• 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

组胺及某些H2拮抗剂对胃“体外”分泌的作用

Action of histamine and of some H2-antagonists on gastric secretion 'in vitro'.

作者信息

Coruzzi G, Adami M, Bertaccini G

出版信息

Agents Actions. 1984 Apr;14(3-4):516-21. doi: 10.1007/BF01973862.

DOI:10.1007/BF01973862
PMID:6145338
Abstract

The effect of histamine and of some H2-antagonists on isolated gastric mucosal preparation from immature (14-18 days) rats, was investigated. Basal secretion varied, in our experimental conditions, between 1.06 and 3.54 mumol cm-2 h-1, reaching higher values (approximately 4.6 mumol cm-2 h-1) only in a small percentage of animals (10%). Histamine exerted a concentration-dependent stimulation of acid secretion in concentrations varying between 2 X 10(-6) and 1.6 X 10(-4) M. The response to histamine was competitively antagonized by ranitidine (pA2 value = 6.78) and by 4(5)-(4- isopropylaminomethyleniminophenyl ) imidazole (compound marked DA 4577) (pA2 value = 7.37). Oxmetidine acted as a competitive antagonist only for concentrations as low as 10(-8) M; higher concentrations (10(-7) and 10(-6) M) determined a non-competitive inhibition. Ranitidine and compound marked DA 4577 did not affect basal secretion up to concentrations of 3 X 10(-4) M. On the contrary oxmetidine exerted a concentration-dependent inhibition starting from 10(-5) M. Since in our experimental conditions the role of calcium ions in the regulation of basal secretion could not be established, the mechanism of action of oxmetidine was not completely clarified, even if an interference in the utilization of calcium ions may be suggested. In any case it is deemed of interest that this H2-antagonist was the only compound capable of inducing a reversible complete inhibition of basal acid secretion (only KSCN, in very high concentrations, had a similar behaviour).

摘要

研究了组胺及一些H2拮抗剂对未成熟(14 - 18天)大鼠离体胃黏膜制剂的作用。在我们的实验条件下,基础分泌量在1.06至3.54 μmol·cm-2·h-1之间变化,仅在一小部分动物(10%)中达到较高值(约4.6 μmol·cm-2·h-1)。组胺在2×10(-6)至1.6×10(-4) M的浓度范围内对胃酸分泌产生浓度依赖性刺激。雷尼替丁(pA2值 = 6.78)和4(5)-(4 - 异丙基氨基亚甲基亚氨基苯基)咪唑(标记为DA 4577的化合物)(pA2值 = 7.37)对组胺的反应具有竞争性拮抗作用。奥美替丁仅在低至10(-8) M的浓度下作为竞争性拮抗剂起作用;较高浓度(10(-7)和10(-6) M)则产生非竞争性抑制。雷尼替丁和标记为DA 4577的化合物在浓度高达3×10(-4) M时不影响基础分泌。相反,奥美替丁从10(-5) M开始产生浓度依赖性抑制。由于在我们的实验条件下无法确定钙离子在基础分泌调节中的作用,奥美替丁的作用机制尚未完全阐明,尽管可能提示其对钙离子利用有干扰。无论如何,值得关注的是,这种H2拮抗剂是唯一能够诱导基础胃酸分泌可逆性完全抑制的化合物(只有高浓度的硫氰酸钾有类似行为)。

