Abstract |
We used Na(+)-Ca(2+) exchanger (NCX) knockout mice to evaluate the effects of NCX in cardiac function and the infarct size after ischemia/reperfusion injury. The contractile function in NCX KO mice hearts was significantly better than that in wild type (WT) mice hearts after ischemia/reperfusion and the infarct size was significantly small in NCX KO mice hearts compared with that in WT mice hearts. NCX is critically involved in the development of ischemia/reperfusion-induced myocardial injury and therefore the inhibition of NCX function may contribute to cardioprotection against ischemia/reperfusion injury.
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Authors | Masashi Ohtsuka, Hiroyuki Takano, Masashi Suzuki, Yunzeng Zou, Hiroshi Akazawa, Masaji Tamagawa, Koji Wakimoto, Haruaki Nakaya, Issei Komuro |
Journal | Biochemical and biophysical research communications
(Biochem Biophys Res Commun)
Vol. 314
Issue 3
Pg. 849-53
(Feb 13 2004)
ISSN: 0006-291X [Print] United States |
PMID | 14741714
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Sodium-Calcium Exchanger
- Tetrazolium Salts
- Calcium
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Topics |
- Animals
- Calcium
(chemistry, metabolism)
- Disease Models, Animal
- Heart
(physiopathology)
- Hemodynamics
(physiology)
- Heterozygote
- Male
- Mice
- Mice, Knockout
- Myocardial Infarction
(metabolism)
- Myocardial Ischemia
(metabolism)
- Myocardial Reperfusion Injury
(metabolism, physiopathology)
- Myocardium
(metabolism, pathology)
- Myocytes, Cardiac
(physiology)
- Sodium-Calcium Exchanger
(genetics, metabolism, physiology)
- Staining and Labeling
(methods)
- Tetrazolium Salts
(chemistry)
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