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质子泵抑制剂对大鼠地塞米松诱导的胃黏膜损伤的影响。

Influence of proton pump inhibitors on dexamethasone-induced gastric mucosal damage in rats.

作者信息

Swamy A H M Viswanatha, Sajjan M, Thippeswamy A H M, Koti B C, Sadiq A J

机构信息

Department of Pharmacology, K. L. E. S College of Pharmacy, Vidyanagar, Hubli-580 031, India.

出版信息

Indian J Pharm Sci. 2011 Mar;73(2):193-8. doi: 10.4103/0250-474x.91582.

DOI:10.4103/0250-474x.91582
PMID:22303063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3267304/
Abstract

The present study was designed to compare the curative role of proton pump inhibitors, omeprazole, rabeprazole and lansoprazole against dexamethasone-induced ulcer model. Dexamethasone (5 mg/kg/day) was used as an ulcerogen. Dexamethasone suspended in 1% CMC in water was given orally to all rats. Omeprazole (20 mg/kg), rabeprazole (20 mg/kg), and lansoprazole (20 mg/kg) were administered by oral route 30 minutes prior to dexamethasone for ulcer protective studies, gastric secretion and mucosal studies. Effects of proton pump inhibitors were determined by the evaluation of various biochemical parameters such as estimation of myeloperoxidase, cortisol, alkaline phosphatase, malondialdehyde, endogenous anti-oxidants like superoxide dismutase, catalase and reduced glutathione. In dexamethasone induced ulcer model, omeprazole showed significant decrease in malondialdehyde, myeloperoxidase, alkaline phosphatase level and increase in superoxide dismutase, catalase and reduced glutathione level as compared to rabeprazole and lansoprazole. Omeprazole showed significant reduction in cortisol content where as rabeprazole and lansoprazole did not show significant changes as compared to control. The result indicates that omeprazole is the most effective and selective proton pump inhibitor in dexamethasone induced ulcer model as compared to rabeprazole and lansoprazole.

摘要

本研究旨在比较质子泵抑制剂奥美拉唑、雷贝拉唑和兰索拉唑对醋酸地塞米松诱导的溃疡模型的治疗作用。醋酸地塞米松(5毫克/千克/天)用作致溃疡剂。将悬浮于1%羧甲基纤维素钠水溶液中的醋酸地塞米松口服给予所有大鼠。在进行溃疡保护研究、胃分泌和黏膜研究时,在给予醋酸地塞米松前30分钟经口给予奥美拉唑(20毫克/千克)、雷贝拉唑(20毫克/千克)和兰索拉唑(20毫克/千克)。通过评估各种生化参数来确定质子泵抑制剂的作用,这些参数包括髓过氧化物酶、皮质醇、碱性磷酸酶、丙二醛的测定,以及内源性抗氧化剂如超氧化物歧化酶、过氧化氢酶和还原型谷胱甘肽的测定。在醋酸地塞米松诱导的溃疡模型中,与雷贝拉唑和兰索拉唑相比,奥美拉唑使丙二醛、髓过氧化物酶、碱性磷酸酶水平显著降低,超氧化物歧化酶、过氧化氢酶和还原型谷胱甘肽水平升高。奥美拉唑使皮质醇含量显著降低,而与对照组相比,雷贝拉唑和兰索拉唑未显示出显著变化。结果表明,与雷贝拉唑和兰索拉唑相比,奥美拉唑在醋酸地塞米松诱导的溃疡模型中是最有效和最具选择性的质子泵抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8097/3267304/49283e1c7516/IJPhS-73-193-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8097/3267304/49283e1c7516/IJPhS-73-193-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8097/3267304/49283e1c7516/IJPhS-73-193-g006.jpg

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