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一种在豚鼠回肠中快速产生阿片类药物耐受性的方法。

A method for the rapid development of opiate tolerance in the guinea pig ileum.

作者信息

Rezvani A, Huidobro-Toro J P, Way E L

出版信息

Life Sci. 1982;31(20-21):2367-70. doi: 10.1016/0024-3205(82)90158-8.

Abstract

The rate and degree of in vitro tolerance development to morphine, normorphine and d,1-methadone were assessed on the excised guinea pig ileum. Agonists in fixed concentrations at 1/4, 1/2, 1 and 2 x IC50 were incubated with the tissue for 1, 2 or 4 hours. The degree of tolerance development was expressed as a ratio of the IC50 after and before incubation. A high degree of tolerance developed to all three agonists and the effect could be prevented by co-incubation with naloxone. Tolerance development was stereo-specific; levorphanol and 1-methadone developed much higher degrees of tolerance than their respective d-isomers. Furthermore, under the same conditions, subsensitivity to acetylcholine, norepinephrine, and adenosine monophosphate did not develop. The in vitro tolerance was accompanied by physical dependence development as evidenced by the fact that naloxone elicited muscular contracture in the tolerant ileum. cAMP enhanced the development of tolerance to normorphine and cycloheximide could reduce this phenomenon. It is concluded that the procedure may facilitate studies on the mechanisms involved in the development of opiate tolerance and physical dependence.

摘要

在离体豚鼠回肠上评估了对吗啡、去甲吗啡和消旋美沙酮的体外耐受性发展速率和程度。将固定浓度为1/4、1/2、1和2×IC50的激动剂与组织孵育1、2或4小时。耐受性发展程度以孵育前后IC50的比值表示。对所有三种激动剂都产生了高度耐受性,并且这种效应可通过与纳洛酮共同孵育来预防。耐受性发展具有立体特异性;左啡诺和L-美沙酮产生的耐受性程度比它们各自的右旋异构体高得多。此外,在相同条件下,对乙酰胆碱、去甲肾上腺素和单磷酸腺苷未产生敏感性降低。体外耐受性伴随着身体依赖性的发展,这一事实表明纳洛酮在耐受性回肠中引发了肌肉挛缩。环磷酸腺苷增强了对去甲吗啡的耐受性发展,环己酰亚胺可减少这种现象。得出的结论是,该程序可能有助于研究阿片类药物耐受性和身体依赖性发展所涉及的机制。

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