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非甾体抗炎药(NSAID)对大鼠钠和水的肾排泄以及体液量的影响。

Effects of nonsteroidal anti-inflammatory drugs (NSAID) on renal excretion of sodium and water, and on body fluid volume in rats.

作者信息

Kadokawa T, Hosoki K, Takeyama K, Minato H, Shimizu M

出版信息

J Pharmacol Exp Ther. 1979 May;209(2):219-24.

PMID:438997
Abstract

Effects of nonsteroidal anti-inflammatory drugs (NSAID) on urine volume and urinary sodium excretion, and on plasma volume and extracellular fluid volume were examined in conscious rats. The basal urine volume and urinary sodium excretion were decreased and the increased urine volume and urinary sodium excretion elicited by saline load (25 ml/kg) and by hydrochlorothiazide (10 mg/kg) were inhibited after oral administration of NSAID in doses which inhibited the rat carrageenin-induced hind paw edema (indomethacin, 1--10 mg/kg; tolmetin, 3--30 mg/kg; phenylbutazone, 3--30 mg/kg; aspirin, 30--300 mg/kg), but aminopyrine (30--300 mg/kg) did not show such an effect. The inhibitory activity on renal function was diminished gradually with repeated administration of NSAID. NSAID (indomethacin, 3 mg/kg; tolmetin, 10 mg/kg; phenoxybenzamin, 10 mg/kg; aspirin, 100 mg/kg) increased plasma volume and extracellular fluid volume of rats after repeated medication for 3 or 5 days, but the body fluid volume expansion disappeared with further repeated administration of NSAID. These results suggest that NSAID may inhibit the intrarenal role of prostaglandins and decrease sodium and water excretion in urine with resulting increased body fluid volume. Tolerance to these actions of NSAID developed after repeated administration.

摘要

在清醒大鼠中研究了非甾体抗炎药(NSAID)对尿量、尿钠排泄、血浆容量和细胞外液容量的影响。口服能抑制大鼠角叉菜胶诱导的后爪水肿的剂量的NSAID(吲哚美辛,1 - 10mg/kg;托美汀,3 - 30mg/kg;保泰松,3 - 30mg/kg;阿司匹林,30 - 300mg/kg)后,基础尿量和尿钠排泄减少,盐水负荷(25ml/kg)和氢氯噻嗪(10mg/kg)引起的尿量增加和尿钠排泄增加受到抑制,但氨基比林(30 - 300mg/kg)未显示出这种作用。随着NSAID的重复给药,对肾功能的抑制活性逐渐减弱。重复给药3或5天后,NSAID(吲哚美辛,3mg/kg;托美汀,10mg/kg;苯氧苄胺,10mg/kg;阿司匹林,100mg/kg)增加了大鼠的血浆容量和细胞外液容量,但随着NSAID的进一步重复给药,体液容量扩张消失。这些结果表明,NSAID可能抑制前列腺素在肾内的作用,减少尿中钠和水的排泄,从而导致体液容量增加。重复给药后对NSAID的这些作用产生了耐受性。

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