Memo M, Pizzi M, Nisoli E, Missale C, Carruba M O, Spano P
Eur J Pharmacol. 1987 Jun 12;138(1):45-51. doi: 10.1016/0014-2999(87)90335-9.
We studied the possible functional modifications of both D-1 and D-2 dopamine (DA) receptor subtypes following repeated administration of DA antagonists that act selectively on a single class of DA receptors. The functional state of D-1 and D-2 DA receptors in particular was evaluated by measuring SKF 82526-stimulated and bromocriptine-inhibited adenylate cyclase activity in different brain regions of rats treated with saline, SCH 23390, or (-)sulpiride for 21 days. The results indicate that chronic blockade of D-1 DA receptors in striatum, nucleus accumbens, and substantia nigra by SCH 23390 induced up-regulation of the D-1 receptors without changing the functional activity of D-2 receptors. Likewise, chronic blockade of D-2 DA receptors by (-)sulpiride caused up-regulation of D-2 but not D-1 DA receptors in striatum, nucleus accumbens, substantia nigra and pituitary. SCH 23390 or (-)sulpiride did not modify the functional activity of either D-1 or D-2 DA receptors located in frontal cortex and hippocampus. In conclusion, these results indicate that chronic treatment with selective D-1 or D-2 DA receptor blockers induces a receptor-specific up-regulation which involves the DA receptors located in the nigrostriatal system and pituitary but not those in the limbic-cortical areas.
我们研究了在重复给予选择性作用于单一类型多巴胺(DA)受体的DA拮抗剂后,D-1和D-2多巴胺受体亚型可能发生的功能改变。通过测量用生理盐水、SCH 23390或(-)舒必利处理21天的大鼠不同脑区中SKF 82526刺激和溴隐亭抑制的腺苷酸环化酶活性,特别评估了D-1和D-2 DA受体的功能状态。结果表明,SCH 23390对纹状体、伏隔核和黑质中D-1 DA受体的慢性阻断诱导了D-1受体的上调,而未改变D-2受体的功能活性。同样,(-)舒必利对D-2 DA受体的慢性阻断导致纹状体、伏隔核、黑质和垂体中D-2而非D-1 DA受体的上调。SCH 23390或(-)舒必利未改变位于额叶皮质和海马中的D-1或D-2 DA受体的功能活性。总之,这些结果表明,用选择性D-1或D-2 DA受体阻滞剂进行慢性治疗会诱导受体特异性上调,这涉及黑质纹状体系统和垂体中的DA受体,但不涉及边缘-皮质区域中的DA受体。