Sloan J W, Martin W R, Bostwick M
Department of Pharmacology, University of Kentucky, Lexington 40536.
Pharmacol Biochem Behav. 1989 Nov;34(3):559-64. doi: 10.1016/0091-3057(89)90558-3.
In the urethane-pentobarbital anesthetized rat, the respiratory depressant and lethal effects of intravenously infused (-)-nicotine (120 micrograms/kg/min) or (+)-nicotine (600 micrograms/kg/min) were effectively prevented by pretreatment with the opioid antagonist, naltrexone, whereas the lethal effect of (-)-nicotine (120 micrograms/kg/min) was not altered by bilateral adrenalectomy. Further, pretreatment with either the nicotinic ganglion-blocker, mecamylamine, a secondary amine, or the quarternary nicotinic ganglion-blocker, hexamethonium, completely prevented the lethal effects of (-)-nicotine (120 micrograms/kg/min). These data suggest that central opioidergic and nicotinic processes are involved in nicotine's respiratory depressant and lethal effects.
在氨基甲酸乙酯-戊巴比妥麻醉的大鼠中,阿片类拮抗剂纳曲酮预处理可有效预防静脉输注(-)-尼古丁(120微克/千克/分钟)或(+)-尼古丁(600微克/千克/分钟)的呼吸抑制和致死作用,而双侧肾上腺切除并未改变(-)-尼古丁(120微克/千克/分钟)的致死作用。此外,用烟碱型神经节阻滞剂美加明(一种仲胺)或季铵型烟碱型神经节阻滞剂六甲铵预处理,可完全预防(-)-尼古丁(120微克/千克/分钟)的致死作用。这些数据表明,中枢阿片能和烟碱能过程参与了尼古丁的呼吸抑制和致死作用。