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Biochemistry (Mosc). 2012 Jun;77(6):671-8. doi: 10.1134/S0006297912060156.

Cerebral ischemia-reperfusion induces GAPDH S-nitrosylation and nuclear translocation.

Author information

1
Jiangsu Province Key Laboratory of Brain Disease Bioinformation and Research Center of Biochemistry and Molecular Biology, Xuzhou Medical College, Xuzhou 221002, Jiangsu, China.

Abstract

Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a glycolytic enzyme, plays an important role in glycolysis. It was reported that GAPDH undergoes S-nitrosylation, which facilitated its binding to Siah1 and resulted in nuclear translocation and cell apoptosis. The results of this study show that GAPDH S-nitrosylation, Siah1 binding, translocation to nucleus, and concomitant neuron death occur during the early stages of reperfusion in the rat four-vessel occlusion ischemic model. N-Methyl-D-aspartate receptor antagonist MK801, neuronal nitric oxide synthase inhibitor 7-nitroindazole, or monoamine oxidase-B inhibitor (R)-(-)-deprenyl hydrochloride could inhibit GAPDH S-nitrosylation and translocation and exert neuroprotective effects.

PMID:
22817468
DOI:
10.1134/S0006297912060156
[Indexed for MEDLINE]
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