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Departments of 1 Physiology and
2 Medicine,
The anorexic agents dexfenfluramine and
fenfluramine plus phentermine have been associated with outbreaks of
pulmonary hypertension. The fenfluramines release serotonin and reduce
serotonin reuptake in neurons. They also inhibit potassium current
(IK), causing membrane potential depolarization in pulmonary arterial smooth muscle
cells. The recent withdrawal of the fenfluramines has led to the use of
fluoxetine and phentermine as an alternative anorexic combination.
Because fluoxetine and venlafaxine reduce serotonin reuptake, we
compared the effects of these agents with those of phentermine and
dexfenfluramine on pulmonary arterial pressure, IK, and membrane
potential. Fluoxetine, venlafaxine, and phentermine caused minimal
increases in pulmonary arterial pressure at concentrations < 100 µM
but did cause a dose-dependent inhibition of
IK. The order of
potency for inhibition of
IK at +50 mV was
fluoxetine > dexfenfluramine = venlafaxine > phentermine. Despite
the inhibitory effect on
IK at more
positive membrane potentials, fluoxetine, venlafaxine, and phentermine,
in contrast to dexfenfluramine, had minimal effects on the cell resting
membrane potential (all at a concentration of 100 µM). However,
application of 100 µM fluoxetine to cells that had been depolarized
to
30 mV by current injection elicited a further depolarization
of >18 mV. These results suggest that fluoxetine, venlafaxine, and
phentermine do not inhibit IK at the resting
membrane potential. Consequently, they may present less risk of
inducing pulmonary hypertension than the fenfluramines, at least by
mechanisms involving membrane depolarization.
anorexic; serotonin; potassium channels; pulmonary hypertension; membrane potential
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