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大鼠经肠胃外和肠内营养后戊巴比妥药代动力学的变化。

Alterations in pentobarbital pharmacokinetics in response to parenteral and enteral alimentation in the rat.

作者信息

Knodell R G, Spector M H, Brooks D A, Keller F X, Kyner W T

出版信息

Gastroenterology. 1980 Dec;79(6):1211-6.

PMID:6777235
Abstract

Recent in vitro observations suggest that the intestine, in addition to the liver, may be an important organ of first-pass drug metabolism. While a variety of changes in intestinal morphology and function in response to continuous parenteral and enteral nutrition have been documented, the effect of different routes of alimentation on intestinal drug metabolism has not been previously investigated. Objectives of this study were to assess the contribution of intestinal pentobarbital metabolism to overall in vivo pentobarbital pharmacokinetics in the rat and to determine if differences in pentobarbital pharmacokinetics were seen between parenterally and enterally nourished animals. After 7 days of continuous infusion of amino acid-glucose mixture via a gastric or jugular vein catheter, pharmacokinetic parameters were determined after 40 mg/kg of pentobarbital was given orally or into the portal or femoral vein. Reduced systemic availability of pentobarbital after oral administration as compared to portal vein injection was seen in both alimentation groups indicating that significant intestinal metabolism of pentobarbital occurred in vivo. Total area under the pentobarbital plasma concentration-time curve was significantly greater in parenterally nourished animals as compared with enterally alimented animals after oral, portal vein and systemic vein drug administration. Differences in pentobarbital, pharmacokinetics between the two alimentation groups appeared to be primarly due to effects on hepatic pentobarbital metabolism. While the mechanism producing these changes has not been defined, differences in gut hormones release and/or pancreatic secretion in response to the two routes of alimentation may be contributory. The widespread use of enteral and parenteral alimentation in clinical medicine suggests that studies to determine if nutrition route of administration similarly influences drug metabolism in humans may be indicated.

摘要

最近的体外观察表明,除肝脏外,肠道可能是药物首过代谢的重要器官。虽然已有文献记载了肠道形态和功能因持续肠外营养和肠内营养而发生的各种变化,但不同营养途径对肠道药物代谢的影响此前尚未得到研究。本研究的目的是评估肠道戊巴比妥代谢对大鼠体内戊巴比妥整体药代动力学的贡献,并确定肠外营养和肠内营养动物之间戊巴比妥药代动力学是否存在差异。通过胃导管或颈静脉导管持续输注氨基酸 - 葡萄糖混合物7天后,在给予40mg/kg戊巴比妥口服、门静脉注射或股静脉注射后测定药代动力学参数。在两个营养组中,口服给药后戊巴比妥的全身可用性均低于门静脉注射,这表明戊巴比妥在体内发生了显著的肠道代谢。在口服、门静脉和全身静脉给药后,肠外营养动物的戊巴比妥血浆浓度 - 时间曲线下总面积显著大于肠内营养动物。两个营养组之间戊巴比妥药代动力学的差异似乎主要是由于对肝脏戊巴比妥代谢的影响。虽然产生这些变化的机制尚未明确,但两种营养途径引起的肠道激素释放和/或胰腺分泌的差异可能起了作用。临床实践中广泛使用肠内营养和肠外营养表明,可能需要开展研究以确定营养给药途径是否同样会影响人体的药物代谢。

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