相似文献

1
Action of histamine and of some H2-antagonists on gastric secretion 'in vitro'.组胺及某些H2拮抗剂对胃“体外”分泌的作用
Agents Actions. 1984 Apr;14(3-4):516-21. doi: 10.1007/BF01973862.
2
Action of the new H2-antagonist, DA 4577, on different in vitro and in vivo preparations.新型H2拮抗剂DA 4577对不同体外和体内制剂的作用。
Agents Actions. 1984 Apr;14(3-4):510-5. doi: 10.1007/BF01973861.
3
Some in vitro and in vivo actions of the new histamine H2-receptor antagonist, ranitidine.新型组胺H2受体拮抗剂雷尼替丁的一些体外和体内作用。
Br J Pharmacol. 1981 Jan;72(1):49-54. doi: 10.1111/j.1476-5381.1981.tb09103.x.
4
Pharmacology of JB-9315, a new selective histamine H2-receptor antagonist.新型选择性组胺H2受体拮抗剂JB-9315的药理学
Gen Pharmacol. 1998 Feb;30(2):181-9. doi: 10.1016/s0306-3623(97)00157-2.
5
FR145715, a novel histamine H2 receptor antagonist, with specific anti-Helicobacter pylori activities.FR145715,一种新型组胺H2受体拮抗剂,具有特异性抗幽门螺杆菌活性。
Eur J Pharmacol. 1999 Aug 13;378(3):299-310. doi: 10.1016/s0014-2999(99)00466-5.
6
Rat gastric secretion "in vitro": interaction between histamine and various antisecretagogues acting by different mechanisms.大鼠胃分泌“体外”:组胺与通过不同机制起作用的各种抗分泌剂之间的相互作用。
Pharmacol Res Commun. 1985 Nov;17(11):1027-41. doi: 10.1016/0031-6989(85)90109-2.
7
Comparative study with oxmetidine and ranitidine on acid secretion and gastrin release in the dog.奥美替丁与雷尼替丁对犬胃酸分泌和胃泌素释放影响的比较研究。
Int J Tissue React. 1984;6(2):181-4.
8
Pharmacological analysis of the CCKB/gastrin receptors mediating pentagastrin-stimulated gastric acid secretion in the isolated stomach of the immature rat.对介导未成熟大鼠离体胃中五肽胃泌素刺激胃酸分泌的CCKB/胃泌素受体的药理学分析。
Br J Pharmacol. 1996 Dec;119(7):1401-10. doi: 10.1111/j.1476-5381.1996.tb16052.x.
9
Effects of H2-receptor antagonists on prolactin secretion: specificity and mediation of the response.
Acta Endocrinol (Copenh). 1987 Aug;115(4):461-8. doi: 10.1530/acta.0.1150461.
10
Gastric acid response to topical or intravenous histamine and topical H2-receptor blockade in dogs.犬胃酸对局部或静脉注射组胺及局部H2受体阻断的反应。
Agents Actions. 1981 Nov;11(5):437-41. doi: 10.1007/BF02004703.

引用本文的文献

1
Effects of cannabinoid receptor agonists on rat gastric acid secretion: discrepancy between in vitro and in vivo data.大麻素受体激动剂对大鼠胃酸分泌的影响:体外和体内数据的差异
Dig Dis Sci. 2006 Feb;51(2):310-7. doi: 10.1007/s10620-006-3130-2.
2
Cardiac and gastric effects of histamine H2 receptor antagonists: no evidence for a correlation between lipophilicity and receptor affinity.组胺H2受体拮抗剂对心脏和胃部的作用:没有证据表明亲脂性与受体亲和力之间存在相关性。
Br J Pharmacol. 1996 Aug;118(7):1813-21. doi: 10.1111/j.1476-5381.1996.tb15608.x.
3
Different activities of impromidine and related phenyl-(pyridylalkyl)guanidines at cardiac and gastric H2 receptors.

