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Effect of the nonpeptide NK-1 receptor antagonist CP-96,345 on the morphine withdrawal response of guinea-pigs.

作者信息

Chahl L A, Johnston P A

机构信息

Neuropharmacology Laboratory, Faculty of Medicine, University of Newcastle, Australia.

出版信息

Regul Pept. 1993 Jul 2;46(1-2):373-5. doi: 10.1016/0167-0115(93)90090-u.

DOI:10.1016/0167-0115(93)90090-u
PMID:7692540
Abstract
摘要

相似文献

1
Effect of the nonpeptide NK-1 receptor antagonist CP-96,345 on the morphine withdrawal response of guinea-pigs.非肽类NK-1受体拮抗剂CP-96,345对豚鼠吗啡戒断反应的影响。
Regul Pept. 1993 Jul 2;46(1-2):373-5. doi: 10.1016/0167-0115(93)90090-u.
2
RP 67580, a selective antagonist of neurokinin-1 receptors, modifies some of the naloxone-precipitated morphine withdrawal signs in rats.RP 67580,一种神经激肽-1受体的选择性拮抗剂,可改变大鼠中一些纳洛酮诱发的吗啡戒断症状。
Neurosci Lett. 1993 Jun 25;156(1-2):135-40. doi: 10.1016/0304-3940(93)90457-v.
3
Neurokinin-1, -2 and -3 receptors are candidates for a role in the opiate withdrawal response in guinea-pigs.神经激肽-1、-2和-3受体可能在豚鼠的阿片类戒断反应中起作用。
Regul Pept. 1993 Jul 2;46(1-2):376-8. doi: 10.1016/0167-0115(93)90091-l.
4
Role of NK-1 receptor in central cardiovascular regulation in rats: studies on a novel non-peptide antagonist, CP-96,345, of substance P NK-1 receptor.NK-1受体在大鼠中枢心血管调节中的作用:对P物质NK-1受体新型非肽拮抗剂CP-96,345的研究
Regul Pept. 1993 Jul 2;46(1-2):293-6. doi: 10.1016/0167-0115(93)90064-f.
5
Different behavioral profiles of the non-peptide substance P (NK-1) antagonists CP-96,345 and RP 67580.非肽类P物质(NK-1)拮抗剂CP-96,345和RP 67580的不同行为特征。
Regul Pept. 1993 Jul 2;46(1-2):346-8. doi: 10.1016/0167-0115(93)90081-i.
6
Chronic treatment with ascorbic acid inhibits the morphine withdrawal response in guinea-pigs.用抗坏血酸进行长期治疗可抑制豚鼠的吗啡戒断反应。
Neurosci Lett. 1992 Jan 20;135(1):23-7. doi: 10.1016/0304-3940(92)90127-s.
7
Tachykinin antagonists inhibit the morphine withdrawal response in guinea-pigs.
Naunyn Schmiedebergs Arch Pharmacol. 1991 Mar;343(3):283-8. doi: 10.1007/BF00251127.
8
Role of spinal and supraspinal muscarinic receptors in the expression of morphine withdrawal symptoms in the rat.脊髓和脊髓上毒蕈碱受体在大鼠吗啡戒断症状表达中的作用。
Neuropharmacology. 1993 Dec;32(12):1387-95. doi: 10.1016/0028-3908(93)90035-2.
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Distribution of Fos-like immunoreactivity in guinea-pig brain following administration of the neurokinin-1 receptor agonist, [SAR9,MET(O2)11]substance P.给予神经激肽-1受体激动剂[ SAR9,MET(O2)11]P物质后豚鼠脑内Fos样免疫反应性的分布
Neuroscience. 1999;94(2):663-73. doi: 10.1016/s0306-4522(99)00283-3.
10
Constitutive mu opioid receptor activation as a regulatory mechanism underlying narcotic tolerance and dependence.
Life Sci. 1994;54(20):PL339-50. doi: 10.1016/0024-3205(94)90022-1.

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Opioid-like effects of the neurokinin 1 antagonist aprepitant in patients maintained on and briefly withdrawn from methadone.阿瑞匹坦作为神经激肽 1 拮抗剂对美沙酮维持治疗并短期撤药患者的类阿片样效应。
Am J Drug Alcohol Abuse. 2013 Mar;39(2):86-91. doi: 10.3109/00952990.2012.762372.
2
An in vitro model of morphine withdrawal manifests the enhancing effect on human immunodeficiency virus infection of human T lymphocytes through the induction of substance P.吗啡戒断的体外模型通过诱导P物质表现出对人类T淋巴细胞感染人类免疫缺陷病毒的增强作用。
Am J Pathol. 2006 Nov;169(5):1663-70. doi: 10.2353/ajpath.2006.060358.
3
Comparative behavioural profile of centrally administered tachykinin NK1, NK2 and NK3 receptor agonists in the guinea-pig.
豚鼠中枢给予速激肽NK1、NK2和NK3受体激动剂的比较行为特征
Br J Pharmacol. 1995 Nov;116(5):2496-502. doi: 10.1111/j.1476-5381.1995.tb15101.x.