In: Anatomy and Physiology
Furosemide (Frusemide)
Because it is a HIGH CEILING (LOOP) DIURETIC. Diuretics
(natriuretics) are drugs which cause a net loss of Na+ and water in
urine.
Prototype drug The development of this rapidly acting highly
efficacious oral diuretic was a breakthrough. Its maximal
natriuretic effect is much greater than that of other classes. The
diuretic response goes on increasing with increasing dose: upto 10
L of urine may be produced in a day. It is active even in patients
with relatively severe renal failure. The onset of action is prompt
(i.v. 2–5 min., i.m. 10–20 min., oral 20–40 min.) and duration
short (3–6 hours).
The major site of action is the thick AscLH (therefore called loop
diuretics) where furosemide inhibits Na+- K+-2Cl ̄ cotransport . A
minor component of action on PT has also been indicated. It is
secreted in PT by organic anion transport and reaches AscLH where
it acts from luminal side of the membrane. The cortico- medullary
osmotic gradient is abolished and positive as well as negative free
water clearance is blocked. K+ excretion is increased mainly due to
high Na+ load reaching DT. However, at equinatri- uretic doses, K+
loss is less than that with thiazides.
Furosemide has weak CAse inhibitory action;
increases HCO ̄ excretion as well; urinary pH 3
may rise but the predominant urinary anion is Cl ̄. Therefore,
acidosis does not develop. The diuretic action is independent of
acid-base balance of the body and it causes little distortion of
the same; mild alkalosis occurs at high doses.