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View Full Version : Drug 'tricks body to lose weight'



broken7
11-11-2008, 10:45 PM
http://news.bbc.co.uk/2/hi/health/7707876.stm

5151
19-11-2008, 05:31 PM
this link reminded me why I hate mainstream media so much. how do you print an article like that without a reference to the study, ****ing ridiculous. I'm going to see what I can find on pubmed. Resveratol gets talked about a lot especially since it made it into 6-oxo hardcore but I'm still not convinced. I also liked the "even while on a high fat diet" part, it truly amazes me how little mainstream media understands when it comes to diet.

Thanks for the link I'm off to search medline

5151
19-11-2008, 05:38 PM
I don't think it's the same article but I came up with this:



Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes.
Milne JC, Lambert PD, Schenk S, Carney DP, Smith JJ, Gagne DJ, Jin L, Boss O, Perni RB, Vu CB, Bemis JE, Xie R, Disch JS, Ng PY, Nunes JJ, Lynch AV, Yang H, Galonek H, Israelian K, Choy W, Iffland A, Lavu S, Medvedik O, Sinclair DA, Olefsky JM, Jirousek MR, Elliott PJ, Westphal CH.

Sirtris Pharmaceuticals Inc., 790 Memorial Drive, Cambridge, Massachusetts 02139, USA.

Calorie restriction extends lifespan and produces a metabolic profile desirable for treating diseases of ageing such as type 2 diabetes. SIRT1, an NAD+-dependent deacetylase, is a principal modulator of pathways downstream of calorie restriction that produce beneficial effects on glucose homeostasis and insulin sensitivity. Resveratrol, a polyphenolic SIRT1 activator, mimics the anti-ageing effects of calorie restriction in lower organisms and in mice fed a high-fat diet ameliorates insulin resistance, increases mitochondrial content, and prolongs survival. Here we describe the identification and characterization of small molecule activators of SIRT1 that are structurally unrelated to, and 1,000-fold more potent than, resveratrol. These compounds bind to the SIRT1 enzyme-peptide substrate complex at an allosteric site amino-terminal to the catalytic domain and lower the Michaelis constant for acetylated substrates. In diet-induced obese and genetically obese mice, these compounds improve insulin sensitivity, lower plasma glucose, and increase mitochondrial capacity. In Zucker fa/fa rats, hyperinsulinaemic-euglycaemic clamp studies demonstrate that SIRT1 activators improve whole-body glucose homeostasis and insulin sensitivity in adipose tissue, skeletal muscle and liver. Thus, SIRT1 activation is a promising new therapeutic approach for treating diseases of ageing such as type 2 diabetes.

seems like great for therapeutic approach but for weight lifters who are already plenty insulin sensitive I doubt it holds much merit.

5151
26-11-2008, 01:25 PM
I have the full text if anyone is interested.