Reue Karen
Department of Human Genetics, David Geffen School of Medicine at UCLA, United States; Molecular Biology Institute, University of California, Los Angeles, United States.
Physiol Behav. 2017 Jul 1;176:174-182. doi: 10.1016/j.physbeh.2017.02.040. Epub 2017 Mar 8.
Obesity is a world-wide problem, and a risk factor for cardiovascular disease, diabetes, cancer and other diseases. It is well established that sex differences influence fat storage. Males and females exhibit differences in anatomical fat distribution, utilization of fat stores, levels of adipose tissue-derived hormones, and obesity co-morbidities. The basis for these sex differences may be parsed into the effects of male vs. female gonadal hormones and the effects of XX vs. XY chromosome complement. Studies employing mouse models that allow the distinction of gonadal from chromosomal effects have revealed that X chromosome dosage influences food intake, which in turn affects adiposity and the occurrence of adverse metabolic conditions such as hyperinsulinemia, hyperlipidemia, and fatty liver. The identification of X chromosome dosage as a player in the behavior and physiology related to obesity suggests novel molecular mechanisms that may underlie sex differences in obesity and metabolism.
肥胖是一个全球性问题,也是心血管疾病、糖尿病、癌症和其他疾病的危险因素。众所周知,性别差异会影响脂肪储存。男性和女性在解剖学上的脂肪分布、脂肪储备的利用、脂肪组织衍生激素的水平以及肥胖合并症方面存在差异。这些性别差异的基础可以分为男性与女性性腺激素的影响以及XX与XY染色体组成的影响。采用小鼠模型的研究能够区分性腺效应和染色体效应,结果显示X染色体剂量会影响食物摄入量,进而影响肥胖以及诸如高胰岛素血症、高脂血症和脂肪肝等不良代谢状况的发生。将X染色体剂量确定为与肥胖相关的行为和生理过程中的一个因素,提示了肥胖和代谢性别差异可能潜在的新分子机制。