Herceg R, Bräunlich H, Bartha J
Arch Int Pharmacodyn Ther. 1985 May;275(1):151-9.
Imidazole, an inhibitor of thromboxane synthetase, reduced the renal excretion of sodium in saline loaded rats. Urine volume was also reduced, whereas the renal excretion of potassium and osmotically active substances was less influenced following imidazole administration. There was also a distinct effect of imidazole (0.5, 5, 10 mg/100 g b.wt. i.p., respectively) on renal excretion of p-aminohippurate. These effects are demonstrable if the urine collecting period begins 10 or 60 min after imidazole administration, but not after a longer time interval (120 min). Both renal excretion of sodium and p-aminohippurate were more diminished in adult rats compared with young animals. The renal effects observed following administration of an inhibitor of thromboxane synthetase are quite similar to effects of the cyclooxygenase inhibitors indomethacin and naproxen.
咪唑作为血栓素合成酶的抑制剂,可减少生理盐水负荷大鼠的肾钠排泄。尿量也减少,而给予咪唑后,钾和渗透活性物质的肾排泄受影响较小。咪唑(分别以0.5、5、10mg/100g体重腹腔注射)对对氨基马尿酸的肾排泄也有明显作用。如果在给予咪唑后10或60分钟开始收集尿液,这些作用是可证实的,但在更长的时间间隔(120分钟)后则不然。与幼龄动物相比,成年大鼠的钠和对氨基马尿酸的肾排泄减少得更多。给予血栓素合成酶抑制剂后观察到的肾脏作用与环氧化酶抑制剂吲哚美辛和萘普生的作用非常相似。