Role of nitric oxide in hypoxia inhibition of fever

被引:2
作者
Almeida, MC
Carnio, EC
Branco, LGS [1 ]
机构
[1] Univ Sao Paulo, Fac Odontol Ribeirao Preto, BR-14040904 Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Escola Enfermagem Ribeirao Preto, BR-14040904 Ribeirao Preto, SP, Brazil
关键词
endothelium-derived relaxing factor; temperature; nitric oxide synthase; lipopolysaccharide;
D O I
10.1152/jappl.1999.87.6.2186
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Hypoxia causes a regulated decrease in body temperature (T-b), and nitric oxide (NO) is now known to participate in hypoxia-induced hypothermia. Hypoxia also inhibits Lipopolysaccharide (LPS)-induced fever. We tested the hypothesis that NO may participate in the hypoxia inhibition of fever. The rectal temperature of awake, unrestrained rats was measured before and after injection of LPS, with or without concomitant exposure to hypoxia, in an experimental group treated with N-omega-nitro-L-arginine (L-NNA) for 4 consecutive days before the experiment and in a saline-treated group (control). L-NNA is a nonspecific NO synthase inhibitor that blocks NO production. LPS caused a dose-dependent typical biphasic rise in T-b that was completely prevented by hypoxia (7% inspired oxygen). L-NNA caused a significant drop in T-b during days 2-4 of treatment. When LPS was injected into L-NNA-treated rats, inhibition of fever was observed. Moreover, the effect of hypoxia during fever was significantly reduced. The data indicate that the NO pathway plays a role in hypoxia inhibition of fever.
引用
收藏
页码:2186 / 2190
页数:5
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