Schweigert Florian J, Trüpschuch Annett, Hantschel Claudia
Institute of Nutritional Science, University of Potsdam, Potsdam-Rehbrücke, Germany.
Ann Nutr Metab. 2002;46(5):200-4. doi: 10.1159/000065407.
BACKGROUND/AIMS: The absorption of beta-carotene is closely associated with the absorption of dietary fats in the duodenum. Aim of the study was to evaluate two different surfactants, taurocholate and Pluronic L-81, which are known to stimulate or inhibit the absorption of dietary fats, respectively with regard to the absorption of beta-carotene and tissue accumulation of beta-carotene and vitamin A.
Rats were kept on a vitamin-A- deficient diet for 4 weeks and then either kept on this diet or fed this diet enriched with beta-carotene (200 mg/kg feed) alone or in combination with taurocholate (10 g/kg) or Pluronic L-81 (5 ml/kg) for another two weeks.
beta-carotene was not detectable in liver or plasma of rats fed the deficient diet. The supplementation of beta-carotene alone led to an increase of beta-carotene in plasma and organs (p < 0.05) and resulted in an increase of vitamin A in the liver (p < 0.01), indicating its conversion. The addition of taurocholate enhanced the absorption of beta-carotene (p < 0.01), but had little affect on the levels of total vitamin A in the liver. In contrast, Pluronic L-81 caused a reduced uptake of beta-carotene as indicated by lower concentrations in plasma and liver (p < 0.01) as well as reduced total vitamin A levels in the liver (p < 0.01) either caused by the reduced availability of beta-carotene or a reduced conversion into vitamin A.
The study shows that surfactants can modulate beta-carotene absorption differently. The results for taurocholate confirm known observations concerning an enhanced absorption of beta-carotene. Pluronic L-81 might diminish the uptake of beta-carotene into the enterocyte, which would be in disagreement with regard to its function in the absorption of total lipids in general, or might effect the excretion into the blood by modulation chylomicron secretion.
背景/目的:β-胡萝卜素的吸收与十二指肠中膳食脂肪的吸收密切相关。本研究的目的是评估两种不同的表面活性剂,牛磺胆酸盐和普朗尼克L-81,已知它们分别刺激或抑制膳食脂肪的吸收,观察其对β-胡萝卜素吸收以及β-胡萝卜素和维生素A在组织中的蓄积情况的影响。
将大鼠置于维生素A缺乏饮食4周,然后继续维持该饮食,或单独给予富含β-胡萝卜素(200mg/kg饲料)的饮食,或与牛磺胆酸盐(10g/kg)或普朗尼克L-81(5ml/kg)联合使用,再持续两周。
喂食缺乏饮食的大鼠肝脏或血浆中未检测到β-胡萝卜素。单独补充β-胡萝卜素导致血浆和器官中β-胡萝卜素增加(p<0.05),并使肝脏中维生素A增加(p<0.01),表明其发生了转化。添加牛磺胆酸盐增强了β-胡萝卜素的吸收(p<0.01),但对肝脏中总维生素A水平影响不大。相比之下,普朗尼克L-81导致β-胡萝卜素摄取减少,表现为血浆和肝脏中浓度较低(p<0.01),以及肝脏中总维生素A水平降低(p<0.01),这可能是由于β-胡萝卜素可用性降低或转化为维生素A减少所致。
该研究表明表面活性剂可不同程度地调节β-胡萝卜素的吸收。牛磺胆酸盐的结果证实了关于β-胡萝卜素吸收增强的已知观察结果。普朗尼克L-81可能会减少β-胡萝卜素进入肠细胞的摄取,这与其在一般总脂质吸收中的功能不一致,或者可能通过调节乳糜微粒分泌影响其向血液中的排泄。