AI Article Synopsis

  • The study explored how the Xianziyizhen recipe capsule (XRC) affects the PGI2-PPARδ signaling pathway in mice with embryo implantation dysfunction (EID).
  • The method involved administering XRC and estradiol to EID mice and analyzing changes in specific gene and protein expressions in their endometrium.
  • The results indicated that XRC treatment improved gene expression and protein levels associated with embryo implantation compared to untreated EID mice, suggesting its potential benefits in treating EID by regulating the PGI2-PPARδ pathway.

Article Abstract

Problem: We investigated the effect of Xianziyizhen recipe capsule (XRC), a kidney-tonifying herb, on the PGI2-PPARδ signaling pathway at the maternal-fetal interface in embryo implantation dysfunction (EID) mice.

Method Of Study: Intragastric administration of Progynova (estradiol) or XRC was performed in EID mouse model, following experimental induction of kidney deficiency by co-treatment with chemotherapy drug hydroxyurea and antiprogesterone mifepristone. The PPARδ and IL-11 mRNA expression in endometrium were detected by real-time relative reverse transcription-polymerase chain reaction (RT-PCR). Further, the protein expression of COX-2, PGI2, MMP-9, and TIMP-3 was detected in endometrial glandular epithelium and in stromal cells by immunohistochemical (IHC) assay.

Results: The results showed that hydroxyurea and mifepristone-induced EID were associated with significantly lower PPARδ and IL-11 mRNA levels in endometrium and reduced COX-2, PGI2, MMP-9, and TIMP-3 levels in endometrial glandular epithelium, compared with normal controls. However, XRC and Progynova treatment reversed these effects, leading to significant increases in PPARδ and IL-11 mRNA expression, and COX-2, PGI2, MMP-9 and TIMP-3 protein levels, when compared with the levels observed in EID mice.

Conclusion: These results strongly suggested that XRC is beneficial in EID treatment and that XRC may mediate its effects through regulation of the PGI2-PPARδ signaling pathway.

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Source
http://dx.doi.org/10.1111/aji.12361DOI Listing

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