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知母皂苷 AIII 通过抑制炎症反应和调节子宫微生物群落结构对大肠杆菌诱导的小鼠子宫内膜炎的保护作用。

Protective effect of Timosaponin AIII on Escherichia coli-induced endometritis in mice through inhibiting inflammatory response and regulating uterine microbiota structure.

机构信息

China-Japan Union Hospital, Jilin University, Jilin, China.

China-Japan Union Hospital, Jilin University, Jilin, China.

出版信息

Int Immunopharmacol. 2024 Mar 30;130:111649. doi: 10.1016/j.intimp.2024.111649. Epub 2024 Feb 16.

Abstract

Endometritis is a sort of general reproductive disease, which can lead to infertility in both humans and animals. Escherichia coli (E. coli) is recognised as the main bacterial etiology of endometritis among livestock and causes huge economic losses to dairy farming industry. Antibiotics are frequently used in the clinical treatment of endometritis; nevertheless, long-term use may result in adverse effects, including bacterial resistance and food safety concerns. TSAIII, one of the active pharmacological components of A. asphodeloides, has exhibited multiple biological activities, including anticancer, anti-angiogenesis, and anti-inflammatory properties. However, the protective effects of TSAIII in E. coli-challenged endometritis remain unclear. This study aimed to clarify the role of TSAIII in E. coli-induced endometritis in mice and elucidate its specific molecular mechanisms. In the present research, TSAIII treatment markedly alleviated the E. coli-induced uterine histopathological injury, and decreased myeloperoxidase (MPO) activity and pro-inflammatory cytokines levels in uterine tissue. Our results further demonstrated that TSAIII improved uterine epithelial barrier function by restoring the expressions of tight junction proteins. Furthermore, TSAIII administration noticeably suppressed the activation of the TLR4/NF-κB pathway and the NLRP3 inflammasome. Importantly, we found that TSAIII could regulate the uterine microbiota structure and composition in E. coli-induced mouse endometritis. In conclusion, these data demonstrate that treatment with TSAIII protects against E. coli-induced endometritis via modulating uterine microbiota composition, inhibiting TLR4/NF-κB pathway and NLRP3 inflammasome activation, in addition to improving uterine epithelial barrier function. Therefore, the results of this study provide a new therapeutic to potentially prevent endometritis.

摘要

子宫内膜炎是一种常见的生殖系统疾病,可导致人类和动物不孕。大肠杆菌(E. coli)被认为是家畜子宫内膜炎的主要细菌病因,给奶牛养殖业造成了巨大的经济损失。抗生素常被用于子宫内膜炎的临床治疗;然而,长期使用可能会导致细菌耐药性和食品安全问题。天山雪莲中的活性药理成分 TSAIII 具有多种生物活性,包括抗癌、抗血管生成和抗炎特性。然而,TSAIII 在大肠杆菌引起的子宫内膜炎中的保护作用尚不清楚。本研究旨在阐明 TSAIII 在大肠杆菌诱导的小鼠子宫内膜炎中的作用及其具体的分子机制。在本研究中,TSAIII 治疗显著减轻了大肠杆菌引起的子宫组织病理损伤,降低了子宫组织中髓过氧化物酶(MPO)活性和促炎细胞因子水平。我们的结果进一步表明,TSAIII 通过恢复紧密连接蛋白的表达来改善子宫上皮屏障功能。此外,TSAIII 给药明显抑制了 TLR4/NF-κB 途径和 NLRP3 炎性小体的激活。重要的是,我们发现 TSAIII 可以调节大肠杆菌诱导的小鼠子宫内膜炎中的子宫微生物群结构和组成。总之,这些数据表明,TSAIII 通过调节子宫微生物群组成、抑制 TLR4/NF-κB 途径和 NLRP3 炎性小体的激活以及改善子宫上皮屏障功能来预防大肠杆菌引起的子宫内膜炎。因此,本研究结果为预防子宫内膜炎提供了一种新的治疗方法。

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