肠道微生物群通过破坏小鼠血液-睾酮屏障促进 LPS 诱导的睾丸炎的发展

IF 2.6 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Reproductive Sciences Pub Date : 2024-11-01 Epub Date: 2024-06-10 DOI:10.1007/s43032-024-01613-9
Qing Guo, Ye Cheng, Tianfeng Li, Jiang Huang, Jinchun Li, Zecai Zhang, Yongli Qu
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引用次数: 0

摘要

睾丸炎是一种常见的生殖系统炎症,会导致男性不育和精子质量下降。肠道微生物群可调节全身和局部炎症、精子发生和血睾酮屏障(BTB)。本研究通过建立抗生素(ABX)治疗诱导的小鼠肠道微生物群失衡模型和脂多糖(LPS)感染诱导的睾丸炎模型,研究了肠道微生物群与睾丸炎之间的相关性。在这两个模型的基础上,结合16s rRNA测序和粪便微生物群移植(FMT)实验,研究肠道微生物群在宿主防御睾丸炎中的功能和调控机制。与对照组小鼠相比,肠道微生物群失衡导致炎症反应增加,调节氧化应激相关酶活性、睾酮水平和血睾酮屏障的通透性,而FMT后这些功能均得到恢复。随后,我们检测了睾丸炎患者肠道微生物群失衡与睾丸炎严重程度之间的关系。结果发现,与 LPS 处理的小鼠相比,ABX 和 LPS 联合处理的小鼠炎症反应更严重,睾酮水平更低,BTB 的通透性更高,但这些变化可通过肠道微生物群移植得到部分恢复。总之,上述结果首次证明了肠道微生物群参与了睾丸炎的发病机制,为后续开发抗睾丸炎药物和针对肠道菌群的益生菌奠定了良好的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The Gut Microbiota Contributes to the Development of LPS-Induced Orchitis by Disrupting the Blood-Testosterone Barrier in Mice.

Orchitis is a frequent inflammatory reproductive disease that causes male infertility and a decline in sperm quality. Gut microbiota can regulate systemic and local inflammation, spermatogenesis and blood-testosterone barrier (BTB). In this study, we investigated correlation between gut microbiota and orchitis by establishing a mouse gut microbiota imbalance model induced by antibiotics (ABX) treatment and orchitis model induced by lipopolysaccharide (LPS) infection. Based on these two models, 16s rRNA sequencing and feces microbiota transplantation (FMT) experiments were combined to examine the function and regulatory mechanisms of the gut microbiota in host defense against orchitis. Compared with control mice, gut microbiota imbalance resulted in increasing inflammatory responses, modulating oxidative stress related enzyme activity, testosterone levels and the permeability of blood testosterone barrier, which are restored after FMT. Subsequently, we tested the relationship between the gut microbiota imbalance and testicular inflammation severity in orchitis. It was found that the ABX and LPS co-treated mice had more severe inflammatory responses, lower testosterone levels and greater permeability of the BTB than the LPS-treated mice, but these changes could be partially recovered by gut microbiota transplantation. In conclusion, these above results proved for the first time that gut microbiota is involved in the pathogenesis of orchitis, which laid a good foundation for the subsequent development of anti-orchitis drugs and probiotic targeting intestinal flora.

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来源期刊
Reproductive Sciences
Reproductive Sciences 医学-妇产科学
CiteScore
5.50
自引率
3.40%
发文量
322
审稿时长
4-8 weeks
期刊介绍: Reproductive Sciences (RS) is a peer-reviewed, monthly journal publishing original research and reviews in obstetrics and gynecology. RS is multi-disciplinary and includes research in basic reproductive biology and medicine, maternal-fetal medicine, obstetrics, gynecology, reproductive endocrinology, urogynecology, fertility/infertility, embryology, gynecologic/reproductive oncology, developmental biology, stem cell research, molecular/cellular biology and other related fields.
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