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L-色氨酸对吗啡镇痛、耐受性及身体依赖性的影响。

Influence of L-tryptophan on morphine analgesia, tolerance and physical dependence.

作者信息

Ho I K, Brase D A, Loh H H, Way E L

出版信息

J Pharmacol Exp Ther. 1975 Apr;193(1):35-43.

PMID:124349
Abstract

Four hours after the acute administration of L-tryptophan (75 mg/kg) to either, nontolerant or morphine-tolerant mice, the antinociceptive effect of morphine was partially and significantly antagonized. Daily tryptophan administration to rats and mice during a 3-day morphine pellet implantation period increased the rates of both morphine tolerance development and development of physical dependence. The accelerating effect of tryptophan on tolerance and dependence development in mice was antagonized by pretreatment with the tryptophan hydroxylase inhibitor, p-chlorophenylalanine. Acute tryptophan administration (75 mg/kg) significantly increased mouse brain 5-hydroxytryptamine levels for at least 4 hours. Although chronic tryptophan treatment increased 5-hydroxytryptamine turnover in morphine-treated mice, no effect of chronic morphine or tryptophan treatment on the particulate tryptophan hydroxylase activity of whole mouse brain was observed. Slight increases in tryptophan hydroxylase activity were observed in the caudate-putamen and septal areas of rat brain 3 and 6 days, respectively, after s.c. morphine pellet implantation. These and previous studies from our laboratory indicate that the development of morphine tolerance and dependence can be modified by agents affecting serotonergic mechanisms.

摘要

在向未耐受或吗啡耐受的小鼠急性给予L-色氨酸(75毫克/千克)4小时后,吗啡的镇痛作用受到部分且显著的拮抗。在为期3天的吗啡植入丸剂期间,每日向大鼠和小鼠给予色氨酸会增加吗啡耐受性发展和身体依赖性发展的速率。色氨酸对小鼠耐受性和依赖性发展的加速作用可被色氨酸羟化酶抑制剂对氯苯丙氨酸预处理所拮抗。急性给予色氨酸(75毫克/千克)可使小鼠脑内5-羟色胺水平显著升高至少4小时。虽然慢性色氨酸治疗可增加吗啡处理小鼠的5-羟色胺周转率,但未观察到慢性吗啡或色氨酸治疗对全小鼠脑微粒体色氨酸羟化酶活性有影响。皮下植入吗啡丸剂后,分别在大鼠脑的尾状核-壳核和隔区观察到色氨酸羟化酶活性在第3天和第6天略有增加。我们实验室的这些研究以及之前的研究表明,影响5-羟色胺能机制的药物可改变吗啡耐受性和依赖性的发展。

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