Tayo F M
West Afr J Pharmacol Drug Res. 1979;5(1):45-53.
Dopamine, noradrenaline, tyramine, amantadine and apomorphine produced concentration-related contractions of the rat vas deferens "in vitro". pD2 values of 5.35 +/- 0.12, 5.20 +/- 0.08, 4.50 +/- 0.06, and 4.50 +/- 0.10 were obtained for dopamine, noradrenaline, tyramine and apomorphine respectively. Phentolamine, haloperidol and pimozide blocked the effects of dopamine, tyramine, amantadine and apomorphine, however, noradrenaline-induced contractions were resistant to pimozide. Guanethidine (4 micrograms/ml) induced supersensitivity towards noradrenaline, almost abolished the effect of tyramine, but did not influence the effects of dopamine, amantadine and apomorphine at this concentration. These results confirm earlier reports that there are distinct dopaminoceptors in the rat vas deferens in addition to the conventional noradrenoceptors.
多巴胺、去甲肾上腺素、酪胺、金刚烷胺和阿扑吗啡在体外可引起大鼠输精管产生浓度相关的收缩。多巴胺、去甲肾上腺素、酪胺和阿扑吗啡的pD2值分别为5.35±0.12、5.20±0.08、4.50±0.06和4.50±0.10。酚妥拉明、氟哌啶醇和匹莫齐特可阻断多巴胺、酪胺、金刚烷胺和阿扑吗啡的作用,然而,去甲肾上腺素诱导的收缩对匹莫齐特具有抗性。胍乙啶(4微克/毫升)可诱导对去甲肾上腺素的超敏反应,几乎消除酪胺的作用,但在此浓度下不影响多巴胺、金刚烷胺和阿扑吗啡的作用。这些结果证实了早期的报道,即除了传统的去甲肾上腺素受体外,大鼠输精管中还存在不同的多巴胺受体。