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神经连接与丙戊酸:髓鞘假说。

Neuroconnectivity and valproic acid: the myelin hypothesis.

机构信息

Academic Unit of Sleep and Department of Psychiatry, Royal Brompton Hospital, London, UK.

出版信息

Neurosci Biobehav Rev. 2012 Sep;36(8):1848-56. doi: 10.1016/j.neubiorev.2012.05.006. Epub 2012 May 28.

Abstract

Neuropsychiatric medications that directly alter the epigenome, such as valproic acid, can under certain conditions reactivate critical developmental periods and thus impact adult neuroconnectivity. In animal models valproic acid was shown to inhibit the process of postnatal myelination and to replicate age-dependent decline in remyelination efficiency. The human central nervous system's myelination process, unlike that of non-human primates commonly used in the experimental models, is an intricate heterochronous process that continues well into adult life and which probably underlies later life neurocognitive changes and plasticity. Chronic exposure to valproic acid, especially in patients with epilepsy and neuropsychiatric disorders, may profoundly affect this process and its developmental trajectory. Further studies using novel MRI methods that allow in vivo mapping of myelination trajectories across the lifespan are urgently required to address the potential effects of valproic acid on brain development.

摘要

神经精神药物可以直接改变表观基因组,如丙戊酸,在某些情况下可以重新激活关键的发育阶段,从而影响成年后的神经连接。在动物模型中,丙戊酸被证明可以抑制出生后的髓鞘形成过程,并复制随年龄增长而髓鞘再生效率下降的现象。与实验模型中常用的非人类灵长类动物不同,人类中枢神经系统的髓鞘形成过程是一个复杂的异时过程,一直持续到成年期,这可能是晚年神经认知变化和可塑性的基础。慢性暴露于丙戊酸,特别是在癫痫和神经精神疾病患者中,可能会深刻影响这个过程及其发育轨迹。迫切需要使用新的 MRI 方法进行进一步研究,这些方法可以在体内对整个生命周期的髓鞘化轨迹进行映射,以解决丙戊酸对大脑发育的潜在影响。

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