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Timing of cognitive deficits following neonatal seizures: relationship to histological changes in the hippocampus.

机译:新生儿惊厥后认知功能障碍的时机:与海马组织学变化的关系。

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Neonatal seizures are frequently associated with cognitive impairment and reduced seizure threshold. Previous studies in our laboratory have demonstrated that rats with recurrent neonatal seizures have impaired learning, lower seizure thresholds, and sprouting of mossy fibers in CA3 and the supragranular region of the dentate gyrus in the hippocampus when studied as adults. The goal of this study was to determine the age of onset of cognitive dysfunction and alterations in seizure susceptibility in rats subjected to recurrent neonatal seizures and the relation of this cognitive impairment to mossy fiber sprouting and expression of glutamate receptors. Starting at postnatal day (P) 0, rats were exposed to 45 flurothyl-induced seizures over a 9-day period of time. Visual-spatial learning in the water maze and seizure susceptibility were assessed in subsets of the rats at P20 or P35. Brains were evaluated for cell loss, mossy fiber distribution, and AMPA (GluR1) and NMDA (NMDAR1) subreceptor expression at these same time points. Rats with neonatal seizures showed significant impairment in the performance of the water maze and increased seizure susceptibility at both P20 and P35. Sprouting of mossy fibers into the CA3 and supragranular region of the dentate gyrus was seen at both P20 and P35. GluR1 expression was increased in CA3 at P20 and NMDAR1 was increased in expression in CA3 and the supragranular region of the dentate gyrus at P35. Our findings indicate that altered seizure susceptibility and cognitive impairment occurs prior to weaning following a series of neonatal seizures. Furthermore, these alterations in cognition and seizure susceptibility are paralleled by sprouting of mossy fibers and increased expression of glutamate receptors. To be effective, our results suggest that strategies to alter the adverse outcome following neonatal seizures will have to be initiated during, or shortly following, the seizures.
机译:新生儿癫痫发作通常与认知障碍和癫痫发作阈值降低有关。我们实验室先前的研究表明,成年后反复发作的新生大鼠癫痫会损害学习能力,降低癫痫发作阈值,并在CA3和海马齿状回的上核区中长出苔藓纤维。这项研究的目的是确定反复发作的新生鼠的认知功能障碍发作年龄和癫痫发作易感性改变,以及这种认知障碍与苔藓纤维发芽和谷氨酸受体表达的关系。从出生后第0天(P)开始,在9天的时间段内,大鼠经历了45次氟尿嘧啶诱发的癫痫发作。在P20或P35的大鼠子集中评估了水迷宫中的视觉空间学习和癫痫发作易感性。在这些相同的时间点评估大脑的细胞丢失,苔藓纤维分布以及AMPA(GluR1)和NMDA(NMDAR1)亚受体表达。在P20和P35处,患有新生儿惊厥的大鼠表现出水迷宫性能的显着损害,并且癫痫发作敏感性增加。在P20和P35处都可以看到长满苔藓的纤维发芽到齿状回的CA3和颗粒上区。在P20,CA3中的GluR1表达增加,而在P35,NMDAR1在CA3和齿状回上皮区的表达增加。我们的研究结果表明,一系列新生儿发作后,断奶前癫痫发作易感性和认知障碍发生了改变。此外,这些认知和癫痫发作易感性的改变与苔藓纤维的发芽和谷氨酸受体表达的增加平行。为有效起见,我们的结果表明,在惊厥发作期间或之后不久必须采取改变新生儿惊厥的不良结局的策略。

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