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“强效镇痛药”是否等于“强效阿片类药物”?盐酸他喷他多与“μ-负荷”概念。

Does 'Strong Analgesic' Equal 'Strong Opioid'? Tapentadol and the Concept of 'µ-Load'.

机构信息

College of Pharmacy, University of Arizona, Tucson, AZ, USA.

Temple University, Philadelphia, PA, USA.

出版信息

Adv Ther. 2018 Oct;35(10):1471-1484. doi: 10.1007/s12325-018-0778-x. Epub 2018 Sep 11.

Abstract

INTRODUCTION

The distinct properties of the centrally-acting analgesic tapentadol derive from the combined contributions of an opioid component and a nonopioid component. However, the opioid component's relative contribution to analgesic and adverse effects has not previously been elucidated. Tapentadol's analgesic effect derives from the combined contribution of an opioid mechanism and a nonopioid mechanism, the extent of which can vary for different pains. Likewise, the interaction can vary for various adverse effects. Hence, the contribution of each mechanism to adverse effects can be different from the contribution to analgesia. We here estimate the percent contribution of each component of the mechanism of action to analgesia and to adverse effects.

AREAS COVERED

Several approaches to in vitro and in vivo data to estimate the contribution of tapentadol's opioid component to analgesia and to the two important opioid adverse effects, respiratory depression and constipation. The results are then compared with clinical data.

EXPERT OPINION

Traditional opioids, such as morphine, oxycodone, and others, produce their analgesic effects primarily through a single mechanism-the activation of µ-opioid receptors (MOR). Therefore, the contribution of the opioid component to adverse effects is 100%. In contrast, the newer strong analgesic tapentadol produces its analgesic effect via two separate and complementary analgesic mechanisms, only one of which is µ-opioid. We applied standard drug-receptor theory and novel techniques to in vitro and in vivo data to estimate by several different ways the μ-load of tapentadol (the % contribution of the opioid component to the adverse effect magnitude relative to a pure/classical µ-opioid at equianalgesia) in respiratory depression and constipation, and we compared the results to clinical evidence. The estimate is remarkably consistent over the various approaches and indicates that the μ-load of tapentadol is ≤ 40% (relative to pure MOR agonists, which have, by definition, a µ-load of 100%).

FUNDING

Grünenthal GmbH.

摘要

简介

中枢作用镇痛药酒石酸布托啡诺的独特性质源于阿片类成分和非阿片类成分的共同作用。然而,阿片类成分对镇痛和不良反应的相对贡献此前尚未阐明。酒石酸布托啡诺的镇痛作用源自阿片类机制和非阿片类机制的共同作用,其程度因不同疼痛而有所不同。同样,相互作用也因各种不良反应而有所不同。因此,每种机制对不良反应的贡献可能与对镇痛的贡献不同。我们在此估计作用机制的每个成分对镇痛和两种重要阿片类不良反应(呼吸抑制和便秘)的贡献百分比。

涵盖的领域

几种评估酒石酸布托啡诺阿片类成分对镇痛和两种重要阿片类不良反应(呼吸抑制和便秘)的体外和体内数据的方法,并将结果与临床数据进行比较。

专家意见

传统阿片类药物,如吗啡、羟考酮等,主要通过单一机制——激活μ-阿片受体(MOR)产生镇痛作用。因此,阿片类成分对不良反应的贡献为 100%。相比之下,新型强效镇痛药酒石酸布托啡诺通过两种独立且互补的镇痛机制发挥镇痛作用,其中只有一种是μ-阿片类。我们应用标准药物受体理论和新技术对体外和体内数据进行评估,通过几种不同的方法估计酒石酸布托啡诺的μ-负荷(阿片类成分对不良反应严重程度的相对贡献与等镇痛时的纯/经典μ-阿片类药物的百分比)在呼吸抑制和便秘方面,并将结果与临床证据进行比较。各种方法的估计结果非常一致,表明酒石酸布托啡诺的μ-负荷(相对于定义为 100%的纯 MOR 激动剂)≤40%。

资助

Grünenthal GmbH。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2827/6182641/b94e9107b080/12325_2018_778_Fig1_HTML.jpg

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