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奎尼丁在实验性急性肾衰竭中的血清结合情况。

Serum binding of quinidine in experimental acute renal failure.

作者信息

Belpaire F, Bogaert M, De Broe M, Mussche M

出版信息

Pharmacology. 1977;15(4):311-7. doi: 10.1159/000136704.

Abstract

Quinidine serum binding is increased in some patients with acute renal failure, but in animals with renal failure conflicting results were published. Therefore, serum binding of quinidine, papaverine and phenylbutazone was studied by equilibrium dialysis in rabbits and rats with acute renal failure induced either by injection of uranyl nitrate or ligation of the ureters. From the results it appears that, in animals, quinidine binding changes are different according to the model used for induction of the renal failure, regardless of the species studied. After ligation of the ureters, lipoprotein concentration increases, but the meaning of this increase for increased serum quinidine binding is not clear.

摘要

急性肾衰竭患者中,奎尼丁的血清结合率会升高,但关于肾衰竭动物的研究结果却相互矛盾。因此,通过平衡透析法,对注射硝酸铀或结扎输尿管诱导急性肾衰竭的家兔和大鼠体内奎尼丁、罂粟碱和保泰松的血清结合情况进行了研究。结果表明,在动物中,无论所研究的物种如何,奎尼丁结合率的变化因用于诱导肾衰竭的模型而异。输尿管结扎后,脂蛋白浓度升高,但这种升高对血清奎尼丁结合率增加的意义尚不清楚。

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引用本文的文献

1
Influence of acute renal failure on the protein binding of drugs in animals and in man.
Eur J Clin Pharmacol. 1977;11(1):27-32. doi: 10.1007/BF00561784.

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