K. Tsuchida et al., CALCIUM CURRENT IN RAT DIABETIC VENTRICULAR MYOCYTES, American journal of physiology. Heart and circulatory physiology, 36(6), 1994, pp. 80002280-80002289
The magnitude and kinetics of the L-type calcium current were compared
in single left ventricular myocytes isolated from 8-mo-old (8M) and 1
9-mo-old (19M) genetically diabetic rats (WBN/Kob rats) and age-matche
d control rats. A diabetic state occurred at 19M but not at 8M. The le
ft ventricular contractility was reduced in 19M WBN/Kob rats compared
with age-matched control rats. The duration of the action potential wa
s longer in 19M WBN/Kob rats than in the age-matched control rats. Pea
k inward current density was similar between diabetic rats and age-mat
ched control rats. In addition, aging did not affect the current densi
ty at 8M or 19M. The various kinetic parameters of the L-type calcium
current were not different between 19M diabetic and control cell types
. The percent increase in the amplitude of the calcium current induced
by isoproterenol was less in diabetic cells at the age of 19M, but no
t at the age of 8M, compared with age-matched control cells. Forskolin
(10(-5) M), intracellularly applied adenosine 3',5'-cyclic monophosph
ate (5 x 10(-5) M), and guanosine 5'-[gamma-thio]triphosphate (10(-4)
M) were equally effective in increasing the current in 19M diabetic an
d age-matched control cell types. The present study demonstrates that
the basal calcium current density and kinetic parameters of the curren
t were not altered. However, a decrease in response to beta-stimulatio
n occurred in genetically diabetic rats compared with control rats.