...
首页> 外文期刊>Biochemical and Biophysical Research Communications >Calcitonin gene-related peptide attenuates angiotensin II-induced ROS-dependent apoptosis in vascular smooth muscle cells by inhibiting the CaMKII/CREB signalling pathway
【24h】

Calcitonin gene-related peptide attenuates angiotensin II-induced ROS-dependent apoptosis in vascular smooth muscle cells by inhibiting the CaMKII/CREB signalling pathway

机译:Calcitonin基因相关肽通过抑制Camkii / Creb信号通路抑制血管平滑肌细胞中的血管紧张素II诱导的ROS依赖性凋亡

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Apoptosis is associated with various cardiovascular diseases. CGRP exerts a variety of effects within the cardiovascular system, and protects against the onset and development of angiotensin (Ang) II-induced vascular dysfunction and remodelling. However, it is not known whether CGRP has a direct effect on Ang II-induced apoptosis in vascular smooth muscle cells (VSMCs), and the mechanism underlying the antiapoptotic role remains unclear. In this study, CGRP significantly suppressed reactive oxygen species (ROS) and apoptosis in Ang II-induced VSMCs. In VSMCs pre-treated with a CGRP receptor antagonist (CGRP(8-37)), the CGRP-mediated inhibition of Ang II-induced ROS and apoptosis was completely abolished. Moreover, pre-treatment with N-acetyl-L cysteine (NAC), an ROS scavenger, blocked the effects of CGRP on Ang II-induced apoptosis. In addition, the activation of CaMKII and the downstream transcription factor CREB stimulated by Ang II was abrogated by CGRP. Importantly, in both CGRP and NAC-treated VSMCs, CGRP failed to further attenuate CaMKII and CREB activation. The results demonstrate that CGRP attenuated Ang II-induced ROS-dependent apoptosis in VSMCs by inhibiting the CaMKII/CREB signalling pathway. (C) 2019 Elsevier Inc. All rights reserved.
机译:细胞凋亡与各种心血管疾病有关。 CGRP在心血管系统内施加各种影响,并防止血管紧张素(Ang)II诱导的血管功能障碍和重塑的发作和发育。然而,尚不清楚CGRP是否对血管平滑肌细胞(VSMCs)中的Ang II诱导的细胞凋亡有直接影响,并且抗曝气角色依赖的机制仍然不清楚。在该研究中,CGRP在致敏VSMC中显着抑制了活性氧物质(ROS)和细胞凋亡。在用CGRP受体拮抗剂预处理的VSMC中(CGRP(8-37)),CGRP介导的Ang II诱导的ROS和细胞凋亡被完全被废除。另外,用N-乙酰基-1半胱氨酸(NAC),ROS清除剂预处理阻断了CGRP对古偶联凋亡的影响。此外,CACKII的激活和由Ang II刺激的下游转录因子Creb被CGRP消除。重要的是,在CGRP和NAC处理的VSMC中,CGRP未能进一步衰减CAMKII和CREB活化。结果表明,通过抑制Camkii / Creb信号通路,CGRP衰减了VSMC中的ROS依赖性凋亡。 (c)2019 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号