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1
Opiate binding and effect in ileum preparations from normal and morphine pretreated guinea-pigs.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
Br J Pharmacol. 1977 Oct;61(2):271-8. doi: 10.1111/j.1476-5381.1977.tb08415.x.
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。
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3
Morphine-tolerant longitudinal muscle strip from guinea-pig ileum.豚鼠回肠的吗啡耐受纵向肌条
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4
Assessment of the potential agonistic and antagonistic properties of ketamine at opiate receptors in the guinea-pig ileum.氯胺酮对豚鼠回肠阿片受体潜在激动和拮抗特性的评估。
Neuropharmacology. 1982 Jul;21(7):605-11. doi: 10.1016/0028-3908(82)90001-6.
5
Beta-endorphin fragments DTgammaE and DEgammaE reduced morphine inhibition of electrically-induced contractions and opiate withdrawal.β-内啡肽片段DTγE和DEγE可减轻吗啡对电诱发收缩的抑制作用以及阿片类药物戒断反应。
Med Chem. 2009 Mar;5(2):165-70. doi: 10.2174/157340609787582864.
6
Effect of cinitapride in isolated ileum obtained from guinea-pigs treated with morphine.西尼必利对用吗啡处理的豚鼠离体回肠的作用。
Gen Pharmacol. 1991;22(5):863-6. doi: 10.1016/0306-3623(91)90220-z.
7
Dynorphin inhibition of the neurotensin contractile activity on the myenteric plexus.强啡肽对神经降压素在肌间神经丛收缩活性的抑制作用。
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8
An analysis of the phenomenon of acute tolerance to morphine in the guinea-pig isolated ileum.豚鼠离体回肠对吗啡急性耐受性现象的分析。
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9
Substance P and opioid interaction on stimulated and non-stimulated guinea pig ileum.P物质与阿片类药物对刺激和未刺激的豚鼠回肠的相互作用。
Eur J Pharmacol. 1978 Dec 15;53(1):21-7. doi: 10.1016/0014-2999(78)90263-7.
10
Contractile effect of morphine and related opioid alkaloids, beta-endorphin and methionine enkephalin on the isolated colon from Long Evans rats.吗啡及相关阿片生物碱、β-内啡肽和甲硫氨酸脑啡肽对长 Evans 大鼠离体结肠的收缩作用。
Br J Pharmacol. 1981 Nov;74(3):681-94. doi: 10.1111/j.1476-5381.1981.tb10479.x.

引用本文的文献

1
Opiate receptor binding studies in the mouse vas deferens exhibiting tolerance without dependence.在小鼠输精管中进行的阿片受体结合研究显示出耐受性但无依赖性。
Naunyn Schmiedebergs Arch Pharmacol. 1982 May;319(2):142-6. doi: 10.1007/BF00503928.
2
The dependence of excitatory junction potential amplitude on the external calcium concentration in mouse vas deferens during narcotic withdrawal.麻醉戒断期间小鼠输精管中兴奋性突触后电位幅度对外源钙浓度的依赖性。
Br J Pharmacol. 1984 Dec;83(4):863-70. doi: 10.1111/j.1476-5381.1984.tb16525.x.
3
Opioid receptor reserve in normal and morphine-tolerant guinea pig ileum myenteric plexus.正常及吗啡耐受豚鼠回肠肌间神经丛中的阿片受体储备
Proc Natl Acad Sci U S A. 1984 Nov;81(22):7253-7. doi: 10.1073/pnas.81.22.7253.
4
Morphine tolerance and nonspecific subsensitivity of the longitudinal muscle myenteric plexus preparation of the guinea-pig to inhibitory agonists.豚鼠纵肌-肠肌丛制备物对抑制性激动剂的吗啡耐受性和非特异性亚敏感性
Naunyn Schmiedebergs Arch Pharmacol. 1988 Nov;338(5):553-9. doi: 10.1007/BF00179329.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
The action of morphine and related substances on contraction and on acetylcholine output of coaxially stimulated guinea-pig ileum.吗啡及相关物质对同轴刺激的豚鼠回肠收缩和乙酰胆碱释放的作用。
Br J Pharmacol Chemother. 1957 Mar;12(1):119-27. doi: 10.1111/j.1476-5381.1957.tb01373.x.
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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.
4
Agonist and antagonist actions of morphine-like drugs on the guinea-pig isolated ileum.吗啡样药物对豚鼠离体回肠的激动剂和拮抗剂作用。
Br J Pharmacol Chemother. 1966 Sep;27(3):514-27. doi: 10.1111/j.1476-5381.1966.tb01864.x.
5
The effect of analgesic drugs on the release of acetylcholine from electrically stimulated guinea-pig ileum.镇痛药对电刺激豚鼠回肠乙酰胆碱释放的影响。
Br J Pharmacol Chemother. 1966 May;27(1):81-92. doi: 10.1111/j.1476-5381.1966.tb01643.x.
6
XIX. Enzyme expansion theory of drug tolerance and physical dependence.十九、药物耐受性和身体依赖性的酶扩张理论。
Res Publ Assoc Res Nerv Ment Dis. 1968;46:265-7.
7
Kinetic parameters of narcotic agonists and antagonists, with particular reference to N-allylnoroxymorphone (naloxone).麻醉性激动剂和拮抗剂的动力学参数,尤其涉及N-烯丙基去甲羟吗啡酮(纳洛酮)。
Br J Pharmacol Chemother. 1968 Jun;33(2):266-76. doi: 10.1111/j.1476-5381.1968.tb00988.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.
9
The increased efficacy of narcotic antagonists induced by various narcotic analgesics.各种麻醉性镇痛药引起的麻醉性拮抗剂效力增强。
J Pharmacol Exp Ther. 1974 Sep;190(3):395-400.
10
Narcotic receptor sites in morphine-dependent rats.吗啡依赖大鼠体内的阿片受体位点
Nature. 1974 Mar 1;248(5443):61-3. doi: 10.1038/248061a0.

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.

DOI:10.1111/j.1476-5381.1977.tb08415.x
PMID:200298
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1667503/
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。