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抗酸剂对结合胆汁酸的体外结合特性

Binding properties in vitro of antacids for conjugated bile acids.

作者信息

Clain J E, Malagelada J R, Chadwick V S, Hofmann A F

出版信息

Gastroenterology. 1977 Sep;73(3):556-9.

PMID:19335
Abstract

The binding properties of various commercial antacids for pure conjugated bile acids in an aqueous solution or the bile acids present in human gallbladder bile were characterized. Aluminum hydroxide was a potent binding agent, similar in affinity and capacity to cholestyramine. With aluminum hydroxide, dihydroxy bile acid conjugates were bound more strongly than trihydroxy bile acid conjugates, and glycine conjugates were bound more strongly than taurine conjugates; pH had no effect per se on binding. Magnesium hydroxide and aluminum phosphate bound bile acids much more weakly. Aluminum hydroxide warrants exploration in therapeutic situations in which bile acid binding is sought.

摘要

对各种市售抗酸剂与水溶液中纯共轭胆汁酸或人胆囊胆汁中存在的胆汁酸的结合特性进行了表征。氢氧化铝是一种有效的结合剂,其亲和力和结合能力与消胆胺相似。对于氢氧化铝,二羟基胆汁酸共轭物的结合比三羟基胆汁酸共轭物更强,甘氨酸共轭物的结合比牛磺酸共轭物更强;pH本身对结合没有影响。氢氧化镁和磷酸铝对胆汁酸的结合要弱得多。在寻求胆汁酸结合的治疗情况下,氢氧化铝值得探索。

相似文献

1
Binding properties in vitro of antacids for conjugated bile acids.抗酸剂对结合胆汁酸的体外结合特性
Gastroenterology. 1977 Sep;73(3):556-9.
2
Adsorption of bile acids by sucralfate, antacids, and cholestyramine in vitro.硫糖铝、抗酸剂和考来烯胺在体外对胆汁酸的吸附作用。
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[Binding of bile acids to antacids].[胆汁酸与抗酸剂的结合]
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Effects of bile acids, antacids, and cholestyramine on transmural electrical potential difference in man.胆汁酸、抗酸剂和消胆胺对人体跨壁电位差的影响。
Acta Hepatogastroenterol (Stuttg). 1978 Oct;25(5):369-75.
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Mechanistic study of inhibition of levofloxacin absorption by aluminum hydroxide.氢氧化铝对左氧氟沙星吸收抑制作用的机制研究
Antimicrob Agents Chemother. 1993 Oct;37(10):2173-8. doi: 10.1128/AAC.37.10.2173.
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Effects of cholestyramine and synthetic hydrotalcite on acute gastric or intestinal lesion formation in rats and dogs.
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In vitro adsorption of bile salts and aspirin to sucralfate.硫糖铝对胆盐和阿司匹林的体外吸附作用
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In vitro bile acid adsorption by bismuth subsalicylate and montmorillonite.次水杨酸铋和蒙脱石对胆汁酸的体外吸附作用
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