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实现无副作用阿片类镇痛的进展。

Advances in Achieving Opioid Analgesia Without Side Effects.

作者信息

Machelska Halina, Celik Melih Ö

机构信息

Department of Experimental Anesthesiology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.

出版信息

Front Pharmacol. 2018 Nov 29;9:1388. doi: 10.3389/fphar.2018.01388. eCollection 2018.

Abstract

Opioids are the most effective drugs for the treatment of severe pain, but they also cause addiction and overdose deaths, which have led to a worldwide opioid crisis. Therefore, the development of safer opioids is urgently needed. In this article, we provide a critical overview of emerging opioid-based strategies aimed at effective pain relief and improved side effect profiles. These approaches comprise biased agonism, the targeting of (i) opioid receptors in peripheral inflamed tissue (by reducing agonist access to the brain, the use of nanocarriers, or low pH-sensitive agonists); (ii) heteromers or multiple receptors (by monovalent, bivalent, and multifunctional ligands); (iii) receptor splice variants; and (iv) endogenous opioid peptides (by preventing their degradation or enhancing their production by gene transfer). Substantial advancements are underscored by pharmaceutical development of new opioids such as peripheral κ-receptor agonists, and by treatments augmenting the action of endogenous opioids, which have entered clinical trials. Additionally, there are several promising novel opioids comprehensively examined in preclinical studies, but also strategies such as biased agonism, which might require careful rethinking.

摘要

阿片类药物是治疗重度疼痛最有效的药物,但它们也会导致成瘾和过量用药死亡,这已引发了一场全球阿片类药物危机。因此,迫切需要开发更安全的阿片类药物。在本文中,我们对旨在有效缓解疼痛并改善副作用的新型阿片类药物策略进行了批判性综述。这些方法包括偏向性激动作用,靶向(i)外周炎症组织中的阿片受体(通过减少激动剂进入大脑、使用纳米载体或低pH敏感激动剂);(ii)异聚体或多种受体(通过单价、二价和多功能配体);(iii)受体剪接变体;以及(iv)内源性阿片肽(通过防止其降解或通过基因转移增强其产生)。新型阿片类药物(如外周κ受体激动剂)的药物研发以及增强内源性阿片肽作用的治疗方法(已进入临床试验)突出了实质性进展。此外,在临床前研究中全面研究了几种有前景的新型阿片类药物,还有偏向性激动作用等策略,可能需要仔细重新思考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67df/6282113/f911a548c000/fphar-09-01388-g001.jpg

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