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花青素在大鼠体内可从小肠被有效吸收。

Anthocyanins are efficiently absorbed from the small intestine in rats.

作者信息

Talavéra Séverine, Felgines Catherine, Texier Odile, Besson Catherine, Manach Claudine, Lamaison Jean-Louis, Rémésy Christian

机构信息

Laboratoire de Pharmacognosie, Faculté de Pharmacie, 63001 Clermont-Ferrand, France.

出版信息

J Nutr. 2004 Sep;134(9):2275-9. doi: 10.1093/jn/134.9.2275.

Abstract

Anthocyanins are natural pigments that possess antioxidant activities and are implicated in various health effects. Recent studies showed that the stomach is a site of anthocyanin absorption. However, the fate of anthocyanins in the small intestine remains unknown. We therefore investigated anthocyanin absorption after in situ perfusion of the jejunum + ileum in rats. The intestine was perfused for 45 min with a physiological buffer supplemented with various anthocyanins. Purified anthocyanin glycosides (9.2 nmol/min) or blackberry (9.0 nmol/min) or bilberry (45.2 nmol/min) anthocyanins were perfused. A high proportion of anthocyanin glycosides was absorbed through the small intestine after perfusion. The rate of absorption was influenced by the chemical structure of the anthocyanin and varied from 10.7 (malvidin 3-glucoside) to 22.4% (cyanidin 3-glucoside). Regardless of the anthocyanins perfused, only glycosides were recovered in the intestinal lumen. After perfusion of a high amount of blackberry anthocyanins (600 nmol/min), native cyanidin 3-glucoside was recovered in urine and plasma from the aorta and mesenteric vein. Methylated and/or glucuronidated derivatives were also identified. Analysis of bile samples revealed that cyanidin 3-glucoside and its methylated derivatives (peonidin 3-glucoside + peonidin glucuronide) quickly appeared in bile. This study demonstrated that anthocyanin glycosides are rapidly and efficiently absorbed from the small intestine. Furthermore, anthocyanins are quickly metabolized and excreted into bile and urine as intact glycosides as well as methylated forms and glucuronidated derivatives.

摘要

花青素是具有抗氧化活性的天然色素,与多种健康效应有关。最近的研究表明,胃是花青素吸收的部位。然而,花青素在小肠中的命运仍不清楚。因此,我们研究了大鼠空肠+回肠原位灌注后花青素的吸收情况。用补充了各种花青素的生理缓冲液对肠道进行45分钟的灌注。灌注了纯化的花青素糖苷(9.2纳摩尔/分钟)或黑莓(9.0纳摩尔/分钟)或越橘(45.2纳摩尔/分钟)花青素。灌注后,高比例的花青素糖苷通过小肠被吸收。吸收速率受花青素化学结构的影响,从10.7%(矢车菊素3-葡萄糖苷)到22.4%(花青素3-葡萄糖苷)不等。无论灌注何种花青素,在肠腔中只回收了糖苷。在灌注大量黑莓花青素(600纳摩尔/分钟)后,在主动脉和肠系膜静脉的尿液和血浆中回收了天然的花青素3-葡萄糖苷。还鉴定出了甲基化和/或葡萄糖醛酸化衍生物。胆汁样本分析显示,花青素3-葡萄糖苷及其甲基化衍生物(芍药素3-葡萄糖苷+芍药素葡萄糖醛酸苷)迅速出现在胆汁中。这项研究表明,花青素糖苷能从小肠快速有效地吸收。此外,花青素会迅速代谢,并以完整的糖苷以及甲基化形式和葡萄糖醛酸化衍生物的形式排泄到胆汁和尿液中。

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