Considerable experimental evidence has accumulated over the past years that proinflammatory cytokines, especially TNF-α and IL-1β, impair myocardial function in different animal species. On the other hand, several prospective clinical trials studying TNF-α antagonist in patients with chronic heart failure were not able to demonstrate a benefit. As there might be a relevant species-related discrepancy, we intended to prove our previous results demonstrating impaired myocardial economy after exogenous administration of recombinant TNF-α in rat myocardium. In the present study, both TNF-α and IL-1β not only revealed an immediate negative inotropic effect but also increased specific oxygen demand in human right-atrial myocardium. Enhanced oxygen consumption was not caused by an elevated basal metabolism but an impaired economy of contraction. Our results suggest that proinflammatory cytokines have a considerable effect on myocardial mechano-energetic parameters in human myocardium as well.