The Modulation of Chitosan Oligosaccharides on High-fat and High-fructose Corn Syrup Induced Hepatic Manifestations of the Metabolic Syndrome in Murine Model

碩士 === 東海大學 === 畜產與生物科技學系 === 104 === In recent years, changes in Taiwanese dietary may cause hepatic manifestations of the metabolic syndrome (HMMS). It is associated with the increased fat and fructose consumption observed in the Western diet. Non-alcoholic fatty liver disease (NAFLD) accounts...

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Main Authors: Chia-Hao Hsu, 許家豪
Other Authors: Chang-Chi Hsieh
Format: Others
Language:zh-TW
Published: 2016
Online Access:http://ndltd.ncl.edu.tw/handle/88042727767149751958
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spelling ndltd-TW-104THU002890032016-08-12T04:14:41Z http://ndltd.ncl.edu.tw/handle/88042727767149751958 The Modulation of Chitosan Oligosaccharides on High-fat and High-fructose Corn Syrup Induced Hepatic Manifestations of the Metabolic Syndrome in Murine Model 殼寡糖對高脂與高果糖玉米糖漿誘導肝代謝綜合症小鼠模式之調節作用 Chia-Hao Hsu 許家豪 碩士 東海大學 畜產與生物科技學系 104 In recent years, changes in Taiwanese dietary may cause hepatic manifestations of the metabolic syndrome (HMMS). It is associated with the increased fat and fructose consumption observed in the Western diet. Non-alcoholic fatty liver disease (NAFLD) accounts for the majority of chronic liver diseases. It shows high prevalence in almost one third of adults and most obese individuals in those countries. In this study, we want to evaluate of chitosan oligosaccharides (COS) against the onset of HMMs induced by 60% high-fat diet and 30% high-fructose corn syrup in drinking water (HFFD). Mice were divided into five groups, the naive group, the HFFD control group and HFFD with oral chitosan oligosaccharides (150, 300, 600 mg/kg) group, respectively. Serum aspartate transaminase (sAST), triglyceride (TG), total cholesterol (TC) determination in serum or liver and oral glucose tolerance test (OGTT), cytokines in liver, and lipid accumulation in liver tissue sections were determinate by Oil-Red O staining, H&E staining and immunohistochemistry staining for 4-hydroxynonenal (4-HNE), Toll-like receptor (TLR-4) and thymic stromal lymphopoietin (TSLP). Our result indicated COS could reduce mice weight, lipid weight, sAST, sTG and hepatic TG. Furthermore, COS could regulate hepatic interleukin-1β (IL-1β), interleukin 6 (IL-6), tumor necrosis factor α (TNF-α), transforming growth factor β1 (TGF-β1), thymic stromal lymphopoietin (TSLP), interferon γ (IFN-γ) and interleukin 4 (IL-4). In addition, the histology stained by Oil-Red O staining, H&E staining and immunohistochemistry staining for 4-hydroxynonenal (4-HNE), Toll-like receptor (TLR-4) and thymic stromal lymphopoietin (TSLP) revealed COS could decreased lipid accumulation and oxidative stress. According to these results, it is suggested that COS could improve lipid accumulation and inflammatory in HMMS. Chang-Chi Hsieh 謝長奇 2016 學位論文 ; thesis 98 zh-TW
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description 碩士 === 東海大學 === 畜產與生物科技學系 === 104 === In recent years, changes in Taiwanese dietary may cause hepatic manifestations of the metabolic syndrome (HMMS). It is associated with the increased fat and fructose consumption observed in the Western diet. Non-alcoholic fatty liver disease (NAFLD) accounts for the majority of chronic liver diseases. It shows high prevalence in almost one third of adults and most obese individuals in those countries. In this study, we want to evaluate of chitosan oligosaccharides (COS) against the onset of HMMs induced by 60% high-fat diet and 30% high-fructose corn syrup in drinking water (HFFD). Mice were divided into five groups, the naive group, the HFFD control group and HFFD with oral chitosan oligosaccharides (150, 300, 600 mg/kg) group, respectively. Serum aspartate transaminase (sAST), triglyceride (TG), total cholesterol (TC) determination in serum or liver and oral glucose tolerance test (OGTT), cytokines in liver, and lipid accumulation in liver tissue sections were determinate by Oil-Red O staining, H&E staining and immunohistochemistry staining for 4-hydroxynonenal (4-HNE), Toll-like receptor (TLR-4) and thymic stromal lymphopoietin (TSLP). Our result indicated COS could reduce mice weight, lipid weight, sAST, sTG and hepatic TG. Furthermore, COS could regulate hepatic interleukin-1β (IL-1β), interleukin 6 (IL-6), tumor necrosis factor α (TNF-α), transforming growth factor β1 (TGF-β1), thymic stromal lymphopoietin (TSLP), interferon γ (IFN-γ) and interleukin 4 (IL-4). In addition, the histology stained by Oil-Red O staining, H&E staining and immunohistochemistry staining for 4-hydroxynonenal (4-HNE), Toll-like receptor (TLR-4) and thymic stromal lymphopoietin (TSLP) revealed COS could decreased lipid accumulation and oxidative stress. According to these results, it is suggested that COS could improve lipid accumulation and inflammatory in HMMS.
author2 Chang-Chi Hsieh
author_facet Chang-Chi Hsieh
Chia-Hao Hsu
許家豪
author Chia-Hao Hsu
許家豪
spellingShingle Chia-Hao Hsu
許家豪
The Modulation of Chitosan Oligosaccharides on High-fat and High-fructose Corn Syrup Induced Hepatic Manifestations of the Metabolic Syndrome in Murine Model
author_sort Chia-Hao Hsu
title The Modulation of Chitosan Oligosaccharides on High-fat and High-fructose Corn Syrup Induced Hepatic Manifestations of the Metabolic Syndrome in Murine Model
title_short The Modulation of Chitosan Oligosaccharides on High-fat and High-fructose Corn Syrup Induced Hepatic Manifestations of the Metabolic Syndrome in Murine Model
title_full The Modulation of Chitosan Oligosaccharides on High-fat and High-fructose Corn Syrup Induced Hepatic Manifestations of the Metabolic Syndrome in Murine Model
title_fullStr The Modulation of Chitosan Oligosaccharides on High-fat and High-fructose Corn Syrup Induced Hepatic Manifestations of the Metabolic Syndrome in Murine Model
title_full_unstemmed The Modulation of Chitosan Oligosaccharides on High-fat and High-fructose Corn Syrup Induced Hepatic Manifestations of the Metabolic Syndrome in Murine Model
title_sort modulation of chitosan oligosaccharides on high-fat and high-fructose corn syrup induced hepatic manifestations of the metabolic syndrome in murine model
publishDate 2016
url http://ndltd.ncl.edu.tw/handle/88042727767149751958
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