Parameters |
Regadenoson |
Adenosine |
Potency |
10 times more potent than adenosine |
Less potent |
Receptor selectivity |
Selective A2a adenosine receptor agonist |
Nonselective agonist |
Dose |
400 ug as a single dose |
140 ug/kg/min |
Duration of infusion |
10 seconds bolus |
4 – 6 min |
Radiotracer injection |
30s after bolus |
Third minute of infusion |
Time to peak plasma concentration (Tmax ) |
33s |
30s |
Metabolism |
No hepatic metabolism |
Deaminated to inosine by adenosine deaminase |
Excretion |
57% appears unchanged in urine |
Cellular uptake |
Half-life |
1st phase: 2 – 4 min 2nd phase: 30 min 3rd phase: 2 h |
< 10 s |
Duration of action |
2.3 min* |
6 s* |
Coronary blood flow |
Increased to >2 times baseline in 30 s and decreased to < 2 times baseline in 10 min |
Maximum response at 2 – 3 min after infusion onset; return to baseline within 1 – 2 min following cessation of infusion |
Coronary hyperemia |
2 – 5 min longer than adenosine |
Lesser effect |
Heart rate |
Faster and greater peak increase in HR |
Less fast and lesser peak in HR |
Adverse effects |
Less hypotension, AV blocks, bronchoconstriction |
hypotension, AV blocks, bronchoconstriction |