Lee P H, Hong J S
Neuropharmacology Section, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709.
Neuroscience. 1990;35(1):71-7. doi: 10.1016/0306-4522(90)90121-j.
The role of the ventral hippocampal dentate granule neurons in the mu opioid receptor agonist-induced motor seizures and wet dog shakes was examined in this study. [NMe-Phe3-D-Pro4]morphiceptin (9.4 nmol) was injected into the left ventral hippocampus of rats 14 days after unilateral or bilateral colchicine (5 nmol/site) lesions of ventral hippocampal dentate granule cells and the subsequent behavioral and neuropathological responses were observed. [NMe-Phe3-D-Pro4]morphiceptin injected into control animals produced convulsions and numerous wet dog shakes that lasted for less than 1 h. [NMe-Phe-D-Pro4]morphiceptin-induced wet dog shakes were significantly reduced in unilateral colchicine-pretreated rats, and completely inhibited in bilateral colchicine-pretreated animals. In contrast, generalized motor seizures evoked by [NMe-Phe3-D-Pro4]morphiceptin were potentiated and prolonged in colchicine-pretreated animals as status epilepticus (sustained clonus of forepaws and head for more than 1 h) was observed in both unilateral and bilateral colchicine-pretreated animals but not in control rats. No morphological damage of granule or pyramidal cells was found in the ventral hippocampus of control animals following [NMe-Phe3-D-Pro4]morphiceptin injection. Colchicine treatment by itself produced a selective lesion of dentate granule cells. In colchicine-pretreated animals, [NMe-Phe3-D-Pro4]morphiceptin induced widespread seizure-related damage of CA3/CA1 pyramidal cells. These results suggest that dentate granule cells in the ventral hippocampus are essential for the elaboration of wet dog shakes. However, these neurons may play an inhibitory role in the spread of seizure activity within the hippocampus or limbic structures.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究考察了腹侧海马齿状颗粒神经元在μ阿片受体激动剂诱导的运动性癫痫发作和湿狗样抖动中的作用。在腹侧海马齿状颗粒细胞单侧或双侧秋水仙碱(5 nmol/部位)损伤14天后,将[NMe-Phe3-D-Pro4]吗啡肽(9.4 nmol)注射到大鼠左侧腹侧海马,随后观察行为和神经病理学反应。注射到对照动物体内的[NMe-Phe3-D-Pro4]吗啡肽会引发惊厥和大量持续时间少于1小时的湿狗样抖动。在单侧秋水仙碱预处理的大鼠中,[NMe-Phe-D-Pro4]吗啡肽诱导的湿狗样抖动明显减少,而在双侧秋水仙碱预处理的动物中则完全被抑制。相反,在秋水仙碱预处理的动物中,[NMe-Phe3-D-Pro4]吗啡肽诱发的全身性运动性癫痫发作增强且持续时间延长,因为在单侧和双侧秋水仙碱预处理的动物中均观察到癫痫持续状态(前爪和头部持续阵挛超过1小时),而对照大鼠中未观察到。注射[NMe-Phe3-D-Pro4]吗啡肽后,对照动物腹侧海马的颗粒细胞或锥体细胞未发现形态学损伤。秋水仙碱处理本身导致齿状颗粒细胞选择性损伤。在秋水仙碱预处理的动物中,[NMe-Phe3-D-Pro4]吗啡肽诱导CA3/CA1锥体细胞广泛的癫痫相关损伤。这些结果表明,腹侧海马中的齿状颗粒细胞对于湿狗样抖动的产生至关重要。然而,这些神经元可能在癫痫活动在海马或边缘结构内的传播中起抑制作用。(摘要截断于250字)