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1.
J Card Fail ; 14(10): 873-80, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19041052

ABSTRACT

BACKGROUND: In heart failure, alterations in the expression of proteins relevant to calcium homeostasis are involved in depressed contractility and diminished relaxation. However the regulation of genes expression is only partially known. The aim was to assess expression of calcium regulatory proteins in left ventricle (LV) myocardium characterised by a preserved global function in mitral valve stenosis (MVS) model but increased neurohumoral/cytokine (N/C) activation. METHODS AND RESULTS: Plasma N/C activation was evaluated in MVS-patients (n = 27), where expression of calcium regulatory proteins (L-type channel, sarcoplasmic reticulum Ca2+-ATPase type2 - SERCA2, Na+/Ca2+ exchanger -NCX, calsequestrin, phospholamban) in LV myocardium was assessed (Western Blot) in comparison with non-failing hearts (NFH). Out of all proteins assessed in MVS, only SERCA2 and NCX expression revealed highly variable changes between subjects, with significant reduction of SERCA2 (15%) level compared to NFH. Moreover, SERCA2 was negatively correlated with BNP (univariate/regression analysis r = -0.63, P = 0.005/r2 = 0.74, P <0.001, respectively), whereas NCX was positively correlated only with noradrenaline (univariate/stepwise analysis r = 0.59 P = 0.002/r2 = 0.59; P = 0.003). CONCLUSIONS: In MVS-patients LV becomes remodelled, although its global function is preserved. It seems that apart from alterations in LV load and wall stress, also such neurohumoral factors as BNP/noradrenaline may influence the Ca2+ handling proteins expression.


Subject(s)
Calcium-Binding Proteins/biosynthesis , Calcium-Binding Proteins/blood , Gene Expression Regulation/physiology , Mitral Valve Stenosis/blood , Ventricular Function, Left/physiology , Adult , Aged , Calcium Channels, L-Type/biosynthesis , Calcium Channels, L-Type/blood , Calcium Channels, L-Type/genetics , Calsequestrin/biosynthesis , Calsequestrin/blood , Calsequestrin/genetics , Female , Humans , Male , Middle Aged , Mitral Valve Stenosis/metabolism , Sarcoplasmic Reticulum Calcium-Transporting ATPases/biosynthesis , Sarcoplasmic Reticulum Calcium-Transporting ATPases/blood , Sarcoplasmic Reticulum Calcium-Transporting ATPases/genetics , Sodium-Calcium Exchanger/biosynthesis , Sodium-Calcium Exchanger/blood , Sodium-Calcium Exchanger/genetics , Young Adult
2.
Eur J Heart Fail ; 9(6-7): 579-86, 2007.
Article in English | MEDLINE | ID: mdl-17347034

ABSTRACT

BACKGROUND: Reduced myocardial contractility is often attributed to altered Ca(2+) transients and expression of Ca(2+)-ATPase of the SR (SERCA) and Na+/Ca(2+)exchanger (NCX) genes. AIMS: To assess myocardial expression of SERCA and NCX protein levels in left ventricular (LV) remodelling due to chronic severe mitral regurgitation (MR). METHODS: Myocardial expression of SERCA/NCX in biopsy specimens obtained during mitral surgery was assessed in 36 MR patients with LV remodelling and plasma neurohumoral/cytokine activation and in four non-failing hearts (NFH). RESULTS: Myocardial protein levels of SERCA were significantly (20%) lower in the MR group than in NFH group (p=0.016). No significant changes in NCX were observed. However, a lack of homogeneity with regard to SERCA/NCX proteins was observed. Moreover, SERCA was negatively correlated with BNP (r=-0.49, p=0.02), TNFalpha (r=-0.68, p=0.0005) and IL-6 (r=-0.52, p=0.02), whereas NCX was only negatively correlated with TNFalpha (r=-0.62, p=0.002). CONCLUSIONS: MR patients showed wide variations in SERCA/NCX protein expression. Myocardial protein levels of SERCA were significantly lower in the MR population. Moreover, a correlation between BNP, cytokines (IL-6, TNFalpha) and the expression of SERCA/NCX proteins was observed.


Subject(s)
Mitral Valve Insufficiency/genetics , Myocardial Contraction/genetics , Sarcoplasmic Reticulum Calcium-Transporting ATPases/genetics , Sarcoplasmic Reticulum/genetics , Sodium-Calcium Exchanger/genetics , Ventricular Dysfunction, Left/genetics , Ventricular Remodeling/genetics , Aged , Aged, 80 and over , Biopsy , Cytokines/blood , Female , Gene Expression/physiology , Humans , Male , Middle Aged , Mitral Valve Insufficiency/pathology , Mitral Valve Insufficiency/physiopathology , Neurotransmitter Agents/blood , Papillary Muscles/pathology , Papillary Muscles/physiopathology , Sarcoplasmic Reticulum/pathology , Ventricular Dysfunction, Left/pathology , Ventricular Dysfunction, Left/physiopathology , Ventricular Remodeling/physiology
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