Tandon P, Barone S, Mundy W R, Tilson H A
Center for Environmental Medicine and Lung Biology, University of North Carolina, Chapel Hill 27511.
Neurotoxicology. 1994 Fall;15(3):513-24.
Direct infusion of colchicine into the dentate gyrus of the hippocampus kills granule cells and elicits behavioral, neurochemical and neuroanatomical changes. Colchicine-treated rats are less sensitive to the behavioral effects of cholinergic muscarinic receptor antagonists and more sensitive to cholinergic agonists. These behavioral changes are associated with time- and dose-dependent alterations in the cholinergic signal transduction mechanism. Carbachol-stimulated turnover of phosphoinositides is increased in the hippocampus of colchicine-treated rats; similar changes are not observed in the cortex or striatum of colchicine-treated animals. Intradentate colchicine produces a significant increase in choline- acetyltransferase activity and staining for acetylcholinesterase activity in the hippocampus, suggesting reactive synaptogenesis of cholinergic fibers. Other studies have shown that the integrity of the septohippocampal pathway is necessary for these colchicine-induced compensatory changes to occur. It is suggested that the mechanism for these neurochemical changes in colchicine-treated animals may be occurring via alterations in negative feedback control of receptor-G-protein-mediated phosphoinositide hydrolysis.
将秋水仙碱直接注入海马齿状回会杀死颗粒细胞,并引发行为、神经化学和神经解剖学变化。用秋水仙碱处理的大鼠对胆碱能毒蕈碱受体拮抗剂的行为效应不太敏感,而对胆碱能激动剂更敏感。这些行为变化与胆碱能信号转导机制中时间和剂量依赖性的改变有关。在用秋水仙碱处理的大鼠海马中,卡巴胆碱刺激的磷酸肌醇周转率增加;在用秋水仙碱处理的动物的皮质或纹状体中未观察到类似变化。齿状体内注射秋水仙碱会使海马中胆碱乙酰转移酶活性和乙酰胆碱酯酶活性染色显著增加,提示胆碱能纤维发生反应性突触形成。其他研究表明,隔海马通路的完整性是这些秋水仙碱诱导的代偿性变化发生所必需的。有人提出,在用秋水仙碱处理的动物中,这些神经化学变化的机制可能是通过受体-G蛋白介导的磷酸肌醇水解的负反馈控制改变而发生的。