Key result
Dipyridamole spares ST segments in microminipigs compared to dogs, supporting their pre-clinical coronary utility.
Why the study?
The inherent vulnerability of coronary circulation in microminipigs has not been characterized, limiting their evaluation as a cardiovascular pharmacological model.
Does dipyridamole affect electrocardiogram and hemodynamics differently in anesthetized beagle dogs compared to microminipigs?
Does dipyridamole affect electrocardiogram and hemodynamics differently in anesthetized beagle dogs compared to microminipigs?
Microminipigs may be a more useful preclinical model than dogs for evaluating drugs affecting coronary circulation, as their ST-segment response to dipyridamole better mimics humans.
May favor microminipigs over dogs for coronary drug testing; leaves open human translation and validation.
Microminipigs are expected as a novel animal model for cardiovascular pharmacological experiments. Since inherent vulnerability of coronary circulation of microminipigs has not been characterized, we performed dipyridamole-stress test to both microminipigs and beagle dogs, and compared the results. Dipyridamole in doses of 0.056 and 0.56 mg/kg were intravenously infused over 10 min (n = 4 for each animal). Dipyridamole decreased the systolic/diastolic blood pressures and double product in dogs as well as in microminipigs; but it did not significantly alter the heart rate or the global balance between the myocardial oxygen demand and supply in either animal. While organic coronary arterial stenosis was not detected in either animal, dogs have well-developed epicardial intracoronary networks unlike microminipigs. Like in humans, dipyridamole did not affect the ST segment of microminipigs, whereas it substantially depressed that in dogs. The results indicate the onset of subendocardial ischemia by dipyridamole in dogs may be partly associated with their well-developed native coronary collateral channels. Microminipigs would be more useful to evaluate the drugs which may affect the coronary circulation in the pre-clinical study than dogs.
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Ando et al. (2018) studied Cardiovascular pharmacological animal model (n=8). Dipyridamole vs. Beagle dogs (comparative model) was evaluated on Changes in electrocardiogram (ST segment) and hemodynamics. Dipyridamole did not affect the ST segment of microminipigs, whereas it substantially depressed that in dogs, suggesting microminipigs may be a more useful pre-clinical model for coronary circulation.
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