Inhaled furosemide (frusemide), a loop diuretic which inhibits the Na/2Cl-/K+ cotransport system, has been shown to inhibit asthma provoked
by several bronchial stimuli known to induce mediator release from in
flammatory cells. Although other loop diuretics with greater diuretic
potency (e.g. bumetanide, piretanide and torasemide) have been tested,
furosemide provides the widest and most effective antiasthma activity
. Inhaled acetazolamide, a selective inhibitor of carbonic anhydrase,
may have a similar protective profile. The relative antiasthma activit
y of these agents seems to be unrelated to their diuretic potency, but
is likely to be linked to their pharmacokinetic characteristics. The
underlying mechanisms of antiasthma activity are probably a reduction
of mediator release from inflammatory cells and a modulation of bronch
oconstriction mediated by sensory nerve activation. Whether this obser
vation will lead to the development of a new class of antiasthma compo
unds or will be a research tool for the study of asthma pathophysiolog
y remains to be determined.