Inada Y, Shibouta Y, Shimakawa H, Nishikawa K, Kikuchi S
Arzneimittelforschung. 1978;28(7):1105-11.
Diuretic features of 1,4-dimorpholino-7-phenylpyrido[3,4-d]pyridazine (DS-511) were studied in rats and mice. DS-511 was similar in diuretic effect to that of hydrochlorothiazide (HC) in both species, but was more water diuretic and less potassium-releasing than HC. After oral administration of DS-511 to rats the diuretic effect promptly appeared and lasted for 4 to 5 h. These patterns on onset and duration were similar to those of furosemide and acetazolamide (AZ). DS-511 was effective in experimentally induced acidotic and alkalotic rats. When DS-511 was used in combinations with other diuretics such as HC, AZ and triamterene at their maximum effective doses, urine volume and sodium excretion further increased, but potassium did not. Diuretic activity of DS-511 was not reduced by daily oral administration for 10 days to rats. In rats DS-511 reversed antidiuretic hormone (ADH)-induced antidiuresis. These findings suggest that DS-511 differs in mode and/or site of action from the known diuretics.
在大鼠和小鼠中研究了1,4-二吗啉代-7-苯基吡啶并[3,4-d]哒嗪(DS-511)的利尿特性。在这两种动物中,DS-511的利尿作用与氢氯噻嗪(HC)相似,但与HC相比,其利水作用更强,排钾作用较弱。给大鼠口服DS-511后,利尿作用迅速出现,持续4至5小时。这些起效和持续时间的模式与呋塞米和乙酰唑胺(AZ)相似。DS-511对实验诱导的酸中毒和碱中毒大鼠有效。当DS-511与其他利尿剂如HC、AZ和氨苯蝶啶以最大有效剂量联合使用时,尿量和钠排泄进一步增加,但钾排泄没有增加。对大鼠连续10天每日口服DS-511,其利尿活性并未降低。在大鼠中,DS-511可逆转抗利尿激素(ADH)诱导的抗利尿作用。这些发现表明,DS-511在作用方式和/或作用部位上与已知利尿剂不同。