Suppr超能文献

正常和经吗啡预处理的豚鼠回肠制剂中的阿片类药物结合及作用

Opiate binding and effect in ileum preparations from normal and morphine pretreated guinea-pigs.

作者信息

Cox B M, Padhya R

出版信息

Br J Pharmacol. 1977 Oct;61(2):271-8. doi: 10.1111/j.1476-5381.1977.tb08415.x.

Abstract

1 Dose-response curves for normorphine in the absence and presence of naloxone have been obtained from myenteric plexus-longitudinal muscle strip preparations from normal and morphine pretreated guinea-pigs. In addition, the high affinity stereospecific binding of [3H]-etorphine has been measured in homogenates of the same tissue. 2 Higher concentrations of normorphine were required to produce 50% inhibition of the electrically stimulated contractions of strip preparations from morphine pretreated animals. There was also an increase in the slope of linearized dose-response curves in opiate-tolerant preparations. Maximum opiate effect was unchanged, and responses to exogenous acetylcholine were not affected by the pretreatment. 3 There was a slight increase in the apparent equilibrium constant for naloxone after morphine pretreatment. 4 Tolerance to opiate effect was not accompanied by a change in the affinity or number of stereospecific binding sites for [3H]-etorphine. Hill plots of [3H]-etorphine binding in both control and morphine pretreated preparations gave slopes close to unity. 5 Most of these results can be explained by the assumption that in tolerant preparations, a certain fractional opiate receptor occupation threshold must be exceeded before opiate effects become apparent. It is suggested that the tissue adapts toward a threshold equivalent to the mean receptor occupancy attained during the period of opiate drug pretreatment.

摘要
  1. 已从正常和经吗啡预处理的豚鼠的肠肌丛-纵肌条制备物中获得了在不存在和存在纳洛酮的情况下,去甲吗啡的剂量-反应曲线。此外,还测定了同一组织匀浆中[3H]-埃托啡的高亲和力立体特异性结合。2. 对于经吗啡预处理的动物的条制备物,需要更高浓度的去甲吗啡才能产生50%的电刺激收缩抑制。在阿片耐受的制备物中,线性化剂量-反应曲线的斜率也有所增加。最大阿片效应未改变,对外源性乙酰胆碱的反应也不受预处理的影响。3. 吗啡预处理后,纳洛酮的表观平衡常数略有增加。4. 对阿片效应的耐受性并未伴随着[3H]-埃托啡立体特异性结合位点的亲和力或数量的变化。对照和经吗啡预处理的制备物中[3H]-埃托啡结合的希尔图给出的斜率接近1。5. 这些结果大多可以通过以下假设来解释:在耐受的制备物中,在阿片效应变得明显之前,必须超过一定比例的阿片受体占据阈值。有人提出,组织会朝着与阿片类药物预处理期间达到的平均受体占据率相当的阈值适应。

相似文献

2
Model of opiate dependence in the guinea-pig isolated ileum.豚鼠离体回肠阿片类药物依赖模型。
Br J Pharmacol. 1981 Aug;73(4):921-32. doi: 10.1111/j.1476-5381.1981.tb08747.x.
3
Morphine-tolerant longitudinal muscle strip from guinea-pig ileum.豚鼠回肠的吗啡耐受纵向肌条
Br J Pharmacol. 1973 Aug;48(4):655-66. doi: 10.1111/j.1476-5381.1973.tb08254.x.

本文引用的文献

3
A modification of receptor theory.受体理论的一种修正。
Br J Pharmacol Chemother. 1956 Dec;11(4):379-93. doi: 10.1111/j.1476-5381.1956.tb00006.x.
8
Morphine-tolerant longitudinal muscle strip from guinea-pig ileum.豚鼠回肠的吗啡耐受纵向肌条
Br J Pharmacol. 1973 Aug;48(4):655-66. doi: 10.1111/j.1476-5381.1973.tb08254.x.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验