The estrogen receptor-α is required and sufficient to maintain physiological glucose uptake in the mouse heart.

Abstract

Estrogens attenuate cardiac hypertrophy and increase cardiac contractility via their cognate estrogen receptors (ERs) ERα and ERβ. Because female sex hormones enhance global glucose use and because myocardial function and mass are tightly linked to cardiac glucose metabolism, we tested the hypothesis that expression and activation of the ERα might be required and sufficient to maintain physiological cardiac glucose uptake in the murine heart. Cardiac glucose uptake quantified in vivo by 18F-fluorodeoxyglucose positron emission tomography was strongly impaired in ovariectomized compared with gonadal intact female C57BL/6JO mice. The selective ERα agonist 16α-LE2 and the nonselective ERα and ERβ agonist 17β-estradiol completely restored cardiac glucose uptake in ovariectomized mice. Cardiac 18F-fluorodeoxyglucose uptake was strongly decreased in female ERα knockout mice compared with wild-type littermates. Analysis of cardiac mRNA accumulation by quantitative RT-PCR revealed an upregulation of genes involved in glycolisis and tricarboxylic acid cycle by ERα treatment. In conclusion, systemic activation of ERα is sufficient, and its expression is required to maintain physiological glucose uptake in the murine heart, which is likely to contribute to known cardioprotective estrogen effects.

• Authors: Paula-Anahi Arias-Loza, Michael C Kreissl, Susanne Kneitz, Franz R Kaiser, Ina Israel, Kai Hu, Stefan Frantz, Barbara Bayer, Karl-Heinz Fritzemeier, Kenneth S Korach, Theo Pelzer
• Journal: Hypertension (Dallas, Tex. : 1979) (Hypertension) Vol. 60 Issue 4 Pg. 1070-7 (Oct 2012) ISSN: 1524-4563 [Electronic] United States
• PMID: 22892812 (Publication Type: Journal Article, Research Support, N.I.H., Intramural, Research Support, Non-U.S. Gov't)

Chemical References

• Estrogen Receptor alpha
• Estrogen Receptor beta
• Estrogens
• Insulin
• Estradiol
• Glucose

Topics

• Animals
• Estradiol (pharmacology)
• Estrogen Receptor alpha (agonists, genetics, metabolism)
• Estrogen Receptor beta (agonists, genetics, metabolism)
• Estrogens (pharmacology)
• Female
• Glucose (metabolism)
• Heart (drug effects, physiology)
• Hemodynamics (physiology)
• Insulin (metabolism)
• Mice
• Mice, Knockout
• Myocardium (metabolism)
• Ovariectomy