Vezzani A, Schwarzer C, Lothman E W, Williamson J, Sperk G
Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.
Epilepsy Res. 1996 Dec;26(1):267-79. doi: 10.1016/s0920-1211(96)00059-9.
Using immunocytochemistry and in situ hybridization analysis of mRNA, we investigated the changes in the expression of somatostatin and neuropeptide Y (NPY) in the rat hippocampal principal neurons in kindling or after electrically induced status epilepticus (SE), two models of limbic epilepsy associated with different chronic sequelae of seizures and seizure-related neuropathology. At the preconvulsive stage 2 of kindling and after three consecutive tonic-clonic seizures (stage 5) but not after a single-discharge (AD), somatostatin and NPY immunoreactivity (IR) were markedly increased in interneurons of the deep hilus and the polymorphic cell layer and their presumed projections to the outer molecular layer of the dentate gyrus. Increased mRNA levels were observed in the same neurons. NPY IR and mRNA were highly expressed in pyramidal-shaped basket cells at both stages of kindling. IR was similar two days after stages 2 or 5 of kindling while less pronounced effects were observed one week after kindling completion. Peptide-containing neurons in the hilus appeared well preserved in spite of an average of 24% reduction of Nissl stained cells (p < 0.01) in the stimulated and contralateral hippocampus at stage 5. No sprouting of mossy fibres in the inner molecular layer was found as assessed by Timm staining. Thirty days after SE, somatostatin IR was slightly reduced or similar to controls in the ventral dentate gyrus and molecular layer in four or six rats (SE-I group) while in the two other post-SE rats (SE-II), somatostatin IR was lost. These changes were associated with a different extent of neurodegeneration as assessed by cell counting of Nissl stained sections. In the granule cells/mossy fibres NPY-IR was transiently expressed at stage 2 and after a single AD. Differently, NPY-IR was persistently enhanced in the mossy fibres of all post-SE rats particularly in the SE-II group. In these rats, NPY immunoreactive fibres were detected in the infrapyramidal region of the stratum oriens CA3 and in the inner molecular layer of the dentate gyrus very likely labeling sprouted mossy fibres. In the hippocampus proper of kindled rats, somatostatin and NPY IR were respectively enhanced in the stratum lacunosum moleculare, the subiculum and in the alveus while no significant changes were observed after SE. Changes in peptide expression were bilateral and involved both the dorsal and the ventral hippocampus. The lasting modifications in peptides IR and mRNA expression in distinct neuronal populations of the hippocampus may reflect functional modifications neurons and play a role in limbic epileptogenesis.
利用免疫细胞化学和mRNA原位杂交分析,我们研究了点燃或电诱导癫痫持续状态(SE)后大鼠海马主要神经元中生长抑素和神经肽Y(NPY)表达的变化,这两种边缘性癫痫模型与癫痫发作的不同慢性后遗症及癫痫相关神经病理学有关。在点燃的惊厥前期2以及连续三次强直-阵挛性发作后(阶段5),而非单次放电后(AD),深齿状回和多形细胞层的中间神经元及其向齿状回外分子层的推测投射中,生长抑素和NPY免疫反应性(IR)显著增加。在相同神经元中观察到mRNA水平升高。在点燃的两个阶段,NPY IR和mRNA在锥体形篮状细胞中均高表达。点燃阶段2或5后两天IR相似,而在点燃完成一周后观察到的效应较弱。尽管在阶段5时,受刺激海马和对侧海马中Nissl染色细胞平均减少了24%(p < 0.01),但齿状回中的含肽神经元似乎保存良好。通过Timm染色评估,未发现内分子层中有苔藓纤维发芽。SE后30天,在4只或6只大鼠(SE-I组)的腹侧齿状回和分子层中,生长抑素IR略有降低或与对照组相似,而在另外两只SE后大鼠(SE-II组)中,生长抑素IR消失。通过对Nissl染色切片进行细胞计数评估,这些变化与不同程度的神经退行性变有关。在颗粒细胞/苔藓纤维中,NPY-IR在阶段2和单次AD后短暂表达。不同的是,所有SE后大鼠,尤其是SE-II组的苔藓纤维中NPY-IR持续增强。在这些大鼠中,在海马体CA3层的锥体下区域和齿状回的内分子层中检测到NPY免疫反应性纤维,很可能标记的是发芽的苔藓纤维。在点燃大鼠的海马本部,生长抑素和NPY IR分别在分子层腔隙层、海马下脚和脑室下区增强,而SE后未观察到显著变化。肽表达的变化是双侧的,涉及背侧和腹侧海马。海马不同神经元群体中肽IR和mRNA表达的持久改变可能反映了神经元的功能改变,并在边缘性癫痫发生中起作用。