局部应用D3偏好化合物对大鼠大脑离散区域运动活动的影响。

T Kling-Petersen, E Ljung, K Svensson
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引用次数: 39

摘要

在大鼠大脑伏隔核(N Acc)和腹侧被盖区(VTA)局部应用后,测试了对多巴胺D3和D2受体具有体外结合偏好的化合物对运动活动的影响。R-(+)-7- oh - dpat是一种多巴胺D3偏好激动剂,注射到N Acc后,在大剂量范围内抑制自发运动活动。R-(+)-7- oh - dpat和多巴胺D2偏好激动剂(+)-3- ppp局部应用于VTA后,活性在大剂量范围内也有所下降。此外,(+)-3-PPP局部应用于nacc后产生剂量依赖性活性增加。假定的D3拮抗剂U99194A对多巴胺D3受体的偏好是D2受体的30倍,当注射到N Acc中时,其活性增加。注入侧脑室后也出现类似的情况。然而,在VTA中的本地应用并没有产生任何显著的效果。目前的结果支持了多巴胺D3受体(与D2受体相反)主要位于突触后的假设,在那里它们对运动活动表现出抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects on locomotor activity after local application of D3 preferring compounds in discrete areas of the rat brain.

Compounds showing an in vitro binding preference for the dopamine D3 vs. D2 receptors were tested for effects on locomotor activity after local application in the nucleus accumbens (N Acc) and the ventral tegmental area (VTA) of the rat brain. R-(+)-7-OH-DPAT, a dopamine D3 preferring agonist, inhibited spontaneous locomotor activity over a wide dose range after injection into the N Acc. A decrease in activity over a wide dose range was also seen after local application into the VTA of both R-(+)-7-OH-DPAT and the dopamine D2 preferring agonist (+)-3-PPP. Furthermore, (+)-3-PPP produced a dose dependent increase in activity after local application into the N Acc. The putative D3 antagonist, U99194A, with a 30 fold preference for the dopamine D3 vs. D2 receptor, produced an increase in activity when injected into the N Acc. A similar pattern were seen after infusion into the lateral ventricle. Local application into the VTA did, however, not produce any significant effects. The present results support the hypothesis that dopamine D3 receptors (in contrast to the D2 receptors) are mainly postsynaptically located where they display an inhibitory action on locomotor activity.

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