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在锂-匹罗卡品颞叶癫痫模型中大鼠脑代谢型谷氨酸受体基因表达的变化。

Changes in Metabotropic Glutamate Receptor Gene Expression in Rat Brain in a Lithium-Pilocarpine Model of Temporal Lobe Epilepsy.

机构信息

Laboratory of Molecular Mechanisms of Neural Interactions, Sechenov Institute of Evolutionary Physiology and Biochemistry of RAS, 194223 Saint Petersburg, Russia.

出版信息

Int J Mol Sci. 2022 Mar 2;23(5):2752. doi: 10.3390/ijms23052752.

Abstract

Preventing epileptogenesis in people at risk is an unmet medical need. Metabotropic glutamate receptors (mGluRs) are promising targets for such therapy. However, drugs acting on mGluRs are not used in the clinic due to limited knowledge of the involvement of mGluRs in epileptogenesis. This study aimed to analyze the changes in gene expression of mGluR subtypes (1-5, 7, 8) in various rat brain regions in the latent and chronic phases of a lithium-pilocarpine model of epilepsy. For this study, multiplex test systems were selected and optimized to analyze mGluR gene expression using RT-qPCR. Region- and phase-specific changes in expression were revealed. During the latent phase, mGluR5 mRNA levels were increased in the dorsal and ventral hippocampus, and expression of group III genes was decreased in the hippocampus and temporal cortex, which could contribute to epileptogenesis. Most of the changes in expression detected in the latent stage were absent in the chronic stage, but mGluR8 mRNA production remained reduced in the hippocampus. Moreover, we found that gene expression of group II mGluRs was altered only in the chronic phase. The study deepened our understanding of the mechanisms of epileptogenesis and suggested that agonists of group III mGluRs are the most promising targets for preventing epilepsy.

摘要

预防高危人群的癫痫发生是一个尚未满足的医学需求。代谢型谷氨酸受体(mGluRs)是此类治疗的有前途的靶点。然而,由于对 mGluRs 在癫痫发生中的作用的了解有限,作用于 mGluRs 的药物并未在临床上使用。本研究旨在分析锂-匹罗卡品癫痫模型的潜伏和慢性阶段各种大鼠脑区中 mGluR 亚型(1-5、7、8)的基因表达变化。为此,本研究选择了多重测试系统,并对其进行了优化,以使用 RT-qPCR 分析 mGluR 基因表达。揭示了表达的区域和阶段特异性变化。在潜伏阶段,mGluR5 mRNA 水平在背侧和腹侧海马体中增加,而海马体和颞叶皮质中的 III 组基因表达减少,这可能有助于癫痫发生。在潜伏阶段检测到的大多数表达变化在慢性阶段都不存在,但 mGluR8 mRNA 的产生在海马体中仍然减少。此外,我们发现只有在慢性阶段才改变了 II 组 mGluRs 的基因表达。该研究加深了我们对癫痫发生机制的理解,并表明 III 组 mGluRs 的激动剂是预防癫痫最有前途的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d328/8910969/2e00e8978237/ijms-23-02752-g0A1.jpg

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