Mitochondrial NOS upregulation during renal I/R causes apoptosis in a peroxynitrite-dependent manner
Author(s) -
Jose L. Viñas,
Anna Solà,
Georgina Hotter
Publication year - 2006
Publication title -
kidney international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.499
H-Index - 276
eISSN - 1523-1755
pISSN - 0085-2538
DOI - 10.1038/sj.ki.5000361
Subject(s) - peroxynitrite , downregulation and upregulation , nitric oxide , apoptosis , nitric oxide synthase , mitochondrion , microbiology and biotechnology , kidney , cytochrome c , chemistry , hypoxia (environmental) , renal ischemia , biology , ischemia , reperfusion injury , superoxide , medicine , biochemistry , endocrinology , oxygen , enzyme , gene , organic chemistry
In the last decade, various groups have found evidence of nitric oxide production by mitochondrial nitric oxide synthase (mNOS) in a range of experimental models. However, little is known about the role of mNOS in renal ischemia-reperfusion (I/R) injury and its possible involvement in the apoptotic pathway. We analyzed the role of mNOS in apoptosis promotion in rat kidney I/R and its direct implication through experiments in which isolated kidney mitochondria were subjected to hypoxia/reoxygenation. Results showed that neuronal NOS located in the inner mitochondrial membrane is upregulated during renal I/R and that this upregulation, together with the increase in nitric oxide production, is involved in the generation of intramitochondrial peroxynitrite, which in turn leads to cytochrome c release and apoptosis induction in renal I/R.
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