Effects of electroacupuncture on luteal regression and steroidogenesis in ovarian hyperstimulation syndrome model rat

Life Sci. 2018 Mar 15:197:1-9. doi: 10.1016/j.lfs.2018.01.026. Epub 2018 Feb 4.

Abstract

Aims: Electroacupuncture (EA) is an effective and safe therapeutic method widely used for treating clinical diseases. Previously, we found that EA could decrease serum hormones and reduce ovarian size in ovarian hyperstimulation syndrome (OHSS) rat model. Nevertheless, the mechanisms that contribute to these improvements remain unclear.

Materials and methods: HE staining was used to count the number of corpora lutea (CL) and follicles. Immunohistochemical and ELISA were applied to examine luteal functional and structural regression. Immunoprecipitation was used for analyzing the interaction between NPY (neuropeptide Y) and COX-2; western blotting and qRT-PCR were used to evaluate the expressions of steroidogenic enzymes and PKA/CREB pathway.

Key findings: EA treatment significantly reduced the ovarian weight and the number of CL, also decreased ovarian and serum levels of PGE2 and COX-2 expression; increased ovarian PGF2α levels and PGF2α/PGE2 ratio; decreased PCNA expression and distribution; and increased cyclin regulatory inhibitor p27 expression to have further effect on the luteal formation, and promote luteal functional and structural regression. Moreover, expression of COX-2 in ovaries was possessed interactivity increased expression of NPY. Furthermore, EA treatment lowered the serum hormone levels, inhibited PKA/CREB pathway and decreased the expressions of steroidogenic enzymes. Hence, interaction with COX-2, NPY may affect the levels of PGF2α and PGE2 as well as impact the proliferation of granulosa cells in ovaries, thus further reducing the luteal formation, and promoting luteal structural and functional regression, as well as the ovarian steroidogenesis following EA treatment.

Significance: EA treatment could be an option for preventing OHSS in ART.

Keywords: Electroacupuncture; Luteal regression; Neuropeptide Y; OHSS; Steroidogenesis.

MeSH terms

  • Animals
  • Corpus Luteum* / metabolism
  • Corpus Luteum* / pathology
  • Cyclooxygenase 2 / biosynthesis
  • Dinoprost / metabolism*
  • Dinoprostone / biosynthesis*
  • Disease Models, Animal
  • Electroacupuncture*
  • Female
  • Gene Expression Regulation
  • Ovarian Hyperstimulation Syndrome* / metabolism
  • Ovarian Hyperstimulation Syndrome* / pathology
  • Ovarian Hyperstimulation Syndrome* / therapy
  • Proliferating Cell Nuclear Antigen / biosynthesis
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Proliferating Cell Nuclear Antigen
  • Dinoprost
  • Cyclooxygenase 2
  • Ptgs2 protein, rat
  • Dinoprostone