Suppr超能文献

大鼠体内脂肪替代品蔗糖聚酯和三羧酸三酯对秋水仙碱吸收的抑制作用。

Inhibition of colchicine absorption by the fat substitutes, sucrose polyester and tricarballylate triester, in the rat.

作者信息

Benmoussa K, Scherrmann J M, Bourre J M

机构信息

INSERM U26, Hôpital Fernand WIDAL, Paris, France.

出版信息

Life Sci. 1995;56(2):117-24. doi: 10.1016/0024-3205(94)00421-n.

Abstract

The effect of non-absorbable fat substitutes (sucrose polyester (SPE) and tricarballylate triester (TCTE)) on the enterohepatic circulation of colchicine was studied in the rat. In a first experiment, emulsions of either sunflower oil (SFO), SPE, or TCTE, were introduced into the ligated small intestine and compared to a control group receiving physiological saline. All the groups received colchicine as an intravenous bolus. The plasma levels of colchicine in all groups was not affected, and luminal samples indicated that SPE and TCTE have no influence on the biliary excretion of colchicine (a previous experiment in bile duct-cannulated rats showed that SPE and TCTE, introduced by intragastric tube, have no effect on bile flow rate). In a second experiment, colchicine diluted in bile was mixed with saline or emulsions of either SFO, SPE or TCTE, and introduced into the ligated small intestine. The area under the curve and the maximal plasma concentration of colchicine were reduced when the drug was mixed with SPE or TCTE rather than saline (p < 0.0005). After 150 min, luminal samples were taken and showed significantly higher (p < 0.034) concentrations of colchicine in both SPE and TCTE groups compared to the saline group, indicating a significant inhibition of reabsorption of biliary colchicine. In conclusion, the non-absorbable fat substitutes, SPE and TCTE, did not influence biliary excretion of colchicine but reduced its reabsorption, thus altering its enterohepatic circulation.

摘要

在大鼠中研究了不可吸收的脂肪替代品(蔗糖聚酯(SPE)和柠檬酸三酯(TCTE))对秋水仙碱肝肠循环的影响。在第一个实验中,将向日葵油(SFO)、SPE或TCTE的乳剂引入结扎的小肠,并与接受生理盐水的对照组进行比较。所有组均静脉推注秋水仙碱。所有组中秋水仙碱的血浆水平均未受影响,管腔样本表明SPE和TCTE对秋水仙碱的胆汁排泄没有影响(先前在胆管插管大鼠中的实验表明,通过胃管引入的SPE和TCTE对胆汁流速没有影响)。在第二个实验中,将稀释在胆汁中的秋水仙碱与生理盐水或SFO、SPE或TCTE的乳剂混合,并引入结扎的小肠。当药物与SPE或TCTE混合而不是与生理盐水混合时,秋水仙碱的曲线下面积和最大血浆浓度降低(p<0.0005)。150分钟后,采集管腔样本,结果显示与生理盐水组相比,SPE和TCTE组中秋水仙碱的浓度显著更高(p<0.034),表明胆汁中秋水仙碱的重吸收受到显著抑制。总之,不可吸收的脂肪替代品SPE和TCTE不影响秋水仙碱的胆汁排泄,但减少了其重吸收,从而改变了其肝肠循环。

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