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在毛果芸香碱诱导的自发性边缘叶癫痫模型中,海马的α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)和N-甲基-D-天冬氨酸(NMDA)信使核糖核酸(mRNA)水平与齿状回苔藓纤维异常出芽相关。

Hippocampal AMPA and NMDA mRNA levels correlate with aberrant fascia dentata mossy fiber sprouting in the pilocarpine model of spontaneous limbic epilepsy.

作者信息

Mathern G W, Pretorius J K, Mendoza D, Lozada A, Kornblum H I

机构信息

Division of Neurosurgery, University of California-Los Angeles, USA.

出版信息

J Neurosci Res. 1998 Dec 15;54(6):734-53. doi: 10.1002/(SICI)1097-4547(19981215)54:6<734::AID-JNR2>3.0.CO;2-P.

Abstract

There is considerable controversy whether aberrant fascia dentata (FD) mossy fiber sprouting is an epiphenomena related to neuronal loss or a pathologic abnormality responsible for spontaneous limbic seizures. If mossy fiber sprouting contributes to seizures, then reorganized axon circuits should alter postsynaptic glutamate receptor properties. In the pilocarpine-status rat model, this study determined if changes in alpha amino-3-hydroxy-5-methyl-4-isoxazole-propionate (AMPA) and n-methyl-D-aspartic acid (NMDA) receptor subunit mRNA levels correlated with mossy fiber sprouting. Sprague-Dawley rats were injected with pilocarpine (320 mg/kg; i.p.) and maintained in status epilepticus for 6 to 8 hours (pilocarpine-status). Rats were killed during the: (1) latent phase after neuronal loss but before spontaneous limbic seizures (day 11 poststatus; n = 7); (2) early seizure phase after their first seizures (day 25; n = 7); and (3) chronic seizure phase after many seizures (day 85; n = 9). Hippocampi were studied for neuron counts, inner molecular layer (IML) neo-Timm's staining, and GluR1-3 and NMDAR1-2b mRNA levels. Compared with controls, pilocarpine-status rats in the: (1) latent phase showed increased FD GluR3, NMDAR1, and NMDAR2b; greater CA4 and CA1 NMDAR1; and decreased subiculum GluR1 hybridization densities; (2) early seizure phase showed increased FD GluR3, increased CA1 NMDAR1, and decreased subiculum NMDAR2b densities; and (3) chronic seizure phase showed increased FD GluR2; increased FD and CA4 GluR3; decreased CA1 GluR2; and decreased subiculum GluR1, GluR2, NMDAR1, and NMDAR2b levels. In multivariate analyses, greater IML neo-Timm's staining: (1) positively correlated with FD GluR3 and NMDAR1 and (2) negatively correlated with CA1 and subiculum GluR1 and GluR2 mRNA levels. These results indicate that: (1) hippocampal AMPA and NMDA receptor subunit mRNA levels changed as rats progressed from the latent to chronic seizure phase and (2) certain subunit alterations correlated with mossy fiber sprouting. Our findings support the hypothesis that aberrant axon circuitry alters postsynaptic hippocampal glutamate receptor subunit stoichiometry; this may contribute to limbic epileptogenesis.

摘要

齿状回(FD)异常苔藓纤维发芽是与神经元丢失相关的一种附带现象,还是导致自发性边缘叶癫痫发作的一种病理异常,目前存在相当大的争议。如果苔藓纤维发芽导致癫痫发作,那么重新组织的轴突回路应该会改变突触后谷氨酸受体的特性。在匹鲁卡品致癫痫持续状态大鼠模型中,本研究确定α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)和N-甲基-D-天冬氨酸(NMDA)受体亚基mRNA水平的变化是否与苔藓纤维发芽相关。将Sprague-Dawley大鼠注射匹鲁卡品(320mg/kg;腹腔注射),并使其处于癫痫持续状态6至8小时(匹鲁卡品致癫痫持续状态)。在以下阶段处死大鼠:(1)神经元丢失后的潜伏期但在自发性边缘叶癫痫发作之前(癫痫持续状态后第11天;n = 7);(2)首次癫痫发作后的早期癫痫发作阶段(第25天;n = 7);以及(3)多次癫痫发作后的慢性癫痫发作阶段(第85天;n = 9)。对海马体进行神经元计数、内分子层(IML)新Timm染色以及GluR1-3和NMDAR1-2b mRNA水平检测。与对照组相比,匹鲁卡品致癫痫持续状态大鼠在:(1)潜伏期显示FD的GluR3、NMDAR1和NMDAR2b增加;CA4和CA1的NMDAR1增加;以及海马下托的GluR1杂交密度降低;(2)早期癫痫发作阶段显示FD的GluR3增加,CA1的NMDAR1增加,以及海马下托的NMDAR2b密度降低;以及(3)慢性癫痫发作阶段显示FD的GluR2增加;FD和CA4的GluR3增加;CA1的GluR2降低;以及海马下托的GluR1、GluR2、NMDAR1和NMDAR2b水平降低。在多变量分析中,更高的IML新Timm染色:(1)与FD的GluR3和NMDAR1呈正相关,(2)与CA1和海马下托的GluR1和GluR2 mRNA水平呈负相关。这些结果表明:(1)随着大鼠从潜伏期发展到慢性癫痫发作阶段,海马体AMPA和NMDA受体亚基mRNA水平发生变化,(2)某些亚基改变与苔藓纤维发芽相关。我们的研究结果支持这样的假设,即异常的轴突回路改变了突触后海马体谷氨酸受体亚基的化学计量;这可能有助于边缘叶癫痫的发生。

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