Thon K P, Lorenz W, Ohmann C, Weber D, Rohde H, Röher H D
Gut. 1985 Nov;26(11):1165-78. doi: 10.1136/gut.26.11.1165.
Changes in histamine storage in the oxyntic mucosa of duodenal ulcer patients and their reversal by vagotomy and the histamine H2-antagonist cimetidine supported the hypothesis that histamine could be a causal factor in peptic ulcer pathogenesis. The specificity of these findings was impaired by problems in biopsy taking, however, and in the preparative steps before measuring the actual histamine contents in all parts of the gastric mucosa and in the duodenum. A prospective trial was carried out in 190 patients to identify these sources of bias and to overcome them by appropriate study designs. Usually a direct correlation was found between weight of biopsy and mucosal histamine content. This problem was solved by selecting a biopsy forceps producing smaller variations in sample size, by limiting the time of cold ischaemia to four to five minutes only and by taking three biopsy specimens for each single histamine value. The actual histamine content of mucosal biopsies remained constant for about four to five minutes only. The 'disappearance' rate was faster in control subjects than in duodenal ulcer patients. Hence by variation of the cold ischaemia time any artefacts of differences between mucosal histamine levels in controls and duodenal ulcer patients could be produced. Using the optimised sample taking procedure mucosal histamine contents of several gastric regions and the duodenal bulb were measured in 24 patients with duodenal ulcer, after selective proximal vagotomy without drainage and in control subjects without any stomach disease (randomised controlled trial). The histamine content was lower in all parts of the upper gastrointestinal tract in duodenal ulcer patients than in controls and was raised again in all regions after selective proximal vagotomy. As the most likely hypothesis it is suggested that vagal reflexes with afferent fibres coming from the oxyntic mucosa stimulate histamine release in duodenal ulcer patients by efferent peptidergic neurones to all parts of the stomach and the duodenum where the ulcer lesion is situated.
十二指肠溃疡患者胃底黏膜中组胺储存的变化,以及迷走神经切断术和组胺H2拮抗剂西咪替丁对这些变化的逆转,支持了组胺可能是消化性溃疡发病机制中的一个致病因素这一假说。然而,活检取材以及在测量胃黏膜和十二指肠所有部位实际组胺含量之前的制备步骤中存在的问题,削弱了这些发现的特异性。对190名患者进行了一项前瞻性试验,以确定这些偏差来源,并通过适当的研究设计来克服它们。通常在活检组织重量与黏膜组胺含量之间发现直接相关性。通过选择样本大小变化较小的活检钳、将冷缺血时间仅限制在四到五分钟以及为每个组胺值采集三个活检标本,解决了这个问题。黏膜活检的实际组胺含量仅在大约四到五分钟内保持恒定。对照组受试者的“消失”率比十二指肠溃疡患者更快。因此,通过改变冷缺血时间,可以产生对照组和十二指肠溃疡患者黏膜组胺水平差异的任何假象。采用优化的取材程序,在24例十二指肠溃疡患者、行选择性近端迷走神经切断术但不做引流术后以及无任何胃部疾病的对照组受试者(随机对照试验)中,测量了几个胃区域和十二指肠球部的黏膜组胺含量。十二指肠溃疡患者上消化道所有部位的组胺含量均低于对照组,而在选择性近端迷走神经切断术后所有区域的组胺含量又再次升高。作为最有可能的假说,有人提出,来自胃底黏膜的传入纤维引起的迷走神经反射,通过传出肽能神经元刺激十二指肠溃疡患者胃和十二指肠所有溃疡病变部位的组胺释放。