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质子泵抑制剂是治疗酸相关性疾病的首选药物。

Proton-pump inhibitors are the treatment of choice in acid-related disease.

作者信息

Brunner G

机构信息

Department of Medicine, University Medical School, Hannover, Germany.

出版信息

Eur J Gastroenterol Hepatol. 1996 Oct;8 Suppl 1:S9-13. doi: 10.1097/00042737-199610001-00003.

DOI:10.1097/00042737-199610001-00003
PMID:8930574
Abstract

INCREASING INTRAGASTRIC PH

Effective treatment of acid-related disease requires an increase in intragastric pH. The two principal pharmacological methods of attaining this goal are (1) using histamine (H2)-receptor antagonists to block H2-receptors on the parietal cell and (2) using proton-pump inhibitors to stop acid production acid at its source. H2-RECEPTOR ANTAGONISTS: H2-receptor antagonists bind loosely and non-covalently to receptors on the parietal cell. They represented a great advance when they first appeared, bringing relief to many patients and improving the standard of care, with fewer operations and hospitalizations and a generally improved quality of life. However, many patients do not respond to these drugs, either because of the nature of the disease or because of resistance to the agent. PROTON-PUMP INHIBITORS: Proton-pump inhibitors represent an advance in the therapy of acid-related disease because they inhibit all acid production, no matter what the source of the stimulus, by binding covalently to the proton pump. Compared with H2-receptor antagonists, the effect of proton-pump inhibition is longer-lasting, faster-acting, and more effective, curing 99% of patients resistant to H2-receptor antagonist therapy. These properties make proton-pump inhibitors the treatment of choice for acid-related diseases.

摘要

提高胃内pH值:有效治疗酸相关性疾病需要提高胃内pH值。实现这一目标的两种主要药理学方法是:(1)使用组胺(H2)受体拮抗剂阻断壁细胞上的H2受体;(2)使用质子泵抑制剂从源头抑制胃酸分泌。H2受体拮抗剂:H2受体拮抗剂与壁细胞上的受体以非共价方式松散结合。它们首次出现时是一大进步,使许多患者症状缓解,改善了医疗水平,减少了手术和住院次数,总体生活质量得到提高。然而,许多患者对这些药物无反应,原因可能是疾病本身特性或对药物产生耐药性。质子泵抑制剂:质子泵抑制剂是酸相关性疾病治疗的一大进展,因为它们通过与质子泵共价结合,无论刺激源是什么,都能抑制所有胃酸分泌。与H2受体拮抗剂相比,质子泵抑制作用持续时间更长、起效更快且更有效,能治愈99%对H2受体拮抗剂治疗耐药的患者。这些特性使质子泵抑制剂成为酸相关性疾病的首选治疗药物。

相似文献

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Proton-pump inhibitors are the treatment of choice in acid-related disease.质子泵抑制剂是治疗酸相关性疾病的首选药物。
Eur J Gastroenterol Hepatol. 1996 Oct;8 Suppl 1:S9-13. doi: 10.1097/00042737-199610001-00003.
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[Gastric acid secretion inhibitors: H2 receptor antagonists (H2RA), proton pump inhibitors (PPI) or acid pump antagonists (APA)].[胃酸分泌抑制剂:H2受体拮抗剂(H2RA)、质子泵抑制剂(PPI)或酸泵拮抗剂(APA)]
Acta Gastroenterol Latinoam. 1996;26(4):263-5.
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The changing role of H2-receptor antagonists in acid-related diseases.
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Proton pump inhibitors versus H2-antagonists: a meta-analysis of their efficacy in treating bleeding peptic ulcer.质子泵抑制剂与H2拮抗剂:关于它们治疗消化性溃疡出血疗效的荟萃分析
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Pharmacological and pharmacodynamic essentials of H(2)-receptor antagonists and proton pump inhibitors for the practising physician.执业医师使用H2受体拮抗剂和质子泵抑制剂的药理学及药效学要点
Best Pract Res Clin Gastroenterol. 2001 Jun;15(3):355-70. doi: 10.1053/bega.2001.0184.
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[Are proton pump inhibitors superior to H2 receptor antagonists within the scope of H. pylori eradication therapy? Meta analysis of current parallel group comparisons].[在幽门螺杆菌根除治疗范围内,质子泵抑制剂是否优于H2受体拮抗剂?当前平行组比较的荟萃分析]
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Gastroduodenal Ulceration in Small Animals: Part 2. Proton Pump Inhibitors and Histamine-2 Receptor Antagonists.小动物胃十二指肠溃疡:第2部分。质子泵抑制剂和组胺-2受体拮抗剂
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Eradication of Helicobacter pylori does not decrease the long-term use of acid-suppressive medication.根除幽门螺杆菌并不会减少抑酸药物的长期使用。
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Histamine receptor antagonists, proton pump inhibitors and their combination in the treatment of gastro-oesophageal reflux disease.组胺受体拮抗剂、质子泵抑制剂及其联合用药治疗胃食管反流病
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Treatment of peptic ulcer in the elderly. Proton pump inhibitors and histamine H2 receptor antagonists.老年人消化性溃疡的治疗。质子泵抑制剂和组胺H2受体拮抗剂。
Drugs Aging. 1996 Oct;9(4):251-61. doi: 10.2165/00002512-199609040-00003.

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Suppressive effect of antiulcer agents on granulocytes--a role for granulocytes in gastric ulcer formation.抗溃疡药物对粒细胞的抑制作用——粒细胞在胃溃疡形成中的作用
Dig Dis Sci. 2000 Sep;45(9):1786-91. doi: 10.1023/a:1005526126694.
2
Trends in the management of gastro-oesophageal reflux disease.胃食管反流病的管理趋势
Postgrad Med J. 1998 Mar;74(869):145-50. doi: 10.1136/pgmj.74.869.145.