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西式饮食对年轻雌性小鼠发情周期的稳态调节

Homeostatic Regulation of Estrus Cycle of Young Female Mice on Western Diet.

作者信息

Lenert Melissa E, Chaparro Micaela M, Burton Michael D

机构信息

Neuroimmunology and Behavior Group, Department of Neuroscience, School of Behavioral and Brain Sciences, Center for Advanced Pain Studies, University of Texas at Dallas, Richardson, TX, USA.

出版信息

J Endocr Soc. 2021 Feb 1;5(4):bvab010. doi: 10.1210/jendso/bvab010. eCollection 2021 Apr 1.

Abstract

The etiology of reproductive disorders correlates with weight gain in patients, but the link between reproduction, diet, and weight has been difficult to translate in rodents. As rates of childhood obesity and reproductive disorders increase, the need to study the effects of weight and diet on adolescent females is key. Previous studies show that female mice are resistant to high-fat diet-induced weight gain, but the mechanisms are unclear. Literature also suggests that ovarian function is essential to resistance in weight gain, as an ovariectomy leads to a weight-gaining phenotype similar to male mice on a high-fat diet. However, reproductive changes that occur in adolescent mice on high-fat diet have not been assessed. Here, we show that regulation of the estrus cycle via progesterone is critical to metabolic homeostasis in female mice on a high-fat diet. Female mice were put on high-fat diet or control diet for 12 weeks starting at 4 weeks of age. Every 4 weeks, their estrus cycle was tracked and fasting glucose was measured. We found that after 4 weeks on high-fat diet, there was no difference in weight between groups, but an increase in time spent in proestrus and estrus in mice on high-fat diet and an increase in serum progesterone during proestrus. These results show that intact females modulate their estrus cycle in response to a high-fat diet as a mechanism of homeostatic regulation of body weight, protecting them from metabolic abnormalities. Understanding the mechanisms behind this protection may yield therapeutic opportunities for treatment of reproductive disorders in adolescent female patients.

摘要

生殖系统疾病的病因与患者体重增加相关,但生殖、饮食和体重之间的联系在啮齿动物中很难得到验证。随着儿童肥胖率和生殖系统疾病发病率的上升,研究体重和饮食对青春期女性的影响至关重要。以往研究表明,雌性小鼠对高脂饮食诱导的体重增加具有抗性,但其机制尚不清楚。文献还表明,卵巢功能对于体重增加抗性至关重要,因为卵巢切除术会导致类似于高脂饮食雄性小鼠的体重增加表型。然而,高脂饮食的青春期小鼠发生的生殖变化尚未得到评估。在此,我们表明,通过孕酮调节发情周期对于高脂饮食雌性小鼠的代谢稳态至关重要。雌性小鼠从4周龄开始接受高脂饮食或对照饮食12周。每4周跟踪其发情周期并测量空腹血糖。我们发现,高脂饮食4周后,各组体重无差异,但高脂饮食小鼠的发情前期和发情期时间增加,发情前期血清孕酮增加。这些结果表明,完整的雌性小鼠会根据高脂饮食调节其发情周期,作为体重稳态调节的一种机制,保护它们免受代谢异常的影响。了解这种保护背后的机制可能为治疗青春期女性患者的生殖系统疾病带来治疗机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e31/7947973/dbca79dc21bd/bvab010_fig1.jpg

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