Department of Anatomy and Neurobiology, Graduate School of Medicine, Nippon Medical School, Tokyo, 113- 8602, Japan.
Department of Anatomy and Neurobiology, Graduate School of Medicine, Nippon Medical School, Tokyo, 113- 8602, Japan.
Peptides. 2021 Aug;142:170546. doi: 10.1016/j.peptides.2021.170546. Epub 2021 Mar 29.
Metabolic stress resulting from either lack or excess of nutrients often causes infertility in both sexes. Kisspeptin-neurokinin B-dynorphin A (KNDy) neurons in the arcuate nucleus (ARC) has been suggested to be a key players in reproduction via direct stimulation of the pulsatile gonadotropin-releasing hormone (GnRH) and subsequent gonadotropin release in mammalian species. In this study, we investigated the effect of high-fat diet (HFD) on hypothalamic KNDy gene expression to examine the pathogenic mechanism underlying obesity-induced infertility in male and female rats. Male and female rats at 7 weeks of age were fed with either a standard or HFD for 4 months. In the male rats, the HFD caused a significant suppression of ARC Kiss1 and Pdyn gene expressions, but did not affect the plasma luteinizing hormone (LH) levels and sizes of the morphology of the testis and epididymis. In the female rats, 58% of the HFD-fed female rats exhibited irregular estrous cycles, whereas the remaining rats showed regular cycles. Two of the 10 rats that showed HFD-induced irregular estrous cycles showed profound suppression of LH pulse frequency and the number of ARC Kiss1-expressing cells, whereas the other females showed normal LH pulses and ARC Kiss1 expression. Our finding shows that suppression of ARC Kiss1 expression might be the initial pathological change of hypogonadotropic hypogonadism in HFD-fed male rats, while the obese-related infertility in the female rats may be mainly induced by KNDy-independent pathways. Taken together, ARC kisspeptin neurons in male rats may be susceptible to HFD-induced obesity compared with those in female rats.
营养缺乏或过剩引起的代谢应激常常导致两性不孕。弓状核(ARC)中的促性腺激素释放激素(GnRH)脉冲刺激和随后的促性腺激素释放的关键作用,kisspeptin-神经激肽 B-强啡肽 A(KNDy)神经元已经被提出。在本研究中,我们研究了高脂肪饮食(HFD)对下丘脑 KNDy 基因表达的影响,以检查肥胖引起的雄性和雌性大鼠不孕的发病机制。7 周龄雄性和雌性大鼠分别用标准饮食或 HFD 喂养 4 个月。在雄性大鼠中,HFD 显著抑制 ARC Kiss1 和 Pdyn 基因的表达,但不影响血浆黄体生成素(LH)水平和睾丸及附睾的形态大小。在雌性大鼠中,58%的 HFD 喂养雌性大鼠表现出不规则发情周期,而其余大鼠表现出规则发情周期。在 10 只出现 HFD 诱导的不规则发情周期的大鼠中,有 2 只大鼠的 LH 脉冲频率和表达 Kiss1 的 ARC 细胞数量明显减少,而其他雌性大鼠的 LH 脉冲和 ARC Kiss1 表达正常。我们的发现表明,ARC Kiss1 表达的抑制可能是 HFD 喂养雄性大鼠低促性腺激素性性腺功能减退症的初始病理变化,而肥胖相关的雌性大鼠不孕可能主要是由 KNDy 非依赖性途径引起的。综上所述,与雌性大鼠相比,雄性大鼠的 ARC kisspeptin 神经元可能更容易受到 HFD 诱导的肥胖的影响。