Dynamic control of maximal ventricular elastance via the baroreflex and force-frequency relation in awake dogs before and after pacing-induced heart failure

• Published in: American journal of physiology. Heart and circulatory physiology Vol. 299; no. 1; pp. H62 - H69
• Main Authors: Chen, Xiaoxiao, Sala-Mercado, Javier A, Hammond, Robert L, Ichinose, Masashi, Soltani, Soroor, Mukkamala, Ramakrishna, O'Leary, Donal S
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.07.2010
• Subjects: Animals; Baroreflex; Blood Pressure; Cardiac Pacing, Artificial; Disease Models, Animal; Dogs; Elasticity; Heart failure; Heart Failure - etiology; Heart Failure - physiopathology; Heart Rate; Models, Cardiovascular; Myocardial Contraction; Time Factors; Veins & arteries; Ventricular Function; Wakefulness
• ISSN: 0363-6135; 1522-1539
• DOI: 10.1152/ajpheart.00922.2009

We investigated to what extent maximal ventricular elastance (E(max)) is dynamically controlled by the arterial baroreflex and force-frequency relation in conscious dogs and to what extent these mechanisms are attenuated after the induction of heart failure (HF). We mathematically analyzed spontaneous beat-to-beat hemodynamic variability. First, we estimated E(max) for each beat during a baseline period using the ventricular unstressed volume determined with the traditional multiple beat method during vena cava occlusion. We then jointly identified the transfer functions (system gain value and time delay per frequency) relating beat-to-beat fluctuations in arterial blood pressure (ABP) to E(max) (ABP-->E(max)) and beat-to-beat fluctuations in heart rate (HR) to E(max) (HR-->E(max)) to characterize the dynamic properties of the arterial baroreflex and force-frequency relation, respectively. During the control condition, the ABP-->E(max) transfer function revealed that ABP perturbations caused opposite direction E(max) changes with a gain value of -0.023 +/- 0.012 ml(-1), whereas the HR-->E(max) transfer function indicated that HR alterations caused same direction E(max) changes with a gain value of 0.013 +/- 0.005 mmHg.ml(-1).(beats/min)(-1). Both transfer functions behaved as low-pass filters. However, the ABP-->E(max) transfer function was more sluggish than the HR-->E(max) transfer function with overall time constants (indicator of full system response time to a sudden input change) of 11.2 +/- 2.8 and 1.7 +/- 0.5 s (P < 0.05), respectively. During the HF condition, the ABP-->E(max) and HR-->E(max) transfer functions were markedly depressed with gain values reduced to -0.0002 +/- 0.007 ml(-1) and -0.001 +/- 0.004 mmHg.ml(-1).(beats/min)(-1) (P < 0.1). E(max) is rapidly and significantly controlled at rest, but this modulation is virtually abolished in HF.