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抗抑郁药与血浆蛋白结合的个体差异:α1-酸性糖蛋白变体的作用。

Interindividual differences in the binding of antidepressives to plasma proteins: the role of the variants of alpha 1-acid glycoprotein.

作者信息

Tinguely D, Baumann P, Conti M, Jonzier-Perey M, Schöpf J

出版信息

Eur J Clin Pharmacol. 1985;27(6):661-6. doi: 10.1007/BF00547045.

Abstract

Alpha 1-acid glycoprotein (AAG) is one of the plasma proteins that bind basic drugs, like amitriptyline (AT) and its metabolite nortriptyline (NT). Two types of genetic polymorphism have been described for AAG: polymorphic forms which, on electrophoresis of the native protein, give four patterns with 5, 6, 7 or 8 bands, and the variants which on by electrophoresis of the desialysed protein, give three patterns with 2 bands, FF, FS and SS. In 31 depressive patients, treated daily with 150 mg AT for 3 weeks, free and total plasma AT and NT were determined, as well as the AAG polymorphic forms and variants. There was only a weak negative correlation between the free fractions of AT and NT and total plasma AAG, but free AT and NT were strongly correlated with the S form (but not the F form) of AAG variants. The differences in binding might be the expression of a further genetic factor determining the steady-state plasma levels of tricyclic drugs.

摘要

α1-酸性糖蛋白(AAG)是一种能结合碱性药物(如阿米替林(AT)及其代谢产物去甲替林(NT))的血浆蛋白。已发现AAG存在两种遗传多态性:一种是天然蛋白电泳时呈现的多态形式,有4种条带模式,分别为5条、6条、7条或8条带;另一种是去唾液酸蛋白电泳时呈现的变体,有3种条带模式,分别为2条带,即FF、FS和SS。对31例抑郁症患者每日给予150 mg AT治疗3周,测定了血浆中游离和总AT及NT水平,以及AAG的多态形式和变体。AT和NT的游离部分与血浆总AAG之间仅存在微弱的负相关,但游离AT和NT与AAG变体的S型(而非F型)密切相关。结合差异可能是决定三环类药物稳态血浆水平的另一个遗传因素的表现。

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