期刊
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
卷 1757, 期 5-6, 页码 562-566出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbabio.2006.02.014
关键词
mitochondria; reactive oxygen species; nitric oxide
We found that reversible inactivation of mitochondrial complex I by S-nitroso-N-acetyl-D,L-penicillamine (SNAP) in isolated rat heart mitochondria resulted in a three-fold increase in H2O2 production, when mitochondria were respiring on pyruvate and malate, (but not when respiring on succinate or in the absence of added respiratory substrate). The inactivation of complex I and the increased H2O2 production were present in mitochondria, washed free of SNAP or NO, but were partially reversed by light or dithiothreitol, treatments known to reverse Snitrosation. Specific inhibition of complex I with rotenone increased H2O2 production to a similar extent as that caused by SNAP. The results suggest that S-nitrosation of complex I can reversibly increase oxidant production by mitochondria, which is potentially important in cell signalling and/or pathology. (c) 2006 Elsevier B.V. All rights reserved.
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