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RESEARCH PAPER / 2025-07-07

The angiotensin II type 2 receptor attenuates aging-associated arterial stiffness in female mice.

Casey G Turner, Rachel Kenney, Jennifer Vorn, Seung Kyum Kim, Greg Martin, Lakshmi Pulakat, Iris Z Jaffe, Jennifer J DuPont

Molecular Cardiology Research Institute, Tufts Medical Center, Boston, Massachusetts, United States.Molecular Cardiology Research Institute, Tufts Medical Center, Boston, Massachusetts, United States. · pubmed

Abstract

Arterial stiffness is associated with overall and cardiovascular-specific mortality, and this association is exacerbated in women over 55 yr of age. Recent literature supports that stimulation of the angiotensin II type 2 receptor (AT2R) can protect from arterial stiffening, and that AT2R has a greater role in female cardiovascular physiology relative to males. The current study aimed to investigate the role of the AT2R in sex differences in aging-associated arterial stiffness. In female mice, the aging-related increase in arterial stiffness is temporally associated with a loss of aortic AT2R mRNA expression, but this is not observed in males. Chronic AT2R inhibition in vivo increases arterial stiffening in young female and male mice, as well as middle-aged female mice. The inhibition of AT2R is associated with an increase in aortic integrinα5 mRNA expression in young males and an increase in collagen1α1 mRNA expression in middle-aged females. Overall, these findings identify a sex-specific mechanism of aging-associated arterial stiffening in mice involving AT2R attenuation and collagen upregulation in females.

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Research summary

The study claims that the angiotensin II type 2 receptor (AT2R) plays a significant role in sex-specific mechanisms of aging-associated arterial stiffness in female mice. This research is relevant as it addresses a potential underlying mechanism of aging-related cardiovascular issues, particularly in women, which could inform future strategies for longevity and age-related disease prevention.

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