Marin-Grez M
Biochem Pharmacol. 1985 Nov 15;34(22):4013-7. doi: 10.1016/0006-2952(85)90381-8.
The effect of adrenal steroids (mineralo- and glucocorticoids) as well as that of the adrenocorticotrophic peptide tetracosactide (beta 1-24 corticotropin) on the renal kallikrein activity and on the urinary kallikrein excretion of rats was investigated. After the animals had been adapted to metabolic cages, they were injected with deoxycorticosterone acetate (15 mg/kg day), corticosterone (40 mg/kg day), both steroids combined or the vehicle (sesame oil). Additional groups of rats received tetracosactide (0.05, 0.1 or 0.2 mg/day) or the vehicle (100 microliter of 38 X 10(-3) M ZnCl2). After four days of treatment the urinary kallikrein excretion was higher in deoxycorticosterone-treated rats than in their controls. This increase was prevented when corticosterone was administered simultaneously. The renal kallikrein activity of corticosterone as well as that of deoxycorticosterone plus corticosterone-treated rats was subnormal. A dose-related reduction of both the renal kallikrein activity and the urinary kallikrein excretion was observed 2 days after starting the tetracosactide administration. It may be concluded that a stimulation of the endogenous release of glucocorticoids in the rat reduces the renal kallikrein activity and that glucocorticoids can prevent the stimulating effect of mineralocorticoids.
研究了肾上腺类固醇(盐皮质激素和糖皮质激素)以及促肾上腺皮质肽二十四肽促皮质素(β1 - 24促肾上腺皮质激素)对大鼠肾激肽释放酶活性和尿激肽释放酶排泄的影响。动物适应代谢笼后,分别注射醋酸脱氧皮质酮(15毫克/千克·天)、皮质酮(40毫克/千克·天)、两种类固醇联合使用或溶剂(芝麻油)。另外几组大鼠接受二十四肽促皮质素(0.05、0.1或0.2毫克/天)或溶剂(100微升38×10⁻³M氯化锌)。治疗四天后,醋酸脱氧皮质酮处理的大鼠尿激肽释放酶排泄量高于对照组。同时给予皮质酮时,这种增加被阻止。皮质酮以及醋酸脱氧皮质酮加皮质酮处理的大鼠肾激肽释放酶活性低于正常水平。开始给予二十四肽促皮质素两天后,观察到肾激肽释放酶活性和尿激肽释放酶排泄量均呈剂量相关的降低。可以得出结论,大鼠体内糖皮质激素内源性释放的刺激会降低肾激肽释放酶活性,并且糖皮质激素可以阻止盐皮质激素的刺激作用。