Resveratrol restored the structural and functional association between M3 receptor and connexin 43 gap junction proteins in ischemia-reperfusion injury of isolated rat heart.
- Author:
Jing XIAO
1
;
Peng YUE
;
Ying WANG
;
Yong ZHANG
;
Rong HUO
;
Ning WANG
;
Dao-Hong LIN
;
Yan-Jie LÜ
;
Bao-Feng YANG
Author Information
1. Department of Pharmacology, Bio-pharmaceutical Key Laboratory of Heilongjiang Province-Incubator of State Key Laboratory, Harbin Medical University, Harbin 150086, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Connexin 43;
metabolism;
Electrocardiography;
Heart;
drug effects;
physiopathology;
In Vitro Techniques;
Male;
Malondialdehyde;
metabolism;
Myocardial Reperfusion Injury;
metabolism;
physiopathology;
Myocardium;
metabolism;
Phosphorylation;
drug effects;
Protective Agents;
pharmacology;
Random Allocation;
Rats;
Rats, Wistar;
Receptor, Muscarinic M3;
metabolism;
Stilbenes;
pharmacology;
Superoxide Dismutase;
metabolism
- From:
Acta Pharmaceutica Sinica
2007;42(1):19-25
- CountryChina
- Language:Chinese
-
Abstract:
This study is to explore whether the protective effect of resveratrol on ischemia-reperfusion injury is correlated with the structural and functional association between M3 receptor (M3 subtype of muscarinic acetylcholine receptor) and Cx43 (connexin 43 gap junction proteins). Immunoprecipitation, immunoblotting and immunofluorescence were applied to investigate whether resveratrol has an effect on structural and functional association between M3 and Cx43. The effect of resveratrol on electrocardiogram Lead II ex vivo in rats, SOD (superoxide dismutase) activity and MDA (malondialdehyde) content was also observed in order to evaluate the protective effect of resveratrol on ischemia-reperfusion injury. Resveratrol could restore the structural and functional association between M3 receptor and Cx43 gap junction proteins that was partially destroyed under ischemia-reperfusion injury. The phosphorylation and spatial distribution disturbances in Cx43 expression caused by ischemia-reperfusion injury were also restored. Also, the QRS duration, SOD activity and MDA content were restored. Resveratrol could restore the structural and functional association between M3 receptor and Cx43 gap junction proteins.
