Coenzyme Q10 protects against hyperlipidemia-induced cardiac damage in apolipoprotein E-deficient mice

Abstract Background Hyperlipidemia is a well-established risk factor for cardiac damage, which can lead to cardiovascular diseases. Many studies have shown that Coenzyme Q10(CoQ10) protects against cardiac damage in vivo. The aim of this study was to investigate the possible protective effects of Co...

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Main Authors: Xiaoqing Zhang, Hongyang Liu, Yuhua Hao, Lulu Xu, Tiemei Zhang, Yingshu Liu, Lipeng Guo, Liyue Zhu, Zuowei Pei
Format: Article
Language:English
Published: BMC 2018-12-01
Series:Lipids in Health and Disease
Online Access:http://link.springer.com/article/10.1186/s12944-018-0928-9
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spelling doaj-0a893bb338f5490ab8da3c79e84acf052020-11-25T02:13:56ZengBMCLipids in Health and Disease1476-511X2018-12-011711810.1186/s12944-018-0928-9Coenzyme Q10 protects against hyperlipidemia-induced cardiac damage in apolipoprotein E-deficient miceXiaoqing Zhang0Hongyang Liu1Yuhua Hao2Lulu Xu3Tiemei Zhang4Yingshu Liu5Lipeng Guo6Liyue Zhu7Zuowei Pei8Department of Infection, Affiliated Zhongshan Hospital of Dalian UniversityDepartment of Heart Intensive Care Unit, the First Affiliated Hospital of Dalian Medical UniversityDepartment of Infection, Affiliated Zhongshan Hospital of Dalian UniversityDepartment of Infection, Affiliated Zhongshan Hospital of Dalian UniversityDepartment of Infection, Affiliated Zhongshan Hospital of Dalian UniversityDepartment of Endocrinology, Dalian Municipal Central HospitalDepartment of Cardiology, Dalian Third People’ Hospital Affiliated to Dalian Medical UniversityRehabilitation Center, Zhejiang HospitalDepartment of Cardiology, Affiliated Zhongshan Hospital of Dalian UniversityAbstract Background Hyperlipidemia is a well-established risk factor for cardiac damage, which can lead to cardiovascular diseases. Many studies have shown that Coenzyme Q10(CoQ10) protects against cardiac damage in vivo. The aim of this study was to investigate the possible protective effects of CoQ10 against cardiac damage in apolipoprotein E-deficient (ApoE−/−) mice. Methods Eight-week-old male C57BL/6 and ApoE−/− mice were randomly divided into four groups: C57BL/6 mice fed a normal diet (C57BL/6 group); C57BL/6 mice fed a normal diet + CoQ10 (C57BL/6 + CoQ10 group); ApoE−/− mice fed a high-fat diet (ApoE−/− HD group), and ApoE−/− mice fed a high-fat diet + CoQ10 (ApoE−/− HD + CoQ10 group). All groups were fed the different diets for 16 weeks. Blood samples were obtained from the inferior vena cava and collected in serum tubes. The samples were then stored at − 80 °C until used. Coronal sections of heart tissues were fixed in 10% formalin and then embedded in paraffin for histological evaluation. The remainder of the heart tissues was snap-frozen in liquid nitrogen for mRNA or immunohistochemical analysis. Results The metabolic parameters such as total cholesterol (TC), low-density lipoprotein-cholesterol (LDL-c), and triglycerides (TG) levels were lower in ApoE−/−HD + CoQ10 mice than in ApoE−/− HD mice. There were significant pathophysiological changes (H&E, PAS, Masson and CD68 staining) in ApoE−/− mice in the HD group compared with those in the HD + CoQ10 group. CoQ10 reduced HD-induced cardiac tissue damage via autophagy (p62 and LC3), as evidenced by immunoblotting, immunohistochemistry, and RT-qPCR. CoQ10 also inhibited inflammation (IL-6 and TNF-α) gene expression in ApoE−/− mice. Conclusions These results indicate that CoQ10 is a potential therapeutic target for cardiac damage caused by hyperlipidemia.http://link.springer.com/article/10.1186/s12944-018-0928-9
