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血管灌注大鼠小肠:一种药物吸收的研究模型

Vascularly perfused rat small intestine: a research model for drug absorption.

作者信息

Sakai K, Akima M, Hinohara Y, Sasaki M, Niki R

出版信息

Jpn J Pharmacol. 1980 Apr;30(2):231-41. doi: 10.1254/jjp.30.231.

Abstract

Rat isolated small intestine was perfused at a fixed flow rate through the superior mesenteric artery with whole rat blood recycled from a devised oxygenator-reservoir. As indicated by perfusion pressure, tissue glucose and oxygen consumption, and histological studies, the perfused intestine remained in a viable state over the perfusion period of 2 hr. Rapid absorption of glucose from the intestinal tract was observed after the intraduodenal injection. When single doses of acetaminophen were injected into the duodenal lumen or poured over the perfused intestine, the absorption was rapid and dose-dependent. Shortly after single intraduodenal injections of salicylamide, salicylamide in free and conjugated forms (sulfate and glucuronide) appeared in the circulating blood. These results indicate that the vascularly perfused intestinal preparation has wide applications in biochemical experimental fields.

摘要

用从特制的氧合器-储液器循环的全鼠血液,以固定流速通过肠系膜上动脉对大鼠离体小肠进行灌注。根据灌注压力、组织葡萄糖和氧消耗以及组织学研究表明,在2小时的灌注期内,灌注的小肠保持存活状态。十二指肠内注射后观察到葡萄糖从肠道快速吸收。当将单剂量对乙酰氨基酚注入十二指肠腔或倾注在灌注的小肠上时,吸收迅速且呈剂量依赖性。在十二指肠单次注射水杨酰胺后不久,游离和结合形式(硫酸盐和葡萄糖醛酸苷)的水杨酰胺出现在循环血液中。这些结果表明,血管灌注的肠道制剂在生化实验领域有广泛应用。

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