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来自天然植物的抗菌敏化剂:对抗耐甲氧西林菌的有力武器。

Antibacterial sensitizers from natural plants: A powerful weapon against methicillin-resistant .

作者信息

Li Xiaoli, Cai Yongqing, Xia Qinchuan, Liao Yongqun, Qin Rongxin

机构信息

Department of Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing, China.

Chongqing Key Laboratory of Drug Metabolism, Chongqing, China.

出版信息

Front Pharmacol. 2023 Feb 24;14:1118793. doi: 10.3389/fphar.2023.1118793. eCollection 2023.

Abstract

Methicillin-resistant (MRSA) is a drug-resistant bacterium that can cause a range of infections with high morbidity and mortality, including pneumonia, Therefore, development of new drugs or therapeutic strategies against MRSA is urgently needed. Increasing evidence has shown that combining antibiotics with "antibacterial sensitizers" which itself has no effect on MRSA, is highly effective against MRSA. Many studies showed the development of antibacterial sensitizers from natural plants may be a promising strategy against MRSA because of their low side effects, low toxicity and multi-acting target. In our paper, we first reviewed the resistance mechanisms of MRSA including "Resistance to Beta-Lactams", "Resistance to Glycopeptide antibiotics", "Resistance to Macrolides, Aminoglycosides, and Oxazolidinones" Moreover, we summarized the possible targets for antibacterial sensitizers against MRSA. Furthermore, we reviewed the synergy effects of active monomeric compounds from natural plants combined with antibiotics against MRSA and their corresponding mechanisms over the last two decades. This review provides a novel approach to overcome antibiotic resistance in MRSA.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)是一种耐药细菌,可导致一系列发病率和死亡率很高的感染,包括肺炎。因此,迫切需要开发针对MRSA的新药或治疗策略。越来越多的证据表明,将抗生素与本身对MRSA无作用的“抗菌增敏剂”联合使用,对MRSA非常有效。许多研究表明,从天然植物中开发抗菌增敏剂可能是一种有前景的抗MRSA策略,因为它们副作用小、毒性低且具有多作用靶点。在我们的论文中,我们首先综述了MRSA的耐药机制,包括“对β-内酰胺类的耐药性”、“对糖肽类抗生素的耐药性”、“对大环内酯类、氨基糖苷类和恶唑烷酮类的耐药性”。此外,我们总结了抗菌增敏剂针对MRSA的可能靶点。此外,我们回顾了过去二十年来天然植物活性单体化合物与抗生素联合对MRSA的协同作用及其相应机制。本综述为克服MRSA中的抗生素耐药性提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2503/9998539/c66da86ad62a/fphar-14-1118793-g001.jpg

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