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[豚鼠脑片青霉素诱发癫痫样后放电的阈值]

[Threshold of penicillin induced epileptiform afterdischarge in brain slices of guinea pig].

作者信息

Yuasa H, Iwata K, Yamazaki A, Mizuno J, Yamada T, Kageyama N, Tasaki F

出版信息

No To Shinkei. 1985 Apr;37(4):371-6.

PMID:4027084
Abstract

Investigation of the regional threshold for epilepsy in many structures in the brain would contribute to the study of epileptogenesis. So we studied the threshold for epileptiform afterdischarge in the neocortex, hippocampus and cerebellar cortex using Na-Penicillin -G (Pc) of which epileptogenesis has been intensively investigated. In order to eliminate the influence from the outside of these structures, the brain slice method was utilized. Procedures for preparation of the tissue and incubation were about the same as those described by Yamamoto. In summary, after sacrifice, brain of the guinea pig was taken out and the hippocampus, neocortex and cerebellum were cut with a razor blade under a microscope. The thickness of the section was about 0.3 mm. Slices were incubated at 37 degrees C for about 30 min in the standard medium perfused with 95% O2 and 0% CO2. The chamber was continuously perfused with the standard medium which composed of NaCl, 124 mM, KCl, 5: KH2PO4, 1.24; MgSO4, 1.3; CaCl2, 2.4; NaHCO3, 26; and glucose, 10. Evoked potentials were elicited by electrical stimulation in the standard medium. Mossy fibers were stimulated and responses were recorded from the CA3 area in the hippocampus by glass pipette microelectrode. Subcortical white matter was stimulated and responses were recorded from the Purkinje cell layer in the cerebellum. Pc was added in the standard medium until epileptiform afterdischarges were superimposed on the evoked potentials. The results of this experiment demonstrated that each structure in the brain has a regional own threshold for Pc induced epileptiform afterdischarge.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究大脑中多个结构的癫痫区域阈值将有助于癫痫发生机制的研究。因此,我们使用已对其癫痫发生机制进行深入研究的青霉素G钠(Pc),研究了新皮层、海马体和小脑皮层中癫痫样放电后电位的阈值。为了消除这些结构外部的影响,采用了脑片法。组织制备和孵育程序与山本所描述的大致相同。简而言之,处死后取出豚鼠的大脑,在显微镜下用剃须刀片切下海马体、新皮层和小脑。切片厚度约为0.3毫米。切片在37摄氏度下于灌注95%氧气和5%二氧化碳的标准培养基中孵育约30分钟。培养室持续灌注由124毫摩尔氯化钠、5毫摩尔氯化钾、1.24毫摩尔磷酸二氢钾、1.3毫摩尔硫酸镁、2.4毫摩尔氯化钙、26毫摩尔碳酸氢钠和10毫摩尔葡萄糖组成的标准培养基。在标准培养基中通过电刺激诱发诱发电位。刺激苔藓纤维,并用玻璃微电极从海马体的CA3区域记录反应。刺激皮层下白质,从小脑的浦肯野细胞层记录反应。向标准培养基中加入Pc,直到癫痫样放电后电位叠加在诱发电位上。该实验结果表明,大脑中的每个结构对Pc诱导的癫痫样放电后电位都有各自的区域阈值。(摘要截断于250字)

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