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麻醉性拮抗剂的人体药理学

Human pharmacology of narcotic antagonists.

作者信息

Jasinski D R

出版信息

Br J Clin Pharmacol. 1979;7 Suppl 3(Suppl 3):287S-290S. doi: 10.1111/j.1365-2125.1979.tb04702.x.

DOI:10.1111/j.1365-2125.1979.tb04702.x
PMID:465291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1429310/
Abstract

1 Human studies at the Addiction Research Center enable narcotic antagonists to be classified into three subgroups: (1) nalorphine-like agents; (2) pure antagonists; and (3) morphine-like agents. 2 Six narcotic antagonists (pentazocine, nalbuphine, cyclazocine, butorphanol, propiram and buprenorphine) developed in recent years seem to have a lesser abuse potential than codeine or propoxyphene. 3 When adjusted for relative availability of the agents, epidemiological data shows that pentazocine is abused less than codeine or propoxyphene in the US. 4 Recent studies with buprenorphine indicate that this agent would find application both as an analgesic of low abuse potential and as a new type of drug for the treatment of addiction.

摘要
  1. 成瘾研究中心开展的人体研究使麻醉拮抗剂能够被分为三个亚组:(1)烯丙吗啡样药物;(2)纯拮抗剂;以及(3)吗啡样药物。2. 近年来研发的六种麻醉拮抗剂(喷他佐辛、纳布啡、环唑辛、布托啡诺、丙哌利定和丁丙诺啡)似乎比可待因或丙氧芬的滥用潜力更低。3. 当根据药物的相对可获得性进行调整时,流行病学数据表明在美国喷他佐辛的滥用情况比可待因或丙氧芬更少。4. 最近关于丁丙诺啡的研究表明,这种药物既可以作为一种低滥用潜力的镇痛药,也可以作为一种新型的成瘾治疗药物。

相似文献

1
Human pharmacology of narcotic antagonists.麻醉性拮抗剂的人体药理学
Br J Clin Pharmacol. 1979;7 Suppl 3(Suppl 3):287S-290S. doi: 10.1111/j.1365-2125.1979.tb04702.x.
2
THE CLINICAL EVALUATION OF MORPHINE AND ITS SUBSTITUTES AS ANALGESICS.吗啡及其替代物作为镇痛药的临床评估
Pharmacol Rev. 1964 Mar;16:47-83.
3
Comparative effects and analgesic efficacy of the agonist-antagonist opioids.
Drug Intell Clin Pharm. 1983 Jun;17(6):411-7. doi: 10.1177/106002808301700601.
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Opioid agonist-antagonist drugs in acute and chronic pain states.阿片类激动剂-拮抗剂药物在急慢性疼痛状态中的应用。
Drugs. 1991 Mar;41(3):326-44. doi: 10.2165/00003495-199141030-00002.
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USE OF WRITHING TEST FOR EVALUATING ANALGESIC ACTIVITY OF NARCOTIC ANTAGONISTS.利用扭体试验评估麻醉性拮抗剂的镇痛活性
Proc Soc Exp Biol Med. 1965 Mar;118:763-6. doi: 10.3181/00379727-118-29963.
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INHIBITION OF PHENYLQUINONE-INDUCED WRITHING BY NARCOTIC ANTAGONISTS.麻醉拮抗剂对苯醌诱发扭体反应的抑制作用。
Nature. 1964 Oct 10;204:189-90. doi: 10.1038/204189a0.
7
SOME NARCOTIC ANTAGONISTS IN THE BENZOMORPHAN SERIES.苯并吗啡烷系列中的一些麻醉拮抗剂。
J Pharmacol Exp Ther. 1964 Feb;143:141-8.
8
ANALGESIC EFFECTS IN MONKEYS OF MORPHINE, NALORPHINE, AND A BENZOMORPHAN NARCOTIC ANTAGONIST.吗啡、烯丙吗啡及一种苯并吗啡烷类麻醉拮抗剂对猴子的镇痛作用
J Pharmacol Exp Ther. 1964 Feb;143:169-73.
9
Subjective effects of narcotic antagonists.麻醉拮抗剂的主观效应。
Adv Biochem Psychopharmacol. 1973;8(0):383-98.
10
Certain theoretical and practical considerations involved in evaluating the overall abuse potential of opiate agonists and antagonists.评估阿片类激动剂和拮抗剂总体滥用可能性时涉及的某些理论和实际考量。
Adv Biochem Psychopharmacol. 1973;8(0):439-53.

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Nalbuphine. A preliminary review of its pharmacological properties and therapeutic efficacy.纳布啡。对其药理特性和治疗效果的初步综述。
Drugs. 1983 Sep;26(3):191-211. doi: 10.2165/00003495-198326030-00002.
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7
Opioid agonist-antagonist drugs in acute and chronic pain states.阿片类激动剂-拮抗剂药物在急慢性疼痛状态中的应用。
Drugs. 1991 Mar;41(3):326-44. doi: 10.2165/00003495-199141030-00002.
8
Mixed agonist-antagonist opiates and physical dependence.混合激动剂-拮抗剂阿片类药物与身体依赖性
Br J Clin Pharmacol. 1979;7 Suppl 3(Suppl 3):291S-296S. doi: 10.1111/j.1365-2125.1979.tb04703.x.

本文引用的文献

1
STUDIES ON THE HUMAN ADDICTION LIABILITY OF 2'-HYDROXY-5-9-DIMETHYL-2-(3,3-DIMETHYLALLYL)-6,7-BENZOMORPHAN (WIN 20,228): A WEAK NARCOTIC ANTAGONIST.2'-羟基-5,9-二甲基-2-(3,3-二甲基烯丙基)-6,7-苯并吗啡烷(WIN 20,228)的人体成瘾性研究:一种弱麻醉拮抗剂
J Pharmacol Exp Ther. 1964 Feb;143:149-56.
2
Physiologic, subjective, and behavioral effects of amphetamine, methamphetamine, ephedrine, phenmetrazine, and methylphenidate in man.苯丙胺、甲基苯丙胺、麻黄碱、芬美曲秦和哌甲酯对人体的生理、主观及行为影响。
Clin Pharmacol Ther. 1971 Mar-Apr;12(2):245-58. doi: 10.1002/cpt1971122part1245.
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Demonstration of tolerance to and physical dependence of N-allylnormorphine (nalorphine).
J Pharmacol Exp Ther. 1965 Dec;150(3):437-42.
4
Studies of the dependence-producing potential of the narcotic antagonist 2-cyclopropylmethyl-2'-hydroxy-5,9-dimethyl-6,7-benzomorphan (cyclazocine, WIN-20,740, ARC II-c-3).对麻醉拮抗剂2-环丙基甲基-2'-羟基-5,9-二甲基-6,7-苯并吗啡烷(环唑辛,WIN-20,740,ARC II-c-3)产生依赖性潜力的研究。
J Pharmacol Exp Ther. 1965 Dec;150(3):426-36.
5
Evaluation of nalbuphine for abuse potential.纳布啡滥用可能性评估。
Clin Pharmacol Ther. 1972 Jan-Feb;13(1):78-90. doi: 10.1002/cpt197213178.
6
Human pharmacology and abuse potential of the analgesic buprenorphine: a potential agent for treating narcotic addiction.
Arch Gen Psychiatry. 1978 Apr;35(4):501-16. doi: 10.1001/archpsyc.1978.01770280111012.