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Earlier this year, a team from UC San Francisco reported on the discovery that a class of commonly prescribed type-2 diabetes drugs, called TZDs thiazolidinediones, such as Actos and Avandiapromoted the conversion of energy-storing white fat cells into energy-burning brown fat cells. Now researchers at Columbia University Medical Center CUMC have identified the mechanism that causes this Browning Cottbus to take place, potentially leading to new Singles dating new Prenzlauer Berg for obesity and type-2 diabetes. While it was known that TZDs have the ability to change Browning Cottbus fat cells to brown fat cells by activating a cell receptor called peroxisome proliferator-activated receptor—gamma ppar-gammathe exact mechanism behind this transformation was unclear. Having previously shown that increasing the activity of a group of enzymes called sirtuins or Sir2 in mice resulted in increased metabolic activity, the CUMC team has now shown that this boost in metabolism is a result of promoting the browning of white fat. Knowing that sirtuins work by severing the chemical bonds between acetyl groups and proteins in a process known as deacetylation, the researchers wanted to uncover whether sirtuins remove acetyl groups from ppar-gamma and if this deacetylation of ppar-gamma is crucial to the browning of white fat. Westend girl beautiful confirmed this is the case by creating a mutant gene of ppar-gamma that, in effect, mimicked the actions of sirtuins and promoted the development of brown fat-like qualities in white fat cells in both mice and human fat tissue.
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