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作 者:贺春波 王丹 杨淑佳[2,3] 周开文 邓怡平 董守良[4,5] HE Chunbo;WANG Dan;YANG Shujia;ZHOU Kaiwen;DENG Yiping;DONG Shouliang(School of Pharmacy,Dezhou University,Shandong Dezhou 253023,China;Shandong Engineering Research Center of Novel Pharmaceutical Excipients,Sustained and Controlled Release Preparations,Shandong Dezhou 253023,China;Medical School of Health,Dezhou University,Shandong Dezhou 253023,China;Dept.of Animal and Biomedical Sciences,School of Life Sciences,Lanzhou University,Lanzhou 730000,China;Key Laboratory of Preclinical Study for New Drugs of Gansu Province,Lanzhou 730000,China)
机构地区:[1]德州学院药学院,山东德州253023 [2]新型药用辅料与缓控释制剂山东省工程研究中心,山东德州253023 [3]德州学院健康医学院,山东德州253023 [4]兰州大学生命科学学院动物学与生物医学系,兰州730000 [5]甘肃省新药临床前研究重点实验室,兰州730000
出 处:《中国药房》2024年第17期2176-2180,共5页China Pharmacy
基 金:山东省自然科学基金项目:(No.ZR2023QH304);德州学院科学研究基金项目:(No.2021xjrc212)。
摘 要:阿片类镇痛药是目前已知疗效最好的镇痛药,然而其便秘、耐受和成瘾等毒副作用严重限制了其临床应用。随着对阿片受体信号转导机制的深入认知和药物设计技术的不断进步,研究者们近年来尝试了许多有前景、不同于传统的改造吗啡骨架结构的全新方法,致力于开发低毒高效的阿片类镇痛药。本文聚焦于目前比较主流的偏向性激动、“一药多靶”和外周激动3种新型研发策略,介绍了各个策略实现镇痛活性与不良反应相对分离的基本原理,并结合相应代表性药物的最新研究进展进行简要综述。其中,近期获批上市的新型阿片类镇痛药奥赛利定和泰吉利定都是偏向性μ阿片受体激动剂,Cebranopadol是典型的“一药多靶”镇痛药,NFEPP是外周阿片受体激动剂的代表性药物。上述几种研发策略相辅相成,为阿片类镇痛新药的研发提供了借鉴与参考。Opioid analgesics are currently known as the best analgesics.However,toxicity and side effects such as constipation,tolerance and addiction severely limit their clinical application.With the in-depth understanding of the signal transduction mechanism of opioid receptors and the continuous advancement of drug design technology,researchers have managed to develop many promising new methods to get low-toxic and more efficient opioid analgesics,which are different from the traditional morphine skeleton structure modifications.This article focuses on three new research strategies of G-protein biased activation,“one drug-multiple targets”and peripheral activation.The basic principles of relative separation of analgesic activity and adverse drug reaction by each strategy are introduced,and the latest research progress of representative drugs is briefly reviewed.Among them,the recently approved novel opioid analgesics oliceridine and tegileridine are G-protein biasedμ-opioid receptor agonists,Cebranopadol is a typical“one drug-multiple targets”analgesic,and NFEPP is a representative drug of peripheral opioid receptor agonists.The above several strategies complement each other and provide reference for the development of new opioid analgesic drugs.
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