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选择性D1和D2受体拮抗剂联合治疗对抑制蔗糖强化的亚相加作用。

Infra-additivity of combined treatments with selective D1 and D2 receptor antagonists for inhibiting sucrose reinforcement.

作者信息

Schneider L H, Watson C A, Gibbs J, Smith G P

机构信息

Department of Psychiatry, New York Hospital-Cornell Medical Center, Edward W. Bourne Behavioral Research Lab, White Plains 10605.

出版信息

Brain Res. 1991 May 31;550(1):122-4. doi: 10.1016/0006-8993(91)90413-p.

Abstract

Selective antagonists of either the D1 receptor (SCH 23390) or of the D2 receptor (raclopride) produce a dose-related inhibition of sucrose sham feeding in the rat. We investigated the effect of combined treatments with these antagonists on sucrose sham feeding and observed infra-additivity of inhibition across a range of doses. On the basis of this observed occlusive relationship, we conclude that the relevant D1 and D2 receptor mechanisms mediating sweet taste reward do not function independently.

摘要

D1受体(SCH 23390)或D2受体(雷氯必利)的选择性拮抗剂均可对大鼠的蔗糖假饲产生剂量相关的抑制作用。我们研究了这些拮抗剂联合治疗对蔗糖假饲的影响,并观察到在一系列剂量下抑制作用的亚加和性。基于这种观察到的闭塞关系,我们得出结论,介导甜味奖励的相关D1和D2受体机制并非独立发挥作用。

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