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对戒断者使用奥昔洛芬(左旋-BC-2605)的临床试验:一种新型麻醉拮抗剂。

Clinical trial in post-addicts with oxilorphan (levo-BC-2605): a new narcotic antagonist.

作者信息

Tennant F S, Tate J A, Ruckel E

出版信息

Drug Alcohol Depend. 1976 Jun;1(5):329-37. doi: 10.1016/0376-8716(76)90035-1.

DOI:10.1016/0376-8716(76)90035-1
PMID:13984
Abstract

Oxilorphan (levo-BC-2605) is a new, long-acting, narcotic antagonist that has agonist properties. Twenty-one (21) heroin addicts in Los Angeles were detoxified and given at least one oral dose of oxilorphan. Only three (14.3%) patients took daily doses for 14 days, which was the maximal time allowed for oxilorphan administration in this study. The remainder discontinued oxilorphan because of subjective side effects or for unknown reasons. Side effects most responsible for dropouts were dysphoria, insomnia, weakness, hallucinations, nausea, drowsiness and anorexia. Oxilorphan provided 24-hour protection with a single, oral dose, but subjective side effects encountered during inductiolinical trials with oxilorphan should be attempted with other addict populations to fully determine its potential therapeutic value.

摘要

氧吗啡烷(左旋-BC-2605)是一种新型长效麻醉拮抗剂,具有激动剂特性。洛杉矶的21名海洛因成瘾者接受了戒毒治疗,并至少口服了一剂氧吗啡烷。只有3名(14.3%)患者连续14天每日服药,这是本研究中允许使用氧吗啡烷的最长时间。其余患者因主观副作用或不明原因停用了氧吗啡烷。导致停药的最主要副作用是烦躁不安、失眠、虚弱、幻觉、恶心、嗜睡和厌食。氧吗啡烷单次口服剂量可提供24小时保护,但在诱导临床试验中遇到的主观副作用,应在其他成瘾人群中进行尝试,以充分确定其潜在治疗价值。

相似文献

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Clinical trial in post-addicts with oxilorphan (levo-BC-2605): a new narcotic antagonist.对戒断者使用奥昔洛芬(左旋-BC-2605)的临床试验:一种新型麻醉拮抗剂。
Drug Alcohol Depend. 1976 Jun;1(5):329-37. doi: 10.1016/0376-8716(76)90035-1.
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Partial agonist properties and toxicity of oral oxilorphan.口服羟吗啡酮的部分激动剂特性及毒性
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Oxilorphan (l-N-cyclopropylmethyl-3,14-dihydroxymorphinan): a new synthetic narcotic antagonist.氧吗啡烷(左旋-N-环丙基甲基-3,14-二羟基吗啡喃):一种新型合成麻醉性拮抗剂。
J Pharmacol Exp Ther. 1975 Apr;193(1):23-34.
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A clinical trial of buprenorphine: I. Comparison with methadone in the detoxification of heroin addicts. II. Examination of its opioid blocking properties.丁丙诺啡的临床试验:I. 与美沙酮在海洛因成瘾者脱毒治疗中的比较。II. 对其阿片类阻断特性的研究。
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Narcotic withdrawal syndrome caused by naltrexone.纳曲酮引起的麻醉药戒断综合征。
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Evidence that nalorphine, butorphanol and oxilorphan are partial agonists at a kappa-opioid receptor.纳洛啡、布托啡诺和奥昔啡烷是κ-阿片受体部分激动剂的证据。
Eur J Pharmacol. 1983 Jan 21;86(3-4):467-70. doi: 10.1016/0014-2999(83)90198-x.
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Studies of EN-1639A (naltrexone): a new narcotic antagonist.对EN - 1639A(纳曲酮)的研究:一种新型麻醉拮抗剂。
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Buprenorphine suppresses heroin use by heroin addicts.丁丙诺啡可抑制海洛因成瘾者对海洛因的使用。
Science. 1980 Feb 8;207(4431):657-9. doi: 10.1126/science.7352279.
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