H. Bjornstad et al., EFFECTS OF TEMPERATURE ON CYCLE LENGTH-DEPENDENT CHANGES AND RESTITUTION OF ACTION-POTENTIAL DURATION IN GUINEA-PIG VENTRICULAR MUSCLE, Cardiovascular Research, 27(6), 1993, pp. 946-950
Objective: The aim was to investigate the effects of temperature on cy
cle length dependent changes of action potential duration and on resti
tution of action potential duration. Methods: Guinea pig papillary mus
cle action potentials were recorded using conventional microelectrode
techniques. Action potential duration was measured at cycle lengths ra
nging from 500 to 2000 ms at both 27-degrees-C and 37-degrees-C. Resti
tution of action potential duration was determined by introducing an e
xtra stimulus at progressively longer diastolic intervals from 40 to 9
000 ms at pacing cycle lengths of 500, 1000, and 2000 ms. Results: At
37-degrees-C, action potential duration measured at 90% of repolarisat
ion (APD90) during continuous pacing and the maximum value of APD90 ac
hieved during restitution (APD90pl) decreased by 18(SEM 6) ms (n=7) an
d 24(7) ms (n=6), respectively, when pacing cycle length was reduced f
rom 2000 to 500 ms. At 27-degrees-C, the magnitude of the shortening o
f APD90 and APD90pl observed when pacing cycle length was similarly re
duced was greater than at 37-degrees-C, ie, 143(21) ms (n=6) and 115(1
1) ms (n=6), respectively. Thus the relation for restitution of action
potential duration shifted downwards with reduction in pacing cycle l
ength, and the magnitude of this shift was greater at 27-degrees-C tha
n at 37-degrees-C. The difference between APD90 at the shortest diasto
lic interval (40 ms) and at diastolic interval of 100 ms (range of pre
mature action potential durations) was much greater at 27-degrees-C th
at at 37-degrees-C at all three pacing cycle lengths. Conclusions: Red
uction in temperature magnifies the cycle length dependent changes in
action potential duration both during abrupt changes in cycle length,
as with an extra stimulus, and during changes of steady state cycle le
ngth. This may indicate a greater dispersion of premature action poten
tial durations during hypothermia, and hence predispose to hypothermia
induced arrhythmias.