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点燃效应会在海马神经元的基因表达中产生持久且具选择性的变化。

Kindling produces long-lasting and selective changes in gene expression of hippocampal neurons.

作者信息

Perlin J B, Gerwin C M, Panchision D M, Vick R S, Jakoi E R, DeLorenzo R J

机构信息

Department of Neurology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298.

出版信息

Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1741-5. doi: 10.1073/pnas.90.5.1741.

Abstract

To test the hypothesis that repeated subconvulsive stimulations required to induce kindling can permanently alter gene expression of hippocampal neurons, we used Northern and in situ hybridization analyses to measure steady-state mRNA levels encoding several phenotypic proteins. mRNA encoding a membrane-bound protein, ligatin, was significantly reduced in kindled brains relative to naive and sham control animals. This change in gene expression persisted for over 4 months after kindling, was associated with a decrease in ligatin protein expression, was not produced by single or multiple seizures that did not induce the kindling phenomena, and was blocked by MK801. These results provide direct evidence that kindling can cause persistent changes in the expression of specific genes in hippocampal neurons and suggest that N-methyl-D-aspartate receptor-activated changes in gene expression may be a basic molecular mechanism underlying some of the long-lasting plasticity changes seen in kindling or models of long-term memory.

摘要

为了验证反复进行亚惊厥刺激以诱导点燃可永久性改变海马神经元基因表达这一假设,我们使用了Northern印迹和原位杂交分析来测量编码几种表型蛋白的稳态mRNA水平。与未处理和假手术对照动物相比,在点燃的大脑中,编码膜结合蛋白连接蛋白的mRNA显著减少。这种基因表达变化在点燃后持续超过4个月,与连接蛋白表达减少有关,不是由未诱导点燃现象的单次或多次癫痫发作引起的,并且被MK801阻断。这些结果提供了直接证据,表明点燃可导致海马神经元中特定基因表达的持续变化,并表明N-甲基-D-天冬氨酸受体激活的基因表达变化可能是在点燃或长期记忆模型中所见的一些持久可塑性变化的基本分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bca7/45955/2c26bf5bafaf/pnas01464-0117-a.jpg

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