Reversible activation of nuclear factor-κB in human end-stage heart failure after left ventricular mechanical support

被引:71
作者
Grabellus, F
Levkau, B
Sokoll, A
Welp, H
Schmid, C
Deng, MC
Takeda, A
Breithardt, G
Baba, HA
机构
[1] Univ Munster, Gerhard Domagk Inst Pathol, D-48149 Munster, Germany
[2] Univ Munster, Inst Arteriosclerosis Res, D-48149 Munster, Germany
[3] Univ Munster, Dept Cardiothorac Surg, D-48149 Munster, Germany
[4] Columbia Univ, Heart Failure Ctr, New York, NY USA
[5] Jikei Univ, Dept Internal Med, Aoto Hosp, Tokyo, Japan
[6] Univ Munster, Dept Cardiol & Angiol, D-48149 Munster, Germany
关键词
heart failure; hypertrophy; myocytes; remodeling; signal transduction;
D O I
10.1016/S0008-6363(01)00433-3
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objective: Left ventricular assist devices (LVAD) have been used to 'bridge' patients with end-stage heart failure to transplantation. Although several reports have suggested that the native ventricular function recovers after long-term LVAD support, a process called 'reverse remodeling', the underlying biological mechanisms are still unknown. As the transcription factor nuclear factor-kappaB (NF-kappaB) has been shown to be active in the failing human heart, we examined whether its activity is altered under LVAD support, and may thus contribute to the dynamic process of 'reverse remodeling'. Methods: The activity of NF-kappaB was studied in 16 patients with end-stage heart failure (eight with dilated cardiomyopathy, six with ischemic heart disease, one with myocarditis, and one with Congenital heart disease) before and after LVAD support by immunohistochemistry using an antibody against active NF-kappaB. Gel-shifts for NF-kappaB DNA-binding activity were performed with paired human myocardial tissue from four patients. The mean cardiomyocyte diameter before and after mechanical unloading was measured with an image analyzer system. Results: 15 patients out of 10 showed a significant decrease in the number of NF-kappaB positive cardiomyocyte nuclei after LVAD support in the left ventricular myocardium. The NF-kappaB DNA-binding activity also decreased after LVAD support as measured by gel-shift analysis. While the number of positive cardiomyocytes. was significantly higher in the subendocardium than in the subepicardium at the time of LVAD implantation, this difference was no longer present at the time of LVAD explantation. The diameter of cardiomyocytes in the left ventricle decreased significantly as a parameter of structural reverse remodeling. Conclusion: LVAD support decreases the extent of NF-kappaB activation in failing human hearts. suggesting that NF-kappaB may be involved in the process of 'reverse remodeling'. (C) 2002 Elsevier Science BY. All right reserved.
引用
收藏
页码:124 / 130
页数:7
相关论文
共 20 条
[1]
Altemose GT, 1997, J HEART LUNG TRANSPL, V16, P765
[2]
Reversal of metallothionein expression is different throughout the human myocardium after prolonged left-ventricular mechanical support [J].
Baba, HA ;
Grabellus, F ;
August, C ;
Plenz, G ;
Takeda, A ;
Tjan, TDT ;
Schmid, C ;
Deng, MC .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2000, 19 (07) :668-674
[3]
Baichwal VR, 1997, CURR BIOL, V7, P94
[4]
Mechanisms of disease - Nuclear factor-kappa b - A pivotal transcription factor in chronic inflammatory diseases [J].
Barnes, PJ ;
Larin, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (15) :1066-1071
[5]
Bartling B, 1999, CIRCULATION, V100, P216
[6]
Unloaded heart in vivo replicates fetal gene expression of cardiac hypertrophy [J].
Depre, C ;
Shipley, GL ;
Chen, WH ;
Han, QY ;
Doenst, T ;
Moore, ML ;
Stepkowski, S ;
Davies, PJA ;
Taegtmeyer, H .
NATURE MEDICINE, 1998, 4 (11) :1269-1275
[7]
Improved left ventricular function after chronic left ventricular unloading [J].
Frazier, OH ;
Benedict, CR ;
Radovancevic, B ;
Bick, RJ ;
Capek, P ;
Springer, WE ;
Macris, MP ;
Delgado, R ;
Buja, LM .
ANNALS OF THORACIC SURGERY, 1996, 62 (03) :675-681
[8]
Medical progress - Implantable left ventricular assist devices [J].
Goldstein, DJ ;
Oz, MC ;
Rose, EA .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (21) :1522-1533
[9]
GRABELLUS F, IN PRESS J PATHOL
[10]
PRESSURE-FLOW RELATIONS IN CORONARY CIRCULATION [J].
HOFFMAN, JIE ;
SPAAN, JAE .
PHYSIOLOGICAL REVIEWS, 1990, 70 (02) :331-390