Sirtuins: To Be or Not To Be in Diabetic Cardiomyopathy

被引:37
作者
Palomer, Xavier [1 ,2 ,3 ,4 ]
Aguilar-Recarte, David [1 ,2 ,3 ,4 ]
Garcia, Raquel [5 ,6 ]
Francisco Nistal, J. [6 ,7 ,8 ,9 ]
Vazquez-Carrera, Manuel [1 ,2 ,3 ,4 ]
机构
[1] Univ Barcelona, Dept Pharmacol Toxicol & Therapeut Chem, Fac Pharm & Food Sci, Barcelona, Spain
[2] Univ Barcelona IBUB, Inst Biomed, Barcelona, Spain
[3] Inst Salud Carlos III, Spanish Biomed Res Ctr Diabet & Associated Metab, Barcelona, Spain
[4] Hosp St Joan de Deu, Pediat Res Inst, Barcelona, Spain
[5] Univ Cantabria, Fac Med, Dept Fisiol & Farmacol, Santander, Spain
[6] Inst Invest Marques de Valdecilla IDIVAL, Santander, Spain
[7] Hosp Univ Marques de Valdecilla, Serv Cirugia Cardiovasc, Santander, Spain
[8] Univ Cantabria, Fac Med, Dept Ciencias Med & Quirurg, Santander, Spain
[9] Inst Salud Carlos III, Ctr Invest Biomed Red Cardiovasc CIBERCV, Santander, Spain
关键词
NF-KAPPA-B; DOXORUBICIN-INDUCED CARDIOTOXICITY; ENDOPLASMIC-RETICULUM STRESS; DEPENDENT GENE-EXPRESSION; IMPROVES CARDIAC-FUNCTION; FATTY-ACID OXIDATION; INDUCED APOPTOSIS; SKELETAL-MUSCLE; AKT ACTIVATION; CELL-SURVIVAL;
D O I
10.1016/j.molmed.2021.03.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diabetic cardiomyopathy is the leading cause of death among people with diabetes. Despite its severity and poor prognosis, there are currently no approved specific drugs to prevent or even treat diabetic cardiomyopathy. There is a need to understand the pathogenic mechanisms underlying the development of diabetic cardiomyopathy to design new therapeutic strategies. These mechanisms are complex and intricate and include metabolic dysregulation, inflammation, oxidative stress, fibrosis, and apoptosis. Sirtuins, a group of deacetylase enzymes, play an important role in all these processes and are, therefore, potential molecular targets for treating this disease. In this review, we discuss the role of sirtuins in the heart, focusing on their contribution to the pathogenesis of diabetic cardiomyopathy and how their modulation could be therapeutically useful.
引用
收藏
页码:554 / 571
页数:18
相关论文
共 131 条
  • [81] SIRT1 Suppresses Doxorubicin-Induced Cardiotoxicity by Regulating the Oxidative Stress and p38MAPK Pathways
    Ruan, Yang
    Dong, Chunlin
    Patel, Jigar
    Duan, Chao
    Wang, Xinyue
    Wu, Xi
    Cao, Yuan
    Pu, Lianmei
    Lu, Dan
    Shen, Tao
    Li, Jian
    [J]. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2015, 35 (03) : 1116 - 1124
  • [82] Metabolomics-assisted proteomics identifies succinylation and SIRT5 as important regulators of cardiac function
    Sadhukhan, Sushabhan
    Liu, Xiaojing
    Ryu, Dongryeol
    Nelson, Ornella D.
    Stupinski, John A.
    Li, Zhi
    Chen, Wei
    Zhang, Sheng
    Weiss, Robert S.
    Locasale, Jason W.
    Auwerx, Johan
    Lin, Hening
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (16) : 4320 - 4325
  • [83] SIRT2 deacetylase represses NFAT transcription factor to maintain cardiac homeostasis
    Sarikhani, Mohsen
    Maity, Sangeeta
    Mishra, Sneha
    Jain, Aditi
    Tamta, Ankit K.
    Ravi, Venkatraman
    Kondapalli, Mrudula S.
    Desingu, Perumal A.
    Khan, Danish
    Kumar, Shweta
    Rao, Swathi
    Inbaraj, Meena
    Pandit, Anwit S.
    Sundaresan, Nagalingam Ravi
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 293 (14) : 5281 - 5294
  • [84] SirT3 is a nuclear NAD+-dependent histone deacetylase that translocates to the mitochondria upon cellular stress
    Scher, Michael B.
    Vaquero, Alejandro
    Reinberg, Danny
    [J]. GENES & DEVELOPMENT, 2007, 21 (08) : 920 - 928
  • [85] Sirtuin 3 deficiency exacerbates diabetic cardiomyopathy via necroptosis enhancement and NLRP3 activation
    Song, Shu
    Ding, Yue
    Dai, Guo-liang
    Zhang, Yue
    Xu, Meng-ting
    Shen, Jie-ru
    Chen, Ting-ting
    Chen, Yun
    Meng, Guo-liang
    [J]. ACTA PHARMACOLOGICA SINICA, 2021, 42 (02) : 230 - 241
  • [86] Sirtuin 3 is essential for hypertension-induced cardiac fibrosis via mediating pericyte transition
    Su, Han
    Zeng, Heng
    Liu, Bo
    Chen, Jian-Xiong
    [J]. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2020, 24 (14) : 8057 - 8068
  • [87] Resveratrol, an activator of SIRT1, upregulates sarcoplasmic calcium ATPase and improves cardiac function in diabetic cardiomyopathy
    Sulaiman, M.
    Matta, M. J.
    Sunderesan, N. R.
    Gupta, M. P.
    Periasamy, M.
    Gupta, M.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2010, 298 (03): : H833 - H843
  • [88] The sirtuin SIRT6 blocks IGF-Akt signaling and development of cardiac hypertrophy by targeting c-Jun
    Sundaresan, Nagalingam R.
    Vasudevan, Prabhakaran
    Zhong, Lei
    Kim, Gene
    Samant, Sadhana
    Parekh, Vishwas
    Pillai, Vinodkumar B.
    Ravindra, P. V.
    Gupta, Madhu
    Jeevanandam, Valluvan
    Cunningham, John M.
    Deng, Chu-Xia
    Lombard, David B.
    Mostoslavsky, Raul
    Gupta, Mahesh P.
    [J]. NATURE MEDICINE, 2012, 18 (11) : 1643 - +
  • [89] The Deacetylase SIRT1 Promotes Membrane Localization and Activation of Akt and PDK1 During Tumorigenesis and Cardiac Hypertrophy
    Sundaresan, Nagalingam R.
    Pillai, Vinodkumar B.
    Wolfgeher, Don
    Samant, Sadhana
    Vasudevan, Prabhakaran
    Parekh, Vishwas
    Raghuraman, Hariharasundaram
    Cunningham, John M.
    Gupta, Madhu
    Gupta, Mahesh P.
    [J]. SCIENCE SIGNALING, 2011, 4 (182)
  • [90] Sirt3 blocks the cardiac hypertrophic response by augmenting Foxo3a-dependent antioxidant defense mechanisms in mice
    Sundaresan, Nagalingam R.
    Gupta, Madhu
    Kim, Gene
    Rajamohan, Senthilkumar B.
    Isbatan, Ayman
    Gupta, Mahesh P.
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (09) : 2758 - 2771