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大豆Δ5-植物甾醇和植物甾烷醇在人体中的胃肠道吸收及血浆动力学

Gastrointestinal absorption and plasma kinetics of soy Delta(5)-phytosterols and phytostanols in humans.

作者信息

Ostlund Richard E, McGill Janet B, Zeng Chun-Min, Covey Douglas F, Stearns Jay, Stenson William F, Spilburg Curtis A

机构信息

Division of Endocrinology, Diabetes and Metabolism, Washington University School of Medicine, Missouri 63017, USA.

出版信息

Am J Physiol Endocrinol Metab. 2002 Apr;282(4):E911-6. doi: 10.1152/ajpendo.00328.2001.

Abstract

Our objective was to measure the systemic absorption of lecithin-emulsified Delta(5)-phytosterols and phytostanols during test meals by use of dual stable isotopic tracers. Ten healthy subjects underwent two single-meal absorption tests in random order 2 wk apart, one with intravenous dideuterated Delta(5)-phytosterols and oral pentadeuterated Delta(5)-phytosterols and the other with the corresponding labeled stanols. The oral-to-intravenous tracer ratio in plasma, a reflection of absorption, was measured by a sensitive negative ion mass spectroscopic technique and became constant after 2 days. Absorption from 600 mg of Delta(5)-soy sterols given with a standard test breakfast was 0.512 +/- 0.038% for sitosterol and 1.89 +/- 0.27% for campesterol. The absorption from 600 mg of soy stanols was 0.0441 +/- 0.004% for sitostanol and 0.155 +/- 0.017% for campestanol. Reduction of the double bond at position 5 decreased absorption by 90%. Plasma t(1/2) for stanols was significantly shorter than that for Delta(5)-sterols. We conclude that the efficiency of phytosterol absorption is lower than what was reported previously and is critically dependent on the structure of both sterol nucleus and side chain.

摘要

我们的目的是通过使用双稳定同位素示踪剂来测量在测试餐期间卵磷脂乳化的Δ⁵ - 植物甾醇和植物甾烷醇的全身吸收情况。10名健康受试者以随机顺序在相隔2周的时间内进行了两次单餐吸收测试,一次是静脉注射双氘代Δ⁵ - 植物甾醇并口服五氘代Δ⁵ - 植物甾醇,另一次是使用相应标记的甾烷醇。通过灵敏的负离子质谱技术测量血浆中口服示踪剂与静脉注射示踪剂的比例,这反映了吸收情况,并且在2天后变得恒定。与标准测试早餐一起给予600毫克Δ⁵ - 大豆甾醇时,谷甾醇的吸收率为0.512±0.038%,菜油甾醇的吸收率为1.89±0.27%。600毫克大豆甾烷醇中,谷甾烷醇的吸收率为0.0441±0.004%,菜油甾烷醇的吸收率为0.155±0.017%。Δ⁵位双键的减少使吸收率降低了90%。甾烷醇的血浆半衰期明显短于Δ⁵ - 甾醇的血浆半衰期。我们得出结论,植物甾醇的吸收效率低于先前报道的水平,并且严重依赖于甾醇核和侧链的结构。

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