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奥美拉唑、尼群地平、法莫替丁与应激性溃疡

Omeprazole, nitrendipine, famotidine and stress-induced ulcers.

作者信息

Inalöz S S, Goral V, Sari I, Canberk Y, Ulak G

机构信息

Department of Histology & Embryology, Dicle University Medical Faculty, Diyarbakir, Turkey.

出版信息

Acta Gastroenterol Belg. 1997 Jul-Sep;60(3):192-6.

PMID:9396173
Abstract

BACKGROUND

Omeprazole inhibits gastric acid secretion by blocking the proton pump of the gastric parietal cell. Nitrendipine is a derivative of the dihydropyridine group of calcium channel blockers and administrated for angina and hypertension. Famotidine is one of the newer histamine H2-receptor antagonists and heals gastric and duodenal ulcers by reducing gastric acid output.

OBJECTIVES

The healing effects of omeprazole, nitrendipine and famotidine on stress-induced gastric ulcers were investigated in rats.

METHODS

Forty male Wistar-albino rats were separated into five groups (n = 8), a control (non-stress) and four experimental (stress) groups. Experimental rats were treated with omeprazole, nitrendipine, famotidine or a placebo after the stresses of starvation and cold-restraint.

RESULT

Macroscopically, the mean area of the affected lesional mucosa was 1/4 of the total gastric mucosa in the famotidine treated group and 1/5 of the total gastric mucosa in the nitrendipine treated group. A considerably decrease was observed in the omeprazole treated group in which the mean area of the lesional mucosa was only in 1/8 of the total gastric mucosa. On microscopic examination, congestive vessels and chronic inflammatory cell infiltrates were significantly reduced in the omeprazole treated group. Tissue regeneration was more prominent in the omeprazole group than the other groups.

CONCLUSION

Omeprazole was found to be superior in terms of the effect on the healing process to nitrendipine and famotidine. Although therapeutic effects of nitrendipine and famotidine were observed, those were less than omeprazole.

摘要

背景

奥美拉唑通过阻断胃壁细胞的质子泵来抑制胃酸分泌。尼群地平是二氢吡啶类钙通道阻滞剂的衍生物,用于治疗心绞痛和高血压。法莫替丁是较新的组胺H2受体拮抗剂之一,通过减少胃酸分泌来治愈胃溃疡和十二指肠溃疡。

目的

研究奥美拉唑、尼群地平及法莫替丁对大鼠应激性胃溃疡的愈合作用。

方法

将40只雄性Wistar白化大鼠分为五组(n = 8),一组为对照(非应激)组,四组为实验(应激)组。实验大鼠在经历饥饿和冷束缚应激后,分别用奥美拉唑、尼群地平、法莫替丁或安慰剂进行治疗。

结果

宏观上,法莫替丁治疗组病变黏膜的平均面积为胃黏膜总面积的1/4,尼群地平治疗组为胃黏膜总面积的1/5。奥美拉唑治疗组病变黏膜的平均面积仅为胃黏膜总面积的1/8,观察到明显减小。显微镜检查显示,奥美拉唑治疗组充血血管和慢性炎性细胞浸润明显减少。奥美拉唑组的组织再生比其他组更显著。

结论

发现奥美拉唑在愈合过程中的效果优于尼群地平及法莫替丁。虽然观察到了尼群地平和法莫替丁的治疗效果,但不如奥美拉唑。

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