Morphological and Molecular Changes of the Myocardium After Left Ventricular Mechanical Support

被引:26
作者
Baba, Hideo A. [1 ]
Wohlschlaeger, Jeremias [1 ]
机构
[1] Univ Duisburg Essen, Univ Hosp Essen, Inst Pathol & Neuropathol, Hufelandstr 55, D-45147 Essen, Germany
关键词
Congestive heart failure (CHF); ventricular unloading; left ventricular assist device (LVAD); reverse cardiac remodeling; morphology; weaning;
D O I
10.2174/157340308785160606
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Left ventricular assist devices (LVAD) are currently used to either "bridge" patients with terminal congestive heart failure (CHF) until cardiac transplantation is possible or optionally for patients with contraindications for transplantation ("destination therapy"). Mechanical support is associated with a marked decrease of cardiac dilation and hypertrophy as well as numerous cellular and molecular changes ("reverse cardiac remodeling"), which can be accompanied by improved cardiac function ("bridge to recovery") in a relatively small subset of patients with heart transplantation no longer necessary even after removal of the device ("weaning"). In the recent past, novel pharmacological strategies have been developed and are combined with mechanical support, which has increased the percentage of patients with improved clinical status and cardiac performance. Gene expression profiles have demonstrated that individuals who recover after LVAD show different gene expression compared to individuals who do not respond to unloading. This methodology holds promise for the future to develop read out frames to identify individuals who can recover after support. Aside from describing the morphological changes associated with "reverse cardiac remodeling", this review will focus on signal transduction, transcriptional regulation, apoptosis, cell stress proteins, matrix remodeling, inflammatory mediators and aspects of neurohormonal activation in the failing human heart before and after ventricular unloading.
引用
收藏
页码:157 / 169
页数:13
相关论文
共 128 条
[1]   THE VASOINHIBITORY ACTIVITY OF BOVINE CHROMOGRANIN-A FRAGMENT (VASOSTATIN) AND ITS INDEPENDENCE OF EXTRACELLULAR CALCIUM IN ISOLATED SEGMENTS OF HUMAN BLOOD-VESSELS [J].
AARDAL, S ;
HELLE, KB .
REGULATORY PEPTIDES, 1992, 41 (01) :9-18
[2]   A glossary of circulating cytokines in chronic heart failure [J].
Adamopoulos, S ;
Parissis, JT ;
Kremastinos, DT .
EUROPEAN JOURNAL OF HEART FAILURE, 2001, 3 (05) :517-526
[3]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[4]   Aldosteronism and a proinflammatory vascular phenotype -: Role of Mg2+, Ca2+, and H2O2 in peripheral blood mononuclear cells [J].
Ahokas, RA ;
Sun, Y ;
Bhattacharya, SK ;
Gerling, IC ;
Weber, KT .
CIRCULATION, 2005, 111 (01) :51-57
[5]   ALTERATIONS IN SARCOPLASMIC-RETICULUM GENE-EXPRESSION IN HUMAN HEART-FAILURE - A POSSIBLE MECHANISM FOR ALTERATIONS IN SYSTOLIC AND DIASTOLIC PROPERTIES OF THE FAILING MYOCARDIUM [J].
ARAI, M ;
ALPERT, NR ;
MACLENNAN, DH ;
BARTON, P ;
PERIASAMY, M .
CIRCULATION RESEARCH, 1993, 72 (02) :463-469
[6]   Inflammatory and anti-inflammatory cytokines in chronic heart failure:: Potential therapeutic implications [J].
Aukrust, P ;
Gullestad, L ;
Ueland, T ;
Damås, JK ;
Yndestad, A .
ANNALS OF MEDICINE, 2005, 37 (02) :74-85
[7]   Elevated circulating levels of C-C chemokines in patients with congestive heart failure [J].
Aukrust, P ;
Ueland, T ;
Müller, F ;
Andreassen, AK ;
Nordoy, I ;
Aas, H ;
Kjekshus, J ;
Simonsen, S ;
Froland, SS ;
Gullestad, L .
CIRCULATION, 1998, 97 (12) :1136-1143
[8]   Cytokine network in congestive heart failure secondary to ischemic or idiopathic dilated cardiomyopathy [J].
Aukrust, P ;
Ueland, T ;
Lien, E ;
Bendtzen, K ;
Müller, F ;
Andreassen, AK ;
Nordoy, I ;
Aass, H ;
Espevik, T ;
Simonsen, S ;
Froland, SS ;
Gullestad, L .
AMERICAN JOURNAL OF CARDIOLOGY, 1999, 83 (03) :376-382
[9]   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
[10]   Dynamic regulation of MEK/Erks and Akt/GSK-3β in human end-stage heart failure after left ventricular mechanical support:: myocardial mechanotransduction-sensitivity as a possible molecular mechanism [J].
Baba, HA ;
Stypmann, J ;
Grabellus, F ;
Kirchhof, P ;
Sokoll, A ;
Schäfers, M ;
Takeda, A ;
Wilhelm, MJ ;
Scheld, HH ;
Takeda, N ;
Breithardt, G ;
Levkau, B .
CARDIOVASCULAR RESEARCH, 2003, 59 (02) :390-399