Mizusawa H, Yamane M, Sakai K
Nihon Yakurigaku Zasshi. 1976 Mar;72(2):185-99.
Effects of ifenprodil tartrate, a potent vasodilator, on the autonomic, peripheral and central nerve system were studied in experimental animals. In isolated vas deferens of guinea pigs, the contraction in response to noradrenaline and sympathetic nerve stimulation was competetively antagonized by ifenprodil 10(-7)--10(-5) M (pA2: 7.69 against noradrenaline). Ifenprodil (50 approximately 1,000 mug/kg i.v.) inhibited the contraction of cat nictitating membrane and dog urinary bladder induced by sympathetic nerve stimulation. Ifenprodil (250 approximately 1,000 mug/kg i.v.) lowered adrenaline-induced lethality (ED50: 360 mug/kg). The drug produced a hypermotility of guinea pig uterus, and showed a transient hypertonus of dog gut which was abolished by atropine. Ifenprodil (10 approximately 20 mg/kg i.v.) inhibited the propulsion of charcoal meal in mice. In Shay rats, more than 10 mg/kg i.m. of the drug inhibited the secretion of acid gastric juice and the ulceration. Ifenprodil showed a potent local anesthetic action in the guinea pig cornea and skin. The spontaneous EEG of rabbits showed a resting pattern (0.25 approximately 2 mg/kg i.v.) followed by an arousal pattern (5 approximately 10 mg/kg). Ifenprodil (20 approximately 100 mg/kg p.o.) potentiated a hypnosis induced by barbital, and potentiated pentylenetetrazol, strychnine and picrotoxin induced convulsion. The drug (20 and 100 mg/kg p.o.) lowered the body temperature of rats. From these results it is concluded that ifenprodil produces a blocking action of alpha-adrenoceptors in various smooth muscle preparations and a direct relaxation of the smooth muscle itself without affecting the motor and central nerve systems.
研究了强效血管扩张剂酒石酸艾芬地尔对实验动物自主神经系统、外周神经系统和中枢神经系统的作用。在豚鼠离体输精管中,10(-7)~10(-5)M的酒石酸艾芬地尔竞争性拮抗去甲肾上腺素和交感神经刺激引起的收缩(对去甲肾上腺素的pA2为7.69)。酒石酸艾芬地尔(静脉注射50~1000μg/kg)抑制交感神经刺激引起的猫瞬膜和狗膀胱收缩。酒石酸艾芬地尔(静脉注射250~1000μg/kg)降低肾上腺素诱导的致死率(半数致死量:360μg/kg)。该药使豚鼠子宫运动增强,并使狗肠管出现短暂的张力亢进,阿托品可消除这种作用。酒石酸艾芬地尔(静脉注射10~20mg/kg)抑制小鼠炭末推进。在沙伊大鼠中,肌肉注射超过10mg/kg的该药可抑制胃酸分泌和溃疡形成。酒石酸艾芬地尔在豚鼠角膜和皮肤中表现出强效局部麻醉作用。家兔的自发脑电图在静脉注射0.25~2mg/kg后呈静息模式,随后在5~10mg/kg时呈觉醒模式。酒石酸艾芬地尔(口服20~100mg/kg)增强巴比妥诱导的催眠作用,并增强戊四氮、士的宁和印防己毒素诱导的惊厥。该药(口服20和100mg/kg)降低大鼠体温。从这些结果得出结论,酒石酸艾芬地尔在各种平滑肌制剂中产生α-肾上腺素受体阻断作用,并直接使平滑肌松弛,而不影响运动和中枢神经系统。