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脂联素可改善血管紧张素II诱导的血管内皮损伤。

Adiponectin ameliorates angiotensin II-induced vascular endothelial damage.

作者信息

Zhi Zuo, Pengfei Zuo, Xiaoyi Tian, Genshan Ma

机构信息

Department of Cardiology, Zhongda Hospital, Medical School of Southeast University, Dingjiaqiao Road No. 87, Nanjing, 210009, Jiangsu Province, China,

出版信息

Cell Stress Chaperones. 2014 Sep;19(5):705-13. doi: 10.1007/s12192-014-0498-3. Epub 2014 Feb 13.

Abstract

Adiponectin is an adipocyte-specific adipocytokine that possesses anti-atherogenic and anti-diabetic properties. It has been shown to have a beneficial effect on the cardiovascular system, but it remains to be elucidated whether adiponectin has a therapeutic effect on vascular damage induced by the potential vasoactive substance angiotensin II (Ang II). In this study, the effects of adiponectin on Ang II-induced vascular endothelial damage were investigated. In cultured human umbilical vein endothelium cells, Ang II stimulation increased generation of ROS and 4-hydroxy-2-nonenal, both of which were clearly restored by administration of adiponectin. In addition, administration of adiponectin was found to increase cell viability and prevent apoptosis. Our results also demonstrate that the protective effects of adiponectin against Ang II-induced vascular endothelial damage are dependent on the binding of adiponectin to its cell surface receptor 1. Importantly, we found that adiponectin treatment modulates the apoptotic pathway by reducing the expression of LOX-1, up-regulating both cIAP-1 and the ratio of Bcl-2/Bax. Finally, our data displayed that the protective effects of adiponectin against Ang II cytotoxicity depend on AMPK activation mediated by the endosomal adaptor protein, adaptor protein with phosphotyrosine binding, pleckstrin homology domains, and leucine zipper motif.

摘要

脂联素是一种脂肪细胞特异性脂肪因子,具有抗动脉粥样硬化和抗糖尿病特性。已证明它对心血管系统有有益作用,但脂联素对潜在血管活性物质血管紧张素II(Ang II)诱导的血管损伤是否具有治疗作用仍有待阐明。在本研究中,研究了脂联素对Ang II诱导的血管内皮损伤的影响。在培养的人脐静脉内皮细胞中,Ang II刺激增加了活性氧(ROS)和4-羟基-2-壬烯醛的生成,而脂联素给药可明显恢复二者水平。此外,发现脂联素给药可增加细胞活力并防止细胞凋亡。我们的结果还表明,脂联素对Ang II诱导的血管内皮损伤的保护作用取决于脂联素与其细胞表面受体1的结合。重要的是,我们发现脂联素处理通过降低LOX-1的表达、上调cIAP-1以及Bcl-2/Bax比值来调节凋亡途径。最后,我们的数据显示,脂联素对Ang II细胞毒性的保护作用取决于由内体衔接蛋白、含磷酸酪氨酸结合结构域、普列克底物蛋白同源结构域和亮氨酸拉链基序的衔接蛋白介导的AMPK激活。

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