Abstract

--- - "Background: The flat or negative force frequency relationship (FFR) is a halltuark of the failing heart. Either decreases in SERCA2a expression, increases in Na+/Ca2+ exchanger (NCX) expression or elevated Na-i(+) have been independently proposed as mediators of the negative FFR." - "Methods and Results: To determine whether each one of these mechanisms is sufficient to account for the negative FFR of the failing heart or on the contrary, various mechanisms, acting in concert are required. SERCA2a was pharmacologically inhibited with thapsigargin (TG) or cyclopiazonic acid (CPA) or by using siRNA technology; Na-i(+), was increased with either ouabain (Oua) or monensin and NCX protein was overexpressed by gene transfer (Ad.NCX), to mimic in nonfailing cat myocytes the phenotype of the failing heart and examine their effect on the FFR. The positive FFR of healthy myocytes remained unaffected after either SERCA2a inhibition, Na-i(+) elevation, or NCX overexpression. However, the combination of TG + Oua, Oua + Ad.NCX, or TG + Ad.NCX, converted the positive FFR to negative. Moreover, the FFR became negative at lower frequencies, when the 3 interventions were combined." - "Conclusions: Ca2+ handling has to be altered at several levels to explain the negative FFR of the failing heart. These anomalies in Ca2+ homeostasis acting in synergy have additive effects."