Stein C
Klinik für Anästhesiologie und operative Intensivmedizin, Charité Universitätsmedizin Berlin, Campus Benjamin Franklin, Hindenburgdamm 30, 12200, Berlin, Deutschland.
Schmerz. 2019 Aug;33(4):295-302. doi: 10.1007/s00482-019-0386-y.
Opioids are the oldest and most potent drugs for the treatment of severe pain but they are burdened by detrimental side effects, such as respiratory depression, addiction potential, sedation, nausea and constipation. Their clinical application is undisputed in the treatment of acute (e.g. perioperative) and cancer pain but their long-term use in chronic pain has met increasing criticism and has contributed to the current "opioid crisis".
This article reviews the pharmacological principles and new research strategies aiming at novel opioids with reduced side effects. The basic mechanisms underlying pain and opioid analgesia and other effects of opioids are outlined. To illustrate the clinical situation and medical problems, the plasticity of opioid receptors, intracellular signaling pathways, endogenous and exogenous opioid receptor ligands, central and peripheral sites of analgesic and side effects are discussed.
The epidemic of opioid misuse has shown that there is a lack of fundamental knowledge about the characteristics and management of chronic pain, that conflicts of interest and validity of models must be more intensively considered in the context of drug development and that novel analgesics with less addictive potential are urgently needed. Currently, the most promising perspectives appear to be augmenting endogenous opioid actions and the selective activation of peripheral opioid receptors.
阿片类药物是治疗重度疼痛最古老且最有效的药物,但它们存在诸如呼吸抑制、成瘾性、镇静、恶心和便秘等有害副作用。它们在治疗急性(如围手术期)和癌症疼痛方面的临床应用无可争议,但在慢性疼痛中的长期使用受到越来越多的批评,并导致了当前的“阿片类药物危机”。
本文综述了旨在研发副作用减少的新型阿片类药物的药理学原理和新研究策略。概述了疼痛和阿片类镇痛的基本机制以及阿片类药物的其他作用。为说明临床情况和医学问题,讨论了阿片受体的可塑性、细胞内信号通路、内源性和外源性阿片受体配体、镇痛和副作用的中枢及外周部位。
阿片类药物滥用的流行表明,对于慢性疼痛的特征和管理缺乏基础知识,在药物研发背景下必须更深入地考虑利益冲突和模型的有效性,并且迫切需要成瘾潜力较小的新型镇痛药。目前,最有前景的方向似乎是增强内源性阿片类作用以及选择性激活外周阿片受体。