Involvement of neuronal nitric oxide synthase in restraint stress-induced fever in rats

被引:16
作者
Sanches, DB
Steiner, AA
Branco, LGS
机构
[1] Univ Sao Paulo, Dent Sch Ribeirao Preto, Dept Morphol Estomatol & Physiol, BR-14040904 Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Physiol, BR-14040904 Ribeirao Preto, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
body temperature; nitric oxide; aminoguanidine; 7-nitroindazole; thermoregulation; psychological stress; hyperthermia; fever;
D O I
10.1016/S0031-9384(01)00657-6
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Nitric oxide (NO) has been shown to be an important modulator of the febrile response to pyrogens and to psychological stress. In the present study, we aimed to identify the nitric oxide synthase (NOS) isoform (neuronal or inducible, nNOS and iNOS, respectively) involved in restraint stress fever. Colonic temperature (Tc) was measured in unanesthetized rats before and after treatment with the more selective nNOS inhibitor 7-nitroindazole or with the selective iNOS inhibitor aminoguanidine (AG) under unrestrained or restrained conditions, Intraperitoneal injection of AG (25 or 50 mg/kg) did not affect restraint fever, indicating that iNOS is unlikely to be involved in restraint fever. On the other hand, intraperitoneal injection of 7-nitroindazole (25 mg/kg) significantly attenuated the rise in the Tc caused by restraint stress, whereas it caused no change in Tc of euthermic animals. These data show that NO produced by nNOS plays an important role in the genesis of restraint stress-induced fever. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:261 / 266
页数:6
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