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人胃黏膜中胃蛋白酶原多态性与胃部疾病的关系。

Pepsinogen polymorphism in human gastric mucosa in relation to gastric diseases.

作者信息

Kucerová Z, Korbová L, Kohout J, Pesková M, Sváb J

机构信息

Department of Pathological Physiology, 1st Medical Faculty, Charles University, Prague.

出版信息

Sb Lek. 1993;94(2):163-8.

PMID:7992009
Abstract

The human stomach mucosa contains two main group of gastric proteinases. Both pepsinogen A (PGA) and pepsinogen C (PGC) consist of molecular variants, isozymogens, which can be separated electrophoretically, PGA was found to consist of five isozymogens (Pg1-Pg2), and PGC of two isozymogens (Pg6 and Pg7). Five hundred zymograms were examined and electrophoretic mobility of pepsinogens from patients with gastric cancer was found to be higher than from other gastric diseases. The ratio of isozymogens Pg3 to Pg5 differs in to great extent in various disease. Patients with ulcer disease have this value higher than 1, but patients with gastric cancer lower than 1. Patients with gastric ulcer have lower occurrence of Pg1 and SMP in antrum. In patients with gastric carcinoma lower concentration of PGA and also ratio PGA to PGC are observed.

摘要

人类胃黏膜含有两类主要的胃蛋白酶。胃蛋白酶原A(PGA)和胃蛋白酶原C(PGC)均由分子变体即同工酶原组成,这些同工酶原可通过电泳分离。已发现PGA由五种同工酶原(Pg1 - Pg2)组成,PGC由两种同工酶原(Pg6和Pg7)组成。检查了500份酶谱,发现胃癌患者胃蛋白酶原的电泳迁移率高于其他胃部疾病患者。同工酶原Pg3与Pg5的比例在各种疾病中差异很大。溃疡病患者该值高于1,而胃癌患者低于1。胃溃疡患者胃窦中Pg1和SMP的发生率较低。胃癌患者中PGA的浓度较低,且PGA与PGC的比例也较低。

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