Honokiol blocks and reverses cardiac hypertrophy in mice by activating mitochondrial Sirt3

被引:367
作者
Pillai, Vinodkumar B. [1 ]
Samant, Sadhana [1 ]
Sundaresan, Nagalingam R. [1 ]
Raghuraman, Hariharasundaram [2 ,3 ]
Kim, Gene [4 ]
Bonner, Michael Y. [5 ]
Arbiser, Jack L. [5 ]
Walker, Douglas I. [6 ]
Jones, Dean P. [6 ]
Gius, David [7 ]
Gupta, Mahesh P. [1 ]
机构
[1] Univ Chicago, Dept Surg, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Biochem, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Mol Biol, Chicago, IL 60637 USA
[4] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[5] Atlanta Vet Adm Hlth Ctr, Dept Dermatol, Atlanta, GA USA
[6] Emory Univ, Dept Biochem & Med, Sch Med, Atlanta, GA 30322 USA
[7] Northwestern Univ, Dept Radiat Oncol, Chicago, IL 60611 USA
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
关键词
SIRT3-MEDIATED DEACETYLATION; CALORIE RESTRICTION; PROTEIN-KINASE; CELL-DEATH; METABOLISM; SIRTUINS; HOMOLOG; PATHWAY; GENE; AKT;
D O I
10.1038/ncomms7656
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Honokiol (HKL) is a natural biphenolic compound derived from the bark of magnolia trees with anti-inflammatory, anti-oxidative, anti-tumour and neuroprotective properties. Here we show that HKL blocks agonist-induced and pressure overload-mediated, cardiac hypertrophic responses, and ameliorates pre-existing cardiac hypertrophy, in mice. Our data suggest that the anti-hypertrophic effects of HKL depend on activation of the deacetylase Sirt3. We demonstrate that HKL is present in mitochondria, enhances Sirt3 expression nearly twofold and suggest that HKL may bind to Sirt3 to further increase its activity. Increased Sirt3 activity is associated with reduced acetylation of mitochondrial Sirt3 substrates, MnSOD and oligomycin-sensitivity conferring protein (OSCP). HKL-treatment increases mitochondrial rate of oxygen consumption and reduces ROS synthesis in wild type, but not in Sirt3-KO cells. Moreover, HKL-treatment blocks cardiac fibroblast proliferation and differentiation to myofibroblasts in a Sirt3-dependent manner. These results suggest that HKL is a pharmacological activator of Sirt3 capable of blocking, and even reversing, the cardiac hypertrophic response.
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页数:16
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