Key result
Aging-induced alterations in responsiveness of the coronary resistance vasculature to endothelin are sex-specific, with ET-induced vasoconstriction reduced with age in males but increased in females.
Why the study?
Do age-induced alterations in responses of coronary arterioles to endothelin differ between male and female rats?
Do age-induced alterations in responses of coronary arterioles to endothelin differ between male and female rats?
Aging induces sex-specific alterations in the responsiveness of coronary resistance vasculature to endothelin, which may contribute to sexual dimorphism in cardiovascular disease risk.
Rat coronary data show sex-specific ET aging effects; hypothesis-generating for human CVD dimorphism, needs clinical validation.
OBJECTIVE: The risk for cardiovascular disease increases with advancing age; however, the chronological development of heart disease differs in males and females. The purpose of this study was to determine whether age-induced alterations in responses of coronary arterioles to the endogenous vasoconstrictor, endothelin, are sex-specific. METHODS: Coronary arterioles were isolated from young and old male and female rats to assess vasoconstrictor responses to endothelin (ET), and ETa and ETb receptor inhibitors were used to assess receptor-specific signaling. RESULTS: In intact arterioles from males, ET-induced vasoconstriction was reduced with age, whereas age increased vasoconstrictor responses to ET in intact arterioles from female rats. In intact arterioles from both sexes, blockade of either ETa or ETb eliminated age-related differences in responses to ET; however, denudation of arterioles from both sexes revealed age-related differences in ETa-mediated vasoconstriction. In arterioles from male rats, ETa receptor protein decreased, whereas ETb receptor protein increased with age. In coronary arterioles from females, neither ETa nor ETb receptor protein changed with age, suggesting age-related changes in ET signaling occur downstream of ET receptors. CONCLUSIONS: Thus, aging-induced alterations in responsiveness of the coronary resistance vasculature to endothelin are sex-specific, possibly contributing to sexual dimorphism in the risk of cardiovascular disease with advancing age.
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LeBlanc et al. (2012) studied Cardiovascular disease risk. Endothelin (ET) and ETa/ETb receptor inhibitors vs. Young vs old, male vs female was evaluated on Vasoconstrictor responses to endothelin. Aging-induced alterations in responsiveness of the coronary resistance vasculature to endothelin are sex-specific, with ET-induced vasoconstriction reduced with age in males but increased in females.
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