de Azeredo F A, Ribeiro M F
Laboratorio de Biociencias, Universidade Federal Fluminense, Niteroi, RJ, Brazil.
Metab Brain Dis. 1992 Dec;7(4):211-21. doi: 10.1007/BF01000247.
The velocity of propagation of the in vitro retinal model of spreading depression is very sensitive to changes in the ionic composition of the extracellular medium and also to the the addition of different drugs. 10 microM of SKF 38393, a D1 agonist, increases the velocity of propagation of the wave while 10 microM of Quinpirole, a D2 agonist, decreases it. Both changes are blocked by their specific antagonists, SCH23390 and 1-sulpiride respectively. This assay can biologically screen potential dopaminergic drugs indicating its physiological D1 and/or D2 preferred effect in the tissue for future analysis by other different methodologies.
扩散性抑制的体外视网膜模型的传播速度对细胞外介质离子组成的变化以及不同药物的添加非常敏感。10微摩尔的SKF 38393(一种D1激动剂)可增加波的传播速度,而10微摩尔的喹吡罗(一种D2激动剂)则会降低其速度。这两种变化分别被它们的特异性拮抗剂SCH23390和舒必利阻断。该检测方法可对潜在的多巴胺能药物进行生物学筛选,表明其在组织中的生理性D1和/或D2偏好效应,以供未来通过其他不同方法进行分析。