Westerink B H, Dijkstra D, Feenstra M G, Horn A S, Rollema H
Eur J Pharmacol. 1980 Jun 13;64(2-3):115-21. doi: 10.1016/0014-2999(80)90034-5.
This study investigates the mechanism of the selective storage of the dopamine agonist 2-amino-5,6-dihydroxytetrahydronaphthalene (5,6-ADTN, used as the esterified prodrug) in densely innervated dopaminergic brain structures. The accumulation of 5,6-ADTN in dopamine-rich areas appeared to be non-saturable at the doses studied. In rats with a unilateral 6-OHDA lesion there was a corresponding unilateral decrease in 5,6-ADTN concentrations which suggests that the agonist interacts with dopamine uptake or storage mechanisms. Apart from an initial decreased penetration in the brain, reserpine-induced depletion of dopamine stores did not influence the accumulation of 5,6-ADTN in dopamine-rich areas, which suggests that 5,6-ADTN is taken up in the so-called 'non-reserpine sensitive DA-pool'. Unexpectedly, reserpine pretreatment caused a long-lasting (at least 170 h) decrease of 5,6-ADTN distribution in non-dopaminergic structures. 5,6-ADTN (used as the prodrug) could have a role to play in the elucidation of the significance of the various dopamine pools.
本研究调查了多巴胺激动剂2-氨基-5,6-二羟基四氢萘(5,6-ADTN,用作酯化前药)在神经密集的多巴胺能脑结构中选择性储存的机制。在所研究的剂量下,5,6-ADTN在富含多巴胺的区域的积累似乎是非饱和的。在单侧6-OHDA损伤的大鼠中,5,6-ADTN浓度相应地单侧降低,这表明该激动剂与多巴胺摄取或储存机制相互作用。除了最初脑内渗透降低外,利血平诱导的多巴胺储存耗竭并不影响5,6-ADTN在富含多巴胺区域的积累,这表明5,6-ADTN被摄取到所谓的“非利血平敏感多巴胺池”中。出乎意料的是,利血平预处理导致5,6-ADTN在非多巴胺能结构中的分布长期(至少170小时)降低。5,6-ADTN(用作前药)在阐明各种多巴胺池的意义方面可能发挥作用。