Degree Name

MS (Master of Science)

Program

Biology

Date of Award

5-2026

Committee Chair or Co-Chairs

Cerrone Foster

Committee Members

Anoop Aruagiri, Sanjay Singh

Abstract

Cardiovascular disease (CVD) is the leading cause of death worldwide and shows important sex differences in incidence and progression. Premenopausal women are relatively protected compared to age-matched men, but this protection declines after menopause, suggesting a key role for estrogen. We hypothesized that prolonged estrogen loss exacerbates cardiac dysfunction under sympathetic stimulation, promoting adverse remodeling. To test this, seven-month post-ovariectomized and sham-operated female mice were treated with isoproterenol (400 μg/kg/hour) for 7 days to model heart failure. Cardiac function was assessed by transthoracic echocardiography. Cardiac hypertrophy, apoptosis, and fibrosis were evaluated using histological staining of heart sections. Prolonged estrogen loss increased mortality by 45% following sympathetic stimulation. Although fractional shortening increased and ejection fraction showed no significant differences, combined estrogen loss and heart failure significantly increased fibrosis, hypertrophy, and apoptosis. These findings demonstrate that prolonged estrogen loss reduces survival and exacerbates pathological cardiac remodeling under chronic sympathetic stress.

Document Type

Thesis - embargo

Copyright

Copyright by the authors.

Available for download on Tuesday, June 15, 2027

Included in

Physiology Commons

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