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首页> 外文期刊>Japanese Journal of Pharmacology >The role of nitrergic system in lidocaine-induced convulsion in the mouse.
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The role of nitrergic system in lidocaine-induced convulsion in the mouse.

机译:硝化系统在利多卡因诱发的小鼠惊厥中的作用。

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摘要

The effects of N-nitro-L-arginine-methyl ester (L-NAME) a nitric oxide (NO) synthase inhibitor and L-arginine, a NO precursor, were investigated on lidocaine-induced convulsions. In the first experiment, four groups of mice received physiological saline (0.9%), L-arginine (300 mg/kg, i.p.), L-NAME (100 mg/kg, i.p.) and diazepam (2 mg/kg), respectively. Thirty minutes after these injections, all mice received lidocaine (50 mg/kg, i.p.). In the second experiment, four groups of mice received similar treatment in the first experiment, and 30 min after these injections, all mice received a higher dose of lidocaine (80 mg/kg). L-NAME (100 mg/kg, i.p.) and diazepam (2 mg/kg) significantly decreased the incidence of lidocaine (50 mg/kg)-induced convulsions. In contrast, the L-arginine treatment increased the incidence of lidocaine (80 mg/kg, i.p.)-induced convulsions significantly. These results may suggest that NO is a proconvulsant mediator in lidocaine-induced convulsions.
机译:研究了N-硝基-L-精氨酸甲酯(L-NAME),一氧化氮(NO)合酶抑制剂和L-精氨酸(NO前体)对利多卡因引起的惊厥的影响。在第一个实验中,四组小鼠分别接受生理盐水(0.9%),L-精氨酸(300 mg / kg,ip),L-NAME(100 mg / kg,ip)和地西epa(2 mg / kg) 。注射后三十分钟,所有小鼠均接受利多卡因(50 mg / kg,腹腔注射)。在第二个实验中,四组小鼠在第一个实验中接受了相似的治疗,这些注射后30分钟,所有小鼠均接受了更高剂量的利多卡因(80 mg / kg)。 L-NAME(100 mg / kg,腹膜内)和地西epa(2 mg / kg)显着降低利多卡因(50 mg / kg)引起的惊厥的发生率。相反,L-精氨酸治疗显着增加了利多卡因(80mg / kg,腹膜内)引起的惊厥的发生。这些结果可能表明NO是利多卡因诱发的惊厥的前惊厥介质。

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