Aix-Marseille University UMR 1249, INSERM (Institut National de la Santé et de la Recherche Médicale) Unité 1249, INMED (Institut de Neurobiologie de la Méditerranée), Marseille, France.
Plateforme Post-Génomique, INMED, Marseille, France.
Elife. 2018 Aug 14;7:e36726. doi: 10.7554/eLife.36726.
Brain computations rely on a proper balance between excitation and inhibition which progressively emerges during postnatal development in rodent. γ-Aminobutyric acid (GABA) neurotransmission supports inhibition in the adult brain but excites immature rodent neurons. Alterations in the timing of the GABA switch contribute to neurological disorders, so unveiling the involved regulators may be a promising strategy for treatment. Here we show that the adipocyte hormone leptin sets the tempo for the emergence of GABAergic inhibition in the newborn rodent hippocampus. In the absence of leptin signaling, hippocampal neurons show an advanced emergence of GABAergic inhibition. Conversely, maternal obesity associated with hyperleptinemia delays the excitatory to inhibitory switch of GABA action in offspring. This study uncovers a developmental function of leptin that may be linked to the pathogenesis of neurological disorders and helps understanding how maternal environment can adversely impact offspring brain development.
大脑计算依赖于兴奋和抑制之间的适当平衡,这种平衡在啮齿动物的出生后发育过程中逐渐出现。γ-氨基丁酸 (GABA) 神经递质在成年大脑中支持抑制,但兴奋不成熟的啮齿动物神经元。GABA 转换时机的改变导致神经发育障碍,因此揭示相关调节因子可能是一种有前途的治疗策略。在这里,我们表明,脂肪细胞激素瘦素为新生啮齿动物海马中的 GABA 能抑制的出现设定了节奏。在缺乏瘦素信号的情况下,海马神经元表现出 GABA 能抑制的提前出现。相反,与高瘦素血症相关的母体肥胖会延迟 GABA 作用的兴奋性向抑制性转换。这项研究揭示了瘦素的一种发育功能,它可能与神经发育障碍的发病机制有关,并有助于理解母体环境如何对后代大脑发育产生不利影响。