RATE-DEPENDENT PROLONGATION OF ACTION-POTENTIAL DURATION IN SINGLE VENTRICULAR MYOCYTES OBTAINED FROM HEARTS OF RATS WITH STREPTOZOTOCIN-INDUCED CHRONIC DIABETES SUSTAINED FOR 30-32 WEEKS
S. Shigematsu et al., RATE-DEPENDENT PROLONGATION OF ACTION-POTENTIAL DURATION IN SINGLE VENTRICULAR MYOCYTES OBTAINED FROM HEARTS OF RATS WITH STREPTOZOTOCIN-INDUCED CHRONIC DIABETES SUSTAINED FOR 30-32 WEEKS, Heart and vessels, 9(6), 1994, pp. 300-306
We examined the characteristics of the action potentials of single ven
tricular myocytes obtained from the hearts of rats with chronically-in
duced diabetes. Male Wistar rats were made diabetic by injecting strep
tozotocin (65 mg/kg) and 30-32 weeks later the hearts were excised and
used for an electrophysiological study. Action potentials were record
ed from isolated right ventricular myocytes by an electrode fabricated
for patch clamp in the whole-cell recording configuration. The action
potential durations (APDs) of steady state chronic diabetic rat myocy
tes were longer than those of age-matched normal rat myocytes at all l
evels of repolarization (APD25, APD50, APD75, and APD90). As the stimu
lation frequency was increased (0.2-2 Hz), the APDs were lengthened in
both diabetic and normal rats, and the difference of APDs between the
groups was greater when the stimulation frequency was higher. When we
examined alterations of APDs under conditions of train stimulation (2
Hz, 20 stimuli), (1) the APDs in both groups were prolonged, and (2)
the degree of prolongation of APD was significantly greater and the ra
te of APD prolongation was significantly faster in myocytes from the d
iabetic rats. The prolongation of APD in these heart cells is probably
secondary to alteration of the transient outward current I(to), and s
heds light on repolarization abnormality in cases of diabetic cardiomy
opathy.