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氨苯蝶啶及其类似物在清醒生理盐水负荷大鼠体内的保钾保镁效能与功效。

Potassium and magnesium retaining potency and efficacy of triamterene and analogues in conscious saline-loaded rats.

作者信息

Priewer H, Ullrich F, Mutschler E

机构信息

Du Pont Pharma GmbH, Bad Homburg, Germany.

出版信息

Magnes Res. 1996 Mar;9(1):33-40.

PMID:8819092
Abstract

The effect of triamterene and analogues on the acute renal excretion of K+ and Mg2+ was investigated in conscious saline-loaded rats. The maximum retention (Emax) value of the potassium and magnesium retaining efficacy is almost independent of the structure of the compound and depends only on the initial basal value of ion excretion (E0). Triamterene and analogues display a comparable magnesium retaining efficacy. This can be explained by activity against the same renal Mg2+ transportation system. There was a relation between the ED50 values for the potassium and magnesium retaining properties of triamterene derivatives. Both the potassium and the magnesium retaining potency are dependent on the basicity as well as on the lipophilicity of the side chain of the triamterene derivatives. The part of the molecule responsible for the antimagnesiuretic properties of the derivatives seems to be sensitive to steric influences.

摘要

在清醒的生理盐水负荷大鼠中研究了氨苯蝶啶及其类似物对钾离子(K⁺)和镁离子(Mg²⁺)急性肾排泄的影响。钾离子和镁离子潴留效能的最大保留值(Emax)几乎与化合物的结构无关,仅取决于离子排泄的初始基础值(E0)。氨苯蝶啶及其类似物表现出相当的镁离子潴留效能。这可以通过对相同的肾脏Mg²⁺转运系统的活性来解释。氨苯蝶啶衍生物的钾离子和镁离子潴留特性的半数有效量(ED50)值之间存在关联。钾离子和镁离子的潴留效力均取决于氨苯蝶啶衍生物侧链的碱性以及亲脂性。衍生物中负责抗利尿镁特性的分子部分似乎对空间影响敏感。

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