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Pronounced expression of the lipolytic inhibitor G0/G1 Switch Gene 2 (G0S2) in adipose tissue from brown bears (Ursus arctos) prior to hibernation

机译:冬眠前棕熊(Ursus arctos)脂肪组织中脂解抑制剂G0 / G1开关基因2(G0S2)的明显表达

摘要

Prior to hibernation, the brown bear (Ursus arctos) exhibits unparalleledweight gain. Unlike humans, weight gain in bears is associated with lowerlevels of circulating free fatty acids (FFA) and increased insulin sensitivity.Understanding how free-ranging brown bears suppress lipolysis when gainingweight may therefore provide novel insight toward the development of humantherapies. Blood and subcutaneous adipose tissue were collected from immobilizedfree-ranging brown bears (fitted with GPS-collars) during hibernationin winter and from the same bears during the active period in summer inDalarna, Sweden. The expression of lipid droplet-associated proteins in adiposetissue was examined under the hypothesis that bears suppress lipolysisduring summer while gaining weight by increased expression of negative regulatorsof lipolysis. Adipose triglyceride lipase (ATGL) expression did not differbetween seasons, but in contrast, the expression of ATGL coactivator Comparativegene identification-58 (CGI-58) was lower in summer. In addition, theexpression of the negative regulators of lipolysis, G0S2 and cell-death inducingDNA fragmentation factor-a-like effector (CIDE)C markedly increased duringsummer. Free-ranging brown bears display potent upregulation of inhibitorsof lipolysis in adipose tissue during summer. This is a potential mechanismfor increased insulin sensitivity during weight gain and G0S2 may serve as atarget to modulate insulin sensitivity.
机译:在冬眠之前,棕熊(Ursus arctos)表现出无与伦比的体重增加。与人类不同,熊的体重增加与循环脂肪酸(FFA)的水平降低和胰岛素敏感性增加有关。了解自由散养的棕熊在增加体重时如何抑制脂解,因此可能为人类疗法的发展提供新颖的见解。在冬天的冬眠期间,从固定的自由活动棕熊(装有GPS项圈)中收集血液和皮下脂肪组织,在瑞典的达拉纳,在夏季的活动期间从相同的熊中收集血液和皮下脂肪组织。假设脂肪在夏季抑制脂解,同时通过增加脂解负调节剂的表达而增加体重,从而检验了脂肪组织中脂滴相关蛋白的表达。脂肪甘油三酯脂肪酶(ATGL)的表达在不同季节之间没有差异,但是相反,ATGL共激活因子Comprehengenegeneidentification-58(CGI-58)的表达在夏季较低。此外,在夏季,脂解,G0S2和细胞死亡诱导DNA片段化因子-a样效应物(CIDE)C的负调控因子的表达明显增加。在夏天,自由放养的棕熊在脂肪组织中显示出脂解抑制剂的有效上调。这是在体重增加期间增加胰岛素敏感性的潜在机制,而G0S2可以作为调节胰岛素敏感性的目标。

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