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Citrus ichangensis Peel Extract Exhibits Anti-Metabolic Disorder Effects by the Inhibition of PPARγ and LXR Signaling in High-Fat Diet-Induced C57BL/6 Mouse

Obesity is a common nutritional disorder associated with type 2 diabetes, cardiovascular diseases, dyslipidemia, and certain cancers. In this study, we investigated the effects of Citrus ichangensis peel extract (CIE) in high-fat (HF) diet-induced obesity mice. Female C57BL/6 mice were fed a chow di...

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Autores principales: Ding, Xiaobo, Fan, Shengjie, Lu, Yan, Zhang, Yu, Gu, Ming, Zhang, Lu, Liu, Gaigai, Guo, Lu, Jiang, Dong, Lu, Xiong, Li, Yiming, Zhou, Zhiqin, Huang, Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3536358/
https://www.ncbi.nlm.nih.gov/pubmed/23320036
http://dx.doi.org/10.1155/2012/678592
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author Ding, Xiaobo
Fan, Shengjie
Lu, Yan
Zhang, Yu
Gu, Ming
Zhang, Lu
Liu, Gaigai
Guo, Lu
Jiang, Dong
Lu, Xiong
Li, Yiming
Zhou, Zhiqin
Huang, Cheng
author_facet Ding, Xiaobo
Fan, Shengjie
Lu, Yan
Zhang, Yu
Gu, Ming
Zhang, Lu
Liu, Gaigai
Guo, Lu
Jiang, Dong
Lu, Xiong
Li, Yiming
Zhou, Zhiqin
Huang, Cheng
author_sort Ding, Xiaobo
collection PubMed
description Obesity is a common nutritional disorder associated with type 2 diabetes, cardiovascular diseases, dyslipidemia, and certain cancers. In this study, we investigated the effects of Citrus ichangensis peel extract (CIE) in high-fat (HF) diet-induced obesity mice. Female C57BL/6 mice were fed a chow diet or an HF diet alone or supplemented with 1% w/w CIE for 8 weeks. We found that CIE treatment could lower blood glucose level and improve glucose tolerance. In the HF+CIE group, body weight gain, serum total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-c) levels, and liver triglyceride (TG) and TC concentrations were significantly (P < 0.05) decreased relative to those in the HF group. To elucidate the mechanism of CIE on the metabolism of glucose and lipid, related genes expression in liver were examined. In liver tissue, CIE significantly decreased the mRNA expression levels of peroxisome proliferator-activated receptor γ (PPARγ) and its target genes, such as fatty acid synthase (FAS) and acyl-CoA oxidase (ACO). Moreover, CIE also decreased the expression of liver X receptor (LXR) α and β which are involved in lipid and glucose metabolism. These results suggest that CIE administration could alleviate obesity and related metabolic disorders in HF diet-induced obesity mice through the inhibition of PPARγ and LXR signaling.
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spelling pubmed-35363582013-01-14 Citrus ichangensis Peel Extract Exhibits Anti-Metabolic Disorder Effects by the Inhibition of PPARγ and LXR Signaling in High-Fat Diet-Induced C57BL/6 Mouse Ding, Xiaobo Fan, Shengjie Lu, Yan Zhang, Yu Gu, Ming Zhang, Lu Liu, Gaigai Guo, Lu Jiang, Dong Lu, Xiong Li, Yiming Zhou, Zhiqin Huang, Cheng Evid Based Complement Alternat Med Research Article Obesity is a common nutritional disorder associated with type 2 diabetes, cardiovascular diseases, dyslipidemia, and certain cancers. In this study, we investigated the effects of Citrus ichangensis peel extract (CIE) in high-fat (HF) diet-induced obesity mice. Female C57BL/6 mice were fed a chow diet or an HF diet alone or supplemented with 1% w/w CIE for 8 weeks. We found that CIE treatment could lower blood glucose level and improve glucose tolerance. In the HF+CIE group, body weight gain, serum total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-c) levels, and liver triglyceride (TG) and TC concentrations were significantly (P < 0.05) decreased relative to those in the HF group. To elucidate the mechanism of CIE on the metabolism of glucose and lipid, related genes expression in liver were examined. In liver tissue, CIE significantly decreased the mRNA expression levels of peroxisome proliferator-activated receptor γ (PPARγ) and its target genes, such as fatty acid synthase (FAS) and acyl-CoA oxidase (ACO). Moreover, CIE also decreased the expression of liver X receptor (LXR) α and β which are involved in lipid and glucose metabolism. These results suggest that CIE administration could alleviate obesity and related metabolic disorders in HF diet-induced obesity mice through the inhibition of PPARγ and LXR signaling. Hindawi Publishing Corporation 2012 2012-12-19 /pmc/articles/PMC3536358/ /pubmed/23320036 http://dx.doi.org/10.1155/2012/678592 Text en Copyright © 2012 Xiaobo Ding et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ding, Xiaobo
Fan, Shengjie
Lu, Yan
Zhang, Yu
Gu, Ming
Zhang, Lu
Liu, Gaigai
Guo, Lu
Jiang, Dong
Lu, Xiong
Li, Yiming
Zhou, Zhiqin
Huang, Cheng
Citrus ichangensis Peel Extract Exhibits Anti-Metabolic Disorder Effects by the Inhibition of PPARγ and LXR Signaling in High-Fat Diet-Induced C57BL/6 Mouse
title Citrus ichangensis Peel Extract Exhibits Anti-Metabolic Disorder Effects by the Inhibition of PPARγ and LXR Signaling in High-Fat Diet-Induced C57BL/6 Mouse
title_full Citrus ichangensis Peel Extract Exhibits Anti-Metabolic Disorder Effects by the Inhibition of PPARγ and LXR Signaling in High-Fat Diet-Induced C57BL/6 Mouse
title_fullStr Citrus ichangensis Peel Extract Exhibits Anti-Metabolic Disorder Effects by the Inhibition of PPARγ and LXR Signaling in High-Fat Diet-Induced C57BL/6 Mouse
title_full_unstemmed Citrus ichangensis Peel Extract Exhibits Anti-Metabolic Disorder Effects by the Inhibition of PPARγ and LXR Signaling in High-Fat Diet-Induced C57BL/6 Mouse
title_short Citrus ichangensis Peel Extract Exhibits Anti-Metabolic Disorder Effects by the Inhibition of PPARγ and LXR Signaling in High-Fat Diet-Induced C57BL/6 Mouse
title_sort citrus ichangensis peel extract exhibits anti-metabolic disorder effects by the inhibition of pparγ and lxr signaling in high-fat diet-induced c57bl/6 mouse
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3536358/
https://www.ncbi.nlm.nih.gov/pubmed/23320036
http://dx.doi.org/10.1155/2012/678592
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