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尿素对血清胆碱酯酶的抑制作用。作用机制及其在异常基因分型中的应用。

The inhibition of serum cholinesterase by urea. Mechanism of action and application in the typing of abnormal genes.

作者信息

Hanel H K, Viby-Mogensen J

出版信息

Br J Anaesth. 1977 Dec;49(12):1251-7. doi: 10.1093/bja/49.12.1251.

Abstract

The mechanism of action of urea on serum cholinesterase and the application of the inhibition by urea in the typing of the abnormal genes of this enzyme were investigated. Urea caused a competitive, irreversible inhibition of serum cholinesterase, which was most pronounced for the abnormal enzymes. Urea inhibition, used with dibucaine inhibition, allowed differentiation between all the known genotypes of locus E1. In the differentiation of rarer genotypes, the combination of urea numbers (percentage inhibition of serum cholinesterase activity caused by urea 5 mol litre-1) and dibucaine numbers was found, in certain situations, to be superior to the classical combination of fluroide and dibucaine numbers.

摘要

研究了尿素对血清胆碱酯酶的作用机制以及尿素抑制作用在该酶异常基因分型中的应用。尿素对血清胆碱酯酶产生竞争性、不可逆抑制,对异常酶的抑制作用最为明显。将尿素抑制与丁卡因抑制结合使用,可区分E1位点的所有已知基因型。在区分罕见基因型时,发现在某些情况下,尿素值(5摩尔/升尿素引起的血清胆碱酯酶活性抑制百分比)与丁卡因值的组合优于传统的氟化物与丁卡因值的组合。

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