Increase of peroxynitrite production in the rat brain following transient forebrain ischemia.
- Author:
Hee Joon KIM
1
;
Seong Yun KIM
Author Information
1. Department of Pharmacology, College of Medicine, Catholic University of Korea, Seoul, South Korea. syk@cmc.cuk.ac.kr
- Publication Type:Original Article
- MeSH:
Animals;
Brain*;
Cell Death;
Ischemia*;
Neurons;
Nitric Oxide;
Oxygen;
Peroxynitrous Acid*;
Prosencephalon*;
Rats*;
Reperfusion;
Septal Nuclei;
Superoxides;
Viola
- From:The Korean Journal of Physiology and Pharmacology
2001;5(3):205-212
- CountryRepublic of Korea
- Language:English
-
Abstract:
It has been proposed that nitric oxide is involved in the pathogenesis of cerebral ischemia-reperfusion. Because superoxide production is also enhanced during reperfusion, the cytotoxic oxidant peroxynitrite could be formed, but it is not known if this occurs following global forebrain ischemia-reperfusion. We examined whether peroxynitrite generation is increased in the vulnerable regions after forebrain ischemia-reperfusion. Transient forebrain ischemia was produced in the conscious rat by four-vessel occlusion. Rats were subjected to 10 or 15 min of forebrain ischemia. Immunohistochemical method was used to detect 3-nitrotyrosine, a marker of peroxynitrite production. 3-Nitrotyrosine immunoreactivity was enhanced in the hippocampal CA1 area 3 days after reperfusion. Furthermore, in rats subjected to ischemia for 15 min, this change was also observed in the lateral striatal region and the lateral septal nucleus 2apprx3 days after reperfusion. The cresyl violet staining of adjacent sections showed that neuronal cell death was induced in parallel with the nitrotyrosine immunoreactivity in the hippocampal CA1 area and the lateral striatal region. Our findings suggest that oxygen free radical accumulation and consequent peroxynitrite production play a role in neuronal death caused by cerebral ischemia-reperfusion.
