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大鼠杏仁核点燃的发展不伴有苔藓纤维发芽和海马神经元变性。

Amygdala kindling develops without mossy fiber sprouting and hippocampal neuronal degeneration in rats.

作者信息

Osawa M, Uemura S, Kimura H, Sato M

机构信息

National Epilepsy Center, Shizuoka Higashi Hospital, Shizuoka, Urushiyama, Japan.

出版信息

Psychiatry Clin Neurosci. 2001 Dec;55(6):549-57. doi: 10.1046/j.1440-1819.2001.00905.x.

Abstract

Repeated electrical stimulation of limbic structures has been reported to produce the kindling effect together with morphological changes in the hippocampus such as mossy fiber sprouting and/or neuronal loss. However, to argue against a causal role of these neuropathological changes in the development of kindling-associated seizures, we examined mossy fiber sprouting in amygdala (AM)-kindled rats using Timm histochemical staining, and evaluated the hippocampal neuronal degeneration in AM-kindled rats by terminal deoxynucleotidyl transferase-mediated digoxigenin-11-dUTP nick end labelling (TUNEL). Amygdala kindling was established by 10.3 +/- 0.7 electrical stimulations, and no increase in Timm granules (neuronal sprouting) was observed up to the time of acquisition of a fully kindled state. However, the density and distribution of Timm granules increased significantly in the dentate gyrus compared with unkindled rats after 29 after-discharges or more than 10 kindled convulsions. In addition, no significant increase in TUNEL-positive cells was found in the hilar polymorphic neurons or in CA3 pyramidal neurons of the kindled rats that had fewer than 29 after-discharges. However, a significant increase of TUNEL-positive cells was found in the granule cell layer in the dentate gyrus of the stimulated side after 18 after-discharges or 10 kindled convulsions. Our result show that AM kindling develops without evidence of mossy fiber sprouting, and that mossy fiber sprouting may appear after repeated kindled convulsions, following death of the granule cells in the dentate gyrus.

摘要

据报道,反复电刺激边缘系统结构会产生点燃效应,并伴有海马体的形态学变化,如苔藓纤维发芽和/或神经元丢失。然而,为了反驳这些神经病理学变化在点燃相关癫痫发展中的因果作用,我们使用Timm组织化学染色检查了杏仁核(AM)点燃大鼠的苔藓纤维发芽,并通过末端脱氧核苷酸转移酶介导的地高辛配基-11-dUTP缺口末端标记(TUNEL)评估了AM点燃大鼠的海马神经元变性。通过10.3±0.7次电刺激建立杏仁核点燃,在达到完全点燃状态之前未观察到Timm颗粒(神经元发芽)增加。然而,在29次放电后或超过10次点燃惊厥后,与未点燃大鼠相比,齿状回中Timm颗粒的密度和分布显著增加。此外,在放电次数少于29次的点燃大鼠的海马门多形神经元或CA3锥体神经元中,未发现TUNEL阳性细胞显著增加。然而,在18次放电或10次点燃惊厥后,在受刺激侧齿状回的颗粒细胞层中发现TUNEL阳性细胞显著增加。我们的结果表明,AM点燃在没有苔藓纤维发芽证据的情况下发展,并且苔藓纤维发芽可能在反复点燃惊厥后出现,继齿状回颗粒细胞死亡之后。

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