Is rate-pressure product of any use in the isolated rat heart? Assessing cardiac "effort' and oxygen consumption in the Langendorff-perfused heart

New Findings What is the central question of this study? Rate-pressure product (RPP) is commonly used as an index of cardiac effort'. In canine and human hearts (which have a positive force-frequency relationship), RPP is linearly correlated with oxygen consumption and has therefore been widely adopted as a species-independent index of cardiac work. However, given that isolated rodent hearts demonstrate a negative force-frequency relationship, its use in this model requires validation. What is the main finding and its importance? Despite its widespread use, RPP is not correlated with oxygen consumption (or cardiac effort') in the Langendorff-perfused isolated rat heart. This lack of correlation was also evident when perfusions included a range of metabolic substrates, insulin or -adrenoceptor stimulation. Langendorff perfusion of hearts isolated from rats and mice has been used extensively for physiological, pharmacological and biochemical studies. The ability to phenotype these hearts reliably is, therefore, essential. One of the commonly used indices of function is rate-pressure product (RPP); a rather ill-defined index of work' or, more correctly, effort'. Rate-pressure product, as originally described in dog or human hearts, was shown to be correlated with myocardial oxygen consumption (MVover dotO(2)). Despite its widespread use, the application of this index to rat or mouse hearts (which, unlike the dog or human, have a negative force-frequency relationship) has not been characterized. The aim of this study was to examine the relationship between RPP and MVover dotO(2) in Langendorff-perfused rat hearts. Paced hearts (300-750beatsmin(-1)) were perfused either with Krebs-Henseleit (KH) buffer (11mm glucose) or with buffer supplemented with metabolic substrates and insulin. The arteriovenous oxygen consumption (MVover dotO(2)) was recorded. Metabolic status was assessed using P-31 magnetic resonance spectroscopy and lactate efflux. Experiments were repeated in the presence of isoprenaline and in unpaced hearts where heart rate was increased by cumulative isoprenaline challenge. In KH buffer-perfused hearts, MVover dotO(2) increased with increasing heart rate, but given that left ventricular developed pressure decreased with increases in rate, RPP was not correlated with MVover dotO(2), lactate production or phosphocreatine/ATP ratio. Although the provision of substrates or -adrenoceptor stimulation changed the shape of the RPP-MVover dotO(2) relationship, neither intervention resulted in a positive correlation between RPP and oxygen consumption. Rate-pressure product is therefore an unreliable index of oxygen consumption or cardiac effort' in the isolated rat heart.