Thyroid hormone signalling is altered in response to physical training in patients with end-stage heart failure and mechanical assist devices: potential physiological consequences?

被引:30
作者
Adamopoulos, Stamatios [1 ]
Gouziouta, Aggeliki [1 ]
Mantzouratou, Polixeni [2 ]
Laoutaris, Ioannis D. [1 ]
Dritsas, Athanasios [1 ]
Cokkinos, Dennis V. [3 ]
Mourouzis, Iordanis [2 ]
Sfyrakis, Petros [1 ]
Iervasi, Giorgio [4 ]
Pantos, Constantinos [2 ]
机构
[1] Onassis Cardiac Surg Ctr, Dept Cardiol, Athens, Greece
[2] Univ Athens, Dept Pharmacol, Athens 11527, Greece
[3] Acad Athens, Biomed Res Fdn, Athens, Greece
[4] CNR, Inst Clin Physiol, Fdn Toscana G Monasterio, I-56100 Pisa, Italy
关键词
Thyroid hormone; Heart failure; Exercise training; Thyroid hormone receptor alpha1; Kinase signalling; MYOCARDIAL-INFARCTION; CARDIOMYOCYTE; HYPERTROPHY; EXPRESSION; RECOVERY; AKT;
D O I
10.1093/icvts/ivt294
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The present study investigated the potential of the failing myocardium of patients with ventricular assist devices (VAD) to respond to physiological growth stimuli, such as exercise, by activating growth signalling pathways. This may be of therapeutic relevance in identifying novel pharmacological targets for therapies that could facilitate recovery after VAD implantation. Twenty-two patients bridged to heart transplantation (HTx) with VAD were included in the study. A group of patients underwent moderate intensity aerobic exercise (GT), while another group of patients did not receive exercise training (CG). Thyroid hormone receptor alpha1 (TR alpha 1) protein and total (t) and phosphorylated (p) protein kinase B (Akt) and c-Jun N-terminal kinase (JNK) kinase signalling were measured in myocardial tissue by western blotting at pre-VAD and pre-HTx period. In addition, Thyroid hormone (TH) levels were measured in plasma. Peak oxygen consumption (VO2) at pre-HTx period was higher in patients subjected to training protocol [18.0 (0.8) for GT when compared with 13.7 (0.7) for CG group, P = 0.002]. N-terminal-prohormone of brain natriuretic peptide (NT-proBNP) levels were 1068 (148) for CG vs 626 (115) for GT group, P = 0.035. A switch towards up-regulation of physiological growth signalling was observed: the ratio of p-Akt/t-Akt was 2-fold higher in GT vs CG, P < 0.05 while p-JNK/t-JNK was 2.5-fold lower (P < 0.05) in GT vs CG, in pre-HTx samples. This response was accompanied by a 2.0-fold increase in TR alpha 1 expression in pre-HTx samples with concomitant increase in circulating T3 in GT vs CG, P < 0.05. No differences in peak VO2, NT-proBNP, T3, TR alpha 1, p/t-AKT and p/t-JNK were found between groups in the pre-VAD period. The unloaded failing myocardium responded to physical training by enhancing thyroid hormone signalling. This response was associated with an up-regulation of Akt and suppression of JNK activation.
引用
收藏
页码:664 / 668
页数:5
相关论文
共 15 条
[1]
Reverse Remodeling With Left Ventricular Assist Devices A Review of Clinical, Cellular, and Molecular Effects [J].
Ambardekar, Amrut V. ;
Buttrick, Peter M. .
CIRCULATION-HEART FAILURE, 2011, 4 (02) :224-233
[2]
Adeno-associated virus-mediated expression of thyroid-hormone-receptor isoforms-α1 and -β1 improves contractile function in pressure overload-induced cardiac hypertrophy [J].
Belke, Darrell D. ;
Gloss, Bernd ;
Swanson, Eric A. ;
Dillmann, Wolfgang H. .
ENDOCRINOLOGY, 2007, 148 (06) :2870-2877
[3]
JNK modulates FOXO3a for the expression of the mitochondrial death and mitophagy marker BNIP3 in pathological hypertrophy and in heart failure [J].
Chaanine, A. H. ;
Jeong, D. ;
Liang, L. ;
Chemaly, E. R. ;
Fish, K. ;
Gordon, R. E. ;
Hajjar, R. J. .
CELL DEATH & DISEASE, 2012, 3 :e265-e265
[4]
Thyroid hormone stimulates protein synthesis in the cardiomyocyte by activating the Akt-mTOR and p70S6K pathways [J].
Kenessey, Agnes ;
Ojamaa, Kaie .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (30) :20666-20672
[5]
Benefits of physical training on exercise capacity, inspiratory muscle function, and quality of life in patients with ventricular assist devices long-term postimplantation [J].
Laoutaris, Ioannis D. ;
Dritsas, Athanasios ;
Adamopoulos, Stamatis ;
Manginas, Athanassios ;
Gouziouta, Aggeliki ;
Kallistratos, Manolis S. ;
Koulopoulou, Maria ;
Voudris, Vasilis ;
Cokkinos, Dennis V. ;
Sfirakis, Petros .
EUROPEAN JOURNAL OF CARDIOVASCULAR PREVENTION & REHABILITATION, 2011, 18 (01) :33-40
[6]
Thyrotoxicosis-facilitated bridge to recovery with a continuous-flow left ventricular assist device [J].
Letsou, George V. ;
Reverdin, Stephane ;
Frazier, O. H. .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2013, 44 (03) :573-574
[7]
Phenotypic spectrum caused by transgenic overexpression of activated Akt in the heart [J].
Matsui, T ;
Li, L ;
Wu, JC ;
Cook, SA ;
Nagoshi, T ;
Picard, MH ;
Liao, RL ;
Rosenzweig, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (25) :22896-22901
[8]
Inhibition of thyroid hormone receptor α1 impairs post-ischemic cardiac performance after myocardial infarction in mice [J].
Mourouzis, Iordanis ;
Kostakou, Erietta ;
Galanopoulos, Georgios ;
Mantzouratou, Polixeni ;
Pantos, Constantinos .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2013, 379 (1-2) :97-105
[9]
Dose-dependent effects of thyroid hormone on post-ischemic cardiac performance: potential involvement of Akt and ERK signalings [J].
Mourouzis, Iordanis ;
Mantzouratou, Polixeni ;
Galanopoulos, Georgios ;
Kostakou, Erietta ;
Roukounakis, Nikolaos ;
Kokkinos, Alexandros D. ;
Cokkinos, Dennis V. ;
Pantos, Constantinos .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2012, 363 (1-2) :235-243
[10]
Pantos C, 2008, J PHYSIOL PHARMACOL, V59, P253