Department of Molecular and Integrative Physiology, University of Illinois Urbana-Champaign, Urbana, Illinois 61801.
Department of Molecular and Integrative Physiology, University of Illinois Urbana-Champaign, Urbana, Illinois 61801
eNeuro. 2024 Oct 21;11(10). doi: 10.1523/ENEURO.0324-24.2024. Print 2024 Oct.
Temporal lobe epilepsy (TLE) is the most common focal epilepsy in adults, and people with TLE exhibit higher rates of reproductive endocrine dysfunction. Hypothalamic gonadotropin-releasing hormone (GnRH) neurons regulate reproductive function in mammals by regulating gonadotropin secretion from the anterior pituitary. Previous research demonstrated GnRH neuron hyperexcitability in both sexes in the intrahippocampal kainic acid (IHKA) mouse model of TLE. Fast-inactivating A-type ( ) and delayed rectifier K-type ( ) K currents play critical roles in modulating neuronal excitability, including in GnRH neurons. Here, we tested the hypothesis that GnRH neuron hyperexcitability is associated with reduced and conductances. At 2 months after IHKA or control saline injection, when IHKA mice exhibit chronic epilepsy, we recorded GnRH neuron excitability, , and using whole-cell patch-clamp electrophysiology. GnRH neurons from both IHKA male and diestrus female GnRH-GFP mice exhibited hyperexcitability compared with controls. In IHKA males, although maximum current density was increased, recovery from inactivation was significantly slower, consistent with a hyperexcitability phenotype. In IHKA females, however, both and were unchanged. Sex differences were not observed in or properties in controls, but IHKA mice exhibited sex effects in properties. These results indicate that although the emergent phenotype of increased GnRH neuron excitability is similar in IHKA males and diestrus females, the underlying mechanisms are distinct. This study thus highlights sex-specific changes in voltage-gated K currents in GnRH neurons in a mouse model of TLE and suggesting potential sex differences in GnRH neuron ion channel properties.
颞叶癫痫(TLE)是成人中最常见的局灶性癫痫,TLE 患者表现出更高的生殖内分泌功能障碍发生率。下丘脑促性腺激素释放激素(GnRH)神经元通过调节垂体前叶促性腺激素的分泌来调节哺乳动物的生殖功能。先前的研究表明,TLE 的海马内海人酸(IHKA)小鼠模型中,GnRH 神经元在两性中均表现出兴奋性过高。快速失活的 A 型()和延迟整流的 K 型()K 电流在调节神经元兴奋性方面起着关键作用,包括 GnRH 神经元。在这里,我们检验了 GnRH 神经元兴奋性过高与减少和电导有关的假设。在 IHKA 或对照生理盐水注射后 2 个月,当 IHKA 小鼠表现出慢性癫痫时,我们使用全细胞膜片钳电生理学记录 GnRH 神经元兴奋性、、和。与对照组相比,来自 IHKA 雄性和动情期雌性 GnRH-GFP 小鼠的 GnRH 神经元表现出兴奋性过高。在 IHKA 雄性中,尽管最大电流密度增加,但失活的恢复明显变慢,与兴奋性过高表型一致。然而,在 IHKA 雌性中,和都没有改变。在对照组中,和的特性没有观察到性别差异,但 IHKA 小鼠在特性中表现出性别效应。这些结果表明,尽管 IHKA 雄性和动情期雌性中增加的 GnRH 神经元兴奋性的新兴表型相似,但潜在的机制是不同的。因此,本研究强调了 TLE 小鼠模型中 GnRH 神经元电压门控 K 电流的性别特异性变化,并提示 GnRH 神经元离子通道特性可能存在潜在的性别差异。