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Nutrients 2015, 7(3), 1992-2000;

Alcohol: A Nutrient with Multiple Salutary Effects

Department of Cardiology, Division of Atherosclerosis, Houston Methodist Research Institute, Fondren F8-047, 6670 Bertner St., Houston, TX 77030, USA
Department of Medicine, Weill Cornell Medical College, 1305 York Ave. Y-805, New York, NY 10021, USA
Author to whom correspondence should be addressed.
Received: 10 February 2015 / Accepted: 11 March 2015 / Published: 18 March 2015
(This article belongs to the Special Issue Lipoprotein Metabolism and Atherosclerosis)
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Numerous studies have shown that cardiovascular disease is lower among alcohol consumers than among nonconsumers. Many of the metabolic effects of alcohol are mediated by its terminal metabolite, acetate, which has reported insulinemic properties. There have been few rational metabolic targets that underly its cardioprotective effects until it was reported that acetate, the terminal product of alcohol metabolism, is the ligand for G-protein coupled receptor 43 (GPCR43), which is highly expressed in adipose tissue. Here, we recast much of some of the major lipid and lipoprotein effects of alcohol in the context of this newly discovered G-protein and develop a mechanistic model connecting the interaction of acetate with adipose tissue-GPCR43 with these effects. According to our model, ingestions of acetate could replace alcohol as a means of improving plasma lipid risk factors, improving glucose disposal, and reducing cardiovascular disease. Future studies should include biochemical, cell, animal, and human tests of acetate on energy metabolism. View Full-Text
Keywords: Alcohol; acetate; insulin resistance; HDL; atherosclerosis Alcohol; acetate; insulin resistance; HDL; atherosclerosis

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Pownall, H.J.; Rosales, C.; Gillard, B.K.; Gotto, A.M., Jr. Alcohol: A Nutrient with Multiple Salutary Effects. Nutrients 2015, 7, 1992-2000.

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