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D1多巴胺拮抗剂的药理和行为效应。

Pharmacological and behavioral effects of D1 dopamine antagonists.

作者信息

Barnett A, Iorio L C, McQuade R, Chipkin R E

机构信息

Schering-Plough Corporation, Bloomfield, NJ 07003.

出版信息

Adv Exp Med Biol. 1988;235:137-44. doi: 10.1007/978-1-4899-2723-1_9.

Abstract

This work includes the effects of SCH 23390 and related benzazepines on behavior and attempts to relate these effects to their D1 dopamine antagonist action. Effects on conditioned avoidance responding (CAR) in rats were studied under the same conditions in which in vivo binding of the radioiodinated D1 specific benzazepine 125I-SCH 38840 was measured. It was found that there is very close agreement between the time-course for antagonism of CAR and for in vivo displacement of 125I-SCH 38840 from rat striatum. The effect of SCH 23390 in CAR in monkeys was compared with standard anti-psychotics and although its oral potency was reasonable, its duration was very short (1-2 hours at 5 times its minimal effective dose for statistically significant reduction of avoidance). It is concluded from this and prior work that SCH 23390 and other D1 specific benzazepines inhibit CAR at the same doses that bind to D1 receptors in the CNS and that D1 specific antagonists are behaviorally effective at doses that do not produce D2 receptor effects (e.g. increased plasma prolactin levels, catalepsy).

摘要

这项研究包括SCH 23390及相关苯并氮杂卓类药物对行为的影响,并试图将这些影响与其D1多巴胺拮抗剂作用联系起来。在测量放射性碘化D1特异性苯并氮杂卓125I-SCH 38840体内结合的相同条件下,研究了其对大鼠条件性回避反应(CAR)的影响。结果发现,CAR拮抗作用的时间进程与125I-SCH 38840从大鼠纹状体的体内置换时间进程非常一致。将SCH 23390对猴子CAR的影响与标准抗精神病药物进行了比较,尽管其口服效力合理,但其作用持续时间非常短(在其最小有效剂量的5倍时为1-2小时,可使回避反应有统计学意义的显著降低)。基于此项研究及之前的工作得出结论,SCH 23390和其他D1特异性苯并氮杂卓类药物在与中枢神经系统D1受体结合的相同剂量下抑制CAR,且D1特异性拮抗剂在不产生D2受体效应(如血浆催乳素水平升高、僵住症)的剂量下具有行为学效应。

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