Hamilton M G, Hirst M
Eur J Pharmacol. 1976 Oct;39(2):237-43. doi: 10.1016/0014-2999(76)90131-x.
Isolated smooth muscle tissues from rats, guinea pigs and rabbits were used to investigate pharmacological effects of salsolinol (1-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline). By itself, salsolinol did not produce any profound or sustained sympathomimetic or 5-hydroxytryptamine-like activity in the concentrations used in these experiments (7.7 and 77 muM). Salsolinol was found to antagonize the contraction of the rabbit aorta induced by noradrenaline but did not affect the adrenaline-induced relaxation of the guinea pig tracheal chain. On both the rat fundus and oestrus rat uterus, salsolinol exhibited significant anti-5-hydroxytryptamine activity but responses of these tissues to acetylcholine and histamine remained unaffected, indicating that the action was not non-specific. These results suggest that in vivo formation of salsolinol after ethanol ingestion could produce significant pharmacological effects.
使用来自大鼠、豚鼠和兔子的离体平滑肌组织来研究salsolinol(1-甲基-6,7-二羟基-1,2,3,4-四氢异喹啉)的药理作用。在这些实验中所使用的浓度(7.7和77μM)下,salsolinol自身不会产生任何显著或持续的拟交感神经或5-羟色胺样活性。发现salsolinol可拮抗去甲肾上腺素诱导的兔主动脉收缩,但不影响肾上腺素诱导的豚鼠气管链舒张。在大鼠胃底和发情期大鼠子宫上,salsolinol均表现出显著的抗5-羟色胺活性,但这些组织对乙酰胆碱和组胺的反应未受影响,表明该作用并非非特异性的。这些结果表明,乙醇摄入后体内形成的salsolinol可能产生显著的药理作用。