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重复给予(-)舒必利和SCH 23390对大鼠中脑纹状体区域的D-1和D-2多巴胺受体功能有不同的上调作用,但对皮质-边缘脑区无此作用。

Repeated administration of (-)sulpiride and SCH 23390 differentially up-regulate D-1 and D-2 dopamine receptor function in rat mesostriatal areas but not in cortical-limbic brain regions.

作者信息

Memo M, Pizzi M, Nisoli E, Missale C, Carruba M O, Spano P

出版信息

Eur J Pharmacol. 1987 Jun 12;138(1):45-51. doi: 10.1016/0014-2999(87)90335-9.

DOI:10.1016/0014-2999(87)90335-9
PMID:2887436
Abstract

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.

摘要

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。

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1
Repeated administration of (-)sulpiride and SCH 23390 differentially up-regulate D-1 and D-2 dopamine receptor function in rat mesostriatal areas but not in cortical-limbic brain regions.重复给予(-)舒必利和SCH 23390对大鼠中脑纹状体区域的D-1和D-2多巴胺受体功能有不同的上调作用,但对皮质-边缘脑区无此作用。
Eur J Pharmacol. 1987 Jun 12;138(1):45-51. doi: 10.1016/0014-2999(87)90335-9.
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Eur J Pharmacol. 1990 Jan 25;176(1):85-90. doi: 10.1016/0014-2999(90)90135-s.
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Prog Neuropsychopharmacol Biol Psychiatry. 1991;15(6):861-72. doi: 10.1016/0278-5846(91)90014-r.

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J Neural Transm (Vienna). 1997;104(4-5):341-62. doi: 10.1007/BF01277656.
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Chronic treatment with the D1 receptor antagonist, SCH 23390, and the D2 receptor antagonist, raclopride, in cebus monkeys withdrawn from previous haloperidol treatment. Extrapyramidal syndromes and dopaminergic supersensitivity.
对先前停用氟哌啶醇治疗的卷尾猴长期给予 D1 受体拮抗剂 SCH 23390 和 D2 受体拮抗剂雷氯必利治疗。锥体外系综合征和多巴胺能超敏反应。
Psychopharmacology (Berl). 1993;112(2-3):389-97. doi: 10.1007/BF02244938.
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Effects of long-term administration of antidepressants and neuroleptics on receptors in the central nervous system.长期服用抗抑郁药和抗精神病药对中枢神经系统受体的影响。
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