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大鼠梨状前皮质深层点燃模型发育过程中脑内前脑啡肽原和前强啡肽原mRNA及相关肽的变化

Changes of proenkephalin and prodynorphin mRNAs and related peptides in rat brain during the development of deep prepyriform cortex kindling.

作者信息

Lee P H, Zhao D, Xie C W, McGinty J F, Mitchell C L, Hong J S

机构信息

Laboratory of Molecular and Integrative Neuroscience, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.

出版信息

Brain Res Mol Brain Res. 1989 Dec;6(4):263-73. doi: 10.1016/0169-328x(89)90072-7.

DOI:10.1016/0169-328x(89)90072-7
PMID:2593781
Abstract

The effects of deep prepyriform cortex (DPC) kindling on the amount of proenkephalin and prodynorphin mRNAs, Met5-enkephalin (ME) and dynorphin (DYN) in rat brain were examined. Animals received electrical stimulation of the DPC until two consecutive stage 2 seizures (S2) or stage 5 seizures (S5) were attained. The proenkephalin mRNA and ME contents in the entorhinal cortex were increased 24 h after S2 and also 5 min and 24 h post S5. In the hippocampus, the proenkephalin mRNA level was reduced 24 h after S2 but increased 5 min and 24 h after S5. Elevated hippocampal ME concentration was observed 24 h after S2 and S5. Similarly, the ME level in the frontal cortex was increased 24 h after S2 and S5 but the proenkephalin mRNA content was only elevated at S5. In the striatum, the proenkephalin mRNA level was slightly increased 24 h after S2 and S5, but no change in ME content was found. The amount of prodynorphin mRNA in the hippocampus was attenuated only at 24 h after S5, whereas DYN concentration was reduced 5 min after S5. No change in striatal DYN concentration was observed despite a slight elevation of prodynorphin mRNA 24 h post S2 and S5. Six weeks after the last seizure, no difference in ME and DYN was found between kindled and control animals. These findings indicate that the enkephalin-containing perforant pathway in the entorhinal cortex-hippocampal region is particularly sensitive to electrical stimulations applied to the DPC. Its role and importance in the development of kindling are discussed.

摘要

研究了大鼠脑内深梨状前皮质(DPC)点燃对脑啡肽原和强啡肽原mRNA含量以及甲硫氨酸脑啡肽(ME)和强啡肽(DYN)含量的影响。动物接受DPC的电刺激,直至达到连续两次2期癫痫发作(S2)或5期癫痫发作(S5)。内嗅皮质中的脑啡肽原mRNA和ME含量在S2后24小时以及S5后5分钟和24小时均增加。在海马中,脑啡肽原mRNA水平在S2后24小时降低,但在S5后5分钟和24小时升高。S2和S5后24小时观察到海马ME浓度升高。同样,额叶皮质中的ME水平在S2和S5后24小时升高,但脑啡肽原mRNA含量仅在S5时升高。在纹状体中,脑啡肽原mRNA水平在S2和S5后24小时略有升高,但ME含量未发现变化。海马中的强啡肽原mRNA量仅在S5后24小时减弱,而DYN浓度在S5后5分钟降低。尽管S2和S5后24小时强啡肽原mRNA略有升高,但纹状体DYN浓度未观察到变化。最后一次癫痫发作六周后,点燃动物和对照动物之间的ME和DYN没有差异。这些发现表明,内嗅皮质-海马区域中含脑啡肽的穿通通路对施加于DPC的电刺激特别敏感。讨论了其在点燃发展中的作用和重要性。

相似文献

1
Changes of proenkephalin and prodynorphin mRNAs and related peptides in rat brain during the development of deep prepyriform cortex kindling.大鼠梨状前皮质深层点燃模型发育过程中脑内前脑啡肽原和前强啡肽原mRNA及相关肽的变化
Brain Res Mol Brain Res. 1989 Dec;6(4):263-73. doi: 10.1016/0169-328x(89)90072-7.
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Deep prepyriform cortex kindling differentially alters the levels of prodynorphin mRNA in rat hippocampus and striatum.梨状前皮质深层点燃对大鼠海马体和纹状体中前强啡肽原mRNA水平的影响存在差异。
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Perforant path stimulation differentially alters prodynorphin mRNA and proenkephalin mRNA levels in the entorhinal cortex-hippocampal region.
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Perforant path kindling induces differential alterations in the mRNA levels coding for prodynorphin and proenkephalin in the rat hippocampus.穿通通路点燃诱导大鼠海马中编码前强啡肽和前脑啡肽的mRNA水平发生不同改变。
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Single or repeated electroconvulsive shocks alter the levels of prodynorphin and proenkephalin mRNAs in rat brain.单次或重复电休克会改变大鼠脑中前强啡肽原和前脑啡肽原mRNA的水平。
Brain Res Mol Brain Res. 1989 Jul;6(1):11-9. doi: 10.1016/0169-328x(89)90023-5.
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Early changes in prodynorphin mRNA and ir-dynorphin A levels after kindled seizures in the rat.
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Changes in the dynamic state of brain proenkephalin-derived peptides during amygdaloid kindling.杏仁核点燃过程中脑前脑啡肽衍生肽动态状态的变化。
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Response of rat pituitary anterior lobe prodynorphin products to changes in gonadal steroid environment.大鼠垂体前叶前强啡肽产物对性腺类固醇环境变化的反应。
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Region-specific changes in prodynorphin mRNA and ir-dynorphin A levels after kindled seizures.点燃性癫痫发作后前强啡肽原mRNA和免疫反应性强啡肽A水平的区域特异性变化。
J Mol Neurosci. 1999 Aug-Oct;13(1-2):69-75. doi: 10.1385/JMN:13:1-2:69.

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