collection DOAJ
language English
format Article
sources DOAJ
author Xiaoqing Zhang
Hongyang Liu
Yuhua Hao
Lulu Xu
Tiemei Zhang
Yingshu Liu
Lipeng Guo
Liyue Zhu
Zuowei Pei
spellingShingle Xiaoqing Zhang
Hongyang Liu
Yuhua Hao
Lulu Xu
Tiemei Zhang
Yingshu Liu
Lipeng Guo
Liyue Zhu
Zuowei Pei
Coenzyme Q10 protects against hyperlipidemia-induced cardiac damage in apolipoprotein E-deficient mice
Lipids in Health and Disease
author_facet Xiaoqing Zhang
Hongyang Liu
Yuhua Hao
Lulu Xu
Tiemei Zhang
Yingshu Liu
Lipeng Guo
Liyue Zhu
Zuowei Pei
author_sort Xiaoqing Zhang
title Coenzyme Q10 protects against hyperlipidemia-induced cardiac damage in apolipoprotein E-deficient mice
title_short Coenzyme Q10 protects against hyperlipidemia-induced cardiac damage in apolipoprotein E-deficient mice
title_full Coenzyme Q10 protects against hyperlipidemia-induced cardiac damage in apolipoprotein E-deficient mice
title_fullStr Coenzyme Q10 protects against hyperlipidemia-induced cardiac damage in apolipoprotein E-deficient mice
title_full_unstemmed Coenzyme Q10 protects against hyperlipidemia-induced cardiac damage in apolipoprotein E-deficient mice
title_sort coenzyme q10 protects against hyperlipidemia-induced cardiac damage in apolipoprotein e-deficient mice
publisher BMC
series Lipids in Health and Disease
issn 1476-511X
publishDate 2018-12-01
description Abstract Background Hyperlipidemia is a well-established risk factor for cardiac damage, which can lead to cardiovascular diseases. Many studies have shown that Coenzyme Q10(CoQ10) protects against cardiac damage in vivo. The aim of this study was to investigate the possible protective effects of CoQ10 against cardiac damage in apolipoprotein E-deficient (ApoE−/−) mice. Methods Eight-week-old male C57BL/6 and ApoE−/− mice were randomly divided into four groups: C57BL/6 mice fed a normal diet (C57BL/6 group); C57BL/6 mice fed a normal diet + CoQ10 (C57BL/6 + CoQ10 group); ApoE−/− mice fed a high-fat diet (ApoE−/− HD group), and ApoE−/− mice fed a high-fat diet + CoQ10 (ApoE−/− HD + CoQ10 group). All groups were fed the different diets for 16 weeks. Blood samples were obtained from the inferior vena cava and collected in serum tubes. The samples were then stored at − 80 °C until used. Coronal sections of heart tissues were fixed in 10% formalin and then embedded in paraffin for histological evaluation. The remainder of the heart tissues was snap-frozen in liquid nitrogen for mRNA or immunohistochemical analysis. Results The metabolic parameters such as total cholesterol (TC), low-density lipoprotein-cholesterol (LDL-c), and triglycerides (TG) levels were lower in ApoE−/−HD + CoQ10 mice than in ApoE−/− HD mice. There were significant pathophysiological changes (H&E, PAS, Masson and CD68 staining) in ApoE−/− mice in the HD group compared with those in the HD + CoQ10 group. CoQ10 reduced HD-induced cardiac tissue damage via autophagy (p62 and LC3), as evidenced by immunoblotting, immunohistochemistry, and RT-qPCR. CoQ10 also inhibited inflammation (IL-6 and TNF-α) gene expression in ApoE−/− mice. Conclusions These results indicate that CoQ10 is a potential therapeutic target for cardiac damage caused by hyperlipidemia.
url http://link.springer.com/article/10.1186/s12944-018-0928-9
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