Development and prenatal exposure to androgens alter potassium currents in gonadotropin-releasing hormone neurons from female mice

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Jennifer Jaime, R. Anthony DeFazio, Suzanne M. Moenter
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引用次数: 0

Abstract

Pulsatile gonadotropin-releasing hormone (GnRH) release is critical for reproduction. Disruptions to GnRH secretion patterns may contribute to polycystic ovary syndrome (PCOS). Prenatally androgenized (PNA) female mice recapitulate many neuroendocrine abnormalities observed in PCOS patients. PNA and development induce changes in spontaneous GnRH neuron firing rate, response to synaptic input, and the afterhyperpolarization potential of the action potential. We hypothesized potassium currents are altered by PNA treatment and/or development. Whole-cell patch-clamp recordings were made of transient and residual potassium currents of GnRH neurons in brain slices from 3-week-old and adult control and PNA females. At 3 weeks of age, PNA treatment increased transient current density versus controls. Development and PNA altered voltage-dependent activation and inactivation of the transient current. In controls, transient current activation and inactivation were depolarized at 3 weeks of age versus in adulthood. In GnRH neurons from 3-week-old mice, transient current activation and inactivation were more depolarized in control than PNA mice. Development and PNA treatment interacted to shift the time-dependence of inactivation and recovery from inactivation. Notably, in cells from adult PNA females, recovery was prolonged compared to all other groups. Activation of the residual current occurred at more depolarized membrane potentials in 3-week-old than adult controls. PNA depolarized activation of the residual current in adults. These findings demonstrate the properties of GnRH neuron potassium currents change during typical development, potentially contributing to puberty, and further suggest PNA treatment may both alter some typical developmental changes and induce additional modifications, which together may underlie aspects of the PNA phenotype. There was not any clinical trial involved in this work.

Abstract Image

Abstract Image

发育和产前暴露于雄激素会改变雌性小鼠促性腺激素释放激素神经元的钾电流
促性腺激素释放激素(GnRH)的脉冲式释放对生殖至关重要。GnRH分泌模式的紊乱可能会导致多囊卵巢综合征(PCOS)。产前雄激素化(PNA)雌性小鼠再现了在多囊卵巢综合症患者身上观察到的许多神经内分泌异常。PNA 和发育诱导 GnRH 神经元自发发射率、对突触输入的反应以及动作电位的超极化后电位发生变化。我们假设钾电流会因 PNA 治疗和/或发育而改变。我们对对照组和 PNA 组 3 周大和成年雌性 GnRH 神经元脑切片的瞬时和残余钾电流进行了全细胞贴片钳记录。与对照组相比,在 3 周大时,PNA 处理会增加瞬时电流密度。发育和 PNA 改变了瞬时电流的电压依赖性激活和失活。在对照组中,瞬时电流的激活和失活在 3 周龄时与成年时相比都是去极化的。在3周龄小鼠的GnRH神经元中,对照组比PNA小鼠的瞬时电流激活和失活的去极化程度更高。发育和 PNA 处理相互作用,改变了失活和失活恢复的时间依赖性。值得注意的是,在成年 PNA 雌性小鼠的细胞中,恢复时间比其他所有组别都要长。与成年对照组相比,3周龄雌性细胞的残余电流激活发生在更多的去极化膜电位上。PNA 可使成年雌鼠的残余电流去极化激活。这些研究结果表明,GnRH神经元钾电流的特性在典型发育过程中会发生变化,这可能是青春期的原因之一,并进一步表明PNA治疗可能会改变一些典型的发育变化,并诱发更多的改变,这些改变可能是PNA表型的某些方面的基础。本研究未涉及任何临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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