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对一种独特的真性血钙过少利尿剂ICI 206,970的肾脏作用部位的微穿刺研究。

A micropuncture study on the renal site of action of ICI 206,970, a unique eukalemic diuretic.

作者信息

Johnston P A, Kau S T

机构信息

Department of Pharmacology, ICI Pharmaceuticals Group, A Business Unit of ICI Americans Inc., Wilmington, Delaware.

出版信息

J Pharmacol Exp Ther. 1993 Feb;264(2):604-8.

PMID:8437111
Abstract

The site of action of ICI 206,970, an aminomethylphenol pyrazine derivative, with effects on Na+ and water excretion similar to hydrochlorothazide, was determined using free-flow micropuncture and in vivo microperfusion techniques. Furosemide and ICI 206,970 were perfused into the loop of Henle, at a concentration of 10(-4) M. Furosemide reduced water, Na+ and K+ reabsorption by the loop, but ICI 206,970 had little effect. Amiloride and ICI 206,970 were perfused into the distal nephron at a concentration of 10(-4) M. Both compounds reduced the reabsorption of Na+ and secretion of K+, ICI 206,970 having a somewhat greater effect than amiloride at this dose. ICI 206,970 also reduced water reabsorption by the distal tubule. ICI 206,970 was infused i.v. at a dose of 10 mg/kg/hr into anesthetized rats, and its effect on reabsorption by various nephron segments was determined. This compound tended to reduce proximal reabsorption of Na+, K+ and water, but had little effect on reabsorption of electrolytes and water by the loop of Henle, or distal tubule reabsorption of Na+ and water. Distal K+ secretion decreased after administration of ICI 206,970. Reabsorption of electrolytes and water beyond the late distal nephron was not affected by the drug. Urinary excretion of Na+ and water was elevated, but K+ excretion remained unchanged after treatment with ICI 206,970. The sites of action of ICI 206,970 appear to be the proximal and distal nephron. Urinary excretion of Na+ and water was largely dependent on the effect of ICI 206,970 on proximal reabsorption, as this compound had little effect on loop of Henle or distal tubule reabsorption.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

ICI 206,970是一种氨基甲基苯酚吡嗪衍生物,其作用部位通过自由流动微穿刺和体内微灌注技术来确定,该药物对钠和水排泄的影响与氢氯噻嗪相似。将速尿和ICI 206,970以10(-4) M的浓度灌注到亨氏袢。速尿减少了亨氏袢对水、钠和钾的重吸收,但ICI 206,970影响很小。将氨氯吡咪和ICI 206,970以10(-4) M的浓度灌注到远端肾单位。两种化合物都减少了钠的重吸收和钾的分泌,在此剂量下ICI 206,970的作用比氨氯吡咪稍大。ICI 206,970还减少了远端小管对水的重吸收。以10 mg/kg/hr的剂量将ICI 206,970静脉注射到麻醉大鼠体内,并确定其对各个肾单位节段重吸收的影响。该化合物倾向于减少近端对钠、钾和水的重吸收,但对亨氏袢的电解质和水重吸收或远端小管对钠和水的重吸收影响很小。给予ICI 206,970后远端钾分泌减少。该药物不影响远端肾单位晚期之后的电解质和水重吸收。ICI 206,9后的钠和水的尿排泄增加,但钾排泄保持不变。ICI 206,970的作用部位似乎是近端和远端肾单位。钠和水的尿排泄很大程度上取决于ICI 206,970对近端重吸收的影响,因为该化合物对亨氏袢或远端小管重吸收影响很小。(摘要截短于250字)

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