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癫痫发作活动会使大鼠海马体内的腺苷A1受体产生不同变化。

Seizure activity produces differential changes in adenosine A1 receptors within rat hippocampus.

作者信息

Vanore G, Giraldez L, Rodríguez de Lores Arnaiz G, Girardi E

机构信息

Instituto de Biologia Celular y Neurociencias Prof. E. De Robertis, Facultad de Medicina, Universidad de Buenos Aires, Argentina.

出版信息

Neurochem Res. 2001 Mar;26(3):225-30. doi: 10.1023/a:1010912516299.

DOI:10.1023/a:1010912516299
PMID:11495545
Abstract

Specific ligand binding to rat hippocampal adenosine A1 receptor after administration of the convulsant drug 3-mercaptopropionic acid (MP) was studied by means of a quantitative autoradiographic method. 2-Chloro-N6-[cyclopentyl-2,3,4,5-3H adenosine] ([3H]CCPA), a potent and selective A1 receptor ligand, was selected for binding studies. MP administration (150 mg/kg, i.p.), at seizure, caused significant increases in the following CA1 layers: pyramidal (45%), radiatum (18%) and lacunosum molecular (35%); in CA2 area, a significant decrease in stratum oriens (36%) and an increase in stratum radiatum (14%) and lacunosum molecular (33%) layers was observed. In CA3 area a rise in pyramidal (40%) and radiatum layers (26%), as well as in hillus (97%) was found. At postseizure, changes were restricted to CA1, CA2 and CA3 pyramidal layers and to CA1 lacunosum molecular layer, with increases ranging from 22 to 50%. These results show that [3H]CCPA binding is modified diversely in intrahippocampal layers and areas, thus indicating their dissimilar role in seizure activity.

摘要

采用定量放射自显影法研究了惊厥药3-巯基丙酸(MP)给药后大鼠海马腺苷A1受体的特异性配体结合情况。选择强效且选择性的A1受体配体2-氯-N6-[环戊基-2,3,4,5-3H腺苷]([3H]CCPA)进行结合研究。在癫痫发作时腹腔注射MP(150mg/kg)后,CA1层的以下区域出现显著增加:锥体层(45%)、辐射层(18%)和分子层(35%);在CA2区域,观察到原层显著减少(36%),辐射层增加(14%),分子层增加(33%)。在CA3区域,锥体层(40%)、辐射层(26%)以及海马齿状回(97%)出现增加。癫痫发作后,变化仅限于CA1、CA2和CA3锥体层以及CA1分子层,增加幅度在22%至50%之间。这些结果表明,[3H]CCPA结合在海马内各层和区域发生不同程度的改变,从而表明它们在癫痫活动中发挥不同作用。

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本文引用的文献

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