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

Citation
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
Citations number
NO
Categorie Soggetti
Cardiac & Cardiovascular System
Journal title
ISSN journal
09108327
Volume
9
Issue
6
Year of publication
1994
Pages
300 - 306
Database
ISI
SICI code
0910-8327(1994)9:6<300:RPOADI>2.0.ZU;2-R
Abstract
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.