TY - JOUR
T1 - Improved exercise tolerance by IV frucose-1,6-diphosphate in chronic, stable angina pectoris
AU - Marchionni, N.
AU - Moschi, G.
AU - Di Bari, M.
AU - Ferrucci, L.
AU - Paoletti, M.
AU - Salani, B.
AU - Fattirolli, F.
PY - 1988
Y1 - 1988
N2 - The effect of IV fructose-1,6-diphosphate (FDP) on transient, reproducible myocardial ischemia was evaluated in ten patients, aged 50 to 66 years, with chronic, stable exertional angina. FDP or placebo (glucose) were administered between basal and posttreatment ergometric stress testing; an identical procedure was repeated in each patient with the second treatment on the following day according to a single-blind, cross-over design. FDP improved exercise tolerance and total work capacity, significantly delaying the onset of ST-segment depression and angina. Nevertheless, the critical level of the rate x pressure (R x P) product, causing appearance of myocardial ischemia, was not remarkably changed. However, the R x P procuct at same workload was significantly lower after FDP. These results suggest that improved exercise tolerance might have resulted from peripheral (increased oxygen delivery to skeletal muscle) rather than from central (cardiac) effects of FDP.
AB - The effect of IV fructose-1,6-diphosphate (FDP) on transient, reproducible myocardial ischemia was evaluated in ten patients, aged 50 to 66 years, with chronic, stable exertional angina. FDP or placebo (glucose) were administered between basal and posttreatment ergometric stress testing; an identical procedure was repeated in each patient with the second treatment on the following day according to a single-blind, cross-over design. FDP improved exercise tolerance and total work capacity, significantly delaying the onset of ST-segment depression and angina. Nevertheless, the critical level of the rate x pressure (R x P) product, causing appearance of myocardial ischemia, was not remarkably changed. However, the R x P procuct at same workload was significantly lower after FDP. These results suggest that improved exercise tolerance might have resulted from peripheral (increased oxygen delivery to skeletal muscle) rather than from central (cardiac) effects of FDP.
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M3 - Article
C2 - 3230148
AN - SCOPUS:0024235427
SN - 0091-2700
VL - 28
SP - 807
EP - 811
JO - Journal of Clinical Pharmacology
JF - Journal of Clinical Pharmacology
IS - 9
ER -