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评估抗组胺药卢帕他定单独使用或联合使用对分枝杆菌的疗效。

Assessment of the Efficacy of the Antihistamine Drug Rupatadine Used Alone or in Combination against Mycobacteria.

作者信息

Tian Xirong, Ma Wanli, Yusuf Buhari, Su Biyi, Hu Jinxing, Zhang Tianyu

机构信息

State Key Laboratory of Respiratory Disease, Guangdong-Hong Kong-Macao Joint Laboratory of Respiratory Infectious Diseases, China-New Zealand Joint Laboratory on Biomedicine and Health, Guangzhou Institutes of Biomedicine and Health (GIBH), Chinese Academy of Sciences (CAS), Guangzhou 510530, China.

University of Chinese Academy of Sciences (UCAS), Beijing 100049, China.

出版信息

Pharmaceutics. 2024 Aug 7;16(8):1049. doi: 10.3390/pharmaceutics16081049.

Abstract

The emergence of drug-resistant mycobacteria has rendered many clinical drugs and regimens ineffective, imposing significant economic and healthcare burden on individuals and society. Repurposing drugs intended for treating other diseases is a time-saving, cost-effective, and efficient approach for identifying excellent antimycobacterial candidates or lead compounds. This study is the first to demonstrate that rupatadine (RTD), a drug used to treat allergic rhinitis, possesses excellent activity against mycobacteria without detectable resistance, particularly and , with a minimal inhibitory concentration as low as 3.13 µg/mL. Furthermore, RTD exhibited moderate activity against nonreplicating with minimal inhibitory concentrations lower than drugs targeting the cell wall, suggesting that RTD has great potential to be modified and used for the treatment of nonreplicating . Additionally, RTD exhibits partial synergistic effects when combined with clofazimine, pretomanid, and TB47 against , providing the theoretical foundation for the development of treatment regimens. Transcriptomic profiling leads us to speculate that eight essential genes may be the targets of RTD or may be closely associated with mycobacterial resistance to RTD. In summary, RTD may be a promising hit for further antimycobacterial drug or regimen optimization, especially in the case of nonreplicating mycobacteria.

摘要

耐药分枝杆菌的出现使许多临床药物和治疗方案失效,给个人和社会带来了巨大的经济和医疗负担。重新利用用于治疗其他疾病的药物是一种省时、经济高效的方法,可用于识别优秀的抗分枝杆菌候选药物或先导化合物。本研究首次证明,用于治疗过敏性鼻炎的药物卢帕他定(RTD)对分枝杆菌具有优异的活性且未检测到耐药性,尤其是对结核分枝杆菌和牛分枝杆菌,其最低抑菌浓度低至3.13 µg/mL。此外,RTD对非复制型结核分枝杆菌表现出中等活性,其最低抑菌浓度低于靶向细胞壁的药物,这表明RTD具有很大的被修饰并用于治疗非复制型结核分枝杆菌的潜力。此外,RTD与氯法齐明、pretomanid和TB47联合使用时对结核分枝杆菌表现出部分协同作用,为治疗方案的开发提供了理论基础。转录组分析使我们推测八个必需基因可能是RTD的靶点,或者可能与分枝杆菌对RTD的耐药性密切相关。总之,RTD可能是进一步优化抗分枝杆菌药物或治疗方案的一个有前景的研究对象,特别是在非复制型分枝杆菌的情况下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/11359651/e8c1e6ec5155/pharmaceutics-16-01049-g001.jpg

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