Resveratrol Arrests and Regresses the Development of Pressure Overload- but Not Volume Overload-Induced Cardiac Hypertrophy in Rats

被引:65
|
作者
Wojciechowski, Peter [1 ,2 ]
Juric, Danijel [1 ,2 ]
Louis, Xavier Lieben [1 ,2 ]
Thandapilly, Sijo Joseph [1 ,2 ]
Yu, Liping [1 ,2 ]
Taylor, Carla [3 ]
Netticadan, Thomas [1 ,2 ]
机构
[1] Univ Manitoba, St Boniface Gen Hosp, Res Ctr,Heart Failure Res Lab, Canadian Ctr Agrifood Res Hlth & Med, Winnipeg, MB R2H 2A6, Canada
[2] Univ Manitoba, St Boniface Gen Hosp, Dept Physiol, Res Ctr, Winnipeg, MB R2H 2A6, Canada
[3] Univ Manitoba, Dept Human Nutr Sci, Winnipeg, MB R3T 2N2, Canada
基金
加拿大健康研究院;
关键词
HEART-FAILURE; CONTRACTILE DYSFUNCTION; MECHANISMS; PREVENTION; PATHWAYS;
D O I
10.3945/jn.109.115006
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Cardiac hypertrophy is a compensatory enlargement of the heart due to either volume overload (VO) and/or pressure overload (PO) that develops into heart failure if left untreated. The polyphenol resveratrol has been reported to regress PO-induced cardiac hypertrophy in rats. Our aim in this study was to assess the effectiveness of resveratrol on VO-induced cardiac hypertrophy. Sprague Dawley rats were subjected to aortocaval shunt and abdominal aortic banding surgeries to create VO and PO, respectively; sham-operated rats served as controls. To arrest the development of cardiac hypertrophy, daily resveratrol treatment (2.5 mg/kg body weight) was started 2 d postsurgery for 26 d and assessed by echocardiography at 2, 14, and 28 d postsurgery. Similarly, to regress cardiac hypertrophy resveratrol treatment was started after structural and functional abnormalities developed (14 d postsurgery) for 14 d and assessed by echocardiography at 14 and 28 d postsurgery. VO surgeries induced eccentric hypertrophy characterized by increased left ventricle internal dimensions (LVID) without wall thickening. Conversely, PO induced concentric hypertrophy with increased wall thickness without change in LVID. Lipid peroxidation, a marker for oxidative stress, was significantly elevated in both PO and VO rats. Resveratrol treatment arrested the development and regressed abnormalities in cardiac structure and function in PO but not VO rats. Treatment with resveratrol also significantly reduced oxidative stress in cardiac tissue of PO and VO rats. The results on cardiac structure and function demonstrate a potential for resveratrol in the treatment of cardiac hypertrophy due to PO but not VO. J. Nutr. 140: 962-968, 2010.
引用
收藏
页码:962 / 968
页数:7
相关论文
共 50 条
  • [1] Autophagy and pressure overload-induced cardiac hypertrophy
    Zeng, Yong
    Ren, Wei-Qiong
    Wen, Ai-Zhen
    Zhang, Wen
    Fan, Fu-Yuan
    Chen, Ou-Ying
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2022, 24 (12) : 1101 - 1108
  • [2] Cinnamaldehyde attenuates pressure overload-induced cardiac hypertrophy
    Yang, Liu
    Wu, Qing-Qing
    Liu, Yuan
    Hu, Zhe-Fu
    Bian, Zhou-Yan
    Tang, Qi-Zhu
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2015, 8 (11): : 14345 - 14354
  • [3] Naringenin attenuates pressure overload-induced cardiac hypertrophy
    Zhang, Ning
    Yang, Zheng
    Yuan, Yuan
    Li, Fangfang
    Liu, Yuan
    Ma, Zhenguo
    Liao, Haihan
    Bian, Zhouyan
    Zhang, Yao
    Zhou, Heng
    Deng, Wei
    Zhou, Mengqiao
    Tang, Qizhu
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2015, 10 (06) : 2206 - 2212
  • [4] Resveratrol Ameliorates Pressure Overload-induced Cardiac Dysfunction and Attenuates Autophagy in Rats
    Wang, Lingjun
    Gao, Mengxi
    Chen, Jie
    Yang, Zhongqi
    Sun, Jinghe
    Wang, Zhaohui
    Huang, Xiwen
    Yuan, Tianhui
    Shen, Xiaoxiao
    Xian, Shaoxiang
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2015, 66 (04) : 376 - 382
  • [5] Puerarin attenuates pressure overload-induced cardiac hypertrophy
    Yuan, Yuan
    Zong, Jing
    Zhou, Heng
    Bian, Zhou-Yan
    Deng, Wei
    Dai, Jia
    Gan, Hua-Wen
    Yang, Zheng
    Li, Hongliang
    Tang, Qi-Zhu
    JOURNAL OF CARDIOLOGY, 2014, 63 (1-2) : 73 - 81
  • [6] Pharmacological inhibition of DNA methylation attenuates pressure overload-induced cardiac hypertrophy in rats
    Stenzig, Justus
    Schneeberger, Yvonne
    Loeser, Alexandra
    Peters, Barbara S.
    Schaefer, Andreas
    Zhao, Rong-Rong
    Ng, Shi Ling
    Hoeppner, Grit
    Geertz, Birgit
    Hirt, Marc N.
    Tan, Wilson
    Wong, Eleanor
    Reichenspurner, Hermann
    Foo, Roger S-Y
    Eschenhagen, Thomas
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2018, 120 : 53 - 63
  • [7] Ryanodine Receptor Type 2 Is Required for the Development of Pressure Overload-Induced Cardiac Hypertrophy
    Zou, Yunzeng
    Liang, Yanyan
    Gong, Hui
    Zhou, Ning
    Ma, Hong
    Guan, Aili
    Sun, Aijun
    Wang, Ping
    Niu, Yuhong
    Jiang, Hong
    Takano, Hiroyuki
    Toko, Haruhiro
    Yao, Atsushi
    Takeshima, Hiroshi
    Akazawa, Hiroshi
    Shiojima, Ichiro
    Wang, Yuqi
    Komuro, Issei
    Ge, Junbo
    HYPERTENSION, 2011, 58 (06) : 1099 - U363
  • [8] Innate Immune Cells in Pressure Overload-Induced Cardiac Hypertrophy and Remodeling
    Liu, Xin
    Shi, Guo-Ping
    Guo, Junli
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 9
  • [9] Cathepsin K Knockout Alleviates Pressure Overload-Induced Cardiac Hypertrophy
    Hua, Yinan
    Xu, Xihui
    Shi, Guo-Ping
    Chicco, Adam J.
    Ren, Jun
    Nair, Sreejayan
    HYPERTENSION, 2013, 61 (06) : 1184 - +
  • [10] Gene profiling during regression of pressure overload-induced cardiac hypertrophy
    Yang, Dong Kwon
    Choi, Bo Youn
    Lee, Young-Hoon
    Kim, Young-Gyu
    Cho, Myeong-Chan
    Hong, Seong-Eui
    Kim, Do Han
    Hajjar, Roger J.
    Park, Woo Jin
    PHYSIOLOGICAL GENOMICS, 2007, 30 (01) : 1 - 7