Abstract

Since many nutrients, including the three major ones of glucose, dipeptides, and cholesterol, are mainly absorbed in the small intestine, the assessment of their effects on intestinal tissue is important for the study of food absorption. However, cultured intestinal cell lines, such as Caco-2 cells, or animal models, which differ from normal human physiological conditions, are generally used for the evaluation of intestinal absorption and digestion. Therefore, it is necessary to develop an alternative in vitro method for more accurate analyses. In this study, we demonstrate inhibitory effects on nutrient absorption through nutrient transporters using three-dimensional xenogeneic-free human intestinal organoids (XF-HIOs), with characteristics of the human intestine, as we previously reported. We first show that the organoids absorbed glucose, dipeptide, and cholesterol in a transporter-dependent manner. Next, we examine the inhibitory effect of natural ingredients on the absorption of glucose and cholesterol. We reveal that glucose absorption was suppressed by epicatechin gallate or nobiletin, normally found in green tea catechin or citrus fruits, respectively. In comparison, cholesterol absorption was not inhibited by luteolin and quercetin, contained in some vegetables. Our findings highlight the usefulness of screening for the absorption of functional food substances using XF-HIOs.

Highlights

  • The small intestine is an organ that is involved many functions, such as absorption, digestion, metabolism, peristalsis, and immune responses [1,2,3,4]

  • Uchida et al have previously reported the successful development of an in vitro intestinal organoid system under xenogeneic-free conditions using human embryonic stem cells or human-induced pluripotent stem cells [14]

  • We showed that xenogeneic-free human intestinal organoids (XF-Human intestinal organoids (HIOs)) had a unique cell structure, similar to that found in previous experiments

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Summary

Introduction

The small intestine is an organ that is involved many functions, such as absorption, digestion, metabolism, peristalsis, and immune responses [1,2,3,4]. Nutrients are mainly assimilated through transporters expressed on the brush border membrane of intestinal epithelial cells. Sodium/Glucose Cotransporter 1 (SGLT1) is a sodium ion gradient-dependent cotransporter and Glucose Transporter Type 2 (GLUT2) facilitates diffusion transport for the absorption of monosaccharide glucose. GLUT2 is present in the intestinal basolateral membrane [5]. With regard to cholesterol absorption, Niemann-Pick C-1-like-1 (NPC1L1) and diffusion transport pathways by micelle formation exist, but about 70% of cholesterol is absorbed via the former [8]. Further details on transporters are required to more fully understand nutrient absorption in the small intestine

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