Physiological effects of food ingredients on intestinal epithelial cell function.

[1]  H. Inui,et al.  Oenothein B in Eucalyptus Leaf Extract Suppresses Fructose Absorption in Caco-2 Cells , 2021, Molecules.

[2]  M. Shimizu,et al.  Inhibitory Effect of Tangeretin and Cardamonin on Human Intestinal SGLT1 Activity In Vitro and Blood Glucose Levels in Mice In Vivo , 2021, Nutrients.

[3]  M. Koziołkiewicz,et al.  Phenolics-Rich Extracts of Dietary Plants as Regulators of Fructose Uptake in Caco-2 Cells via GLUT5 Involvement , 2021, Molecules.

[4]  H. Satsu Regulation of Detoxification Enzymes by Food Components in Intestinal Epithelial Cells , 2019, Food Science and Technology Research.

[5]  M. Himmelsbach,et al.  In Vitro and In Vivo Inhibition of Intestinal Glucose Transport by Guava (Psidium Guajava) Extracts , 2018, Molecular nutrition & food research.

[6]  M. Shimizu,et al.  Suppressive effect of nobiletin and epicatechin gallate on fructose uptake in human intestinal epithelial Caco-2 cells , 2018, Bioscience, biotechnology, and biochemistry.

[7]  H. Satsu Molecular and cellular studies on the absorption, function, and safety of food components in intestinal epithelial cells , 2017, Bioscience, biotechnology, and biochemistry.

[8]  T. Inakuma,et al.  Establishment of a stable aryl hydrocarbon receptor-responsive HepG2 cell line , 2015, Cytotechnology.

[9]  H. Daniel,et al.  Gymnemic acids inhibit sodium-dependent glucose transporter 1. , 2014, Journal of agricultural and food chemistry.

[10]  T. Inakuma,et al.  6-shogaol, a major compound in ginger, induces aryl hydrocarbon receptor-mediated transcriptional activity and gene expression. , 2014, Journal of agricultural and food chemistry.

[11]  M. Shimizu,et al.  Analysis of flavonoids regulating the expression of UGT1A1 via xenobiotic receptors in intestinal epithelial cells. , 2014, BioFactors.

[12]  M. Shimizu,et al.  Induction of NAD(P)H:quinone oxidoreductase 1 expression by cysteine via Nrf2 activation in human intestinal epithelial LS180 cells , 2012, Amino Acids.

[13]  Y. Sugita‐Konishi,et al.  Metabolites of galangin by 2,3,7,8-tetrachlorodibenzo-p-dioxin-inducible cytochrome P450 1A1 in human intestinal epithelial Caco-2 cells and their antagonistic activity toward aryl hydrocarbon receptor. , 2010, Journal of agricultural and food chemistry.

[14]  L. Tappy,et al.  Metabolic effects of fructose and the worldwide increase in obesity. , 2010, Physiological reviews.

[15]  T. Akiyama,et al.  Aryl hydrocarbon receptor suppresses intestinal carcinogenesis in ApcMin/+ mice with natural ligands , 2009, Proceedings of the National Academy of Sciences.

[16]  Bernadette P Marriott,et al.  National estimates of dietary fructose intake increased from 1977 to 2004 in the United States. , 2009, The Journal of nutrition.

[17]  M. Shimizu,et al.  Activation of pregnane X receptor and induction of MDR1 by dietary phytochemicals. , 2008, Journal of agricultural and food chemistry.

[18]  H. Ashida,et al.  TCDD-induced CYP1A1 expression, an index of dioxin toxicity, is suppressed by flavonoids permeating the human intestinal Caco-2 cell monolayers. , 2006, Journal of agricultural and food chemistry.

[19]  A. Kong,et al.  Induction of phase I, II and III drug metabolism/transport by xenobiotics , 2005, Archives of pharmacal research.

[20]  Timothy M Willson,et al.  The nuclear pregnane X receptor: a key regulator of xenobiotic metabolism. , 2002, Endocrine reviews.

[21]  M. E. Hahn,et al.  Aryl hydrocarbon receptors: diversity and evolution. , 2002, Chemico-biological interactions.

[22]  Thomas J. Raub,et al.  Characterization of the human colon carcinoma cell line (Caco-2) as a model system for intestinal epithelial permeability. , 1989, Gastroenterology.