Probiotics Combined with Metformin Improves Sperm Parameters in Obese Male Mice through Modulation of Intestinal Microbiota Equilibrium.

IF 2.6 3区 医学 Q2 OBSTETRICS & GYNECOLOGY
Reproductive Sciences Pub Date : 2025-01-01 Epub Date: 2024-12-02 DOI:10.1007/s43032-024-01748-9
Dan Liu, Xiaolong Han, Wenda Zou, Zhenyu Yang, Juan Peng, Yukun Li, Yuli Liu, Man Jia, Weijun Liu, Hui Li, Qianyin Zhou, Zhirong Tan, Juan Zhang
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Abstract

The decline in sperm parameters among obese males has attracted significant scholarly interest. The intestinal microbiota plays a crucial role in obesity, and investigating the intestinal-reproductive axis may offer a novel molecular approach to addressing the decline in male sperm parameters caused by obesity. To clarify whether probiotics, either alone or in conjunction with metformin, can enhance sperm parameters in obese male mice and assess the underlying mechanisms involved. 6-week-old male mice were constructed as obese models. Probiotics and metformin were used as intervention conditions. Changes in inflammatory factors and ROS content were detected by ELISA, morphological changes in testicular and colon tissues were observed by H&E staining, changes in intestinal microbiota abundance were detected by 16SrRNA gene sequencing, and changes in metabolites such as blood glucose, blood lipids, and lipopolysaccharide were detected by biochemical testing to investigate the mechanism of probiotics, metformin, and their combination to ameliorate reproductive impairment in obese male mice. Our results revealed that high-fat diet would result in reduced testicular spermatogenic tubule hierarchy, decreased spermatogenic cell counts, decreased sperm concentration and motility, and altered abundance of intestinal microbiota, whereas the combination of probiotics and metformin could restore high-fat-mediated pathophysiological alterations thereby ameliorating spermatogenic disorders in mice. The combination of probiotics and metformin can attenuate inflammation and oxidative stress, while enhancing androgen production to improve testicular spermatogenic function by re-construction intestinal microbiota equilibrium in HFD mice.

益生菌联合二甲双胍通过调节肠道菌群平衡改善肥胖雄性小鼠精子参数。
肥胖男性精子参数的下降引起了重大的学术兴趣。肠道微生物群在肥胖中起着至关重要的作用,研究肠道-生殖轴可能为解决肥胖引起的男性精子参数下降提供一种新的分子方法。阐明益生菌单独使用或与二甲双胍联合使用是否能提高肥胖雄性小鼠的精子参数,并评估其中的潜在机制。以6周龄雄性小鼠为肥胖模型。以益生菌和二甲双胍作为干预条件。ELISA检测炎症因子和ROS含量变化,H&E染色观察睾丸和结肠组织形态变化,16SrRNA基因测序检测肠道菌群丰度变化,生化检测血糖、血脂、脂多糖等代谢产物变化,探讨益生菌、二甲双胍、以及它们的组合改善肥胖雄性小鼠的生殖障碍。我们的研究结果表明,高脂肪饮食会导致睾丸生精小管层次减少,生精细胞数量减少,精子浓度和活力降低,肠道微生物群丰度改变,而益生菌和二甲双胍联合使用可以恢复高脂肪介导的病理生理改变,从而改善小鼠的生精障碍。益生菌与二甲双胍联合使用可以减轻HFD小鼠的炎症和氧化应激,同时通过重建肠道菌群平衡来增强雄激素的产生,改善睾丸生精功能。
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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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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