Abstract | AIMS: Our previous studies have shown that myocardial ischemia-reperfusion (I/R) injury is related closely with early growth response (Egr)-1 overexpression. The present study is to confirm thoroughly the effects of Egr-1 on the occurrance and development of myocardial I/R injury. METHODS: RESULTS: In vivo, Egr-1 AS-ODN significantly attenuated injury and inflammation of myocardial tissues caused by I/R evidenced by the amelioration of hemodynamics and the reduction in MPO activity. In vitro, Egr-1 AS-ODN significantly relieved injury and inflammation of cultured cardiomyocyte caused by H/R evidenced by the improvement in morphology, structure and beat as well as the decrease in leakage of cTnI and release of TNF-alpha from cultured cardiomyocyte. CONCLUSIONS: These data suggest that Egr-1 plays a vital role in the pathogenesis of myocardial I/R injury and Egr-1 AS-ODN could protect the myocardium from I/R injury.
|
Authors | Yanmei Zhang, Ganggang Shi, Jinhong Zheng, Yanqiu Lv, Ping Gao, Zhanqin Huang, Fenfei Gao, Yanqiong Zhou |
Journal | Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
(Cell Physiol Biochem)
Vol. 22
Issue 5-6
Pg. 645-52
( 2008)
ISSN: 1421-9778 [Electronic] Germany |
PMID | 19088446
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | Copyright 2008 S. Karger AG, Basel. |
Chemical References |
- Culture Media
- Early Growth Response Protein 1
- Egr1 protein, rat
- Oligodeoxyribonucleotides, Antisense
- Protective Agents
- Troponin I
- Tumor Necrosis Factor-alpha
- Peroxidase
- Oxygen
|
Topics |
- Animals
- Cell Hypoxia
(drug effects)
- Cell Shape
(drug effects)
- Cell Survival
(drug effects)
- Cells, Cultured
- Culture Media
- Early Growth Response Protein 1
(metabolism)
- Hemodynamics
(drug effects)
- Male
- Myocardial Reperfusion Injury
(physiopathology, prevention & control)
- Myocardium
(enzymology, pathology)
- Myocytes, Cardiac
(drug effects, pathology)
- Oligodeoxyribonucleotides, Antisense
(metabolism, pharmacology)
- Oxygen
(pharmacology)
- Peroxidase
(metabolism)
- Protective Agents
(pharmacology)
- Rats
- Rats, Sprague-Dawley
- Subcellular Fractions
(metabolism)
- Troponin I
(metabolism)
- Tumor Necrosis Factor-alpha
(metabolism)
|