首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >D1-D2 dopamine receptor interaction within the nucleus accumbens mediates long-loop negative feedback to the ventral tegmental area (VTA).
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D1-D2 dopamine receptor interaction within the nucleus accumbens mediates long-loop negative feedback to the ventral tegmental area (VTA).

机译:伏伏核内的D1-D2多巴胺受体相互作用介导长腹负反馈到腹侧被盖区(VTA)。

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摘要

The objective of the present study was to examine the effects of perfusion of dopamine (DA) D1- and D2-like receptor agonists in the nucleus accumbens (ACB) on the long-loop negative feedback regulation of mesolimbic somatodendritic DA release in the ventral tegmental area (VTA) of Wistar rats employing ipsilateral dual probe in vivo microdialysis. Perfusion of the ACB for 60 min with the D1-like receptor agonist SKF 38393 (SKF, 1-100 microM) dose-dependently reduced the extracellular levels of DA in the ACB, whereas the extracellular levels of DA in the VTA were not changed. Similarly, application of the D2-like receptor agonist quinpirole (Quin, 1-100 microM) through the microdialysis probe in the ACB reduced the extracellular levels of DA in the ACB in a concentration-dependent manner, whereas extracellular levels of DA in the VTA were not altered. Co-application of SKF (100 microM) and Quin (100 microM) produced concomitant reductions in the extracellular levels of DA in the ACB and VTA. The reduction in extracellular levels of DA in the ACB and VTA produced by co-infusion of SKF and Quin was reversed in the presence of either 100 microM SCH 23390 (D1-like antagonist) or 100 microM sulpiride (D2-like antagonist). Overall, the results suggest that (a) activation of dopamine D1- or D2-like receptors can independently regulate local terminal DA release in the ACB, whereas stimulation of both subtypes is required for activation of the negative feedback pathway to the VTA.
机译:本研究的目的是研究伏隔核(ACB)中多巴胺(DA)D1和D2样受体激动剂的灌注对腹侧被盖中的中脑边缘树突状DA释放的长环负反馈调节的影响。同侧双探针体内微透析的Wistar大鼠大面积(VTA)。用D1样受体激动剂SKF 38393(SKF,1-100 microM)灌注ACB 60分钟可以剂量依赖性地降低ACB中DA的细胞外水平,而VTA中DA的细胞外水平没有改变。同样,通过微透析探针在ACB中应用D2样受体激动剂喹吡罗(Quin,1-100 microM)以浓度依赖的方式降低了ACB中DA的细胞外水平,而VTA中DA的细胞外水平没有改变。 SKF(100 microM)和Quin(100 microM)的共同应用可降低ACB和VTA中DA的细胞外水平。在100 microM SCH 23390(D1样拮抗剂)或100 microM舒必利(D2样拮抗剂)的存在下,通过SKF和Quin的共注入产生的ACB和VTA中DA胞外水平的降低被逆转。总体而言,结果表明(a)多巴胺D1或D2样受体的激活可以独立调节ACB中局部末端DA的释放,而激活这两种亚型是激活通往VTA的负反馈途径所必需的。

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