Tissue-selective estrogen complexes with bazedoxifene prevent metabolic dysfunction in female mice

被引:108
作者
Kim, Jun Ho
Meyers, Matthew S.
Khuder, Saja S.
Abdallah, Simon L.
Muturi, Harrison T.
Russo, Lucia
Tate, Chandra R.
Hevener, Andrea L.
Najjar, Sonia M.
Leloup, Corinne
Mauvais-Jarvis, Franck [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Div Endocrinol Metab & Mol Med, Dept Med, Chicago, IL 60611 USA
关键词
Tissue selective estrogen complexes; Bazedoxiiene; Menopause; Metabolic syndrome; Insulin resistance; Type; 2; diabetes;
D O I
10.1016/j.molmet.2013.12.009
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Pairing the selective estrogen receptor modulator bazedoxifene (BZA) with estrogen as a tissue-selective estrogen complex (TSEC) is a novel menopausal therapy. We investigated estrogen, BZA and TSEC effects in preventing diabetisity in ovariectomized mice during high-fat feeding. Estrogen, BZA or TSEC prevented fat accumulation in adipose tissue, liver and skeletal muscle, and improved insulin resistance and glucose intolerance without stimulating uterine growth. Estrogen, BZA and TSEC improved energy homeostasis by increasing lipid oxidation and energy expenditure, and promoted insulin action by enhancing insulin-stimulated glucose disposal and suppressing hepatic glucose production. While estrogen improved metabolic homeostasis, at least partially, by increasing hepatic production of FGF21, BZA increased hepatic expression of Sirtuint PPARa and AMPK activity. The metabolic benefits of BZA were lost in estrogen receptor-a deficient mice. Thus, BZA alone or in TSEC produces metabolic signals of fasting and caloric restriction and improves energy and glucose homeostasis in female mice. (C) 2014 The Authors. Published by Elsevier GmbH.
引用
收藏
页码:177 / 190
页数:14
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