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香芹酚和百里香酚对碳酸酐酶的选择性抑制作用可能会损害生物膜的产生和外膜囊泡的释放。

Selective Inhibition of Carbonic Anhydrases by Carvacrol and Thymol Could Impair Biofilm Production and the Release of Outer Membrane Vesicles.

机构信息

Department of Pharmacy, "G. d'Annunzio" University of Chieti-Pescara, 66100 Chieti, Italy.

Neurofarba Department, University of Florence, 50019 Sesto Fiorentino, Italy.

出版信息

Int J Mol Sci. 2021 Oct 27;22(21):11583. doi: 10.3390/ijms222111583.

Abstract

, a Gram-negative neutrophilic pathogen, is the cause of chronic gastritis, peptic ulcers, and gastric cancer in humans. Current therapeutic regimens suffer from an emerging bacterial resistance rate and poor patience compliance. To improve the discovery of compounds targeting bacterial alternative enzymes or essential pathways such as carbonic anhydrases (CAs), we assessed the anti- activity of thymol and carvacrol in terms of CA inhibition, isoform selectivity, growth impairment, biofilm production, and release of associated outer membrane vesicles-eDNA. The microbiological results were correlated by the evaluation in vitro of CA inhibition, in silico analysis of the structural requirements to display such isoform selectivity, and the assessment of their limited toxicity against three probiotic species with respect to amoxicillin. Carvacrol and thymol could thus be considered as new lead compounds as alternative CA inhibitors or to be used in association with current drugs for the management of infection and limiting the spread of antibiotic resistance.

摘要

幽门螺杆菌,一种革兰氏阴性嗜中性病原体,是导致人类慢性胃炎、消化性溃疡和胃癌的原因。目前的治疗方案存在细菌耐药率上升和患者顺应性差的问题。为了提高针对细菌替代酶或碳酸酐酶(CA)等必需途径的化合物的发现率,我们评估了百里香酚和香芹酚在 CA 抑制、同工型选择性、生长抑制、生物膜生成和相关外膜囊泡- eDNA 释放方面的活性。通过体外评估 CA 抑制、显示这种同工型选择性的结构要求的计算分析以及相对于阿莫西林对三种益生菌物种的有限毒性评估,对微生物学结果进行了相关性分析。因此,香芹酚和百里香酚可以被认为是新的先导化合物,可作为替代 CA 抑制剂,或与现有药物联合用于治疗 感染和限制抗生素耐药性的传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723d/8584244/71ccfd51ce5d/ijms-22-11583-g001.jpg

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