L-Carnitine suppresses oleic acid-induced membrane permeability transition of mitochondria

被引:22
|
作者
Oyanagi, Eri [2 ]
Yano, Hiromi [1 ]
Kato, Yasuko [3 ]
Fujita, Hirofumi [2 ]
Utsumi, Kozo [2 ]
Sasaki, Junzo [2 ]
机构
[1] Kawasaki Univ Med Welfare, Dept Hlth & Sport Sci, Kurashiki, Okayama 7010193, Japan
[2] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Cytol & Histol, Okayama, Japan
[3] Kawasaki Med Sch Welfare, Dept Clin Nutr, Kurashiki, Okayama, Japan
关键词
ATP; CoA; beta-oxidation; fatty acid; cytochrome c; apoptosis; rat liver;
D O I
10.1002/cbf.1506
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Membrane permeability transition (MPT) of mitochondria has an important role in apoptosis of various cells. The classic type of MPT is characterized by increased Ca2+ transport, membrane depolarization, swelling, and sensitivity to cyclosporin A. In this study, we investigated whether L-carnitine suppresses oleic acid-induced MPT using isolated mitochondria from rat liver. Oleic acid-induced MPT in isolated mitochondria, inhibited endogenous respiration, caused membrane depolarization, and increased large amplitude swelling, and cytochrome c (Cyt. c) release from mitochondria. L-Carnitine was indispensable to beta-oxidation of oleic acid in the mitochondria, and this reaction required ATP and coenzyme A (CoA). In the presence of ATP and CoA, L-carnitine stimulated oleic acid oxidation and suppressed the oleic acid-induced depolarization, swelling, and Cyt. c release. L-Carnitine also contributed to maintaining mitochondrial function, which was decreased by the generation of free fatty acids with the passage of time after isolation. These results suggest that L-carnitine acts to maintain mitochondrial function and suppresses oleic acid-mediated MPT through acceleration of beta-oxidation. Copyright (c) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:778 / 786
页数:9
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