Nishiyama S, Kanno K, Yoneda H, Yano K, Yamaguchi I
Pharmacological Research Laboratory, Tanabe Seiyaku Co., Ltd., Saitama, Japan.
Arzneimittelforschung. 1992 Apr;42(4):451-6.
The effects of a new angiotensin-converting enzyme (ACE) inhibitor, imidapril hydrochloride ((-)-(4S)-3-[(2S)-2- [[(1S)-1-ethoxycarbonyl-3-phenylpropyl]amino]propionyl]- 1-methyl-2-oxoimidazolidine-4-carboxylic acid hydrochloride, imidapril, TA-6366, CAS 89396-94-1) and of its active metabolite, 6366 A (CAS 89371-44-8) on renal function were studied in anesthetized dogs and compared to the effects of enalapril and its active metabolite, enalaprilat. Intravenous (i.v.) administration of 6366 A at 30 micrograms/kg strongly inhibited angiotensin I-induced renal vasoconstrictive and pressor responses. 6366 A promptly lowered blood pressure and renal vascular resistance, and caused clear increases in renal blood flow and glomerular filtration rate. It also increased urine volume and urinary excretion of sodium and chloride. These renal effects were also produced by intraduodenal (i.d.) administration of 2 mg/kg of imidapril. However, the effects of i.d. imidapril began later, developed gradually and reached a plateau after 2 to 3 h. Enalaprilat (30 micrograms/kg i.v.) and enalapril (2 mg/kg i.d.) had renal effects similar to 6366 A and imidapril. In conclusion, the ACE inhibitor imidapril has beneficial effects on renal function via its active metabolite, and the effects appear to be essentially identical to those of enalapril.
在麻醉犬身上研究了一种新型血管紧张素转换酶(ACE)抑制剂盐酸咪达普利((-)-(4S)-3-[(2S)-2-[[(1S)-1-乙氧羰基-3-苯基丙基]氨基]丙酰基]-1-甲基-2-氧代咪唑烷-4-羧酸盐酸盐,咪达普利,TA-6366,CAS 89396-94-1)及其活性代谢物6366 A(CAS 89371-44-8)对肾功能的影响,并与依那普利及其活性代谢物依那普利拉的作用进行了比较。以30微克/千克静脉注射(i.v.)6366 A可强烈抑制血管紧张素I诱导的肾血管收缩和升压反应。6366 A迅速降低血压和肾血管阻力,并使肾血流量和肾小球滤过率明显增加。它还增加尿量以及钠和氯的尿排泄量。十二指肠内(i.d.)给予2毫克/千克咪达普利也产生这些肾脏效应。然而,i.d.咪达普利的作用开始较晚,逐渐发展,并在2至3小时后达到平台期。依那普利拉(30微克/千克i.v.)和依那普利(2毫克/千克i.d.)具有与6366 A和咪达普利相似的肾脏作用。总之,ACE抑制剂咪达普利通过其活性代谢物对肾功能具有有益作用,且这些作用似乎与依那普利基本相同。