Angiotensin IV protects against angiotensin II-induced cardiac injury via AT4 receptor.

Abstract

Angiotensin II (Ang II) is an important regulator of cardiac function and injury in hypertension. The novel Ang IV peptide/AT4 receptor system has been implicated in several physiological functions and has some effects opposite to those of Ang II. However, little is known about the role of this system in Ang II-induced cardiac injury. Here we studied the effect of Ang IV on Ang II-induced cardiac dysfunction and injury using isolated rat hearts, neonatal cardiomyocytes and cardiac fibroblasts. We found that Ang IV significantly improved Ang II-induced cardiac dysfunction and injury in the isolated heart in response to ischemia/reperfusion (I/R). Moreover, Ang IV inhibited Ang II-induced cardiac cell apoptosis, cardiomyocyte hypertrophy, and proliferation and collagen synthesis of cardiac fibroblasts; these effects were mediated through the AT4 receptor as confirmed by siRNA knockdown. These findings suggest that Ang IV may have a protective effect on Ang II-induced cardiac injury and dysfunction and may be a novel therapeutic target for hypertensive heart disease.

• Authors: Hui Yang, Xiang-Jun Zeng, Hong-Xia Wang, Li-Ke Zhang, Xiao-Li Dong, Shubin Guo, Jie Du, Hui-Hua Li, Chao-Shu Tang
• Journal: Peptides (Peptides) Vol. 32 Issue 10 Pg. 2108-15 (Oct 2011) ISSN: 1873-5169 [Electronic] United States
• PMID: 21963909 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2011 Elsevier Inc. All rights reserved.

Chemical References

• AT4 receptor
• RNA, Small Interfering
• Receptor, Angiotensin, Type 1
• Receptors, Angiotensin
• Angiotensin II
• angiotensin II, des-Asp(1)-des-Arg(2)-Ile(5)-

Topics

• Angiotensin II (analogs & derivatives, metabolism, pharmacology)
• Animals
• Cell Proliferation
• Cells, Cultured
• Fibroblasts (cytology, drug effects, physiology)
• Heart (drug effects)
• Hypertrophy
• Male
• Myocardium (metabolism, pathology)
• Myocytes, Cardiac (cytology, drug effects, physiology)
• RNA, Small Interfering (genetics, metabolism)
• Rats
• Rats, Sprague-Dawley
• Receptor, Angiotensin, Type 1 (genetics, metabolism)
• Receptors, Angiotensin (genetics, metabolism)
• Reperfusion Injury (metabolism, pathology)