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Apple Polyphenols Decrease Atherosclerosis and Hepatic Steatosis in ApoE(−/−) Mice through the ROS/MAPK/NF-κB Pathway

In this study, we examined the effects of apple polyphenols (APs) on hyperlipidemia, atherosclerosis, hepatic steatosis and endothelial function and investigated the potential mechanisms. ApoE(−/−) mice were fed a western-type diet and orally treated with APs (100 mg/kg) or atorvastatin (10 mg/kg) f...

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Autores principales: Xu, Zhe-Rong, Li, Jin-You, Dong, Xin-Wei, Tan, Zhong-Ju, Wu, Wei-Zhen, Xie, Qiang-Min, Yang, Yun-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555163/
https://www.ncbi.nlm.nih.gov/pubmed/26305254
http://dx.doi.org/10.3390/nu7085324
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author Xu, Zhe-Rong
Li, Jin-You
Dong, Xin-Wei
Tan, Zhong-Ju
Wu, Wei-Zhen
Xie, Qiang-Min
Yang, Yun-Mei
author_facet Xu, Zhe-Rong
Li, Jin-You
Dong, Xin-Wei
Tan, Zhong-Ju
Wu, Wei-Zhen
Xie, Qiang-Min
Yang, Yun-Mei
author_sort Xu, Zhe-Rong
collection PubMed
description In this study, we examined the effects of apple polyphenols (APs) on hyperlipidemia, atherosclerosis, hepatic steatosis and endothelial function and investigated the potential mechanisms. ApoE(−/−) mice were fed a western-type diet and orally treated with APs (100 mg/kg) or atorvastatin (10 mg/kg) for 12 weeks. Hyperlipidemia and atherosclerosis in the aortic sinuses and, and hepatic lipidosis were measured. The treatment with APs or atorvastatin induced a remarkable reduction in the atherosclerotic lesions and hepatic steatosis and decreased the levels of low-density lipoprotein, triglyceride, CCL-2 and VCAM-1 levels in the plasma. Conversely, the APs significantly increased the plasma levels of high-density lipoprotein (HDL) cholesterol and markedly up-regulated the glutathione peroxidase (GPx), catalase (CAT) and superoxide dismutase (SOD) levels in liver tissues. Moreover, the APs treatment modulated lipid metabolism by up-regulating the transcription of associated hepatic genes including PPARα, while down-regulating the transcription of SCAP and its downstream genes associated with lipid synthesis in the liver. Histological assessment showed that the APs treatment also reduced the macrophage infiltration in the aortic root plaque and the inflammatory cells infiltrations to the liver tissues. Moreover, we confirmed that the APs treatment greatly reduced the ox-LDL-induced endothelial dysfunction and monocyte adhesion to rat aortic endothelial cells (RAECs). Mechanistically, the APs treatment suppressed the ROS/MAPK/NF-κB signaling pathway, and consequently, reduced CCL-2, ICAM-1 and VCAM-1 expression. Our results suggest that the APs are a beneficial nutritional supplement for the attenuation of atherosclerosis.
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spelling pubmed-45551632015-09-01 Apple Polyphenols Decrease Atherosclerosis and Hepatic Steatosis in ApoE(−/−) Mice through the ROS/MAPK/NF-κB Pathway Xu, Zhe-Rong Li, Jin-You Dong, Xin-Wei Tan, Zhong-Ju Wu, Wei-Zhen Xie, Qiang-Min Yang, Yun-Mei Nutrients Article In this study, we examined the effects of apple polyphenols (APs) on hyperlipidemia, atherosclerosis, hepatic steatosis and endothelial function and investigated the potential mechanisms. ApoE(−/−) mice were fed a western-type diet and orally treated with APs (100 mg/kg) or atorvastatin (10 mg/kg) for 12 weeks. Hyperlipidemia and atherosclerosis in the aortic sinuses and, and hepatic lipidosis were measured. The treatment with APs or atorvastatin induced a remarkable reduction in the atherosclerotic lesions and hepatic steatosis and decreased the levels of low-density lipoprotein, triglyceride, CCL-2 and VCAM-1 levels in the plasma. Conversely, the APs significantly increased the plasma levels of high-density lipoprotein (HDL) cholesterol and markedly up-regulated the glutathione peroxidase (GPx), catalase (CAT) and superoxide dismutase (SOD) levels in liver tissues. Moreover, the APs treatment modulated lipid metabolism by up-regulating the transcription of associated hepatic genes including PPARα, while down-regulating the transcription of SCAP and its downstream genes associated with lipid synthesis in the liver. Histological assessment showed that the APs treatment also reduced the macrophage infiltration in the aortic root plaque and the inflammatory cells infiltrations to the liver tissues. Moreover, we confirmed that the APs treatment greatly reduced the ox-LDL-induced endothelial dysfunction and monocyte adhesion to rat aortic endothelial cells (RAECs). Mechanistically, the APs treatment suppressed the ROS/MAPK/NF-κB signaling pathway, and consequently, reduced CCL-2, ICAM-1 and VCAM-1 expression. Our results suggest that the APs are a beneficial nutritional supplement for the attenuation of atherosclerosis. MDPI 2015-08-24 /pmc/articles/PMC4555163/ /pubmed/26305254 http://dx.doi.org/10.3390/nu7085324 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Xu, Zhe-Rong
Li, Jin-You
Dong, Xin-Wei
Tan, Zhong-Ju
Wu, Wei-Zhen
Xie, Qiang-Min
Yang, Yun-Mei
Apple Polyphenols Decrease Atherosclerosis and Hepatic Steatosis in ApoE(−/−) Mice through the ROS/MAPK/NF-κB Pathway
title Apple Polyphenols Decrease Atherosclerosis and Hepatic Steatosis in ApoE(−/−) Mice through the ROS/MAPK/NF-κB Pathway
title_full Apple Polyphenols Decrease Atherosclerosis and Hepatic Steatosis in ApoE(−/−) Mice through the ROS/MAPK/NF-κB Pathway
title_fullStr Apple Polyphenols Decrease Atherosclerosis and Hepatic Steatosis in ApoE(−/−) Mice through the ROS/MAPK/NF-κB Pathway
title_full_unstemmed Apple Polyphenols Decrease Atherosclerosis and Hepatic Steatosis in ApoE(−/−) Mice through the ROS/MAPK/NF-κB Pathway
title_short Apple Polyphenols Decrease Atherosclerosis and Hepatic Steatosis in ApoE(−/−) Mice through the ROS/MAPK/NF-κB Pathway
title_sort apple polyphenols decrease atherosclerosis and hepatic steatosis in apoe(−/−) mice through the ros/mapk/nf-κb pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555163/
https://www.ncbi.nlm.nih.gov/pubmed/26305254
http://dx.doi.org/10.3390/nu7085324
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