Berretta N, Berton F, Bianchi R, Capogna M, Francesconi W, Brunelli M
Department of Physiology and Biochemistry G. Moruzzi, University of Pisa, Italy.
Exp Brain Res. 1990;83(1):124-30. doi: 10.1007/BF00232200.
In hippocampal pyramidal cells (HPCs), Dopamine (DA) application (1 microM) produced, in 50% of recorded cells, an hyperpolarization of the resting membrane potential (r.m.p.) and an increase of the afterhyperpolarization (AHP) amplitude and duration in 79% of recorded cells. DA-induced effects on both the r.m.p. and AHP were mimicked by bath application of a D-1 selective agonist, SKF 38393 (20 microM). In addition, we have observed that a D-1 selective antagonist such as SCH 23390 (1 microM) abolished the action of both DA and SKF 38393. In contrast, the activation of D-2 receptors through LY 171555 (10 microns) produced, in 50% of cells, a depolarization of the r.m.p. and a depression of the AHP in 67% of recorded cells. These results suggest that the effects observed in hippocampal pyramidal neurons after DA application of micromolar concentration are mediated by D-1 subtype of receptors.
在海马锥体细胞(HPCs)中,施加多巴胺(DA,1微摩尔)后,在50%的记录细胞中引起静息膜电位(r.m.p.)超极化,在79%的记录细胞中引起后超极化(AHP)幅度和时程增加。通过浴槽施加D-1选择性激动剂SKF 38393(20微摩尔)可模拟DA对r.m.p.和AHP的影响。此外,我们观察到,D-1选择性拮抗剂如SCH 23390(1微摩尔)可消除DA和SKF 38393的作用。相反,通过LY 171555(10微摩尔)激活D-2受体后,在50%的细胞中引起r.m.p.去极化,在67%的记录细胞中引起AHP降低。这些结果表明,在微摩尔浓度的DA作用于海马锥体细胞后所观察到的效应是由D-1受体亚型介导的。