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Lycium barbarum L. Polysaccharide (LBP) Reduces Glucose Uptake via Down-Regulation of SGLT-1 in Caco2 Cell

Lycium barbarum L. polysaccharide (LBP) is prepared from Lycium barbarum L. (L. barbarum), which is a traditional Chinese medicine. LPB has been shown to have hypoglycemic effects. In order to gain some mechanistic insights on the hypoglycemic effects of LBP, we investigated the uptake of LBP and it...

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Autores principales: Cai, Huizhen, Yang, Xiaohui, Cai, Qian, Ren, Binbin, Qiu, Hongyan, Yao, Zhiqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155582/
https://www.ncbi.nlm.nih.gov/pubmed/28241438
http://dx.doi.org/10.3390/molecules22020341
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author Cai, Huizhen
Yang, Xiaohui
Cai, Qian
Ren, Binbin
Qiu, Hongyan
Yao, Zhiqing
author_facet Cai, Huizhen
Yang, Xiaohui
Cai, Qian
Ren, Binbin
Qiu, Hongyan
Yao, Zhiqing
author_sort Cai, Huizhen
collection PubMed
description Lycium barbarum L. polysaccharide (LBP) is prepared from Lycium barbarum L. (L. barbarum), which is a traditional Chinese medicine. LPB has been shown to have hypoglycemic effects. In order to gain some mechanistic insights on the hypoglycemic effects of LBP, we investigated the uptake of LBP and its effect on glucose absorption in the human intestinal epithelial cell line Caco2 cell. The uptake of LBP through Caco2 cell monolayer was time-dependent and was inhibited by phloridzin, a competitive inhibitor of SGLT-1. LPB decreased the absorption of glucose in Caco2 cell, and down-regulated the expression of SGLT-1. These results suggest that LBP might be transported across the human intestinal epithelium through SGLT-1 and it inhibits glucose uptake via down-regulating SGLT-1.
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spelling pubmed-61555822018-11-13 Lycium barbarum L. Polysaccharide (LBP) Reduces Glucose Uptake via Down-Regulation of SGLT-1 in Caco2 Cell Cai, Huizhen Yang, Xiaohui Cai, Qian Ren, Binbin Qiu, Hongyan Yao, Zhiqing Molecules Article Lycium barbarum L. polysaccharide (LBP) is prepared from Lycium barbarum L. (L. barbarum), which is a traditional Chinese medicine. LPB has been shown to have hypoglycemic effects. In order to gain some mechanistic insights on the hypoglycemic effects of LBP, we investigated the uptake of LBP and its effect on glucose absorption in the human intestinal epithelial cell line Caco2 cell. The uptake of LBP through Caco2 cell monolayer was time-dependent and was inhibited by phloridzin, a competitive inhibitor of SGLT-1. LPB decreased the absorption of glucose in Caco2 cell, and down-regulated the expression of SGLT-1. These results suggest that LBP might be transported across the human intestinal epithelium through SGLT-1 and it inhibits glucose uptake via down-regulating SGLT-1. MDPI 2017-02-22 /pmc/articles/PMC6155582/ /pubmed/28241438 http://dx.doi.org/10.3390/molecules22020341 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cai, Huizhen
Yang, Xiaohui
Cai, Qian
Ren, Binbin
Qiu, Hongyan
Yao, Zhiqing
Lycium barbarum L. Polysaccharide (LBP) Reduces Glucose Uptake via Down-Regulation of SGLT-1 in Caco2 Cell
title Lycium barbarum L. Polysaccharide (LBP) Reduces Glucose Uptake via Down-Regulation of SGLT-1 in Caco2 Cell
title_full Lycium barbarum L. Polysaccharide (LBP) Reduces Glucose Uptake via Down-Regulation of SGLT-1 in Caco2 Cell
title_fullStr Lycium barbarum L. Polysaccharide (LBP) Reduces Glucose Uptake via Down-Regulation of SGLT-1 in Caco2 Cell
title_full_unstemmed Lycium barbarum L. Polysaccharide (LBP) Reduces Glucose Uptake via Down-Regulation of SGLT-1 in Caco2 Cell
title_short Lycium barbarum L. Polysaccharide (LBP) Reduces Glucose Uptake via Down-Regulation of SGLT-1 in Caco2 Cell
title_sort lycium barbarum l. polysaccharide (lbp) reduces glucose uptake via down-regulation of sglt-1 in caco2 cell
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155582/
https://www.ncbi.nlm.nih.gov/pubmed/28241438
http://dx.doi.org/10.3390/molecules22020341
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