Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), 14004 Cordoba, Spain; Departament of Cell Biology, Physiology and Immunology, University of Cordoba, 14004 Cordoba, Spain; Hospital Universitario Reina Sofía, 14004 Cordoba, Spain.
Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), 14004 Cordoba, Spain; Departament of Cell Biology, Physiology and Immunology, University of Cordoba, 14004 Cordoba, Spain; Hospital Universitario Reina Sofía, 14004 Cordoba, Spain; CIBER Fisiopatología de la Obesidad y Nutrición (CIBEROBN), Instituto de Salud Carlos III, 14004 Córdoba, Spain.
Metabolism. 2021 Feb;115:154460. doi: 10.1016/j.metabol.2020.154460. Epub 2020 Dec 4.
Reproduction is tightly coupled to body energy and metabolic status. GnRH neurons, master elements and final output pathway for the brain control of reproduction, directly or indirectly receive and integrate multiple metabolic cues to regulate reproductive function. Yet, the molecular underpinnings of such phenomenon remain largely unfolded. AMP-activated protein kinase (AMPK), the fundamental cellular sensor that becomes activated in conditions of energy deficit, has been recently shown to participate in the control of Kiss1 neurons, essential gatekeepers of the reproductive axis, by driving an inhibitory valence in situations of energy scarcity at puberty. However, the contribution of AMPK signaling specifically in GnRH neurons to the metabolic control of reproduction remains unknown.
Double immunohistochemistry (IHC) was applied to evaluate expression of active (phosphorylated) AMPK in GnRH neurons and a novel mouse line, named GAMKO, with conditional ablation of the AMPK α1 subunit in GnRH neurons, was generated. GAMKO mice of both sexes were subjected to reproductive characterization, with attention to puberty and gonadotropic responses to kisspeptin and metabolic stress.
A vast majority (>95%) of GnRH neurons co-expressed pAMPK. Female (but not male) GAMKO mice displayed earlier puberty onset and exaggerated LH (as surrogate marker of GnRH) responses to kisspeptin-10 at the prepubertal age. In adulthood, GAMKO females retained increased LH responsiveness to kisspeptin and showed partial resilience to the inhibitory effects of conditions of negative energy balance on the gonadotropic axis. The modulatory role of AMPK in GnRH neurons required preserved ovarian function, since the differences in LH pulsatility detected between GAMKO and control mice subjected to fasting were abolished in ovariectomized animals.
Altogether, our data document a sex-biased, physiological role of AMPK signaling in GnRH neurons, as molecular conduit of the inhibitory actions of conditions of energy deficit on the female reproductive axis.
生殖与机体能量和代谢状态紧密相关。作为大脑控制生殖的主要元素和最终输出途径,GnRH 神经元直接或间接接收并整合多种代谢信号来调节生殖功能。然而,这种现象的分子基础在很大程度上仍未阐明。AMP 激活的蛋白激酶(AMPK)是细胞的基本感受器,在能量缺乏的情况下被激活,最近的研究表明,它通过在青春期能量匮乏时驱动 Kiss1 神经元的抑制性变化,参与了生殖轴关键门控因子 Kiss1 神经元的调控。然而,AMPK 信号在 GnRH 神经元中对生殖代谢控制的具体贡献仍不清楚。
采用双重免疫组织化学(IHC)评估 GnRH 神经元中活性(磷酸化)AMPK 的表达,并生成一种新的小鼠品系,称为 GAMKO,其 GnRH 神经元中 AMPKα1 亚基条件性缺失。对 GAMKO 雌雄小鼠进行生殖特征分析,重点关注青春期和促性腺激素对 kisspeptin 和代谢应激的反应。
超过 95%的 GnRH 神经元共表达 pAMPK。雌性(而非雄性)GAMKO 小鼠表现出更早的青春期启动和青春期前 kisspeptin-10 刺激时 LH(作为 GnRH 的替代标志物)反应增强。成年后,GAMKO 雌性小鼠保留了对 kisspeptin 的 LH 反应性增强,并对负能平衡状态对促性腺激素轴的抑制作用具有部分抗性。AMPK 在 GnRH 神经元中的调节作用需要保留卵巢功能,因为在禁食状态下,GAMKO 小鼠和对照小鼠之间检测到的 LH 脉冲频率差异在卵巢切除动物中被消除。
综上所述,我们的数据证明了 AMPK 信号在 GnRH 神经元中的性别偏倚、生理性作用,作为能量缺乏状态对雌性生殖轴抑制作用的分子途径。