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Am J Physiol Heart Circ Physiol. 2013 Mar 15;304(6):H796-805. doi: 10.1152/ajpheart.00712.2012. Epub 2013 Jan 18.
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Adiponectin receptors in energy homeostasis and obesity pathogenesis.脂联素受体在能量平衡和肥胖发病机制中的作用。
Prog Mol Biol Transl Sci. 2013;114:317-42. doi: 10.1016/B978-0-12-386933-3.00009-1.
3
Angiotensin (1-7) ameliorates angiotensin II-induced inflammation by inhibiting LOX-1 expression.血管紧张素 (1-7) 通过抑制 LOX-1 的表达来减轻血管紧张素 II 引起的炎症。
Inflamm Res. 2013 Feb;62(2):219-28. doi: 10.1007/s00011-012-0571-2. Epub 2012 Dec 12.
4
Endothelial Kruppel-like factor 4 protects against atherothrombosis in mice.内皮型 Kruppel 样因子 4 可保护小鼠免于动脉血栓形成。
J Clin Invest. 2012 Dec;122(12):4727-31. doi: 10.1172/JCI66056. Epub 2012 Nov 19.
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Angiotensin II regulates activation of Bim via Rb/E2F1 during apoptosis: involvement of interaction between AMPKβ1/2 and Cdk4.血管紧张素 II 通过 Rb/E2F1 调节 Bim 的激活,从而在细胞凋亡中发挥作用:涉及 AMPKβ1/2 和 Cdk4 之间的相互作用。
Am J Physiol Lung Cell Mol Physiol. 2012 Aug 1;303(3):L228-38. doi: 10.1152/ajplung.00087.2012. Epub 2012 Jun 1.
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Counteraction between angiotensin II and angiotensin-(1-7) via activating angiotensin type I and Mas receptor on rat renal mesangial cells.血管紧张素II与血管紧张素-(1-7)通过激活大鼠肾系膜细胞上的血管紧张素I型受体和Mas受体产生的拮抗作用。
Regul Pept. 2012 Aug 20;177(1-3):12-20. doi: 10.1016/j.regpep.2012.04.002. Epub 2012 May 1.
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Therapeutic strategies targeting endothelial function in humans: clinical implications.针对人类内皮功能的治疗策略:临床意义。
Curr Vasc Pharmacol. 2012 Jan;10(1):77-93. doi: 10.2174/157016112798829751.
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Impaired mitochondrial biogenesis contributes to mitochondrial dysfunction in Alzheimer's disease.阿尔茨海默病中线粒体生物发生受损导致线粒体功能障碍。
J Neurochem. 2012 Feb;120(3):419-29. doi: 10.1111/j.1471-4159.2011.07581.x. Epub 2011 Dec 8.
9
Globular adiponectin protects human umbilical vein endothelial cells against apoptosis through adiponectin receptor 1/adenosine monophosphate-activated protein kinase pathway.球形脂联素通过脂联素受体 1/腺苷酸活化蛋白激酶通路保护人脐静脉内皮细胞免于凋亡。
Chin Med J (Engl). 2011 Aug;124(16):2540-7.
10
Angiotensin II activates AMPK for execution of apoptosis through energy-dependent and -independent mechanisms.血管紧张素 II 通过能量依赖和非依赖机制激活 AMPK 以执行细胞凋亡。
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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.

DOI:10.1007/s12192-014-0498-3
PMID:24523033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4147077/
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。