• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

胶体次枸橼酸铋细胞保护作用机制的认识进展。

Advances in the understanding of the mechanism of cytoprotective action by colloidal bismuth subcitrate.

作者信息

Konturek S J, Radecki T, Piastucki I, Drozdowicz D

出版信息

Scand J Gastroenterol Suppl. 1986;122:6-10. doi: 10.3109/00365528609102578.

DOI:10.3109/00365528609102578
PMID:3465028
Abstract

This study was designed to compare the gastroprotective effects of colloidal bismuth subcitrate (CBS) with those of sucralfate and methylated analog of prostaglandin E2 (PGE2) against acute gastric lesions induced by absolute ethanol, acidified aspirin (ASA), and water immersion and restraint stress in rats. When given orally, both CBS and sucralfate prevented in a dose-dependent way the formation of gastric lesions induced by all three ulcerogens, CBS being about 7, 2, and 20 times more potent, respectively on a weight-to-weight basis than sucralfate. Methylated PGE2 was also highly effective against these ulcerogens. Bismuth subnitrate was ineffective against acute gastric lesions induced by stress conditions. The protection of both CBS and sucralfate was reversible when the animals were pretreated with indomethacin to suppress the generation of endogenous prostaglandins. Since CBS and sucralfate increased the production of PGE2 in the gastric mucosa, we postulate that their gastric protective action may be mediated, at least partly, by mucosal prostaglandins.

摘要

本研究旨在比较枸橼酸铋钾(CBS)、硫糖铝和前列腺素E2(PGE2)甲基化类似物对大鼠因无水乙醇、酸化阿司匹林(ASA)、水浸束缚应激诱导的急性胃损伤的胃保护作用。口服给药时,CBS和硫糖铝均能以剂量依赖的方式预防由这三种致溃疡剂诱导的胃损伤形成,以重量对重量计算,CBS的效力分别比硫糖铝高约7倍、2倍和20倍。甲基化PGE2对这些致溃疡剂也非常有效。硝酸铋对由应激条件诱导的急性胃损伤无效。当用吲哚美辛预处理动物以抑制内源性前列腺素的产生时,CBS和硫糖铝的保护作用均可逆转。由于CBS和硫糖铝增加了胃黏膜中PGE2的产生,我们推测它们的胃保护作用可能至少部分是由黏膜前列腺素介导的。

相似文献

1
Advances in the understanding of the mechanism of cytoprotective action by colloidal bismuth subcitrate.胶体次枸橼酸铋细胞保护作用机制的认识进展。
Scand J Gastroenterol Suppl. 1986;122:6-10. doi: 10.3109/00365528609102578.
2
Gastrocytoprotection by colloidal bismuth subcitrate (De-Nol) and sucralfate. Role of endogenous prostaglandins.枸橼酸铋钾(得乐)和硫糖铝的胃细胞保护作用。内源性前列腺素的作用。
Gut. 1987 Feb;28(2):201-5. doi: 10.1136/gut.28.2.201.
3
Studies on the gastroprotective and ulcer-healing effects of colloidal bismuth subcitrate.枸橼酸铋钾的胃保护和溃疡愈合作用研究。
Digestion. 1987;37 Suppl 2:8-15. doi: 10.1159/000199553.
4
Gastric mucosa protection and prostaglandin E2 generation in rats by colloidal bismuth subcitrate (DE-NOL).枸橼酸铋钾(得乐)对大鼠胃黏膜的保护作用及前列腺素E2的生成
Arch Int Pharmacodyn Ther. 1987 Apr;286(2):308-19.
5
Gastric mucosa protective effects of colloidal bismuth subcitrate (DE-NOL).枸橼酸铋钾(得乐)对胃黏膜的保护作用。
Int J Tissue React. 1987;9(5):427-32.
6
Protective properties of colloidal bismuth subcitrate on gastric mucosa.枸橼酸铋钾对胃黏膜的保护作用。
Scand J Gastroenterol Suppl. 1986;122:11-3. doi: 10.3109/00365528609102579.
7
Effect of bismuth subcitrate and sucralfate on rat duodenal and human gastric bicarbonate secretion in vivo.枸橼酸铋钾和硫糖铝对大鼠十二指肠及人胃碳酸氢盐分泌的体内效应。
Gut. 1990 Jan;31(1):26-31. doi: 10.1136/gut.31.1.26.
8
Gastroprotection by an aluminium- and magnesium hydroxide-containing antacid in rats. Role of endogenous prostanoids.含氢氧化铝和氢氧化镁的抗酸剂对大鼠的胃保护作用。内源性前列腺素的作用。
Scand J Gastroenterol. 1989 Nov;24(9):1113-20. doi: 10.3109/00365528909089264.
9
Role of mucus and prostaglandins in the gastric mucosal protective actions of sucralfate against ethanol-induced injury in the rat.黏液和前列腺素在硫糖铝对大鼠乙醇诱导损伤的胃黏膜保护作用中的作用
Am J Med. 1987 Sep 28;83(3B):19-23. doi: 10.1016/0002-9343(87)90822-9.
10
Recent experimental and clinical studies on the pharmacology of colloidal bismuth subcitrate.近期关于枸橼酸铋胶体药理学的实验与临床研究。
Scand J Gastroenterol Suppl. 1986;122:14-6. doi: 10.3109/00365528609102580.

