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SBC3与依布硒啉联合使用对感染的协同活性。

The synergistic activity of SBC3 in combination with Ebselen against infection.

作者信息

Chen Hao, Lu Qianqian, An Haoyue, Li Juntong, Shen Shuchu, Zheng Xi, Chen Wei, Wang Lu, Li Jihong, Du Youqin, Wang Yueqing, Liu Xiaowen, Baumann Marcus, Tacke Matthias, Zou Lili, Wang Jun

机构信息

The Second People's Hospital of China Three Gorges University, Yichang, Hubei, China.

The Second People's Hospital of Yichang, Yichang, Hubei, China.

出版信息

Front Pharmacol. 2022 Dec 15;13:1080281. doi: 10.3389/fphar.2022.1080281. eCollection 2022.

Abstract

ranks as the number one clinical isolate in the past years in China according to The China Antimicrobial Surveillance Network (CHINET), and its multidrug-resistant (MDR) pathogenic strains account for over 160 million cases of dysentery and one million deaths per year. Here, our work demonstrates that is highly sensitive to the synergistic combination of SBC3 [1,3-Dibenzyl-4,5-diphenyl-imidazol-2-ylidene silver (I) acetate] and Ebselen, which shows no synergistic toxicity on mammalian cells. The proposed mechanism for the synergistic antibacterial effect of SBC3 in combination with Ebselen is based on directly inhibiting thioredoxin reductase and rapidly depleting glutathione, resulting in the increase of reactive oxygen species that cause bacterial cell death. Furthermore, the bactericidal efficacy of SBC3 in combination with Ebselen has been confirmed in mild and acute peritonitis mice. In addition, the five most difficult to treat Gram-negative bacteria (including , Acinetobacter baumannii, Enterobacter cloacae, , and ) are also highly sensitive to a synergistic combination of SBC3 and Ebselen. Thus, SBC3 in combination with Ebselen has potential as a treatment for clinically important Gram-negative bacterial infections.

摘要

根据中国抗菌药物监测网(CHINET)的数据,在过去几年中,[细菌名称]在中国临床分离菌中排名第一,其多重耐药(MDR)致病菌株每年导致超过1.6亿例痢疾病例和100万人死亡。在此,我们的研究表明,[细菌名称]对SBC3[1,3-二苄基-4,5-二苯基-咪唑-2-亚基乙酸银(I)]和依布硒仑的协同组合高度敏感,而该组合对哺乳动物细胞没有协同毒性。SBC3与依布硒仑协同抗菌作用的 proposed mechanism 是基于直接抑制[细菌名称]硫氧还蛋白还原酶并迅速消耗谷胱甘肽,导致活性氧增加,从而引起细菌细胞死亡。此外,SBC3与依布硒仑联合使用的杀菌效果已在轻度和急性腹膜炎小鼠中得到证实。此外,五种最难治疗的革兰氏阴性菌(包括[细菌名称]、鲍曼不动杆菌、阴沟肠杆菌、[细菌名称]和[细菌名称])对SBC3和依布硒仑的协同组合也高度敏感。因此,SBC3与依布硒仑联合使用有潜力用于治疗临床上重要的革兰氏阴性菌感染。

原文中“proposed mechanism”未明确给出中文释义,可根据具体语境理解,这里暂保留英文。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a2/9797518/9aed99312a91/fphar-13-1080281-g001.jpg

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