The urinary isoflavonoid genistein inhibits membrane Na-R-CI cotranspo
rters at similar concentrations as furosemide, but the significance of
this action is unknown, Genistein was therefore investigated in rats
for its potential salidiuretic actions, In the isolated, perfused rat
kidney, genistein induced a maximal salidiuretic action similar to tha
t of furosemide but was 3 to 5 times less potent than furosemide In te
rms of active doses (natriuresis EC50, 237+/-92 versus 56+/-20 mu mol/
L for genistein and furosemide, respectively). Genistein and furosemid
e had no additive salidiuretic actions, Genistein had no significant e
ffect on glomerular filtration rate but was able to significantly redu
ce renal vascular resistance with respect to vehicle isolated perfused
kidney, Indomethacin (10 mu mol/L), a blocker of prostaglandin biosyn
thesis, reduced salidiuresis and renal vasorelaxation by genistein, Su
bcutaneous genistein (ii mg/kg) induced a statistically significant in
crease in diuresis and natriuresis with respect to vehicle during the
first 6 hours of administration in rats. In conclusion, genistein comp
ares well with furosemide in vitro for its salidiuretic profile and po
tency in the isolated pet-fused rat kidney and is also natriuretic by
the subcutaneous route in the rat. Further studies are required to inv
estigate potential natriuretic and perhaps hypotensive actions of diet
ary genistein.