부산대학교 도서관

Aging is associated with visceral adiposity, metabolic disorders, and chronic low-grade inflammation. 17[alpha]-estradiol (17[alpha]-E2), a naturally occurring enantiomer of 17[beta]-estradiol (17[beta]-E2), extends life span in male mice through unresolved mechanisms. We tested whether 17[alpha]-E2 could alleviate age-related metabolic dysfunction and inflammation. 17[alpha]-E2 reduced body mass, visceral adiposity, and ectopic lipid deposition without decreasing lean mass. These declines were associated with reductions in energy intake due to the activation of hypothalamic anorexigenic pathways and direct effects of 17[alpha]-E2 on nutrient-sensing pathways in visceral adipose tissue. 17[alpha]-E2 did not alter energy expenditure or excretion. Fasting glucose, insulin, and glycosylated hemoglobin were also reduced by 17[alpha]-E2, and hyperinsulinemic-euglycemic clamps revealed improvements in peripheral glucose disposal and hepatic glucose production. Inflammatory mediators in visceral adipose tissue and the circulation were reduced by 17[alpha]-E2. 17[alpha]-E2 increased AMPK[alpha] and reduced mTOR complex 1 activity in visceral adipose tissue but not in liver or quadriceps muscle, which is in contrast to the generalized systemic effects of caloric restriction. These beneficial phenotypic changes occurred in the absence of feminization or cardiac dysfunction, two commonly observed deleterious effects of exogenous estrogen administration. Thus, 17[alpha]-E2 holds potential as a novel therapeutic for alleviating age-related metabolic dysfunction through tissue-specific effects. Keywords: 17[alpha]-Estradiol--Adipose tissue--Hypothalamus--Inflammation--Metabolism doi:10.1093/gerona/glv309