Cardiac function and tolerance to ischemia/reperfusion injury in a rat model of polycystic ovary syndrome during the postmenopausal period

Life Sci. 2020 Dec 1:262:118394. doi: 10.1016/j.lfs.2020.118394. Epub 2020 Sep 7.

Abstract

Aims: There is much controversy regarding whether cardiovascular events increase in women with polycystic ovary syndrome (PCOS) with aging. Considering the lack of possibility of certain investigations in humans, animal models of PCOS may be suitable resources to obtain the useful data needed. In this study; we aimed to investigate whether cardiac function and tolerance to ischemia/reperfusion (I/R) injury worsen in postmenopausal rats, who had PCOS at younger ages, compared to controls.

Main methods: The hearts of aged rats with a history of PCOS and their controls were isolated and perfused in a Langendorff apparatus. Values of hemodynamic parameters, including left ventricular systolic pressure (LVSP), left ventricular developed pressure (LVDP), rate pressure product (RPP) and peak rates of positive and negative changes in left ventricular pressure (±dp/dt) were recorded using a power lab system. Blood serum levels of total testosterone (TT) and estradiol (E2) were determined by ELISA kits. Generalized Estimating Equation Model and t-student unpaired test results were used to compare the findings documented between two groups.

Key findings: No statistically significant differences were observed in hemodynamic parameters of the heart including, LVSP, LVDP, RPP and ±dp/dt, between the rats of two groups of study, at baseline or before ischemia and after I/R. Nor were any significant differences observed in the levels of two hormones between the two groups (p > 0.05).

Significance: History of PCOS during reproductive ages should not be considered an important risk factor for reduction in cardiac contractile function or less tolerance to I/R injury during the postmenopausal period.

Keywords: Cardiac function; Ischemia/reperfusion injury; Polycystic ovary syndrome; Postmenopausal period; Rat.

MeSH terms

  • Aging / physiology
  • Animals
  • Disease Models, Animal
  • Estradiol / blood
  • Female
  • Hemodynamics / physiology
  • Myocardial Contraction / physiology*
  • Myocardial Reperfusion Injury / physiopathology*
  • Polycystic Ovary Syndrome / physiopathology*
  • Postmenopause*
  • Rats
  • Rats, Wistar
  • Risk Factors
  • Testosterone / blood

Substances

  • Testosterone
  • Estradiol