Shiyan dongwu yu bijiao yixue (Oct 2021)

Relationship Between the Abnormal Expression of PPARs and Insulin Resistance in Uterus of Rats with Polycystic Ovary Syndrome and Insulin Resistance

  • WEI Wei,
  • CHEN Yihua,
  • ZHANG Xiuzhi,
  • LENG Yifu,
  • LI Chun,
  • YIN Tianxiao

DOI
https://doi.org/10.12300/j.issn.1674-5817.2020.206
Journal volume & issue
Vol. 41, no. 5
pp. 435 – 442

Abstract

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ObjectiveTo investigate the relationship between abnormal expression of peroxisome proliferator-activated receptors (PPARs) and insulin resistance in the uterine tissues of rats with polycystic ovary syndrome and insulin resistance (PCOS-IR).MethodsForty female SD rats were randomly divided into normal control and PCOS-IR model groups. PCOS-IR models were established by subcutaneous injection of insulin and human chorionic gonadotropin (INS+hCG) method, and rats in the normal control group were injected with equal amounts of normal saline. Fasting insulin (FINS) and fasting plasma glucose (FPG) levels were measured by enzyme-linked immunosorbent assay (ELISA), and the insulin resistance index (HOMA-IR) was calculated. Uterine tissues of rats were stained with hematoxylin-eosin (HE), PPARs were detected by immunohistochemistry, and the expressions of PPARs, insulin receptors (IRS), glucose transporter 4 (GLUT-4), and insulin-like growth factor-1 (IGF-1) were detected by Western blotting.ResultsFPG and FINS levels and HOMA-IR in the model group were significantly higher than those in the normal control group (P 0.05). Western blotting results showed that the expression of PPARα, PPARγ, IRS, and GLUT-4 in the rat uterus of the model group was significantly lower than that of the normal control group (P < 0.05), while the expression of IGF-1 was higher than that of the normal control group (P < 0.05).ConclusionThe expression of IRS and GLUT-4 is down-regulated and the expression of IGF-1 is up-regulated in the uterine tissue of PCOS-IR rats. The existence of IR is confirmed in the uterine tissue of PCOS-IR rats, and it may be related to the down-regulation of PPARα and PPARγ expression in the uterine tissues.

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