Winson J, Dahl D
Exp Brain Res. 1985;59(3):497-506. doi: 10.1007/BF00261340.
The effects of iontophoretic application of 1-norepinephrine (NE) and related drugs on granule cell responses evoked by a stimulus pulse applied to the medial perforant pathway were studied in anesthetized rats. Drugs were applied and responses recorded at successive dorso-ventral positions along the dendrites and at the cell body layer. 1. Reciprocal actions of alpha and beta receptors were revealed in the cell body region. The beta agonist isoproterenol decreased the population spike while the beta antagonist sotalol increased it. In contrast, the alpha agonists phenylephrine and clonidine increased the population spike whereas the alpha antagonist prazosin decreased it. The action of the drugs was rapid, dose dependent and reversible. NE itself had no effect when applied in the granule cell layer. 2. In contrast to the failure of NE to elicit a short term response, and in confirmation of a previous report (Neuman and Harley 1983), the prolonged application of NE in the granule cell layer produced a longterm enhancement of the population spike. However, this effect was also observed after the application of d-NE. 3. NE affected granule cell responses in the middle third of the dendrites where it reduced the evoked synaptic potential (ESP, current flow produced by excitatory synaptic activity) in a dose-dependent manner. Recordings taken simultaneously in the cell body region revealed a reduction of the population spike and no change in the ESP at the cell body layer (the positive-going ESP reflecting an outward current flow from the cell). In an attempt to delineate receptor specificity, a series of alpha and beta agonists and antagonists were applied to the mid-dendritic region. All drugs reduced the ESP in a manner similar to NE. Such lack of specificity in the action of NE has been previously reported in the spinal motoneuron (Engberg et al. 1976; Marshall 1983). The function of NE in the dentate gyrus is discussed in the light of these and previous results.
在麻醉大鼠中,研究了离子电渗法应用1-去甲肾上腺素(NE)及相关药物对施加于内侧穿通通路的刺激脉冲所诱发的颗粒细胞反应的影响。在沿树突的连续背腹位置以及细胞体层施加药物并记录反应。1. 在细胞体区域揭示了α和β受体的相互作用。β激动剂异丙肾上腺素降低群体峰电位,而β拮抗剂索他洛尔则使其增加。相反,α激动剂去氧肾上腺素和可乐定增加群体峰电位,而α拮抗剂哌唑嗪则使其降低。药物的作用迅速、剂量依赖性且可逆。NE本身施加于颗粒细胞层时无作用。2. 与NE未能引发短期反应相反,并且正如先前报道(纽曼和哈雷,1983年)所证实的,在颗粒细胞层中长时间应用NE会使群体峰电位产生长期增强。然而,应用d-NE后也观察到了这种效应。3. NE影响树突中部三分之一处的颗粒细胞反应,在此处它以剂量依赖性方式降低诱发的突触电位(ESP,由兴奋性突触活动产生的电流)。同时在细胞体区域进行的记录显示群体峰电位降低,而细胞体层的ESP无变化(正向ESP反映细胞外向电流)。为了确定受体特异性,将一系列α和β激动剂及拮抗剂应用于树突中部区域。所有药物均以与NE相似的方式降低ESP。NE作用缺乏特异性这一情况先前在脊髓运动神经元中已有报道(恩伯格等人,1976年;马歇尔,1983年)。根据这些及先前的结果讨论了NE在齿状回中的功能。