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用于治疗慢性阻塞性肺疾病的长效毒蕈碱拮抗剂:当前及正在研发药物的综述

Long acting muscarinic antagonists for the treatment of chronic obstructive pulmonary disease: a review of current and developing drugs.

作者信息

Mastrodicasa Mark A, Droege Christopher A, Mulhall Aaron M, Ernst Neil E, Panos Ralph J, Zafar Muhammad A

机构信息

a Division of Pulmonary and Critical Care Medicine , University of Cincinnati Medical Center , Cincinnati , OH , USA.

c Department of Medicine , Cincinnati Veterans Affairs Medical Center , Cincinnati , OH , USA.

出版信息

Expert Opin Investig Drugs. 2017 Feb;26(2):161-174. doi: 10.1080/13543784.2017.1276167. Epub 2017 Jan 9.

Abstract

Long acting muscarinic receptor antagonists (LAMA) reverse airflow obstruction by antagonizing para-sympathetic bronchoconstricting effects within the airways. For years, tiotropium, has been the cornerstone LAMA for chronic obstructive pulmonary disease (COPD) management. Recently, new agents, aclidinium bromide, glycopyrronium bromide, and umeclidinium bromide, have been developed and introduced into clinical practice. Areas covered: This article reviews the clinical efficacy and adverse effects of currently available LAMAs in COPD treatment as well as developing LAMAs in early clinical trials and preclinical studies (V0162, TD-4208, CHF 5407, AZD9164, AZD8683, bencycloquidium). In addition, a new class of molecule that combines muscarinic antagonist and β2-adrenergic properties (MABA) is described and current developmental progress discussed (GSK-961081, THRX-200495). Expert opinion: Future key areas for developing drugs for the management of COPD include prolonged duration of action, optimal delivery systems, synergistic combinations with other drugs, maximization of benefits and minimization of adverse effects. The development of new LAMA and MABA molecules provides exciting progress towards simpler and more effective COPD management.

摘要

长效毒蕈碱受体拮抗剂(LAMA)通过拮抗气道内副交感神经的支气管收缩作用来逆转气流阻塞。多年来,噻托溴铵一直是慢性阻塞性肺疾病(COPD)管理中的基石LAMA。最近,新的药物,如阿地溴铵、格隆溴铵和乌美溴铵,已被开发并引入临床实践。涵盖领域:本文综述了目前可用的LAMA在COPD治疗中的临床疗效和不良反应,以及处于早期临床试验和临床前研究阶段的正在研发的LAMA(V0162、TD - 4208、CHF 5407、AZD9164、AZD8683、苯环喹溴铵)。此外,还描述了一类结合毒蕈碱拮抗剂和β2 - 肾上腺素能特性的新型分子(MABA),并讨论了当前的研发进展(GSK - 961081、THRX - 200495)。专家意见:未来COPD管理药物研发的关键领域包括延长作用时间、优化给药系统、与其他药物的协同组合、效益最大化和不良反应最小化。新型LAMA和MABA分子的研发为更简单有效的COPD管理带来了令人兴奋的进展。

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