Funaki H, Tokiyori Y, Hara K, Oshino N
Nihon Yakurigaku Zasshi. 1982 Nov;80(5):349-65.
Pharmacological actions of lisuride hydrogen maleate (lisuride) were studied by using isolated organs. 1) Lisuride at 2.2 microM exerted a negative chronotropic effect on guinea-pig atria, the effect being antagonized completely by 2.9 microM sulpiride. 2) alpha-Adrenolytic action of lisuride was observed in the rat vas deferens and beta-adrenolytic action in the rabbit trachea, respectively. The former (ID50 = 64 nM) was potent and equivalent to that of phentolamine, whereas the latter (ID50 = 26 microM) was only 1/30 as compared to that of propranolol. 3) Anti-5-hydroxytryptamine action (ID50 = 11 nM) was detected in the rat stomach and anti-histamine (ID50 = 15 nM) in the guinea-pig ileum, respectively. In these respective activities, lisuride was equipotent to methysergide and diphenhydramine. 4) Lisuride showed a spasmodic action, which may be categolized as an ergot alkaloid action, on the guinea-pig ileum and on rabbit renal artery. A weak positive inotropic action of lisuride was also observed in guinea-pig atria. In the rat uterus, however, no uterotonic action of lisuride was detected. It is concluded that, in addition to its known effects on the central nervous system, lisuride possesses potent peripheral anti-5-hydroxytryptamine and anti-histamine activities.
采用离体器官研究了马来酸麦角乙脲(麦角乙脲)的药理作用。1)2.2微摩尔的麦角乙脲对豚鼠心房产生负性变时作用,该作用被2.9微摩尔的舒必利完全拮抗。2)在大鼠输精管中观察到麦角乙脲的α-肾上腺素能阻断作用,在兔气管中观察到β-肾上腺素能阻断作用。前者(半数抑制浓度=64纳摩尔)作用较强,与酚妥拉明相当,而后者(半数抑制浓度=26微摩尔)与普萘洛尔相比仅为其1/30。3)在大鼠胃中检测到抗5-羟色胺作用(半数抑制浓度=11纳摩尔),在豚鼠回肠中检测到抗组胺作用(半数抑制浓度=15纳摩尔)。在这些各自的活性中,麦角乙脲与甲基麦角新碱和苯海拉明等效。4)麦角乙脲对豚鼠回肠和兔肾动脉表现出痉挛作用,这可能归类为麦角生物碱作用。在豚鼠心房中也观察到麦角乙脲微弱的正性肌力作用。然而,在大鼠子宫中未检测到麦角乙脲的子宫收缩作用。结论是,除了其对中枢神经系统的已知作用外,麦角乙脲还具有强大的外周抗5-羟色胺和抗组胺活性。