Mourre C, Widmann C, Lazdunski M
Institut de Pharmacologie moléculaire et cellulaire, Valbonne, France.
Brain Res. 1991 Feb 1;540(1-2):340-4. doi: 10.1016/0006-8993(91)90533-2.
The density of glibenclamide (GB) binding sites decreases considerably in the dentate gyrus (greater than 80%), the CA1 field (approximately 75%) and the stratum lucidum of CA3 field (approximately 70%) after intradentate colchicine injections in rat hippocampus. The density of GB receptors is unchanged in kainic acid damaged hippocampus. These data show that GB binding sites associated to adenosine triphosphate-sensitive K+ channels are mainly located in granular cells in both pre- and post-synaptic positions. They are present in mossy fibers.
在大鼠海马齿状回内注射秋水仙碱后,格列本脲(GB)结合位点的密度在齿状回(超过80%)、CA1区(约75%)和CA3区透明层(约70%)显著降低。在 kainic 酸损伤的海马中,GB 受体的密度没有变化。这些数据表明,与三磷酸腺苷敏感钾通道相关的 GB 结合位点主要位于突触前和突触后位置的颗粒细胞中。它们存在于苔藓纤维中。