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Valproic Acid Leads New Neurons Down the Wrong Path

机译:丙戊酸导致错误的新神经元

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摘要

>Ectopic Neurogenesis Induced by Prenatal Antiepileptic Drug Exposure Augments Seizure Susceptibility in Adult Mice Sakai A, Matsuda T, Doi H, Nagaishi Y, Kato K, Nakashima K. Proc Natl Acad Sci U S A. 2018;115(16):4270-4275.Epilepsy is a neurological disorder often associated with seizure that affects ∼0.7% of pregnant women. During pregnancy, most epileptic patients are prescribed antiepileptic drugs (AEDs) such as valproic acid (VPA) to control seizure activity. Here, we show that prenatal exposure to VPA in mice increases seizure susceptibility in adult offspring through mislocalization of newborn neurons in the hippocampus. We confirmed that neurons newly generated from neural stem/progenitor cells (NS/PCs) are integrated into the granular cell layer in the adult hippocampus; however, prenatal VPA treatment altered the expression in NS/PCs of genes associated with cell migration, including CXC motif chemokine receptor 4 (Cxcr4), consequently increasing the ectopic localization of newborn neurons in the hilus. We also found that voluntary exercise in a running wheel suppressed this ectopic neurogenesis and countered the enhanced seizure susceptibility caused by prenatal VPA exposure, probably by normalizing the VPA-disrupted expression of multiple genes including Cxcr4 in adult NS/PCs. Replenishing Cxcr4 expression alone in NS/PCs was sufficient to overcome the aberrant migration of newborn neurons and increased seizure susceptibility in VPA-exposed mice. Thus, prenatal exposure to an AED, VPA, has a long-term effect on the behavior of NS/PCs in offspring, but this effect can be counteracted by a simple physical activity. Our findings offer a step to developing strategies for managing detrimental effects in offspring exposed to VPA in utero.
机译:>由产前抗癫痫药暴露引起的成年小鼠癫痫易感性诱发的异位神经发生 Sakai A,Matsuda T,Doi H,Nagaishi Y,Kato K,Nakashima K.Proc Natl Acad Sci US A.2018; 115( 16):4270-4275。癫痫病是一种神经系统疾病,通常与癫痫发作有关,影响约0.7%的孕妇。在怀孕期间,大多数癫痫患者需要开具抗癫痫药(AED),例如丙戊酸(VPA),以控制癫痫发作的活动。在这里,我们显示小鼠的产前暴露于VPA会通过海马中新生神经元的错误定位而增加成年后代的癫痫发作易感性。我们证实,从神经干/祖细胞(NS / PCs)新产生的神经元已整合到成年海马的颗粒细胞层中。但是,产前VPA治疗改变了与细胞迁移相关的基因(包括CXC基序趋化因子受体4(Cxcr4))在NS / PCs中的表达,从而增加了新生神经元在中的异位定位。我们还发现,在跑轮中进行自愿锻炼可以抑制这种异位神经发生,并抵消由产前VPA暴露引起的癫痫易感性的增强,可能是通过使成年NS / PCs中包括Cxcr4在内的多个基因的VPA破坏表达正常化来实现的。单独补充NS / PC中Cxcr4的表达足以克服新生神经元的异常迁移并增加VPA暴露小鼠的癫痫发作敏感性。因此,产前暴露于AED VPA对子代NS / PC的行为具有长期影响,但是这种影响可以通过简单的体育活动来抵消。我们的发现为制定策略以管理宫内暴露于VPA的后代带来的有害影响迈出了一步。

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