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Vol. 299, Issue 1, 290-296, October 2001
Drug Safety Evaluation, Aventis Pharmaceuticals, Inc., Bridgewater,
New Jersey
Mefloquine is a quinoline antimalarial drug that is structurally
related to the antiarrhythmic agent quinidine. Mefloquine is widely
used in both the treatment and prophylaxis of Plasmodium falciparum malaria. Mefloquine can prolong cardiac
repolarization, especially when coadministered with halofantrine, an
antagonist of the human ether-a-go-go-related gene
(HERG) cardiac K+ channel. For these reasons we examined
the effects of mefloquine on the slow delayed rectifier K+
channel (KvQT1/minK) and HERG, the K+ channels that
underlie the slow (IKs) and rapid (IKr)
components of repolarization in the human myocardium, respectively.
Using patch-clamp electrophysiology we found that mefloquine inhibited KvLQT1/minK channel currents with an IC50 value of
approximately 1 µM. Mefloquine slowed the activation rate of
KvLQT1/minK and more block was evident at lower membrane potentials
compared with higher ones. When channels were held in the closed state
during drug application, block was immediate and complete with the
first depolarizing step. HERG channel currents were about 6-fold less sensitive to block by mefloquine (IC50 = 5.6 µM).
Block of HERG displayed a positive voltage dependence with maximal
inhibition obtained at more depolarized potentials. In contrast to
structurally related drugs such as quinidine, mefloquine is a more
effective antagonist of KvLQT1/minK compared with HERG. Block of
KvLQT1/minK by mefloquine may involve an interaction with the closed
state of the channel. Inhibition by mefloquine of KvLQT1/minK in the human heart may in part explain the synergistic prolongation of QT
interval observed when this drug is coadministered with the HERG
antagonist halofantrine.
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