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7-Nitroindazole reduces nitric oxide concentration in rat hippocampus after transient forebrain ischemia.
- Source :
-
European journal of pharmacology [Eur J Pharmacol] 1999 Sep 10; Vol. 380 (2-3), pp. 117-21. - Publication Year :
- 1999
-
Abstract
- We investigated the effects of 7-nitroindazole, a specific inhibitor of neuronal nitric oxide (NO) synthase, on NO concentration and on blood flow in rat hippocampus after transient forebrain ischemia which was induced by 4-vessel occlusion for 10 min. NO concentration was measured directly by an NO-selective electrode method. Hippocampal blood flow was also estimated by laser Doppler flowmetry. 7-Nitroindazole [0 (vehicle), 12.5, 25, 50 or 100 mg/kg] was administered intraperitoneally 20 min before ischemia. 7-Nitroindazole at any dose used did not affect basal NO levels before ischemia. 7-Nitroindazole (25, 50 and 100 mg/kg) reduced the NO concentration significantly during post-ischemic early reperfusion. Before 10 min of ischemia and during post-ischemic early reperfusion, there were no significant differences in hippocampal basal blood flow and reactive hyperemia between vehicle- and 7-nitroindazole-treated groups. These results demonstrate that the neuronal NO synthase inhibitor, 7-nitroindazole, can effectively inhibit NO synthesis in rat hippocampus during post-ischemic early reperfusion.
- Subjects :
- Animals
Hippocampus blood supply
Hippocampus metabolism
Hyperemia chemically induced
Hyperemia prevention & control
Male
Prosencephalon physiopathology
Rats
Rats, Wistar
Regional Blood Flow drug effects
Reperfusion Injury prevention & control
Enzyme Inhibitors pharmacology
Hippocampus drug effects
Indazoles pharmacology
Ischemic Attack, Transient physiopathology
Nitric Oxide metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0014-2999
- Volume :
- 380
- Issue :
- 2-3
- Database :
- MEDLINE
- Journal :
- European journal of pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 10513570
- Full Text :
- https://doi.org/10.1016/s0014-2999(99)00555-5