Fernandois Daniela, Cruz Gonzalo, Na Eun Kyung, Lara Hernán E, Paredes Alfonso H
Department of Biochemistry and Molecular BiologyLaboratory of Neurobiochemistry, Faculty of Chemistry and Pharmaceutical Sciences, Universidad de Chile, Santiago, Chile.
Laboratorio de Alteraciones Reproductivas y MetabólicasCentro de Neurobiología y Plasticidad Cerebral (CNPC), Instituto de Fisiología, Facultad de Ciencias, Universidad de Valparaíso, Valparaíso, Chile.
J Endocrinol. 2017 Jan;232(1):97-105. doi: 10.1530/JOE-16-0181.
Previous work has demonstrated that the increase in the activity of sympathetic nerves, which occurs during the subfertility period in female rats, causes an increase in follicular cyst development and impairs follicular development. In addition, the increase in ovarian sympathetic activity of aged rats correlates with an increased expression of kisspeptin (KISS1) in the ovary. This increase in KISS1 could participate in the decrease in follicular development that occurs during the subfertility period. We aimed to determine whether the blockade of ovarian sympathetic tone prevents the increase in KISS1 expression during reproductive aging and improves follicular development. We performed 2 experiments in rats: (1) an in vivo blockade of beta-adrenergic receptor with propranolol (5.0 mg/kg) and (2) an ovarian surgical denervation to modulate the sympathetic system at these ages. We measured Kisspeptin and follicle-stimulating hormone receptor (FSHR) mRNA and protein levels by qRT-PCR and western blot and counted primordial, primary and secondary follicles at 8, 10 and 12 months of age. The results showed that ovarian KISS1 decreased but FSHR increased after both propranolol administration and the surgical denervation in rats of 8, 10 and 12 months of age. An increase in FSHR was related to an increase in the number of smaller secondary follicles and a decreased number of primordial follicles at 8, 10 and 12 months of age. These results suggest that intraovarian KISS1 is regulated by sympathetic nerves via a beta-adrenergic receptor and participates locally in ovarian follicular development in reproductive aging.
先前的研究表明,雌性大鼠在生育力低下期间交感神经活动增加,会导致卵泡囊肿发育增加并损害卵泡发育。此外,老年大鼠卵巢交感神经活动的增加与卵巢中亲吻素(KISS1)表达的增加相关。KISS1的这种增加可能参与了生育力低下期间卵泡发育的减少。我们旨在确定阻断卵巢交感神经张力是否能防止生殖衰老过程中KISS1表达的增加并改善卵泡发育。我们在大鼠中进行了两项实验:(1)用普萘洛尔(5.0mg/kg)对β-肾上腺素能受体进行体内阻断,(2)进行卵巢手术去神经支配以调节这些年龄段的交感神经系统。我们通过qRT-PCR和蛋白质印迹法测量了亲吻素和促卵泡激素受体(FSHR)的mRNA和蛋白质水平,并在8、10和12月龄时对原始卵泡、初级卵泡和次级卵泡进行了计数。结果显示,在8、10和12月龄大鼠中,给予普萘洛尔和进行手术去神经支配后,卵巢KISS1水平降低,但FSHR水平升高。FSHR的增加与8、10和12月龄时较小次级卵泡数量的增加以及原始卵泡数量的减少有关。这些结果表明,卵巢内的KISS1受交感神经通过β-肾上腺素能受体调节,并在生殖衰老过程中局部参与卵巢卵泡发育。