Prospects for macrolide therapy of asthma and COPD.

Q1 Pharmacology, Toxicology and Pharmaceutics
Advances in pharmacology Pub Date : 2023-01-01 Epub Date: 2023-03-30 DOI:10.1016/bs.apha.2023.03.002
Michael J Parnham, Virginia Norris, Jennifer A Kricker, Thorarinn Gudjonsson, Clive P Page
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引用次数: 1

Abstract

Macrolide compounds, many of which are derived from natural sources, all share a lactone ring structure, but of varying sizes. Their biological activities differ with structure and size but tend to overlap. Marketed macrolide drugs include immunosuppressives and antibiotics. Some of the latter have been shown to exert anti-inflammatory activities, due to direct effects on inflammatory cells and processes when used for respiratory infections. Consequently, azithromycin is included in clinical guidelines for COPD and asthma treatment, though it has the disadvantage, as an antibiotic, of increasing bacterial resistance. COPD and asthma, however, like several chronic inflammatory diseases involving other organs, are driven to a large extent by epithelial barrier dysfunction. Recently, azithromycin was shown to directly enhance epithelial barrier function and a new class of derivatives, barriolides, is under development with the lead indication COPD. It is thus likely that by circumventing antibiosis and acting on a crucial etiological disease process, this type of agent will open up a new, safer approach to COPD and asthma therapy with macrolides.

大环内酯类药物治疗哮喘和慢性阻塞性肺病的前景。
大环内酯类化合物,其中许多来源于天然,都具有内酯环结构,但大小不同。它们的生物活动因结构和大小而异,但往往重叠。市场上出售的大环内酯类药物包括免疫抑制剂和抗生素。后者中的一些已被证明具有抗炎活性,因为在用于呼吸道感染时对炎症细胞和过程有直接影响。因此,阿奇霉素被纳入COPD和哮喘治疗的临床指南,尽管它作为一种抗生素有增加细菌耐药性的缺点。然而,与涉及其他器官的几种慢性炎症性疾病一样,COPD和哮喘在很大程度上是由上皮屏障功能障碍引起的。最近,阿奇霉素被证明可以直接增强上皮屏障功能,一类新的衍生物barriolides正在开发中,其主要适应症是COPD。因此,通过绕过抗生素并作用于一个关键的病因过程,这种药物可能会为使用大环内酯类药物治疗COPD和哮喘开辟一种新的、更安全的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in pharmacology
Advances in pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
9.10
自引率
0.00%
发文量
45
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