Division of Endocrinology, Department of Medicine and Department of Neurobiology and Behavior, SUNY Stony Brook, Stony Brook, New York 11794, USA.
Mol Cell Neurosci. 1992 Feb;3(1):79-87. doi: 10.1016/1044-7431(92)90011-p.
The opioid peptide dynorphin (DYN) is expressed normally at high levels in dentate gyrus granule cells in hippocampus and in neurons in entorhinal and neocortex. In the present study, ribonuclease protection and in situ hybridization analyses were used to examine preproDYN mRNA expression in hippocampus and neocortex following recurrent limbic seizure induced by a unilateral electrolytic lesion of the dentate gyrus hilus. In this paradigm, electrographic seizures within hippocampus recur intermittently from 1.6 to 12 h following the hilus lesion (HL). Solution hybridization-ribonuclease protection analysis of preproDYN mRNA levels in hippocampal dentate gyrus/CA1 samples from rats sacrificed 6 and 12 h following HL revealed an approximate 6-fold increase above control values at both times. PreproDYN mRNA levels returned toward control values by 24 h post-HL, were suppressed up to 10-fold below control values at 48 and 96 h post-HL, and then returned to control levels by 10 days post-HL. In situ hybridization analyses confirmed the biphasic nature of seizure-induced changes in preproDYN expression specifically within dentate gyrus granule cells. Additionally, these latter studies demonstrated that seizures induce expression of preproDYN mRNA in a small population of neurons within stratum pyramidale CAL Transient increases in preproDYN mRNA were also detected in subiculum and entorhinal cortex. However, in neocortex hybridization of preproDYN mRNA remained constant through 96 h post-HL. These findings of biphasic seizure-induced alterations in preproDYN mRNA expression can be contrasted with previously described changes in gene expression following limbic seizure activity and suggest that different cellular mechanisms regulate expression of colocalized hippocampal neuropeptides such as dynorphin, Metenkephalin, and neuropeptide Y.
阿片肽强啡肽 (DYN) 在海马齿状回颗粒细胞和内嗅皮质及新皮质神经元中正常高水平表达。在本研究中,采用核糖核酸酶保护和原位杂交分析,检测单侧海马齿状回门区电灼后反复边缘性癫痫发作对海马和新皮质中前强啡肽原 (preproDYN) mRNA 表达的影响。在该模型中,电刺激海马内癫痫在门区损伤后 1.6-12 小时内间歇性复发(HL)。对 HL 后 6 和 12 小时处死大鼠海马齿状回/CA1 样本进行 preproDYN mRNA 水平的溶液杂交-核糖核酸酶保护分析显示,在这两个时间点,其水平比对照值升高约 6 倍。HL 后 24 小时,preproDYN mRNA 水平接近对照值,48 和 96 小时后降至对照值的 10 倍以下,10 天后恢复至对照水平。原位杂交分析证实,癫痫诱导的 preproDYN 表达变化具有双相性,仅发生在齿状回颗粒细胞内。此外,这些后续研究表明,癫痫诱导 preproDYN mRNA 在 CA1 层锥体神经元中的一小部分神经元中表达。在 subiculum 和内嗅皮质中也检测到 preproDYN mRNA 的短暂增加。然而,在新皮质中,preproDYN mRNA 的杂交在 HL 后 96 小时内保持不变。这些双相性癫痫诱导的 preproDYN mRNA 表达变化的发现与先前描述的边缘性癫痫活动后基因表达的变化形成对比,表明不同的细胞机制调节强啡肽、Met-脑啡肽和神经肽 Y 等海马神经肽的共表达。