DeFazio Richard A, Elias Carol F, Moenter Suzanne M
Departments of Molecular and Integrative Physiology,
Departments of Molecular and Integrative Physiology, Obstetrics and Gynecology, and.
J Neurosci. 2014 Dec 3;34(49):16296-308. doi: 10.1523/JNEUROSCI.3057-14.2014.
Gonadotropin-releasing hormone (GnRH) secretion is regulated by estradiol feedback. This feedback switches from negative to positive in females; this switch depends on time of day in many species. Estradiol feedback is likely conveyed via afferents. Kisspeptin neurons of the arcuate nucleus and anteroventral-periventricular region (AVPV) may differentially regulate GnRH neurons during negative and positive feedback, respectively. We tested estradiol and time of day regulation of GABAergic transmission and postsynaptic response to GABA in these two populations using transgenic mice with GFP-identified kisspeptin neurons. Ovariectomized (OVX) mice treated or not with estradiol (E) were studied in the AM (negative feedback) or PM (positive feedback). GABAA receptor reversal potential was unaffected by time of day or estradiol. GABA depolarized the membrane potential of arcuate neurons from OVX+E mice; this response was blunted in cells from OVX mice. GABA hyperpolarized AVPV kisspeptin neurons, except in the OVX PM group in which GABA did not alter membrane potential attributable to a PM hyperpolarization of baseline membrane potential. In both kisspeptin neuron populations from OVX mice, the frequency of GABAergic spontaneous postsynaptic currents was increased in the PM; this increase was blunted by estradiol. In arcuate, but not AVPV, kisspeptin neurons, estradiol reduced miniature postsynaptic current amplitude independent of time of day. Using nonstationary fluctuation analysis and diazepam to manipulate GABAA receptor apparent affinity, the decrease in arcuate miniature postsynaptic current amplitude was attributed to decreased number of receptors bound by GABA. Time of day and estradiol feedback thus both target presynaptic and postsynaptic mechanisms to differentially regulate kisspeptin neurons via GABAergic transmission.
促性腺激素释放激素(GnRH)的分泌受雌二醇反馈调节。在雌性动物中,这种反馈从负反馈转变为正反馈;在许多物种中,这种转变取决于一天中的时间。雌二醇反馈可能通过传入神经传递。弓状核和腹前室周区域(AVPV)的 kisspeptin 神经元可能分别在负反馈和正反馈期间对 GnRH 神经元进行不同的调节。我们使用绿色荧光蛋白(GFP)标记的 kisspeptin 神经元的转基因小鼠,测试了这两个群体中 GABA 能传递的雌二醇和时间调节以及对 GABA 的突触后反应。对去卵巢(OVX)的小鼠在上午(负反馈)或下午(正反馈)进行研究,分别给予或不给予雌二醇(E)处理。GABAA 受体反转电位不受一天中的时间或雌二醇的影响。GABA 使 OVX + E 小鼠的弓状神经元膜电位去极化;在 OVX 小鼠的细胞中,这种反应减弱。GABA 使 AVPV kisspeptin 神经元超极化,但在 OVX 下午组中除外,在该组中 GABA 未改变膜电位,这归因于基线膜电位的下午超极化。在 OVX 小鼠的两个 kisspeptin 神经元群体中,GABA 能自发突触后电流的频率在下午增加;这种增加被雌二醇减弱。在弓状核而非 AVPV 的 kisspeptin 神经元中,雌二醇降低了微小突触后电流幅度,且与一天中的时间无关。使用非平稳波动分析和地西泮来操纵 GABAA 受体的表观亲和力,弓状核微小突触后电流幅度的降低归因于与 GABA 结合的受体数量减少。因此,一天中的时间和雌二醇反馈都靶向突触前和突触后机制,通过 GABA 能传递对 kisspeptin 神经元进行不同的调节。