Naito K, Otsuka M, Harigaya S, Nagao T, Narita H
Arzneimittelforschung. 1985;35(5):833-5.
The relationship between the positive inotropic action and blood levels of (-)-(R)-1-(p-hydroxyphenyl)-2-[(3,4-dimethoxyphenethyl)amino]ethanol (denopamine, TA-064) was studied after intraduodenal administration of 3H-denopamine (100 micrograms/kg) in cats. The increase in cardiac contractile force attained the peak (about 100% increase) 15 min after the administration and the effect persisted for over 90 min. The blood levels of denopamine also reached the peak at 15 min with a concentration of 20 ng/ml and decreased gradually thereafter. Thus, it was indicated that the time courses of the increase in cardiac contractile force were closely related to those of blood levels of the drug. Furthermore, denopamine was distributed to the liver, kidney, parotid gland and heart, followed by being excreted into the urine and bile mostly as metabolites.
在猫经十二指肠给予3H-多巴胺(100微克/千克)后,研究了(-)-(R)-1-(对羟基苯基)-2- [(3,4-二甲氧基苯乙基)氨基]乙醇(多巴胺,TA-064)的正性肌力作用与血药浓度之间的关系。给药后15分钟,心脏收缩力增加达到峰值(约增加100%),且该效应持续超过90分钟。多巴胺血药浓度在15分钟时也达到峰值,为20纳克/毫升,此后逐渐下降。因此,表明心脏收缩力增加的时间进程与药物血药浓度的时间进程密切相关。此外,多巴胺分布于肝脏、肾脏、腮腺和心脏,随后大部分以代谢产物的形式排泄到尿液和胆汁中。