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L-刀豆氨酸抑制一氧化氮生成可减轻内毒素诱导的大鼠血管低反应性。

Inhibition of nitric oxide formation with L-canavanine attenuates endotoxin-induced vascular hyporeactivity in the rat.

作者信息

Cai M, Sakamoto A, Ogawa R

机构信息

Department of Anaesthesiology, Nippon Medical School, Tokyo, Japan.

出版信息

Eur J Pharmacol. 1996 Jan 11;295(2-3):215-20. doi: 10.1016/0014-2999(95)00593-5.

Abstract

L-Canavanine, a selective inhibitor of inducible nitric oxide (NO) synthase, has beneficial effects on the circulatory failure of rats with endotoxin shock. To investigate the direct relationship between these beneficial effects and the inhibition of the formation of NO in response to L-canavanine in endotoxin shock in the rat, we detected changes in venous nitrosyl-hemoglobin (NO-hemoglobin) levels using an electron spin resonance (ESR) assay. Anaesthetized rats were injected with lipopolysaccharide (10 mg/kg i.v.). 1 h after the lipopolysaccharide injection, the rats were divided into four groups: a lipopolysaccharide group receiving 0.3 ml of saline hourly, an L-canavanine 10 or an L-canavanine 20 group receiving L-canavanine 10 or 20 mg/kg i.v. hourly, respectively, and an L-NAME group receiving NG-nitro-L-arginine methyl ester (L-NAME) 15 mg/kg followed by 10 mg/kg i.v. hourly. A sham group received saline instead of lipopolysaccharide, and an L-canavanine group received L-canavanine 20 mg/kg i.v. hourly, 1 h after the saline injection. At 5 h after the lipopolysaccharide or saline injection, pressor responses to noradrenaline (1 microgram/kg i.v.) were obtained. In the lipopolysaccharide group, lipopolysaccharide caused a progressive decrease in mean arterial pressure and an impairment of pressor responsiveness to noradrenaline. Administration of L-canavanine or L-NAME attenuated the endotoxin-induced hypotension and vascular hyporeactivity to noradrenaline. L-Canavanine did not alter mean arterial pressure and the pressor response to noradrenaline in the L-canavanine group. The endotoxin-induced increases in venous levels of NO-hemoglobin were significantly inhibited by L-canavanine or L-NAME. These data indicate that the beneficial hemodynamic effects of L-canavanine are associated with inhibition of the enhanced formation of NO by inducible NO synthase in a rat model of endotoxin shock. L-Canavanine is a potential agent in the treatment of endotoxin shock.

摘要

L-刀豆氨酸是一种诱导型一氧化氮合酶的选择性抑制剂,对患有内毒素休克的大鼠的循环衰竭具有有益作用。为了研究这些有益作用与L-刀豆氨酸抑制大鼠内毒素休克中一氧化氮形成之间的直接关系,我们使用电子自旋共振(ESR)测定法检测了静脉亚硝基血红蛋白(NO-血红蛋白)水平的变化。将麻醉的大鼠静脉注射脂多糖(10 mg/kg)。脂多糖注射后1小时,将大鼠分为四组:每小时接受0.3 ml生理盐水的脂多糖组,分别每小时静脉注射10或20 mg/kg L-刀豆氨酸的L-刀豆氨酸10或L-刀豆氨酸20组,以及接受15 mg/kg NG-硝基-L-精氨酸甲酯(L-NAME)然后每小时静脉注射10 mg/kg的L-NAME组。假手术组接受生理盐水代替脂多糖,L-刀豆氨酸组在注射生理盐水后1小时每小时静脉注射20 mg/kg L-刀豆氨酸。在脂多糖或生理盐水注射后5小时,获得对去甲肾上腺素(1微克/千克静脉注射)的升压反应。在脂多糖组中,脂多糖导致平均动脉压逐渐降低以及对去甲肾上腺素的升压反应性受损。给予L-刀豆氨酸或L-NAME可减轻内毒素诱导的低血压和对去甲肾上腺素的血管反应性降低。L-刀豆氨酸在L-刀豆氨酸组中未改变平均动脉压和对去甲肾上腺素的升压反应。L-刀豆氨酸或L-NAME可显著抑制内毒素诱导的静脉NO-血红蛋白水平升高。这些数据表明,在大鼠内毒素休克模型中,L-刀豆氨酸的有益血流动力学作用与抑制诱导型一氧化氮合酶增强的一氧化氮形成有关。L-刀豆氨酸是治疗内毒素休克的潜在药物。

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