Department of Medicine (Austin Health/Northern Health), Heidelberg Repatriation Hospital, The University of Melbourne, Heidelberg Heights, Melbourne, Victoria 3081, Australia.
J Endocrinol. 2011 Jun;209(3):307-15. doi: 10.1530/JOE-11-0022. Epub 2011 Mar 23.
Infertility, associated with oligo/anovulation, increased ovarian volume, numerous follicular cysts, and metabolic disturbances such as obesity and insulin resistance (IR) are characteristics common to polycystic ovary syndrome (PCOS), the most common endocrine disorder in women of reproductive age. Here, we show that New Zealand obese (NZO) mice display similar metabolic characteristics such as obesity, leptin insensitivity, glucose intolerance, and IR. Importantly, NZO mice are poor breeders; however, the mechanism for this has not been investigated. The aim of this study was to assess the ovarian structure/morphology and sex hormone levels in female NZO and lean C57BL/6J control mice. Twenty-five NZO and twenty female control mice were studied at three different ages (young, adult, and aged). The animals were weighed, an insulin tolerance test was carried out, and blood was collected for measurement of hormone levels. The ovaries were removed for histological analysis. As expected, NZO mice presented higher body weights (P=0.001), increased basal plasma glucose (P=0.007), and insulin levels (P=0.001) as well as IR, compared with control mice. NZO mice showed an increased ovarian volume, reduced numbers of corpora lutea, and higher total follicle numbers (P=0.0001). The number of primordial follicles increased (P=0.02) at the young stage, as well as the amount of atretic follicles (P=0.03), in NZO compared with control mice. NZO mice also displayed reduced plasma LH and increased estradiol levels. In conclusion, NZO mice show a poor breeding performance due to decreased ovulation, increased number of primordial and atretic follicles, and ovarian size. Given that NZO mice are obese, hyperinsulinemic and insulin resistant, they are suitable for investigating pathophysiological mechanisms linking metabolic alterations with reproductive defects.
不孕与稀发排卵/无排卵、卵巢体积增大、多个卵泡囊肿以及肥胖和胰岛素抵抗 (IR) 等代谢紊乱有关,这些都是多囊卵巢综合征 (PCOS) 的共同特征,是育龄妇女最常见的内分泌疾病。在这里,我们发现新西兰肥胖 (NZO) 小鼠表现出类似的代谢特征,如肥胖、瘦素不敏感、葡萄糖不耐受和 IR。重要的是,NZO 小鼠繁殖能力差;然而,其机制尚未得到研究。本研究旨在评估雌性 NZO 和瘦型 C57BL/6J 对照小鼠的卵巢结构/形态和性激素水平。在三个不同年龄(年轻、成年和老年)研究了 25 只 NZO 和 20 只雌性对照小鼠。对动物进行称重,进行胰岛素耐量试验,并采集血液以测量激素水平。切除卵巢进行组织学分析。正如预期的那样,与对照小鼠相比,NZO 小鼠的体重更高(P=0.001),基础血浆葡萄糖(P=0.007)和胰岛素水平(P=0.001)以及 IR 更高。NZO 小鼠的卵巢体积增大,黄体数量减少,总卵泡数量增加(P=0.0001)。与对照小鼠相比,NZO 小鼠的原始卵泡数量增加(P=0.02),闭锁卵泡数量增加(P=0.03)。NZO 小鼠的血浆 LH 减少,雌二醇水平增加。总之,由于排卵减少、原始卵泡和闭锁卵泡数量增加以及卵巢大小增加,NZO 小鼠的繁殖性能较差。鉴于 NZO 小鼠肥胖、高胰岛素血症和胰岛素抵抗,它们适合研究将代谢改变与生殖缺陷联系起来的病理生理机制。