羟考酮:目前对其药理学、滥用和药物治疗发展的展望。

IF 19.3 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Pharmacological Reviews Pub Date : 2023-11-01 Epub Date: 2023-06-15 DOI:10.1124/pharmrev.121.000506
James E Barrett, Aryan Shekarabi, Saadet Inan
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引用次数: 0

摘要

羟考酮是天然蒂巴因的半合成衍生物,蒂巴因是一种阿片类生物碱,已有100多年的历史。尽管蒂巴因在更高剂量下会发生抽搐,因此无法用于治疗,但它已被转化为许多其他广泛使用的化合物,包括纳洛酮、纳曲酮、丁丙诺啡和羟考酮。尽管羟考酮的鉴定很早,但直到20世纪90年代,临床研究才开始探索其镇痛功效。在这些研究之后,进行了几项临床前研究,以检查羟考酮在实验动物中的镇痛作用和滥用责任,以及在人类志愿者中的主观影响。多年来,羟考酮一直处于阿片类药物危机的前沿,在导致阿片类物质滥用和滥用方面发挥了重要作用,有人认为它导致了向其他阿片类化合物的过渡。早在20世纪40年代,人们就表达了一些担忧,认为羟考酮具有类似海洛因和吗啡的巨大滥用潜力。动物和人类虐待责任研究都证实了这些早期警告,在某些情况下甚至放大了这些警告。尽管与吗啡具有相似的结构,并且药理学作用也由μ-阿片受体介导,但羟考酮的药理学和神经生物学存在一些差异。在分析羟考酮的药理学和分子机制的许多努力中产生的数据对其许多作用产生了相当大的见解,本文对此进行了综述,这反过来又为阿片受体药理学提供了新的信息。意义声明:羟考酮是一种μ-阿片受体激动剂,于1916年合成,1917年在德国投入临床使用。它作为一种治疗急性和慢性神经性疼痛的镇痛药,作为吗啡的替代品,已被广泛研究。羟考酮是一种广泛滥用的药物。本文对羟考酮的药理学、疼痛和滥用的临床前和临床研究,以及确定潜在的无滥用责任的阿片类止痛药的最新进展进行了全面、详细的综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oxycodone: A Current Perspective on Its Pharmacology, Abuse, and Pharmacotherapeutic Developments.

Oxycodone, a semisynthetic derivative of naturally occurring thebaine, an opioid alkaloid, has been available for more than 100 years. Although thebaine cannot be used therapeutically due to the occurrence of convulsions at higher doses, it has been converted to a number of other widely used compounds that include naloxone, naltrexone, buprenorphine, and oxycodone. Despite the early identification of oxycodone, it was not until the 1990s that clinical studies began to explore its analgesic efficacy. These studies were followed by the pursuit of several preclinical studies to examine the analgesic effects and abuse liability of oxycodone in laboratory animals and the subjective effects in human volunteers. For a number of years oxycodone was at the forefront of the opioid crisis, playing a significant role in contributing to opioid misuse and abuse, with suggestions that it led to transitioning to other opioids. Several concerns were expressed as early as the 1940s that oxycodone had significant abuse potential similar to heroin and morphine. Both animal and human abuse liability studies have confirmed, and in some cases amplified, these early warnings. Despite sharing a similar structure with morphine and pharmacological actions also mediated by the μ-opioid receptor, there are several differences in the pharmacology and neurobiology of oxycodone. The data that have emerged from the many efforts to analyze the pharmacological and molecular mechanism of oxycodone have generated considerable insight into its many actions, reviewed here, which, in turn, have provided new information on opioid receptor pharmacology. SIGNIFICANCE STATEMENT: Oxycodone, a μ-opioid receptor agonist, was synthesized in 1916 and introduced into clinical use in Germany in 1917. It has been studied extensively as a therapeutic analgesic for acute and chronic neuropathic pain as an alternative to morphine. Oxycodone emerged as a drug with widespread abuse. This article brings together an integrated, detailed review of the pharmacology of oxycodone, preclinical and clinical studies of pain and abuse, and recent advances to identify potential opioid analgesics without abuse liability.

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来源期刊
Pharmacological Reviews
Pharmacological Reviews 医学-药学
CiteScore
34.70
自引率
0.50%
发文量
40
期刊介绍: Pharmacological Reviews is a highly popular and well-received journal that has a long and rich history of success. It was first published in 1949 and is currently published bimonthly online by the American Society for Pharmacology and Experimental Therapeutics. The journal is indexed or abstracted by various databases, including Biological Abstracts, BIOSIS Previews Database, Biosciences Information Service, Current Contents/Life Sciences, EMBASE/Excerpta Medica, Index Medicus, Index to Scientific Reviews, Medical Documentation Service, Reference Update, Research Alerts, Science Citation Index, and SciSearch. Pharmacological Reviews offers comprehensive reviews of new pharmacological fields and is able to stay up-to-date with published content. Overall, it is highly regarded by scholars.
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