TRPV1 and TRPV4 channels: Potential therapeutic targets for ischemic conditioning-induced cardioprotection

被引:39
|
作者
Randhawa, Puneet Kaur [1 ]
Jaggi, Amteshwar Singh [1 ]
机构
[1] Punjabi Univ, Dept Pharmaceut Sci & Drug Res, Patiala 147002, Punjab, India
关键词
Cardioprotection; TRPV1; TRPV4; CGRP Substance P; ALOX; GENE-RELATED PEPTIDE; TRPV4-DEPENDENT CALCIUM INFLUX; VANILLOID; REPERFUSION INJURY; ISCHEMIA/REPERFUSION INJURY; PRECONDITIONING PROTECTS; INDUCED ACTIVATION; MYOCARDIAL INJURY; EXPRESSION; CAPSAICIN;
D O I
10.1016/j.ejphar.2014.11.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Besides the involvement of TRPV channels in exhibiting various cellular functions including thermoregulation, pain perception, maintenance of bone homeostasis and gastrointestinal function; certain studies have also implicated the putative role of these channels in mediating ischemic conditioning induced cardioprotection. The potential role of TRPVI channels in different forms of ischemic conditioning (pre/post/remote)-induced cardioprotection has been described by employing TRPVI knockout mice and various pharmacological modulators. The cardioprotective effects of TRPV1 activation during ischemic conditioning have been linked with increased CGRP, substance P release and augmented ALOX expression. Furthermore, the role of TRPV4 channels in mediating preconditioning-induced preservation of vascular function in terms restoring NO- and further improving EDH(F)-mediated endothelial relaxation has been described. The present review discusses the putative role of TRPV1 and TRPV4 channels in mediating different forms of conditioning (pre/post/remote)-induced carchoprotection along with the possible mechanisms. Future perspectives have also been described to fully understand the cascade of signaling and contribution of TRPV channel activation during myocardial ischemic conditioning. (C) 2014 Elsevier B.V. All rights reserved
引用
收藏
页码:180 / 185
页数:6
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