Anabolic effects of exercise training in patients with advanced chronic heart failure (NYHA IIIb): Impact on ubiquitin-protein ligases expression and skeletal muscle size

被引:29
作者
Hoellriegel, Robert [1 ]
Beck, Ephraim B. [1 ]
Linke, Axel [1 ]
Adams, Volker [1 ]
Moebius-Winkler, Sven [1 ]
Mangner, Norman [1 ]
Sandri, Marcus [1 ]
Gielen, Stephan [1 ]
Gutberlet, Matthias [2 ]
Hambrecht, Rainer [3 ]
Schuler, Gerhard [1 ]
Erbs, Sandra [1 ]
机构
[1] Univ Leipzig, Ctr Heart, Dept Internal Med Cardiol, D-04289 Leipzig, Germany
[2] Univ Leipzig, Ctr Heart, Dept Radiol, D-04289 Leipzig, Germany
[3] Klinikum Links Weser, Heart Ctr Bremen, Bremen, Germany
关键词
Chronic heart failure; Exercise training; Skeletal muscle alterations; E3-ligases; GROWTH-FACTOR-I; PROTEASOME PATHWAY; BODY-COMPOSITION; INDUCTION; MURF-1; MAFBX;
D O I
10.1016/j.ijcard.2012.03.083
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with advanced chronic heart failure (CHF) are characterized by progressive muscle wasting. The two E3-ligases Rnf28 and Atrogin-1 controlling the activation of the ubiquitinproteasome system might be of importance for the regulation of muscle size. Given the convincing effect of regular physical exercise training (ET) in CHF, it was the aim of the present trial to elucidate, whether ET affects both mentioned enzymes in CHF and whether this is associated with an increase in skeletal muscle mass. Methods: 37 patients with severe CHF were randomized to 12 weeks of ET or sedentary lifestyle (control). The expression of Rnf28 and Atrogin-1 in the skeletal muscle was analyzed by RT-PCR and Western blotting. Skeletal muscle cross sectional area (CSA) was measured by computed tomography. Results: In CHF patients ET led to a significant reduction in skeletal muscle mRNA transcription (from 14.3 +/- 2.0 to 8.7 +/- 1.4 arbitrary units; p<0.05 versus baseline and versus control for the change) and protein expression of Rnf28 (from 4.70 +/- 1.35 to 2.84 +/- 0.65 arbitrary units; p<0.05 versus baseline and versus control for the change). This was accompanied by a significant increase in total muscle CSA of both thighs (from 139.9 +/- 5.2 to 149.2 +/- 5.9 cm(2); p<0.05 versus baseline and versus control for the change). On the contrary, Atrogin-1 was not affected. Conclusion: In patients with advanced CHF, regular physical exercise training led to a decrease in Rnf28 expression in the skeletal muscle. This was linked to an increase in skeletal muscle cross sectional area, supporting the notion that ET has anti-catabolic properties in CHF. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:975 / 980
页数:6
相关论文
共 29 条
[1]   Induction of MuRF1 Is Essential for TNF-α-Induced Loss of Muscle Function in Mice [J].
Adams, Volker ;
Mangner, Norman ;
Gasch, Alexander ;
Krohne, Christian ;
Gielen, Stephan ;
Hirner, Stephanie ;
Thierse, Hermann-Josef ;
Witt, Christian C. ;
Linke, Axel ;
Schuler, Gerhard ;
Labeit, Siegfried .
JOURNAL OF MOLECULAR BIOLOGY, 2008, 384 (01) :48-59
[2]   Myocardial expression of Murf-1 and MAFbx after induction of chronic heart failure:: Effect on myocardial contractility [J].
Adams, Volker ;
Linke, Axel ;
Wisloff, Ulrik ;
Doering, Christian ;
Erbs, Sandra ;
Kraenkel, Nicolle ;
Witt, Christian C. ;
Labeit, Siegfried ;
Mueller-Werdan, Ursula ;
Schuler, Gerhard ;
Hambrecht, Rainer .
CARDIOVASCULAR RESEARCH, 2007, 73 (01) :120-129
[3]   Serum from patients with severe heart failure downregulates eNOS and is proapoptotic -: Role of tumor necrosis factor-α [J].
Agnoletti, L ;
Curello, S ;
Bachetti, T ;
Malacarne, F ;
Gaia, G ;
Comini, L ;
Volterrani, M ;
Bonetti, P ;
Parrinello, G ;
Cadei, M ;
Grigolato, PG ;
Ferrari, R .
CIRCULATION, 1999, 100 (19) :1983-1991
[4]   Cytokines and neurohormones relating to body composition alterations in the wasting syndrome of chronic heart failure [J].
Anker, SD ;
Ponikowski, PP ;
Clark, AL ;
Leyva, F ;
Rauchhaus, M ;
Kemp, M ;
Teixeira, MM ;
Hellewell, PG ;
Hooper, J ;
Poole-Wilson, PA ;
Coats, AJS .
EUROPEAN HEART JOURNAL, 1999, 20 (09) :683-693
[5]   Prognostic importance of weight loss in chronic heart failure and the effect of treatment with angiotensin-converting-enzyme inhibitors: an observational study [J].
Anker, SD ;
Negassa, A ;
Coats, AJS ;
Afzal, R ;
Poole-Wilson, PA ;
Cohn, JN ;
Yusuf, S .
LANCET, 2003, 361 (9363) :1077-1083
[6]   Wasting as independent risk factor for mortality in chronic heart failure [J].
Anker, SD ;
Ponikowski, P ;
Varney, S ;
Chua, TP ;
Clark, AL ;
WebbPeploe, KM ;
Harrington, D ;
Kox, WJ ;
PooleWilson, PA ;
Coats, AJS .
LANCET, 1997, 349 (9058) :1050-1053
[7]  
Anker SD, 1997, CIRCULATION, V96, P526
[8]  
BERGSTROM J, 1975, SCAND J CLIN LAB INV, V35, P606
[9]   Identification of ubiquitin ligases required for skeletal muscle atrophy [J].
Bodine, SC ;
Latres, E ;
Baumhueter, S ;
Lai, VKM ;
Nunez, L ;
Clarke, BA ;
Poueymirou, WT ;
Panaro, FJ ;
Na, EQ ;
Dharmarajan, K ;
Pan, ZQ ;
Valenzuela, DM ;
DeChiara, TM ;
Stitt, TN ;
Yancopoulos, GD ;
Glass, DJ .
SCIENCE, 2001, 294 (5547) :1704-1708
[10]   IKKβ/NF-κB activation causes severe muscle wasting in mice [J].
Cai, DS ;
Frantz, JD ;
Tawa, NE ;
Melendez, PA ;
Oh, BC ;
Lidov, HGW ;
Hasselgren, PO ;
Frontera, WR ;
Lee, J ;
Glass, DJ ;
Shoelson, SE .
CELL, 2004, 119 (02) :285-298