Production of Superoxide Anion and Damage of Mitochondria Isolated from Ischemic Repertused Heart.
10.4070/kcj.1991.21.6.1137
- Author:
Chong Yun RIM
;
Young LEE
;
Yun Song LEE
;
Myung Suk KIM
- Publication Type:Original Article
- Keywords:
Superoxide anion;
Mitochondria;
Reperfused myocardium
- MeSH:
Free Radicals;
Glutathione Peroxidase;
Heart*;
Mitochondria*;
Myocardial Reperfusion;
Neutrophils;
Oxidative Stress;
Oxygen;
Phosphorylation;
Respiration;
Superoxide Dismutase;
Superoxides*;
Xanthine Oxidase
- From:Korean Circulation Journal
1991;21(6):1137-1151
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Oxygen free radicals have been implicated as a cause of deleterious effects in the setting of coronary reperfusion, and they are believed to be generated by the xanthine oxidase system, from activated neutrophiles and from mitochondria. We evaluate the contribution of mitochondria to the production of oxygen free radicals and clarify the mechanism of cellular damage in ischemic reperfused hearts. METHODS: Mitochondria isolated from the ischemic rabbit hearts were incubated in the reaction conditions with different oxygen tensions. Generation of superoxide anion and activities of defensive enzymes aginst oxidative stress were mesured. RESULTS: Superoxide anion genertion by mitochondria incubated in 21% oxygen condition were 0.54+/-0.09 and 0.27+/-0.04(O2./min/mg protein) in ischemic mitochondria and in control respectively(P<0.05). Activites of defensive enzymes against oxidative stress, superoxide dismutase and glutathione peroxidase, were significantly reduced in mitochondria isolated from either ischemic or reperfused hearts. With the lapse of respiration in 21% oxygen condition, ADP-stimulated state 3 oxygen consumption(306.4+/-31.5 vs 214.4+/-11.4n atoms O/min/mg protein) at 30 minutes, P : O ratio and phosphorylation rate were significantly decreased in ischemic mitochondria. CONCLUSION: Elevation of oxygen free radical generation as well as the reduction of defensive enzyme activities in ischemic reperfused mitochondria are injurious to mitochondrial respiratory function. It may contribute to the mechanism of cellular damage in ischemic reperfused hearts.
