Abstract

Coronary blood flow adapts to metabolic demand ("metabolic regulation") and remains relatively constant over a range of pressure changes ("autoregulation"). Coronary metabolic regulation and autoregulation are usually studied separately. We developed an intact animal experimental model to explore both regulatory mechanisms of coronary blood flow. Coronary pressure and flow‐velocities were measured in four anesthetized and closed‐chest pigs using an intracoronary Doppler wire. Metabolic regulation was assessed by coronary flow reserve defined as the ratio between the maximally vasodilated and the basal flow, with hyperemia achieved using intracoronary administration of adenosine (90 µg) or bradykinin (10–6 M) as endothelium‐independent and ‐dependent vasodilators respectively. For both vasodilators, we found a healthy coronary flow reserve ≥ 3.0 at baseline, which was maintained at 2.9 ± 0.2 after a 6‐hr period. Autoregulation was assessed by the lower breakpoint of coronary pressure‐flow relationships, with gradual decrease in coronary pressure through the inflation of an intracoronary balloon. We found a lower limit of autoregulation between 42 and 55 mmHg, which was stable during a 6‐hr period. We conclude that this intact animal model is adequate for the study of pharmacological interventions on the coronary circulation in health and disease, and as such suitable for preclinical drug studies.

Highlights

  • Cardiac muscle is characterized by a high oxygen (O2) uptake along with a high O2 extraction with limited anaerobic capacity (Tune, Gorman, & Feigl, 2004)

  • CBF is determined by autonomic nervous system tone and metabolic demand (i.e. "metabolic regulation") (Feigl, Neat, & Huang, 1990; Tune et al, 2004) and remains constant over a wide range of pressures

  • Autoregulation of CBF fails when coronary perfusion pressure drops below a critical value

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Summary

Introduction

Cardiac muscle is characterized by a high oxygen (O2) uptake along with a high O2 extraction with limited anaerobic capacity (Tune, Gorman, & Feigl, 2004). "metabolic regulation") (Feigl, Neat, & Huang, 1990; Tune et al, 2004) and remains constant over a wide range of pressures CBF may increase by up to three times by metabolic regulation. Autoregulation of CBF fails when coronary perfusion pressure drops below a critical value. CBF becomes directly dependent on perfusion pressure (Duncker, Koller, Merkus, & Canty, 2015; Hoffman & Spaan, 1990). Autoregulation of CBF occurs mainly in the microcirculation, which contributes for more than 90% of the coronary vascular resistance (Chilian, 1997). In response to physiological triggers, such as shear stress or metabolic changes, the vascular endothelium regulates arterial smooth muscle tone through a fine balance between vasodilators and vasoconstrictors release. Microvascular and endothelial function play a key role in CBF regulation (Durand & Gutterman, 2013; Furchgott & Zawadzki, 1980)

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