Casolini P, Kabbaj M, Piazza P V, Angelucci L, Simon H, Le Moal M, Maccari S
Laboratoire de Psychobiologie des Comportements Adaptatifs, INSERM U259, Université de Bordeaux II, France.
Neuroscience. 1994 Jun;60(4):939-43. doi: 10.1016/0306-4522(94)90273-9.
Type I and type II brain corticosteroid receptors are regulated by adrenal hormones as well as being under neural control. Recent studies have indicated that neurotransmitters such as serotonin and noradrenaline are also involved in the regulation of corticosteroid receptors. In a previous study, we showed that dopamine also modulates activity of the corticosteroid receptor system. In the present study, we examined the roles of the dopamine D1 and D2 receptor subtypes in the regulation of corticosteroid receptors. Adrenalectomized rats whose corticosterone levels were maintained within normal limits by corticosterone replacement implants, were injected intraperitoneally with the D1 agonist SKF 38393 or the D2 agonist LY 171555. Corticosteroid receptors were assayed in the ventral striatum and hippocampus. We have shown that the D1 agonist SKF 38393 decreased type II receptor affinity in both regions, whereas the D2 agonist LY 171555 had no effects. The results show that the influence of the dopaminergic system on corticosteroid receptors appears to be mediated by D1 receptors.
I型和II型脑皮质类固醇受体受肾上腺激素调节,同时也受神经控制。最近的研究表明,血清素和去甲肾上腺素等神经递质也参与皮质类固醇受体的调节。在之前的一项研究中,我们发现多巴胺也能调节皮质类固醇受体系统的活性。在本研究中,我们研究了多巴胺D1和D2受体亚型在调节皮质类固醇受体中的作用。通过皮质酮替代植入物将皮质酮水平维持在正常范围内的肾上腺切除大鼠,腹腔注射D1激动剂SKF 38393或D2激动剂LY 171555。在腹侧纹状体和海马体中检测皮质类固醇受体。我们发现D1激动剂SKF 38393降低了两个区域中II型受体的亲和力,而D2激动剂LY 171555则没有影响。结果表明,多巴胺能系统对皮质类固醇受体的影响似乎是由D1受体介导的。