Sperk G, Marksteiner J, Gruber B, Bellmann R, Mahata M, Ortler M
Department of Pharmacology, University of Innsbruck, Austria.
Neuroscience. 1992 Oct;50(4):831-46. doi: 10.1016/0306-4522(92)90207-i.
The influence of sustained epileptic seizures evoked by intraperitoneal injection of kainic acid on the gene expression of the neuropeptides somatostatin and neuropeptide Y and on the damage of neurons containing these peptides was studied in the rat brain. Injection of kainic acid induced an extensive loss of somatostatin and, though less pronounced, of neuropeptide Y neurons in the inner part of the hilus of the dentate gyrus. Neuropeptide Y-immunoreactive neurons located in the subgranular layer of the hilus, presumably pyramidal-shaped basket cells, were spared by the treatment. Although neuropeptide Y messenger RNA was not detected in granule cells of control rats, it was found there after kainic acid seizures at all time intervals investigated (12 h to 90 days after injection of kainic acid). High concentrations of neuropeptide Y messenger RNA were especially observed 24 h after injection of kainic acid. At this time neuropeptide Y messenger RNA was also transiently observed in CA1 pyramidal cells. Neuropeptide Y synthesis in granule cells in turn gave rise to an intense immunoreactivity of the peptide in the terminal field of mossy fibers which persisted for the entire time period (90 days) investigated. In addition, neuropeptide Y messenger RNA concentrations were also drastically elevated in presumptive basket cells located at the inner surface of the granule cell layer, especially at the "late" time intervals investigated (30-90 days after kainic acid). These data support the concept that extensive activation of granule cells by limbic seizures contributes to the observed neuronal cell death in CA3 pyramidal neurons and interneurons of the hilus. Consecutively, basket cells containing neuropeptide Y and presumably GABA might be activated and participate in recurrent inhibition of granule cells. Neuropeptide Y-immunoreactive fibers observed in the inner molecular layer at "late" time intervals after kainic acid may result either from collateral sprouting of mossy fibers or from basket cells extensively expressing the peptide. It is speculated that neuropeptide Y synthesized and released at a high rate from granule cells and basket cells may exert a protective action against seizures.
在大鼠脑中研究了腹腔注射海藻酸诱发的持续性癫痫发作对神经肽生长抑素和神经肽Y基因表达以及对含有这些肽的神经元损伤的影响。注射海藻酸导致齿状回门部内侧生长抑素神经元大量丢失,神经肽Y神经元丢失虽不那么明显,但也有发生。位于门部颗粒下层的神经肽Y免疫反应性神经元,推测为锥体形篮状细胞,未受该处理影响。虽然在对照大鼠的颗粒细胞中未检测到神经肽Y信使核糖核酸,但在注射海藻酸后的所有研究时间间隔(注射海藻酸后12小时至90天)均在其中发现了该信使核糖核酸。尤其在注射海藻酸后24小时观察到高浓度的神经肽Y信使核糖核酸。此时,在CA1锥体细胞中也短暂观察到神经肽Y信使核糖核酸。颗粒细胞中神经肽Y的合成进而导致苔藓纤维终末场中该肽的强烈免疫反应性,这种反应在整个研究时间段(90天)持续存在。此外,位于颗粒细胞层内表面的推测篮状细胞中神经肽Y信使核糖核酸浓度也大幅升高,尤其是在研究的“晚期”时间间隔(海藻酸注射后30 - 90天)。这些数据支持这样的概念,即边缘性癫痫发作对颗粒细胞的广泛激活导致了在CA3锥体细胞和门部中间神经元中观察到的神经元细胞死亡。随后,含有神经肽Y且可能含有γ-氨基丁酸的篮状细胞可能被激活并参与颗粒细胞的反复抑制。在注射海藻酸后的“晚期”时间间隔在内分子层观察到的神经肽Y免疫反应性纤维可能是苔藓纤维的侧支发芽或大量表达该肽的篮状细胞所致。推测从颗粒细胞和篮状细胞高速合成和释放的神经肽Y可能对癫痫发作发挥保护作用。