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Obesity reduces methionine sulphoxide reductase activity in visceral adipose tissue.

机译:肥胖会降低内脏脂肪组织中的蛋氨酸亚砜还原酶活性。

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摘要

Visceral obesity is linked to insulin resistance and cardiovascular disease. A recent genetic study indicated that the gene locus for the anti-oxidant defense enzyme methionine sulphoxide reductase A (MsrA) is positively associated with the development of visceral adiposity. This work tested the hypothesis that Msr activity is diminished in visceral fat as a result of obesity. It used two animal models of obesity, wild-type rats fed a high-fat (45% of calories from fat) diet and Zucker rats fed a 10% fat calorie diet. The data indicate that MsrA activity was selectively reduced by approximately 25% in the visceral adipose, but not subcutaneous adipose or liver, of both rat models as compared to control, wild type rats receiving a 10% fat calorie diet. MsrB activity was similarly reduced only in visceral fat. The data indicate that Msr activity is reduced by obesity and may alter oxidative stress signalling of obesity.
机译:内脏肥胖与胰岛素抵抗和心血管疾病有关。最近的一项遗传研究表明,抗氧化防御酶蛋氨酸亚砜还原酶A(MsrA)的基因位点与内脏肥胖的发展呈正相关。这项工作检验了以下假设:肥胖导致内脏脂肪中Msr活性降低。它使用了两种肥胖症动物模型,即以高脂(脂肪中热量的45%)为饮食的野生型大鼠和以脂肪热量为10%的大鼠为Zucker的饮食。数据表明,与接受10%脂肪卡路里饮食的对照野生型大鼠相比,两种大鼠模型的内脏脂肪中MsrA活性选择性降低约25%,但皮下脂肪或肝中没有降低。同样,MsrB活性仅在内脏脂肪中降低。数据表明,肥胖会降低Msr活性,并可能改变肥胖的氧化应激信号。

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