Sachs G, Shin J M, Munson K, Vagin O, Lambrecht N, Scott D R, Weeks D L, Melchers K
UCLA Digestive Research Center, Departments of Physiology and Medicine, University of California, Los Angeles, CA, USA.
Aliment Pharmacol Ther. 2000 Nov;14(11):1383-401. doi: 10.1046/j.1365-2036.2000.00837.x.
This review focuses on the gastric acid pump as a therapeutic target for the control of acid secretion in peptic ulcer and gastro-oesophageal reflux disease. The mechanism of the proton pump inhibitors is discussed as well as their clinical use. The biology of Helicobacter pylori as a gastric denizen is then discussed, with special regard to its mechanisms of acid resistance. Here the properties of the products of the urease gene clusters, ureA, B and ureI, E, F, G and H are explored in order to explain the unique location of this pathogen. The dominant requirement for acid resistance is the presence of a proton gated urea transporter, UreI, which increases access of gastric juice urea to the intrabacterial urease 300-fold. This enables rapid and continuous buffering of the bacterial periplasm to approximately pH 6.0, allowing acid resistance and growth at acidic pH in the presence of 1 mM urea. A hypothesis for the basis of combination therapy for eradication is also presented.
本综述聚焦于胃酸泵作为消化性溃疡和胃食管反流病中控制胃酸分泌的治疗靶点。文中讨论了质子泵抑制剂的作用机制及其临床应用。接着探讨了幽门螺杆菌作为胃部定植菌的生物学特性,特别关注其耐酸机制。在此,研究了脲酶基因簇产物ureA、B以及ureI、E、F、G和H的特性,以解释该病原体的独特定位。耐酸的主要需求是存在质子门控尿素转运体UreI,它可使胃液尿素进入细菌内脲酶的量增加300倍。这能使细菌周质迅速且持续地缓冲至约pH 6.0,从而在存在1 mM尿素的情况下实现耐酸并在酸性pH环境中生长。文中还提出了根除联合治疗基础的假说。