Effect of Xianziyizhen Recipe Capsule on PGI2-PPARδ Signaling Pathway in Embryo Implantation Dysfunction Mice

Min Xu1, Ying-Zhou Tian1, Xiu-Jun Zhu1

  • 1Department of Gynecology, Guangdong Provincial Hospital of TCM, Guangzhou, China.

Abstract

Insights

Xianziyizhen recipe capsule (XRC) treatment improved embryo implantation dysfunction (EID) in mice by regulating the PGI2-PPARδ signaling pathway. XRC increased key protein and mRNA levels, suggesting its therapeutic potential for EID.

Area of Science:

  • Reproductive biology
  • Pharmacology
  • Traditional Chinese Medicine

Background:

  • Embryo implantation dysfunction (EID) poses a significant challenge in reproductive health.
  • The PGI2-PPARδ signaling pathway plays a crucial role in regulating the maternal-fetal interface during implantation.
  • Kidney deficiency is implicated in EID, and traditional herbs are explored for therapeutic benefits.

Purpose of the Study:

  • To investigate the therapeutic effect of Xianziyizhen recipe capsule (XRC) on EID in a mouse model.
  • To elucidate the role of the PGI2-PPARδ signaling pathway in XRC's mechanism of action for EID treatment.

Main Methods:

  • An EID mouse model was established using hydroxyurea and mifepristone.
  • Mice were treated with XRC or Progynova (estradiol).
  • mRNA expression of PPARδ and IL-11, and protein levels of COX-2, PGI2, MMP-9, and TIMP-3 were analyzed using RT-PCR and immunohistochemistry.

Main Results:

  • EID mice exhibited significantly lower endometrial PPARδ and IL-11 mRNA levels, and reduced COX-2, PGI2, MMP-9, and TIMP-3 protein levels.
  • XRC and Progynova treatments reversed these alterations, increasing the expression of these key molecules.
  • These findings indicate XRC's efficacy in restoring normal molecular profiles associated with implantation.

Conclusions:

  • Xianziyizhen recipe capsule (XRC) demonstrates significant therapeutic benefits for embryo implantation dysfunction (EID).
  • XRC appears to exert its effects by modulating the PGI2-PPARδ signaling pathway.
  • These findings support the use of XRC as a potential treatment for EID.

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