Hevener Andrea L, Clegg Deborah J, Mauvais-Jarvis Franck
Department of Medicine, Division of Endocrinology, Diabetes, and Hypertension, David Geffen School of Medicine, Iris Cantor-UCLA Women's Health Center, University of California, Los Angeles, CA 90095, USA.
Department of Biomedical Sciences, Diabetes and Obesity Research Institute Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Mol Cell Endocrinol. 2015 Dec 15;418 Pt 3(Pt 3):306-21. doi: 10.1016/j.mce.2015.05.020. Epub 2015 May 29.
Considering the current trends in life expectancy, women in the modern era are challenged with facing menopausal symptoms as well as heightened disease risk associated with increasing adiposity and metabolic dysfunction for up to three decades of life. Treatment strategies to combat metabolic dysfunction and associated pathologies have been hampered by our lack of understanding regarding the biological underpinnings of these clinical conditions and our incomplete understanding of the effects of estrogens and the tissue-specific functions and molecular actions of its receptors. In this review we provide evidence supporting a critical and protective role for the estrogen receptor α specific form in the maintenance of metabolic homeostasis and insulin sensitivity. Studies identifying the ER-regulated pathways required for disease prevention will lay the important foundation for the rational design of targeted therapeutics to improve women's health while limiting complications that have plagued traditional hormone replacement interventions.
考虑到当前预期寿命的趋势,现代女性面临着更年期症状以及与肥胖增加和代谢功能障碍相关的疾病风险增加的挑战,这种情况会持续长达三十年。由于我们对这些临床病症的生物学基础缺乏了解,以及对雌激素的作用及其受体的组织特异性功能和分子作用认识不全面,对抗代谢功能障碍及相关病症的治疗策略受到了阻碍。在本综述中,我们提供证据支持雌激素受体α特定形式在维持代谢稳态和胰岛素敏感性方面的关键保护作用。确定疾病预防所需的雌激素受体调节途径的研究,将为合理设计靶向治疗药物奠定重要基础,以改善女性健康,同时限制困扰传统激素替代干预措施的并发症。