单胺类神经递质
癫痫持续状态
匹罗卡品
多巴胺
神经化学
血清素
内科学
海马体
化学
内分泌学
海马结构
句号(音乐)
去甲肾上腺素
谷氨酸受体
癫痫
医学
受体
声学
物理
精神科
作者
Ésper A. Cavalheiro,Maria José da Silva Fernandes,L. Turski,Maria da Graça Naffah‐Mazzacoratti
出处
期刊:Epilepsia
[Wiley]
日期:1994-01-01
卷期号:35 (1): 1-11
被引量:257
标识
DOI:10.1111/j.1528-1157.1994.tb02905.x
摘要
Summary: Rats subjected to structural brain damage induced by sustained convulsions triggered by systemic administration of pilocarpine (PILO) are a useful model for investigation of the mechanisms essential for seizure generation and spread in rodents. After PILO administration, three distinct phases are observed: (a) an acute period of 1–2 days’ duration corresponding to a pattern of repetitive limbic seizures and status epilepticus; (b) a seizurefree (silent) period characterized by a progressive return to normal EEG and behavior of 4–44 days’ duration; and (c) a period of spontaneous recurrent seizures (SRS) starting 5‐45 days after PILO administration and lasting throughout the animal's life. PILO (320–350 mgikg intraperitoneally, i.p.) was administered to rats, and the content of hippocampal monoamines and amino acids was measured in the acute, silent, and SRS periods by liquid chromatography. Norepinephrine (NE) level was decreased during all periods whereas dopamine (DA) content was increased. Serotonin (5‐hydroxytryptamine, 5‐HT) was increased only in the acute period. Utilization rate measurement of monoamines showed increased NE consumption and decreased DA consumption during all phases. 5‐HT utilization rate was increased only in the acute period. Amino acid content showed a decrease in aspartate (ASP) and glutamate (GLU) concentrations associated with increased y‐aminobutyric acid (GABA) level during the acute period. The silent phase was characterized by a decrease in glycine (GLY) and GABA levels and an increase in GLU concentration. The SRS period showed an increase in all amino acid concentrations. These findings show important neurochemical changes in the course of establishment of an epileptic focus after brain damage induced by status epilepticus triggered by pilocarpine.
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