Monmaur P, Puma C, Sharif A
Laboratoire de Psychopharmacologie et Processus Cognitifs, Université Paris VII, France.
Brain Res. 1994 Sep 5;656(1):199-204. doi: 10.1016/0006-8993(94)91385-4.
Binding and autoradiographic studies have shown the presence of a rather high density of M2 muscarinic subtype receptors and the apparent absence or low density of the M1 subtype in the septum. We tested the hypothesis that, in the urethane-anesthetized rat, septal M2 receptors are involved in the generation of the hippocampal theta (theta) rhythm induced by intraseptal administration of carbachol, a potent cholinomimetic agent. Carbachol-induced theta was blocked by local infusion of the unspecific muscarinic antagonist agent, atropine (20 micrograms (29.55 nM)), given 10 min prior to carbachol. The intraseptal administration of low to high doses of gallamine (range: 20-180 micrograms (22.43-201.90 nM)), a specific M2 antagonist which displays high affinity for the septal region, resulted in significant changes in the electrophysiological characteristics of carbachol-induced theta but failed to abolish this rhythm. It is suggested that the latter may have resulted from a combined activation of both M2 and non-M2 receptors at septal level.
结合和放射自显影研究表明,在隔区存在相当高密度的M2毒蕈碱亚型受体,而M1亚型明显缺失或密度较低。我们检验了这样一个假设:在氨基甲酸乙酯麻醉的大鼠中,隔区M2受体参与了由强效拟胆碱剂卡巴胆碱经隔区给药诱导的海马θ节律的产生。在给予卡巴胆碱前10分钟,局部注入非特异性毒蕈碱拮抗剂阿托品(20微克(29.55纳摩尔))可阻断卡巴胆碱诱导的θ节律。向隔区内注射低到高剂量的加拉明(范围:20 - 180微克(22.43 - 201.90纳摩尔)),加拉明是一种对隔区具有高亲和力的特异性M2拮抗剂,这导致卡巴胆碱诱导的θ节律的电生理特征发生显著变化,但未能消除该节律。提示后者可能是由于隔区水平的M2和非M2受体的联合激活所致。