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作为联合抑菌治疗的抗生素佐剂的甲氟喹研究进展。

Progress in the study of mefloquine as an antibiotic adjuvant for combination bacterial inhibition treatment.

作者信息

Liang Xiaofang, Liu Zhihong, Wang Yulin, Zhang Yu, Deng Wenbo, Liu Qianqian, Lu Zhangping, Li Keke, Chang Yanbing, Wei Lianhua

机构信息

School of Public Health, Gansu University of Chinese Medicine, Lanzhou, Gansu, China.

Department of Clinical Laboratory, Gansu Provincial Hospital, Lanzhou, Gansu, China.

出版信息

Front Cell Infect Microbiol. 2024 Nov 28;14:1470891. doi: 10.3389/fcimb.2024.1470891. eCollection 2024.

Abstract

Antimicrobial resistance is among the greatest threats to public health globally, and drug repurposing strategies may be advantageous to addressing this problem. Mefloquine, a drug traditionally used to treat malaria, has emerged as a promising antibiotic adjuvant, due to its ability to enhance the effectiveness of conventional antibiotics against resistant bacterial strains. In this paper, we first outline the enhancement properties of mefloquine and its mechanisms of action as an adjuvant antibiotic against multidrug-resistant bacteria. Mefloquine exhibits synergistic bacteriostatic effects when combined with colistin, β-lactams, antituberculosis drugs, quinolones, and linezolid. Potential mechanisms underlying its synergistic effects include inhibition of antibiotic efflux, disruption of bacterial cell membrane integrity, and disturbance of biofilm formation. In addition, we explore the bacteriostatic effects of several mefloquine derivatives against and some fungi. Further, we summarize the findings of recent studies on other aspects of mefloquine activity, including its antiviral and antitumor effects. Finally, the advantages and challenges of mefloquine use as an antibiotic adjuvant in combination with antibiotics for bacterial inhibition are discussed. Overall, mefloquine shows excellent potential as an antibiotic adjuvant therapy against multidrug-resistant bacteria and is a promising candidate for combination therapy; however, further studies are needed to fully elucidate its mechanism of action and address the challenges associated with its clinical application.

摘要

抗菌耐药性是全球公共卫生面临的最大威胁之一,药物重新利用策略可能有利于解决这一问题。甲氟喹是一种传统上用于治疗疟疾的药物,由于其能够增强传统抗生素对耐药菌株的有效性,已成为一种有前景的抗生素佐剂。在本文中,我们首先概述了甲氟喹作为抗多药耐药菌佐剂抗生素的增强特性及其作用机制。甲氟喹与黏菌素、β-内酰胺类、抗结核药物、喹诺酮类和利奈唑胺联合使用时表现出协同抑菌作用。其协同作用的潜在机制包括抑制抗生素外排、破坏细菌细胞膜完整性和干扰生物膜形成。此外,我们还探讨了几种甲氟喹衍生物对某些细菌和一些真菌的抑菌作用。此外,我们总结了近期关于甲氟喹活性其他方面的研究结果,包括其抗病毒和抗肿瘤作用。最后,讨论了甲氟喹作为抗生素佐剂与抗生素联合用于抑制细菌的优点和挑战。总体而言,甲氟喹作为抗多药耐药菌的抗生素佐剂疗法显示出极好的潜力,是联合疗法的一个有前景的候选药物;然而,需要进一步研究以充分阐明其作用机制并应对与其临床应用相关的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c02/11634880/b3d2809fb515/fcimb-14-1470891-g001.jpg

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