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脂联素上调单核细胞激活素A,但在肥胖或2型糖尿病中其全身水平未改变。

Adiponectin upregulates monocytic activin A but systemic levels are not altered in obesity or type 2 diabetes.

作者信息

Weigert Johanna, Neumeier Markus, Wanninger Josef, Schober Franziska, Sporrer Daniela, Weber Markus, Schramm Andrea, Wurm Sylvia, Stögbauer Fabian, Filarsky Michael, Schäffler Andreas, Aslanidis Charalampos, Schölmerich Jürgen, Buechler Christa

机构信息

Department of Internal Medicine I, Regensburg University Hospital, Franz Josef Strauss Allee 11, 93042 Regensburg, Germany.

出版信息

Cytokine. 2009 Feb;45(2):86-91. doi: 10.1016/j.cyto.2008.10.017. Epub 2009 Jan 6.

Abstract

Adiponectin is an adipocyte-derived protein with atheroprotective and immunoregulatory function. Adiponectin and activin A reduce foam cell formation and adiponectin activates the p38 MAPK pathway that is well described to induce activin A. Therefore, it was analyzed whether adiponectin alters activin A in primary human monocytes. Adiponectin dose- and time-dependently induced activin A in the supernatant, and the maximal amount was observed after 12h of incubation. Adiponectin-stimulated release of activin A was blocked by a p38 MAPK inhibitor. Metformin and pioglitazone are drugs frequently used to treat diabetic patients and metformin slightly reduced monocytic activin A release whereas pioglitazone had no effect. Type 2 diabetes is associated with elevated inflammatory systemic cytokines but activin A serum levels were similar in slim probands, overweight controls and type 2 diabetic patients. Furthermore, activin A did not correlate to systemic adiponectin, body mass index, waist to hip ratio or C-reactive protein. These findings indicate that adiponectin upregulates monocytic activin A release via the p38 MAPK pathway, and this may in part explain the immunoregulatory and antiatherosclerotic effects of this adipokine.

摘要

脂联素是一种由脂肪细胞分泌的蛋白质,具有抗动脉粥样硬化和免疫调节功能。脂联素和激活素A可减少泡沫细胞的形成,且脂联素可激活p38丝裂原活化蛋白激酶(MAPK)信号通路,而该信号通路可诱导激活素A的产生。因此,本研究分析了脂联素是否会改变原代人单核细胞中激活素A的水平。脂联素可呈剂量和时间依赖性地诱导上清液中激活素A的产生,孵育12小时后可观察到最大量。p38 MAPK抑制剂可阻断脂联素刺激的激活素A释放。二甲双胍和吡格列酮是常用于治疗糖尿病患者的药物,二甲双胍可轻微降低单核细胞激活素A的释放,而吡格列酮则无此作用。2型糖尿病与全身性炎症细胞因子水平升高有关,但瘦人、超重对照者和2型糖尿病患者的血清激活素A水平相似。此外,激活素A与全身性脂联素、体重指数、腰臀比或C反应蛋白均无相关性。这些研究结果表明,脂联素通过p38 MAPK信号通路上调单核细胞激活素A的释放,这可能部分解释了这种脂肪因子的免疫调节和抗动脉粥样硬化作用。

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