Schneider P G, Rodríguez de Lores Arnaiz G
Instituto de Biología Celular y Neurociencias, Facultad de Medicina, Universidad de Buenos Aires, Paraguay, Argentina.
Mol Chem Neuropathol. 1997 Sep-Dec;32(1-3):213-21. doi: 10.1007/BF02815177.
It has already been shown that the administration of convulsant 3-mercaptopropionic acid at 150 mg/kg enhances binding affinity of muscarinic antagonist [3H]quinuclidinyl benzilate ([3H]QNB) to certain rat CNS membranes without affecting site number. Herein we employed a 100 mg/kg dose and tested [3H]QNB binding to cerebellar, hippocampal, and striatal membranes obtained from rats killed at preseizure, seizure, and postseizure stages. In cerebellum, binding increased 24, 65, and 19% a1 preseizure, seizure, and postseizure stages, respectively; in hippocampus, values were 12 and 20% higher at pre- and seizure stages, but failed to differ from controls at postseizure; in striatum, increases of 10 and 18% were recorded at seizure and postseizure, with no changes at preseizure. Neither a subconvulsant dose (20 mg/kg) nor in vitro drug addition had any effect on binding. Results indicate a differential response to the convulsant, with reversible changes in cerebellum and hippocampus, and a delayed response in striatum, supporting the concept of area-dependent neuronal plasticity.
已经表明,以150mg/kg的剂量给予惊厥剂3-巯基丙酸可增强毒蕈碱拮抗剂[3H]喹核醇基苯甲酸酯([3H]QNB)与某些大鼠中枢神经系统膜的结合亲和力,而不影响位点数量。在此,我们采用100mg/kg的剂量,并测试了[3H]QNB与从处于癫痫发作前、发作期和发作后期处死的大鼠获得的小脑、海马和纹状体膜的结合。在小脑中,结合在癫痫发作前、发作期和发作后期分别增加24%、65%和19%;在海马中,在癫痫发作前和发作期的值分别高出12%和20%,但在发作后期与对照组无差异;在纹状体中,在发作期和发作后期记录到增加10%和18%,在癫痫发作前无变化。惊厥剂的亚惊厥剂量(20mg/kg)或体外添加药物对结合均无任何影响。结果表明对惊厥剂有不同的反应,小脑中的变化是可逆的,海马中的变化也是可逆的,而纹状体中的反应延迟,这支持了区域依赖性神经元可塑性的概念。