Ohl. Bing et al., FLUOROCARBON SIMULATION OF MYOCARDIAL-ISCHEMIA AND REPERFUSION - STUDIES OF RELATIONSHIPS BETWEEN FORCE AND INTRACELLULAR CALCIUM, Cardiovascular Research, 27(10), 1993, pp. 1863-1868
Objective: The aim was to compare the effects of simulated ischaemia-r
eperfusion with those of hypoxia-reoxygenation in isolated muscle prep
arations from the ferret right ventricle. Methods: Ischaemia was simul
ated using fluorocarbon immersion plus hypoxia. Intracellular calcium
transients were determined from aequorin luminescence during isometric
contractions. Results: Hypoxia in fluorocarbon and physiological sali
ne solution resulted in a similar reversible depression of the peak of
the calcium transient. Peak active tension, however, was more depress
ed in fluorocarbon than in physiological salt solution. The dissociati
on between peak light and peak active tension was most pronounced on r
eoxygenation, with near complete recovery of peak light, while there w
as little recovery of tension in fluorocarbon. When fluorocarbon was t
hen replaced by physiological salt solution, peak active tension recov
ered promptly. A prolongation of the decay of the calcium transient wa
s seen in both fluorocarbon and physiological salt solution during hyp
oxia, which shortened promptly on reoxygenation. The time to the peak
of the calcium transient was most prolonged during hypoxia in fluoroca
rbon and there was gradual recovery on reoxygenation. Conclusions: Whi
le some changes in the calcium transient during simulated ischaemia ar
e rapidly reversible with reoxygenation (in fluorocarbon), suggesting
an effect of hypoxia, others are incompletely reversed or only reverse
d with physiological salt solution, suggesting an effect of metabolite
accumulation. The pronounced dissociation between peak light and peak
active tension during reoxygenation in fluorocarbon is promptly rever
sed by changing to physiological salt solution, suggesting that metabo
lite retention in the postischaemic period may contribute to depressed
myocardial function after reperfusion.