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Aging is associated with altered estrogen receptor expression and alters redox protein balance in human female skeletal muscle
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DOI：10.1007/s11357-026-02432-3.png)
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Abstract
En 中文
It has been hypothesized that age‑related declines in skeletal muscle and vascular function in females may be partly estrogen‑dependent. This study investigated skeletal muscle protein expression of estrogen receptor α (ERα), estrogen receptor β (ERβ), and G protein–coupled estrogen receptor 1 (GPER1), and their association with proteins involved in redox regulation and vascular function, in relation to age, menopausal status, and lifelong physical activity. Skeletal muscle biopsies were obtained from 107 healthy females aged 19–70 years, including 26 postmenopausal females who were lifelong exercise trained. Protein expression of ERα, ERβ, GPER1, and downstream redox‑ and vascular‑related proteins was quantified. Age‑ and menopause‑related differences, associations between protein targets, and effects of lifelong exercise were examined. ERα protein expression was lower in older females with a 48% lower expression in the ≥ 55 years age group compared with the < 30-year group. GPER1 protein expression was 22% lower across all older age groups compared with the < 30-year group. ERβ expression was reduced in mid‑life (45–59 years) but not in the oldest age group. Both ERα and ERβ were positively correlated with endothelial nitric oxide synthase (eNOS) expression, whereas GPER1 showed no association with eNOS. ERβ expression was associated with pro‑oxidative NOX2 expression. Aging in females is associated with a lower ERα and GPER1 protein expression in skeletal muscle. Furthermore, lower ER expression by aging is associated with a lower eNOS expression, indicating associations with proteins involved in nitric oxide-related redox regulation in skeletal muscle in aged females. Aging in females was associated with a lower expression of estrogen receptor-α (ERα) and G protein–coupled estrogen receptor 1 (GPER1) in skeletal muscle. This age-related downregulation of estrogen receptors coincided with lower endothelial nitric oxide synthase (eNOS) expression, suggesting a shift toward a diminished antioxidant capacity and a more pro-oxidative skeletal muscle environment in aged females. Figure created with BioRender.
Keywords:
Menopause
Estrogen receptors
Oxidative stress
Females vascular aging
Skeletal muscle
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