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纹状体多巴胺受体发育受损:成人中D-1受体的差异调节

Impaired striatal dopamine receptor development: differential D-1 regulation in adults.

作者信息

Saleh M I, Kostrzewa R M

机构信息

Department of Pharmacology, Quillen-Dishner College of Medicine, East Tennessee State University, Johnson City 37614.

出版信息

Eur J Pharmacol. 1988 Sep 23;154(3):305-11. doi: 10.1016/0014-2999(88)90206-3.

Abstract

Previous reports have indicated that prenatal, but not postnatal, haloperidol impairs the ontogenic development of striatal dopamine D-2 receptors. In the present study a specific D-2 receptor antagonist, spiroperidol (1.0 mg/kg i.p.) and/or a specific D-1 receptor antagonist, SCH 23390 (0.30 mg/kg i.p.), was administered to rats for 32 successive days from birth. Postnatal spiroperidol and SCH 23390 treatments markedly impaired the development of striatal dopamine D-2 and D-1 receptors, respectively, at 12 weeks after birth. Spiroperidol did not affect D-1 receptor development and did not modify the effect of SCH 23390 treatment. Also, SCH 23390 did not affect D-2 receptor development and did not modify the effect of spiroperidol treatment. When rats with impaired development of striatal D-2 receptors were challenged at 12 weeks with spiroperidol (1.0 mg/kg per day i.p. x 17 days) D-2 receptors did not up-regulate. However, when rats with impaired development of striatal D-1 receptors were challenged at 12 weeks with SCH 23390 (0.30 mg/kg per day i.p. x 17 days) D-1 receptors did up-regulate. These findings demonstrate that postnatal treatment with D-1 and D-2 receptor antagonists can permanently impair the development of striatal D-1 and D-2 receptors. Moreover, the ability of developmentally impaired striatal D-1 receptors to up-regulate in adulthood appears to be greater than that for the developmentally impaired striatal D-2 receptors.

摘要

先前的报告表明,产前而非产后给予氟哌啶醇会损害纹状体多巴胺D-2受体的个体发生发育。在本研究中,从出生起连续32天给大鼠腹腔注射特定的D-2受体拮抗剂螺哌啶醇(1.0毫克/千克)和/或特定的D-1受体拮抗剂SCH 23390(0.30毫克/千克)。产后给予螺哌啶醇和SCH 23390处理分别在出生后12周时显著损害了纹状体多巴胺D-2和D-1受体的发育。螺哌啶醇不影响D-1受体的发育,也不改变SCH 23390处理的效果。此外,SCH 23390不影响D-2受体的发育,也不改变螺哌啶醇处理的效果。当纹状体D-2受体发育受损的大鼠在12周时用螺哌啶醇(每天1.0毫克/千克腹腔注射×17天)进行激发时,D-2受体没有上调。然而,当纹状体D-1受体发育受损的大鼠在12周时用SCH 23390(每天0.30毫克/千克腹腔注射×17天)进行激发时,D-1受体确实上调了。这些发现表明,产后用D-1和D-2受体拮抗剂治疗可永久性损害纹状体D-1和D-2受体的发育。此外,发育受损的纹状体D-1受体在成年期上调的能力似乎大于发育受损的纹状体D-2受体。

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