Ct. Hawk et al., AVP AND ALDOSTERONE AT PHYSIOLOGICAL CONCENTRATIONS HAVE SYNERGISTIC EFFECTS ON NA+ TRANSPORT IN RAT CCD, Kidney international, 50, 1996, pp. 35-41
These studies examined whether the previously reported synergism betwe
en pharmacological doses of deoxycorticosterone (DOG) and arginine vas
opressin (AVP) also occur at physiological concentrations of aldostero
ne and AVP. We examined the dose-response of salt transport, as measur
ed by the lumen-to-bath Na-22(+) flux (J(1-->b)) and transepithelial v
oltage (V-T), and of osmotic water permeability (P-f), to AVP in isola
ted perfused cortical collecting ducts (CCDs) from three groups of rat
s: (1) implanted with a 1 mg d-aldosterone pellet, which produced a mo
derately elevated, but physiologically relevant, plasma aldosterone co
ncentration of 18.4 +/- 2.6 ng/dl: (7) implanted with a 2.5 mg DOC pel
let (a high pharmacological dose); and (3) untreated rats. P-f reached
the same maximal value in all three groups, and the concentration of
AVP producing one-half the maximal P-f response (K-0.5) was not signif
icantly different among the three groups, ranging from 5 to 10 pM. The
re was a significantly greater increase in J(1-->b) and hyperpolarizat
ion of V-T with increasing AVP in both groups of treated rats than in
the untreated group. The maximum values of J(1-->) and V-T achieved at
high AVP concentrations were not significantly different in CCDs from
the aldosterone-treated and DOC-treated groups, but they were signifi
cantly higher than in the CCDs from untreated rats. Although maximal V
-T values achieved with DOC and aldosterone treatment were the same, t
he AVP K-0.5 for V-T values were significantly lower in the DOC-treate
d than in the aldosterone-treated group. Although not statistically si
gnificant, the same trend was observed for J(1-->b). We conclude that
AVP and aldosterone synergistically stimulate Na+ reabsorption at phys
iological concentrations of birth hormones: however, V-T (and probably
Na+ reabsorption, which is generally proportional to V-T) reaches max
imum values at lower AVP concentrations when pharmacological doses of
DOC are employed.