of cognitive decline. J Neurol Neurosurg Psychiatry. 2004 Aug;75(8):1093-9. PubMed Abstract

Comments on Related News
  Related News: Sirtuin Inhibitor Boosts Cognition, Reduces Phospho-tau

Comment by:  David Sinclair (Disclosure)
Submitted 11 November 2008  |  Permalink Posted 11 November 2008

One must be careful when calling nicotinamide an "inhibitor" in this experiment. While it is true that our lab showed that nicotinamide is a direct inhibitor of SIRT1 enzyme, it is also a precursor of NAD+, and NAD+ is a co-substrate (i.e., activator) of SIRT1.

In vivo, there is an abundant enzyme called Nampt in cells and serum that initiates the conversion of nicotinamide to NAD+. Therefore we should entertain the possibility that nicotinamide is activating SIRT1 in vivo, not inhibiting it. This would fit with other papers showing that SIRT1 is neuroprotective.

View all comments by David Sinclair


  Related News: Sirtuin Inhibitor Boosts Cognition, Reduces Phospho-tau

Comment by:  William Polsky
Submitted 15 November 2008  |  Permalink Posted 18 November 2008

The experimental dose used in the study was 200 mg/kg/day. This would translate to a daily dose of nearly 14,000 mg for a 70 kg (154 lb.) person. Yet in the proposed clinical trial the experimental group will be receiving a daily dose of 3,000 mg. How does one explain the lower dose being used in the clinical trial?

View all comments by William Polsky

  Related News: Sirtuin Inhibitor Boosts Cognition, Reduces Phospho-tau

Comment by:  Will Block
Submitted 19 November 2008  |  Permalink Posted 21 November 2008

I am responding to William Polsky's comment on computation of the human dose of nicotinamide.

Following the publication of a study on the use of resveratrol in mice to improve their health and maximum lifespan, the press reported that a human would have to consume an enormous amount of wine or supplements to gain similar benefits. This statement shows a lack of understanding of the appropriate criteria for dosage translations between species.

There are a number of acceptable ways to compute the human equivalent dose from animal studies. The key is to consider energy-expenditure differences between species. Energy expenditure is a measure of metabolic rate. The method favored by the FDA (see www.fda.gov/cber/gdlns/dose.htm) uses the body surface area (BSA) normalization method. Basal metabolic rate is directly related to surface area. As the FDA notes, the BSA method correlates well across several mammalian species with several parameters of biology, including oxygen utilization, caloric expenditure, basal...  Read more

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