Obesity and insulin resistance induce early development of diastolic dysfunction in young female mice fed a Western

Camila Manrique1, Vincent G DeMarco, Annayya R Aroor

  • 1MD, Professor of Medicine and Medical Pharmacology and Physiology, University of Missouri, D109 Diabetes Center Health Sciences Center, One Hospital Drive, Columbia, Missouri 65212. sowersj@health.missouri.edu.

Endocrinology
|July 26, 2013
PubMed

Insights

A Western diet causes diastolic dysfunction, an early sign of heart failure, in female mice due to insulin resistance and increased cardiac stiffness. Male mice did not develop this dysfunction.

Area of Science:

  • Cardiovascular physiology
  • Metabolic disease research
  • Sex differences in disease

Background:

  • Cardiovascular disease (CVD) is a leading cause of death, particularly in individuals with diabetes.
  • Women lose cardiovascular protection postmenopause and with diabetes, with heart failure and diastolic dysfunction being key concerns.
  • Insulin resistance and obesity exacerbate heart failure risk in females.

Purpose of the Study:

  • To investigate the mechanisms underlying diastolic dysfunction in insulin-resistant female mice.
  • To compare the cardiac effects of a Western diet (WD) in young female versus male mice.

Main Methods:

  • Eight weeks of a high-fructose/high-fat WD was administered to young female and male C57BL6/J mice.
  • Insulin sensitivity was assessed using hyperinsulinemic-euglycemic clamps.
  • Cardiac structure and function were evaluated via two-dimensional echocardiography and electron microscopy.

Main Results:

  • Both sexes developed systemic insulin resistance after WD exposure.
  • Only female mice exhibited diastolic dysfunction, characterized by increased collagen 1, oxidative stress, and altered mitochondria.
  • Higher baseline aldosterone levels in females, independent of WD, were observed.

Conclusions:

  • A Western diet predisposes females to early diastolic heart failure, independent of overall insulin resistance.
  • Elevated aldosterone in females may interact with insulin resistance to promote myocardial stiffness and diastolic dysfunction under overnutrition.

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