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佐林格-埃利森综合征及奥美拉唑治疗对胃壁细胞内分泌细胞的影响。

The effect of Zollinger-Ellison syndrome and omeprazole therapy on gastric oxyntic endocrine cells.

作者信息

Maton P N, Lack E E, Collen M J, Cornelius M J, David E, Gardner J D, Jensen R T

机构信息

Digestive Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.

出版信息

Gastroenterology. 1990 Oct;99(4):943-50. doi: 10.1016/0016-5085(90)90611-4.

Abstract

In 1983, all trials of omeprazole in humans were stopped because rats given the drug developed gastric endocrine cell hyperplasia and carcinoid tumors. Further studies in rats showed that drug-induced achlorhydria and hypergastrinemia caused these changes. Because data in humans are limited, we compared the numbers of endocrine cells, as judged by silver staining (argyrophilia), in the gastric mucosa of patients with Zollinger-Ellison syndrome, who are hypergastrinemic, and in normogastrinemic patients with idiopathic acid-peptic diseases. In addition, we analyzed the number of gastric endocrine cells in patients with Zollinger-Ellison syndrome given omeprazole for up to 3 years. Patients with Zollinger-Ellison syndrome had 15.7% +/- 6.9% argyrophil cells in biopsies of gastric oxyntic mucosa, and patients with idiopathic acid-peptic disease had 7.8% +/- 2.3% (P less than 0.01). In patients with Zollinger-Ellison syndrome, the percentage of argyrophil cells was not related to serum gastrin concentration, duration of symptoms, time since diagnosis, basal or maximal acid output, extent of tumor, or age. There was a tendency for patients with multiple endocrine neoplasia type 1 to have a greater percent of argyrophil cells than patients with sporadic Zollinger-Ellison syndrome. Considering the biopsies from both normogastrinemic and hypergastrinemic patients, there was a significant relationship between the percentage of argyrophil cells and the serum concentration of gastrin (P less than 0.01). Patients with Zollinger-Ellison syndrome given omeprazole for up to 3 years developed no significant changes in percentage of argyrophil cells, no carcinoid tumors, and no changes in serum concentrations of gastrin. The present study shows that patients with Zollinger-Ellison syndrome have an increased percentage of argyrophil cells in oxyntic mucosa and that omeprazole does not increase this percentage. In periods of up to 3 years, omeprazole had no effects on gastric morphology in patients with Zollinger-Ellison syndrome.

摘要

1983年,所有奥美拉唑人体试验均被停止,因为给大鼠服用该药物后出现了胃内分泌细胞增生和类癌肿瘤。对大鼠的进一步研究表明,药物诱导的胃酸缺乏和高胃泌素血症导致了这些变化。由于人类数据有限,我们比较了高胃泌素血症的佐林格-埃利森综合征患者和正常胃泌素血症的特发性酸相关性疾病患者胃黏膜中通过银染色(嗜银性)判断的内分泌细胞数量。此外,我们分析了接受奥美拉唑治疗长达3年的佐林格-埃利森综合征患者的胃内分泌细胞数量。佐林格-埃利森综合征患者胃泌酸黏膜活检中嗜银细胞占15.7%±6.9%,特发性酸相关性疾病患者为7.8%±2.3%(P<0.01)。在佐林格-埃利森综合征患者中,嗜银细胞百分比与血清胃泌素浓度、症状持续时间、诊断后时间、基础或最大胃酸分泌量、肿瘤范围或年龄无关。1型多发性内分泌腺瘤患者的嗜银细胞百分比有高于散发性佐林格-埃利森综合征患者的趋势。综合正常胃泌素血症和高胃泌素血症患者的活检结果,嗜银细胞百分比与胃泌素血清浓度之间存在显著相关性(P<0.01)。接受奥美拉唑治疗长达3年的佐林格-埃利森综合征患者,嗜银细胞百分比无显著变化,未出现类癌肿瘤,血清胃泌素浓度也无变化。本研究表明,佐林格-埃利森综合征患者胃泌酸黏膜中嗜银细胞百分比增加,而奥美拉唑不会增加该百分比。在长达3年的时间里,奥美拉唑对佐林格-埃利森综合征患者的胃形态无影响。

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