To elucidate possible mechanisms underlying the cardiotoxicity of terf
enadine, the effect of this antihistamine on L-type Ca2+ channel curre
nt (I-Ca,I-L) was studied in adult rat ventricular myocytes using the
whole-cell patch-clamp technique. Myocytes were held at -70 mV and int
ernally dialyzed and externally perfused with Na+- and K+-free solutio
ns; exposure to terfenadine (10(-9) to 5x10(-6) mol/L) resulted in a c
oncentration-dependent inhibition of peak I-Ca,I-L with a half-maximum
inhibition concentration (IC50) Of 142 nmol/L. The terfenadine-induce
d inhibition of I-Ca,I-L was not mediated via effects on histamine H-1
receptors, because 1 mu mol/L triprolidine, a more selective and pote
nt H-1 antagonist, had no effect on I-Ca,I-L. In this study, we found
that terfenadine (1) increased both the fast and slow time constants o
f I-Ca,I-L, inactivation, (2) shifted the steady state inactivation of
I-Ca,I-L to more negative potentials, and (3) elicited a tonic block
and a use-dependent block of I-Ca,I-L. The terfenadine-induced tonic a
nd use-dependent block and the steady state inhibition of I-Ca,I-L wer
e voltage dependent. Both tonic and use-dependent blocks of I-Ca,I-L b
y terfenadine at -40 mV were greater than that at -70 mV, and blocks w
ere partially released by applying a long hyperpolarizing prepulse to
-90 mV. These results suggest that terfenadine binds to L-type Ca2+ ch
annels in inactivated and rested states and inhibits I-Ca,I-L predomin
antly by interacting with the inactivated state with an apparent disso
ciation constant of GO nmol/L. Open-state block could be observed only
at high concentrations of terfenadine. The high-affinity interaction
of terfenadine with the inactivated state of L-type Ca2+ channels may
play an important role in its cardiotoxicity under pathophysiological
conditions, such as ischemia.