Morishita S, Saito T, Mishima Y, Mizutani A, Hirai Y, Kawakami M
Nihon Yakurigaku Zasshi. 1986 Apr;87(4):361-78. doi: 10.1254/fpj.87.361.
General pharmacological properties of two kinds of Senso-containing drugs were studied. There were no prominent differences in the pharmacological profile between the two prescriptions. Inhibition of writhing (60 mg/kg, p.o.), prolongation of hexobarbital-induced hypnosis, hypothermia, antipyretic effect, and inhibition of acetic acid-induced capillary permeability (600 mg/kg, p.o.) in mice were observed after administration of these drugs. These effects were suggested to originate from cinobufagin, a constituent of Senso. Augmentation of blood sugar level and inhibition of gastric juice secretion (600 mg/kg, p.o.) in rats were also observed after administration of these drugs. These effects were suggested to originate from constituents of Senso other than cinobufagin. Isolated ileum and aorta of guinea pigs and vas deferens and fundus strip preparation of rats contracted, and isolated trachea of guinea pigs relaxed after the application of these drugs. The majority of these effects were suggested to originate from epinephrine-like or serotonin-like compounds, constituents of Senso.
对两种含蟾酥药物的一般药理学特性进行了研究。两种方剂之间的药理学特征没有显著差异。给药后观察到对小鼠扭体反应的抑制(60mg/kg,口服)、延长己巴比妥诱导的催眠时间、体温降低、解热作用以及对乙酸诱导的毛细血管通透性的抑制(600mg/kg,口服)。这些作用提示源自蟾酥的成分华蟾酥毒基。给药后还观察到大鼠血糖水平升高和胃液分泌抑制(600mg/kg,口服)。这些作用提示源自蟾酥中除华蟾酥毒基之外的成分。给予这些药物后,豚鼠离体回肠和主动脉以及大鼠输精管和胃底条制备物收缩,豚鼠离体气管松弛。这些作用大多数提示源自蟾酥中的肾上腺素样或5-羟色胺样化合物成分。