Fernandois D, Na E, Cuevas F, Cruz G, Lara H E, Paredes A H
Laboratory of NeurobiochemistryDepartment of Biochemistry and Molecular Biology, Faculty of Chemistry and Pharmaceutical Sciences, Universidad de Chile, Santiago 8380492, ChileLaboratorio de alteraciones Reproductivas y MetabólicasFacultad de Ciencias, Universidad de Valparaíso, Valparaíso 2360102, Chile.
Laboratory of NeurobiochemistryDepartment of Biochemistry and Molecular Biology, Faculty of Chemistry and Pharmaceutical Sciences, Universidad de Chile, Santiago 8380492, ChileLaboratorio de alteraciones Reproductivas y MetabólicasFacultad de Ciencias, Universidad de Valparaíso, Valparaíso 2360102, Chile
J Endocrinol. 2016 Mar;228(3):161-70. doi: 10.1530/JOE-15-0429. Epub 2015 Dec 23.
We have previously reported that kisspeptin (KP) may be under the control of the sympathetic innervation of the ovary. Considering that the sympathetic activity of the ovary increases with aging, it is possible that ovarian KP also increases during this period and participates in follicular development. To evaluate this possibility, we determined ovarian KP expression and its action on follicular development during reproductive aging in rats. We measured ovarian KP mRNA and protein levels in 6-, 8-, 10- and 12-month-old rats. To evaluate follicular developmental changes, intraovarian administration of KP or its antagonist, peptide 234 (P234), was performed using a mini-osmotic pump, and to evaluate FSH receptor (FSHR) changes in the senescent ovary, we stimulated cultured ovaries with KP, P234 and isoproterenol (ISO). Our results shows that KP expression in the ovary was increased in 10- and 12-month-old rats compared with 6-month-old rats, and this increase in KP was strongly correlated with the increase in ovarian norepinephrine observed with aging. The administration of KP produced an increase in corpora lutea and type III follicles in 6- and 10-month-old rats, which was reversed by P234 administration at 10 months. In addition, KP decreased the number and size of antral follicles in 6- and 10-month-old rats, while P234 administration produced an increase in these structures at the same ages. In ovarian cultures KP prevented the induction of FSHR by ISO. These results suggest that intraovarian KP negatively participates in the acquisition of FSHR, indicating a local role in the regulation of follicular development and ovulation during reproductive aging.
我们之前曾报道, kisspeptin(KP)可能受卵巢交感神经支配的调控。鉴于卵巢的交感神经活动会随着衰老而增加,在此期间卵巢KP也有可能增加,并参与卵泡发育。为评估这种可能性,我们测定了大鼠生殖衰老过程中卵巢KP的表达及其对卵泡发育的作用。我们测量了6、8、10和12月龄大鼠的卵巢KP mRNA和蛋白水平。为评估卵泡发育变化,使用微型渗透泵在卵巢内给予KP或其拮抗剂肽234(P234),为评估衰老卵巢中促卵泡激素受体(FSHR)的变化,我们用KP、P234和异丙肾上腺素(ISO)刺激培养的卵巢。我们的结果显示,与6月龄大鼠相比,10和12月龄大鼠卵巢中的KP表达增加,且这种KP的增加与衰老过程中观察到的卵巢去甲肾上腺素增加密切相关。在6和10月龄大鼠中给予KP可使黄体和III型卵泡数量增加,而在10月龄时给予P234可逆转这种增加。此外,在6和10月龄大鼠中,KP可减少窦状卵泡的数量和大小,而给予P234则会使相同年龄的这些结构增加。在卵巢培养物中,KP可阻止ISO诱导FSHR。这些结果表明,卵巢内的KP在FSHR的获得过程中起负性作用,表明其在生殖衰老过程中对卵泡发育和排卵的调节中发挥局部作用。