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[右旋尼古丁的药效学效应——与左旋尼古丁的比较]

[Pharmacodynamic effects of d-nicotine--Comparison with l-nicotine].

作者信息

Shimada A, Iizuka H, Kawaguchi T, Yanagita T

出版信息

Nihon Yakurigaku Zasshi. 1984 Jul;84(1):1-10.

PMID:6489864
Abstract

The acute toxicity and pharmacological effects of d-nicotine were examined in several species of animals and compared with those of l-nicotine. The LD50s for intravenous administration of d- and l-nicotine were 6.15 and 0.33 mg/kg, respectively. In unanesthetized rhesus monkeys, EEG activity was not influenced by d-nicotine, 64 micrograms/kg, i.v., while the same dose of l-nicotine produced seizure-like waves with some spindles. In rats, d-nicotine increased spontaneous motor activity, and in the experiment under a DRL 20-sec schedule, it increased lever press responding, decreased the number of reinforcements and shortened interresponse time. Similar effects were also observed by administration of l-nicotine at lower doses than for the d-isomer. In anesthetized rats, d-nicotine elevated the blood pressure and increased the heart rate with a potency of about one-eighth that of the l-isomer. Further, tachyphylaxis and cross tachyphylaxis were developed to the blood pressure-raising effect in rats after repeated administration of both isomers. d-Nicotine elicited contraction of isolated rat ileum preparations, but with a potency of about one-tenth that of the l-isomer. Both isomers at the same concentration blocked transmission at the neuromuscular junction in isolated rat phrenic nerve-diaphragm muscle preparations. These results indicate that the pharmacological effects of d-nicotine are qualitatively similar to but quantitatively less potent than those of l-nicotine.

摘要

研究了右旋尼古丁在几种动物中的急性毒性和药理作用,并与左旋尼古丁进行了比较。静脉注射右旋和左旋尼古丁的半数致死量分别为6.15和0.33毫克/千克。在未麻醉的恒河猴中,静脉注射64微克/千克的右旋尼古丁对脑电图活动没有影响,而相同剂量的左旋尼古丁则产生了伴有一些纺锤波的癫痫样波。在大鼠中,右旋尼古丁增加了自发运动活动,在DRL 20秒时间表的实验中,它增加了杠杆按压反应,减少了强化次数并缩短了反应间隔时间。在比右旋异构体更低的剂量下给予左旋尼古丁也观察到了类似的效果。在麻醉的大鼠中,右旋尼古丁升高了血压并增加了心率,其效力约为左旋异构体的八分之一。此外,在两种异构体重复给药后,大鼠对血压升高作用产生了快速耐受性和交叉快速耐受性。右旋尼古丁引起离体大鼠回肠制剂收缩,但其效力约为左旋异构体的十分之一。相同浓度的两种异构体均阻断了离体大鼠膈神经-膈肌制备物中神经肌肉接头处的传递。这些结果表明,右旋尼古丁的药理作用在性质上与左旋尼古丁相似,但在数量上效力较低。

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