本文引用的文献

1
EFFECTS OF REMOVAL OF CALCIUM FROM BATHING MEDIA ON FROG STOMACH.从浴液中去除钙对蛙胃的影响
Am J Physiol. 1965 Jul;209:134-40. doi: 10.1152/ajplegacy.1965.209.1.134.
2
Some quantitative uses of drug antagonists.药物拮抗剂的一些定量应用。
Br J Pharmacol Chemother. 1959 Mar;14(1):48-58. doi: 10.1111/j.1476-5381.1959.tb00928.x.
3
Calcium and stimulus-secretion coupling in gastric fundic mucosa. Effect of inhibition of calcium transport by verapamil on gastric acid secretion in the isolated guinea pig fundic mucosa and in healthy subjects.
脒基丁脲及相关苯基-(吡啶基烷基)胍在心脏和胃H2受体上的不同活性。
Inflamm Res. 1995 Apr;44 Suppl 1:S108-9. doi: 10.1007/BF01674420.
4
The new potent and selective histamine H2 receptor agonist amthamine as a tool to study gastric secretion.新型强效选择性组胺H2受体激动剂安他明作为研究胃分泌的工具。
Naunyn Schmiedebergs Arch Pharmacol. 1993 Jul;348(1):77-81. doi: 10.1007/BF00168540.
5
Action of the new H2-antagonist, DA 4577, on different in vitro and in vivo preparations.新型H2拮抗剂DA 4577对不同体外和体内制剂的作用。
Agents Actions. 1984 Apr;14(3-4):510-5. doi: 10.1007/BF01973861.
6
Inhibitory effect of misoprostol on gastric acid secretion in vitro. Qualitative differences from natural prostaglandins.米索前列醇对胃酸分泌的体外抑制作用。与天然前列腺素的质性差异。
Dig Dis Sci. 1988 Oct;33(10):1265-8. doi: 10.1007/BF01536677.
7
Effects of Ca2+ ions on gastric acid secretion by the rat isolated stomach.钙离子对大鼠离体胃胃酸分泌的影响。
Agents Actions. 1986 Apr;18(1-2):201-4. doi: 10.1007/BF01988021.
8
Pharmacology of the novel H2 antagonist famotidine: in vitro studies.新型H2拮抗剂法莫替丁的药理学:体外研究
Agents Actions. 1986 Nov;19(3-4):180-7. doi: 10.1007/BF01966204.
9
Effect of glucagon on gastric acid secretion by the isolated fundus from immature rats.胰高血糖素对未成熟大鼠离体胃底胃酸分泌的影响。
Agents Actions. 1988 Apr;23(3-4):280-2. doi: 10.1007/BF02142564.
10
Effect of histamine on gastric acid secretion "in vitro": interference with endogenous prostaglandins.
Agents Actions. 1990 Apr;30(1-2):188-90. doi: 10.1007/BF01969034.
胃底黏膜中的钙与刺激-分泌偶联。维拉帕米抑制钙转运对离体豚鼠胃底黏膜及健康受试者胃酸分泌的影响。
Scand J Gastroenterol. 1982 Jun;17(4):533-8. doi: 10.3109/00365528209182245.
4
Action of the new H2-antagonist, DA 4577, on different in vitro and in vivo preparations.新型H2拮抗剂DA 4577对不同体外和体内制剂的作用。
Agents Actions. 1984 Apr;14(3-4):510-5. doi: 10.1007/BF01973861.
5
Cardiac effects of the new H2-receptor antagonists.新型H2受体拮抗剂的心脏效应。
Agents Actions. 1983 Apr;13(2-3):173-8. doi: 10.1007/BF01967325.
6
Effect of some new H2-receptor antagonists on gastrointestinal motility.某些新型H2受体拮抗剂对胃肠动力的影响。
Agents Actions. 1983 Apr;13(2-3):157-62. doi: 10.1007/BF01967321.
7
Estimation of pKB values for histamine H2-receptor antagonists using an in vitro acid secretion assay.使用体外胃酸分泌试验估算组胺H2受体拮抗剂的pKB值。
Br J Pharmacol. 1980 Mar;68(3):413-23. doi: 10.1111/j.1476-5381.1980.tb14555.x.
8
The rat isolated stomach sheet; an in vitro model for the study of the physiology and pharmacology of gastric acid secretion.大鼠离体胃片:一种用于研究胃酸分泌生理和药理学的体外模型。
J Pharmacol Methods. 1982 Nov;8(3):197-212. doi: 10.1016/0160-5402(82)90074-2.
9
Effect of some new Histamine H2-receptor antagonists on the guinea-pig papillary muscle.某些新型组胺H2受体拮抗剂对豚鼠乳头肌的作用。
Naunyn Schmiedebergs Arch Pharmacol. 1981 Nov;317(3):225-7. doi: 10.1007/BF00503821.
10
A comparison of the effects of sympathomimetic agents on gastric acid secretion by the rat stomach in vivo and in vitro.拟交感神经药对大鼠胃体内和体外胃酸分泌影响的比较。
J Physiol. 1981 Jul;316:11-21. doi: 10.1113/jphysiol.1981.sp013768.