Suppr超能文献

二甲双胍增强多西环素疗效:来自体外、体内及形态学研究的证据。

Metformin Enhances Doxycycline Efficacy Against : Evidence from In Vitro, In Vivo, and Morphological Studies.

作者信息

Jiang Nansong, Wang Weiwei, Liang Qizhang, Fu Qiuling, Liu Rongchang, Fu Guanghua, Wan Chunhe, Cheng Longfei, Huang Yu, Chen Hongmei

机构信息

Research Center for Poultry Diseases, Institute of Animal Husbandry and Veterinary Medicine, Fujian Academy of Agricultural Sciences, Fuzhou 350013, China.

Fujian Key Laboratory for Prevention and Control of Avian Diseases, Fuzhou 350013, China.

出版信息

Microorganisms. 2025 Jul 23;13(8):1724. doi: 10.3390/microorganisms13081724.

Abstract

() is a zoonotic pathogen that poses a significant threat to animal health and causes substantial economic losses, further aggravated by rising tetracycline resistance. To restore the efficacy of tetracyclines to , we evaluated the synergistic antibacterial activity of doxycycline combined with metformin, an FDA-approved antidiabetic agent. Among several non-antibiotic adjuvant candidates, metformin exhibited the most potent in vitro synergy with doxycycline, especially against capsular serogroup A strain (A). The combination demonstrated minimal cytotoxicity and hemolysis in both mammalian and avian cells and effectively inhibited resistance development under doxycycline pressure. At 50 mg/kg each, the combination of metformin and doxycycline significantly reduced mortality in mice and ducks acutely infected with A (from 100% to 60%), decreased pulmonary bacterial burdens, and alleviated tissue inflammation and damage. Mechanistic validation confirmed that metformin enhances membrane permeability in without compromising membrane integrity, dissipates membrane potential, increases intracellular doxycycline accumulation, and downregulates the transcription of the tetracycline efflux gene (B). Morphological analyses further revealed pronounced membrane deformation and possible leakage of intracellular contents. These findings highlight metformin as a potent, low-toxicity tetracycline adjuvant with cross-species efficacy, offering a promising therapeutic approach for managing tetracycline-resistant infections.

摘要

(病原体名称未给出)是一种人畜共患病原体,对动物健康构成重大威胁,并造成巨大经济损失,四环素耐药性的上升进一步加剧了这种情况。为了恢复四环素对(病原体名称未给出)的疗效,我们评估了强力霉素与二甲双胍(一种美国食品药品监督管理局批准的抗糖尿病药物)联合使用的协同抗菌活性。在几种非抗生素佐剂候选物中,二甲双胍与强力霉素表现出最强的体外协同作用,尤其是对A群荚膜菌株(A)。该组合在哺乳动物和禽类细胞中均表现出最小的细胞毒性和溶血作用,并在强力霉素压力下有效抑制耐药性的产生。二甲双胍和强力霉素各以50mg/kg的剂量联合使用,可显著降低急性感染A群荚膜菌株(A)的小鼠和鸭子的死亡率(从100%降至60%),减少肺部细菌载量,并减轻组织炎症和损伤。机制验证证实,二甲双胍可增强(病原体名称未给出)的膜通透性而不损害膜完整性,耗散膜电位,增加细胞内强力霉素的积累,并下调四环素外排基因(B)的转录。形态学分析进一步揭示了明显的膜变形和细胞内内容物可能的泄漏。这些发现突出了二甲双胍作为一种高效、低毒的四环素佐剂,具有跨物种疗效,为治疗四环素耐药(病原体名称未给出)感染提供了一种有前景的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed67/12388482/0fe233a91765/microorganisms-13-01724-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验