Ns. Stachenfeld et al., ESTROGEN INFLUENCES OSMOTIC SECRETION OF AVP AND BODY-WATER BALANCE IN POSTMENOPAUSAL WOMEN, American journal of physiology. Regulatory, integrative and comparative physiology, 43(1), 1998, pp. 187-195
To determine if estrogen upregulates osmotic secretion of arginine vas
opressin (AVP) and alters body water balance, we infused hypertonic (3
% NaCl) saline in 6 women (68 +/- 3 yr) after 14 days of 17 beta-estra
diol (transdermal patch, similar to 0.1 mg/day, E-2) and placebo (cont
rol) administration. Hypertonic saline was infused at 0.1 ml.kg(-1).mi
n(-1) for 120 min, and after a 30-min equilibration period, the subjec
ts drank water ad libitum for 180 min. E-2 increased basal plasma estr
adiol concentration from less than or equal to 12 to 80 +/- 12 pg/ml a
nd plasma AVP concentration (P-[AVP]) from 2.1 +/- 0.7 to 3.1 +/- 0.8
pg/ml (P < 0.05), but not plasma osmolality (P-osm, 288 +/- 1 and 287
+/- 1, for control and E-2, respectively). Hypertonic saline infusion
increased P-osm by 18 +/- 1 and 17 +/- 1 mosmol/kgH(2)O and P-[AVP] by
5.2 +/- 0.5 and 4.9 +/- 0.4 pg/ml for control and E-2 treatments, res
pectively. The P-[AVP]-P-osm relationship shifted upward after E-2, wi
th no change in sensitivity (slope, 0.36 +/- 0.02 and 0.33 +/- 0.03 pg
.ml(-1).mosmol(-1) for control and E-2, respectively). Water intake wa
s similar between control and E-2 (24 vs. 22 ml/kg), but by 180 min of
drinking, urine output and free water clearance (C-H2O) were reduced
by 5.6 +/- 2.3 ml/kg and 2.6 +/- 2.0 ml/min, respectively (P < 0.05) a
fter E-2. Plasma aldosterone concentration was unaffected by E-2, but
fractional sodium excretion was reduced from 2.7 +/- 0.5 to 1.7 +/- 0.
4% (P < 0.05) at 180 min of drinking. Our data suggest that E-2 augmen
ts osmotic AVP secretion, thereby implicating elevated AVP as a contri
butor to water retention in high E-2 states; however, an increase in r
enal sodium reabsorption was a major component of the enhanced fluid r
etention.