کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2536110 | 1559141 | 2007 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Early and sharp nitric oxide production and anoxic depolarization in the rat hippocampus during transient forebrain ischemia
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کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب سلولی و مولکولی
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چکیده انگلیسی
This study was designed to characterize nitric oxide (NO) production and anoxic depolarization in the rat hippocampus during transient forebrain ischemia using two NO synthase (NOS) inhibitors, l-N5-(1-iminoethyl)ornithine (l-NIO), a relatively selective endothelial NOS (eNOS) inhibitor, and 7-nitroindazole, a relatively selective neuronal NOS (nNOS) inhibitor, and an NO scavenger, [2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide] (carboxy-PTIO). We measured the mean arterial blood pressure, hippocampal blood flow, NO concentration and direct current potential before, during and after transient forebrain ischemia, which was induced by 4-vessel occlusion for 10Â min. Saline, l-NIO (20Â mg/kg), 7-nitroindazole (25Â mg/kg), l-NIO (20Â mg/kg)Â +Â 7-nitroindazole (25Â mg/kg) or carboxy-PTIO (1Â mg/kg) was administered intraperitoneally 20Â min before the onset of ischemia. We observed early and sharp NO production in the hippocampus during ischemia in the saline group. This NO increase during ischemia was significantly reduced by l-NIO (20Â mg/kg)Â +Â 7-nitroindazole (25Â mg/kg) or carboxy-PTIO (1Â mg/kg), but not l-NIO (20Â mg/kg) or 7-nitroindazole (25Â mg/kg). On the other hand, NO production after ischemia was significantly reduced by 7-nitroindazole (25Â mg/kg), l-NIO (20Â mg/kg)Â +Â 7-nitroindazole (25Â mg/kg) or carboxy-PTIO (1Â mg/kg), but not l-NIO (20Â mg/kg). The peak latency of NO production during ischemia always preceded the onset latency of anoxic depolarization in both the saline group and the carboxy-PTIO group. In the carboxy-PTIO group, the onset latency of anoxic depolarization was significantly longer than that in the saline group. Moreover, carboxy-PTIO significantly reduced the anoxic depolarization amplitude, compared with that of the saline group. These results suggest that both NOS-dependent and-independent NO formation contributes to early and sharp NO production during ischemia, and that this NO increase is, at least in part, related to the triggering of anoxic depolarization.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Pharmacology - Volume 567, Issues 1â2, 12 July 2007, Pages 83-88
Journal: European Journal of Pharmacology - Volume 567, Issues 1â2, 12 July 2007, Pages 83-88
نویسندگان
Min Hai Jiang, Junichi Hada,