Lai Hao, Jia Xiao, Yu Qiuxiao, Zhang Chenglu, Qiao Jie, Guan Youfei, Kang Jihong
Department of Physiology and Pathophysiology, Peking University Health Science Center, Beijing, China.
Department of Obstetrics and Gynecology, Center for Reproductive Medicine, Peking University Third Hospital, Beijing, China.
Biol Reprod. 2014 Nov;91(5):127. doi: 10.1095/biolreprod.114.120063. Epub 2014 Aug 6.
Polycystic ovary syndrome (PCOS) is the most common female endocrinopathy associated with both reproductive and metabolic disorders. Dehydroepiandrosterone (DHEA) is currently used to induce a PCOS mouse model. High-fat diet (HFD) has been shown to cause obesity and infertility in female mice. The possible effect of an HFD on the phenotype of DHEA-induced PCOS mice is unknown. The aim of the present study was to investigate both reproductive and metabolic features of DHEA-induced PCOS mice fed a normal chow or a 60% HFD. Prepubertal C57BL/6 mice (age 25 days) on the normal chow or an HFD were injected (s.c.) daily with the vehicle sesame oil or DHEA for 20 consecutive days. At the end of the experiment, both reproductive and metabolic characteristics were assessed. Our data show that an HFD did not affect the reproductive phenotype of DHEA-treated mice. The treatment of HFD, however, caused significant metabolic alterations in DHEA-treated mice, including obesity, glucose intolerance, dyslipidemia, and pronounced liver steatosis. These findings suggest that HFD induces distinct metabolic features in DHEA-induced PCOS mice. The combined DHEA and HFD treatment may thus serve as a means of studying the mechanisms involved in metabolic derangements of this syndrome, particularly in the high prevalence of hepatic steatosis in women with PCOS.
多囊卵巢综合征(PCOS)是最常见的与生殖和代谢紊乱相关的女性内分泌疾病。脱氢表雄酮(DHEA)目前被用于诱导PCOS小鼠模型。高脂饮食(HFD)已被证明会导致雌性小鼠肥胖和不育。HFD对DHEA诱导的PCOS小鼠表型的可能影响尚不清楚。本研究的目的是调查喂食正常饲料或60%HFD的DHEA诱导的PCOS小鼠的生殖和代谢特征。对处于青春期前的C57BL/6小鼠(25日龄),正常饲料组或HFD组每天皮下注射溶剂芝麻油或DHEA,连续注射20天。在实验结束时,评估生殖和代谢特征。我们的数据表明,HFD不影响DHEA处理小鼠的生殖表型。然而,HFD处理在DHEA处理的小鼠中引起了显著的代谢改变,包括肥胖、葡萄糖不耐受、血脂异常和明显的肝脂肪变性。这些发现表明,HFD在DHEA诱导的PCOS小鼠中诱导了独特的代谢特征。因此,联合使用DHEA和HFD治疗可能作为一种手段来研究该综合征代谢紊乱所涉及的机制,特别是在PCOS女性中肝脂肪变性的高患病率方面。