4.7 Article

Tempol ameliorates polycystic ovary syndrome through attenuating intestinal oxidative stress and modulating of gut microbiota composition-serum metabolites interaction

期刊

REDOX BIOLOGY
卷 41, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.redox.2021.101886

关键词

Polycystic ovary syndrome; Tempol; Gut microbiota; Metabolites

资金

  1. National Natural Science Foundation of China [81801407, 82070250]
  2. Beijing Natural Science Foundation [7184212]
  3. Beijing Hospitals Authority Youth Programme [QML20191401]
  4. Beijing Postdoctoral Research Foundation

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The study demonstrated that treatment with tempol alleviated ovarian dysfunction and glucose tolerance in PCOS rats, reduced intestinal oxidative stress, and modulated gut microbiota composition. Tempol intervention is suggested as a potential therapeutic approach for PCOS due to its ability to improve PCOS phenotype by restoring gut dysbiosis.
Polycystic ovary syndrome (PCOS) is a complex endocrine and metabolic disorder, which is often accompanied by oxidative stress. Tempol, a superoxide dismutase mimetic, protects against several diseases caused by oxidative stress. However, the effect of tempol on PCOS has not been investigated. The present study demonstrated the alleviation of ovarian dysfunction and glucose tolerance in dehydroepiandrosterone (DHEA)-induced PCOS rats treated with tempol. Tempol significantly reduced the intestinal oxidative stress in PCOS rats without affecting the ovarian redox rate. The 16S rDNA sequencing of the intestinal microbiome and non-targeted metabolomics analysis indicated significant differences in gut microbiota composition and serum metabolite profiles between the control and PCOS rats, and most of these differences were reduced after tempol intervention. Tempol alters the gut microbiome by increasing the abundance of genus Ruminococcus_1 and by decreasing the abundance of Ruminococcus_2, Staphylococcus, Ideonella, and Corynebnacterium genera. Tempol also attenuates the reduction of serum bile acid and stachyose levels in PCOS rats, and the serum stachyose level was significantly correlated with the abundance of 15 genera, particularly Ruminococcus_1 and Ruminococcus_2. Moreover, stachyose administration improved ovarian dysfunction in PCOS rats. Thus, our data indicate that tempol ameliorates PCOS phenotype by reducing intestinal oxidative stress, restoring gut dysbiosis, and modulating the interaction between gut microbiota and host metabolite. Therefore, tempol intervention is a potential therapeutic approach for PCOS.

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