Abstract

Samul-tang (SM), a traditional herbal medicine, has been used to treat menstrual irregularities and infertility in women. However, the cellular and molecular mechanisms underlying the effects of SM remain elusive. We investigated the potential protective effect of SM against chronic ovarian dysfunction and used bioinformatics analysis to identify its underlying mechanism in a mouse model of cyclophosphamide (CP)-induced diminished ovarian reserve. Female C57BL/6 mice were intraperitoneally injected with CP three times a week, followed by oral administration of distilled water (CP group) or SM (CP + SM group) for 4 weeks. Four weeks later, the effect of SM was assessed by ovarian tissue histological analysis, steroid hormone measurement, oocyte quality, and mRNA and microRNA microarray analysis in the ovaries. Although SM administration did not prevent CP-induced follicle loss in mice, the quality of oocytes was better in CP + SM mice than in CP mice. Gene expression analysis revealed that the expression of fertilisation- and ovarian follicle development-related genes was altered by CP treatment but normalized after SM administration. Further bioinformatics analysis showed possible interactions between differentially expressed mRNAs and microRNAs. Therefore, we demonstrated the protective effects of SM on ovarian function and oocyte maturation against CP-induced damage via multiple epigenetic mechanisms.

Highlights

  • Samul-tang (SM), a traditional herbal medicine, has been used to treat menstrual irregularities and infertility in women

  • We found that the Bmp[15] mRNA harboured binding sites for miR-200b-3p and miR-665-3p and that the Oas[1] family transcript harboured a binding site for miR-667-3p, of which expressions were changed by SM administration after CP exposure

  • In this study, we investigated the effects of SM as a fertoprotective adjuvant in a CP-induced diminished ovarian reserve (DOR) mouse model

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Summary

Introduction

Samul-tang (SM), a traditional herbal medicine, has been used to treat menstrual irregularities and infertility in women. We investigated the potential protective effect of SM against chronic ovarian dysfunction and used bioinformatics analysis to identify its underlying mechanism in a mouse model of cyclophosphamide (CP)-induced diminished ovarian reserve. SM administration did not prevent CP-induced follicle loss in mice, the quality of oocytes was better in CP + SM mice than in CP mice. Further bioinformatics analysis showed possible interactions between differentially expressed mRNAs and microRNAs. we demonstrated the protective effects of SM on ovarian function and oocyte maturation against CP-induced damage via multiple epigenetic mechanisms. In this study, we investigated the potential protective effect of SM and its underlying molecular mechanism in mice with a CP-induced chronic impairment of ovarian function

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