Cheng H C, Long J P, Van Orden L S, Cannon J G, O'Donnell J P
Res Commun Chem Pathol Pharmacol. 1976 Sep;15(1):89-106.
The dopaminergic activity of ten apomorphine analogs was studied in rats lesioned unilaterally with 6-hydroxydopamine in the nigro-striatal system. Of these ten compounds, N,N-dimethyl-5,6-dihydroxy-2-amino-tetralin (M-7), N-methyl-5,6-dihydroxy-2-aminotetralin (M-8) and N,N-dimethyl-4,5-dihydroxy-2-aminoindan (DDAI) exhibited potent dopaminergic stimulant activity by causing the rat to turn to the unoperated side. The turning behavior of apomorphine, M-7, DDAI and d-amphetamine were antagonized by haloperidol. M-7 and DDAI also induced pecking in pigeons and their effects were also blocked by haloperidol. It is concluded that M-7, M-8 and DDAI are direct acting central dopaminergic agents.
在单侧黑质纹状体系统用6-羟基多巴胺损伤的大鼠中研究了10种阿扑吗啡类似物的多巴胺能活性。在这10种化合物中,N,N-二甲基-5,6-二羟基-2-氨基四氢萘(M-7)、N-甲基-5,6-二羟基-2-氨基四氢萘(M-8)和N,N-二甲基-4,5-二羟基-2-氨基茚满(DDAI)通过使大鼠转向未手术侧而表现出强效的多巴胺能刺激活性。阿扑吗啡、M-7、DDAI和右旋苯丙胺的转向行为被氟哌啶醇拮抗。M-7和DDAI还诱导鸽子啄食,它们的作用也被氟哌啶醇阻断。得出结论,M-7、M-8和DDAI是直接作用的中枢多巴胺能药物。