引用本文的文献

1
Colloidal bismuth subcitrate impedes proton entry into Helicobacter pylori and increases the efficacy of growth-dependent antibiotics.枸橼酸铋胶体可阻止质子进入幽门螺杆菌,并提高依赖生长的抗生素的疗效。
Aliment Pharmacol Ther. 2015 Oct;42(7):922-33. doi: 10.1111/apt.13346. Epub 2015 Aug 4.
2
Utilization of time-kill kinetic methodologies for assessing the bactericidal activities of ampicillin and bismuth, alone and in combination, against Helicobacter pylori in stationary and logarithmic growth phases.利用时间杀菌动力学方法评估氨苄青霉素和铋单独及联合使用对处于稳定期和对数生长期的幽门螺杆菌的杀菌活性。
Antimicrob Agents Chemother. 1995 Jan;39(1):66-9. doi: 10.1128/AAC.39.1.66.
3
De-Nol stimulates gastric and duodenal alkaline secretion through prostaglandin dependent mechanism.
得乐通过前列腺素依赖机制刺激胃和十二指肠碱性分泌。
Gut. 1987 Dec;28(12):1557-63. doi: 10.1136/gut.28.12.1557.
4
Mechanism of action of nonantisecretory agents.
Dig Dis Sci. 1988 Oct;33(10):1342. doi: 10.1007/BF01536693.
5
Colloidal bismuth subcitrate. A review of its pharmacodynamic and pharmacokinetic properties, and its therapeutic use in peptic ulcer disease.枸橼酸铋钾。对其药效学和药代动力学特性及其在消化性溃疡疾病中的治疗应用的综述。
Drugs. 1988 Aug;36(2):132-57. doi: 10.2165/00003495-198836020-00002.
6
Effect of bismuth subcitrate on amphibian gastroduodenal bicarbonate secretion.枸橼酸铋对两栖类动物胃十二指肠碳酸氢盐分泌的影响。
Gut. 1989 Jul;30(7):917-21. doi: 10.1136/gut.30.7.917.
7
Effect of bismuth subcitrate and sucralfate on rat duodenal and human gastric bicarbonate secretion in vivo.枸橼酸铋钾和硫糖铝对大鼠十二指肠及人胃碳酸氢盐分泌的体内效应。
Gut. 1990 Jan;31(1):26-31. doi: 10.1136/gut.31.1.26.
8
Helicobacter pylori: bridging the credibility gap.幽门螺杆菌:弥合可信度差距。
Gut. 1990 Aug;31(8):940-5. doi: 10.1136/gut.31.8.940.
9
Colloidal bismuth subcitrate-induced changes on gastric mucosal hemodynamics in the rat: gastric mucosal blood flow after CBS treatment.枸橼酸铋钾对大鼠胃黏膜血流动力学的影响:CBS治疗后的胃黏膜血流量
Gastroenterol Jpn. 1991 Jun;26(3):283-6. doi: 10.1007/BF02781915.
10
Effect of Helicobacter pylori infection on colloidal bismuth subcitrate concentration in gastric mucus.幽门螺杆菌感染对胃黏液中枸橼酸铋钾浓度的影响。
Gut. 1992 May;33(5):592-6. doi: 10.1136/gut.33.5.592.