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氯拉扎尼降低大鼠尿激肽释放酶排泄及抗利钾作用

Reduced urine kallikrein excretion and antikaliuresis by chlorazanil in rats.

作者信息

Olsen U B, Eilertsen E

出版信息

Acta Pharmacol Toxicol (Copenh). 1981 Sep;49(3):210-4. doi: 10.1111/j.1600-0773.1981.tb00895.x.

Abstract

In normal conscious female Sprague-Dawley rats chlorazanil (3 mg/kg intraperitoneally) reduced urine kallikrein excretion by approximately 80%. Thus, urine kininogenase activity decreased from 54 +/- 5 U/kg/3 hrs to 10 +/- 2 U/kg/3 hrs and urine TAMe-esterase activity decreased from 34 +/- 1.5 mEU/kg/3 hrs to 7.4 +/- 1.0 mEU/kg/3 hrs. In addition kidney kallikrein content decreased by approximately 50% from 0.76 +/- 0.03 U/kidney to 0.40 +/- 0.07 U/kidney at three hours post treatment. Chlorazanil (3 mg/kg intraperitoneally) increased urine sodium excretion from 0.48 +/- 0.04 mmol/kg/3 hrs to 2.48 +/- 0.98 mmol/kg/3 hrs and decreased the potassium excretion from 1.06 +/- 0.45 mmol/kg/3 hrs to 0.29 +/- 0.09 mmol/kg/3 hrs. Comparable antikaliuretic doses of amiloride (5 mg/kg intraperitoneally) or triamterene (10 mg/kg orally) did not change urine kallikrein excretion It is suggested that chlorazanil inhibits kidney kallikrein synthesis perhaps by an innate antimineralocorticoid-like effect.

摘要

在正常清醒的雌性斯普拉格-道利大鼠中,氯扎尼(腹腔注射3毫克/千克)使尿激肽释放酶排泄量减少了约80%。因此,尿激肽原酶活性从54±5单位/千克/3小时降至10±2单位/千克/3小时,尿对甲苯磺酰精氨酸甲酯酯酶活性从34±1.5毫酶单位/千克/3小时降至7.4±1.0毫酶单位/千克/3小时。此外,治疗后3小时,肾脏激肽释放酶含量从0.76±0.03单位/肾脏减少了约50%,降至0.40±0.07单位/肾脏。氯扎尼(腹腔注射3毫克/千克)使尿钠排泄量从0.48±0.04毫摩尔/千克/3小时增加到2.48±0.98毫摩尔/千克/3小时,并使钾排泄量从1.06±0.45毫摩尔/千克/3小时降至0.29±0.09毫摩尔/千克/3小时。同等抗利尿剂量的氨氯地平(腹腔注射5毫克/千克)或氨苯蝶啶(口服10毫克/千克)并未改变尿激肽释放酶的排泄。有人认为,氯扎尼可能通过一种先天性的抗盐皮质激素样作用抑制肾脏激肽释放酶的合成。

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