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产前暴露于丙戊酸引起的局部新皮质微回路的过度连接

Hyperconnectivity of local neocortical microcircuitry induced by prenatal exposure to valproic acid.

作者信息

Rinaldi Tania, Silberberg Gilad, Markram Henry

机构信息

Laboratory of Neural Microcircuitry, Brain Mind Institute, Ecole Polytechnique Fédérale de Lausanne, Lausanne 1015, Switzerland.

出版信息

Cereb Cortex. 2008 Apr;18(4):763-70. doi: 10.1093/cercor/bhm117. Epub 2007 Jul 17.

Abstract

Exposure to valproic acid (VPA) during embryogenesis can cause several teratogenic effects, including developmental delays and in particular autism in humans if exposure occurs during the third week of gestation. We examined the postnatal effects of embryonic exposure to VPA on microcircuit properties of juvenile rat neocortex using in vitro electrophysiology. We found that a single prenatal injection of VPA on embryonic day 11.5 causes a significant enhancement of the local recurrent connectivity formed by neocortical pyramidal neurons. The study of the biophysical properties of these connections revealed weaker excitatory synaptic responses. A marked decrease of the intrinsic excitability of pyramidal neurons was also observed. Furthermore, we demonstrate a diminished number of putative synaptic contacts in connection between layer 5 pyramidal neurons. Local hyperconnectivity may render cortical modules more sensitive to stimulation and once activated, more autonomous, isolated, and more difficult to command. This could underlie some of the core symptoms observed in humans prenatally exposed to valproic acid.

摘要

胚胎发育期间接触丙戊酸(VPA)会导致多种致畸效应,包括发育迟缓,尤其是在妊娠第三周接触VPA时,会导致人类患自闭症。我们使用体外电生理学方法研究了胚胎期接触VPA对幼鼠新皮质微回路特性的产后影响。我们发现,在胚胎第11.5天单次产前注射VPA会显著增强新皮质锥体神经元形成的局部递归连接。对这些连接的生物物理特性的研究揭示了较弱的兴奋性突触反应。还观察到锥体神经元的内在兴奋性显著降低。此外,我们证明了第5层锥体神经元之间连接中假定突触接触的数量减少。局部高连接性可能使皮质模块对刺激更敏感,一旦被激活,就会更自主、孤立,且更难控制。这可能是产前接触丙戊酸的人类所观察到的一些核心症状的基础。

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