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Age-related accumulation of advanced glycation end-products-albumin, S100 beta, and the expressions of advanced glycation end product receptor differ in visceral and subcutaneous fat

机译:内脏和皮下脂肪中晚期糖基化终末产物-白蛋白,S100 beta的年龄相关积累以及晚期糖基化终末产物受体的表达不同

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摘要

Visceral fat induces more inflammation by activating macrophages than subcutaneous fat, and inflammation is an underlying feature of the pathogeneses of various diseases, including cardiovascular disease and diabetes. Advanced glycation end products (AGEs), S100 beta, and their receptors, the receptor for advanced glycation end products (RAGE), lead to macrophage activation. However, little information is available regarding the differential accumulations of AGE-albumin (serum albumin modified by AGEs), sloop, or expressions of RAGE in different adipocyte types in fat tissues. In this study, the authors investigated whether age-related AGE-albumin accumulations S100 beta level, and RAGE expressions differ in subcutaneous and visceral fat tissues. Subcutaneous and visceral fat were harvested from 3- and 28 week -old rats.
机译:内脏脂肪通过激活巨噬细胞比皮下脂肪引起更多的炎症,并且炎症是包括心血管疾病和糖尿病在内的各种疾病的病原体的潜在特征。晚期糖基化终产物(AGEs),S100 beta及其受体,即晚期糖基化终产物(RAGE)的受体,会导致巨噬细胞活化。但是,关于脂肪组织中不同类型脂肪细胞中AGE-白蛋白(经AGEs修饰的血清白蛋白),单反或RAGE的差异积累的信息很少。在这项研究中,作者调查了皮下和内脏脂肪组织中与年龄相关的AGE-白蛋白积累S100β水平和RAGE表达是否不同。从3和28周龄的大鼠中收获皮下和内脏脂肪。

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