Urinary guanosine 3′: 5′-cyclic monophosphate but not tissue kallikrein follows the plasma atrial natriuretic factor response to acute volume expansion with saline
- 1 November 1988
- journal article
- research article
- Published by Portland Press Ltd. in Clinical Science
- Vol. 75 (5) , 489-494
- https://doi.org/10.1042/cs0750489
Abstract
The relationship between plasma immunoreactive atrial natriuretic factor (Ir-ANF) and the urinary excretion of sodium, guanosine 3'':5''-cyclic monophosphate (cyclic GMP) and of tissue kallikrein was examined in seven healthy female volunteers. Each volunteer attended on two occasions, a control and a saline infusion day. On the infusion day saline (2 liters, 0.9% NaCl) was administered over 60 min. Measurement of plasma Ir-ANF and urinary excretion of sodium, cyclic GMP and of tissue kallikrein were made at 30 min intervals during the infusion and for 3 h after the infusion. Mean (.+-. SEM) urinary sodium excretion increased from a basal value (time 0) of 102 .+-. 15 .mu.mol/min to 222 .+-. 47 .mu.mol/min 60-90 min from the start of the infusion and thereafter remained significantly elevated (P < 0.01), above sodium excretion on the control day. In response to saline infusion there was a transient rise in mean (.+-. SEM) plasma Ir-ANF from 6.7 .+-. 0.8 pmol/l to a peak of 22.5 .+-. 3.7 pmol/l at 75 min, falling to 12.7 .+-. 1.9 pmol/l at 135 min. The peak plasma Ir-ANF level on the infusion day was significantly elevated (P < 0.05) above the time-matched measurement on the control day. Similarly, there was a transient rise in mean (.+-. SEM) urinary cycle GMP excretion on the infusion day from 30.9 .+-. 4.4 fmol/min to 64.6 .+-. 11.4 fmol/min during the 60-90 min collection period, returning to 43.7 .+-. 14.5 fmol/min at 210-240 min. Cyclic GMP excretion on the infusion day was significantly elevated (P < 0.05) above the time-matched measurement on the control day during the period 60-180 min. Serum and urinary tissue kallikrein on the infusion day did not differ significantly from time-matched measurements on the control day. Thus urinary cycle GMP but not tissue kallikrein follows the plamsa Ir-ANF response to acute volume expansion with saline, and may be a useful marker of the activity of this peptide.This publication has 2 references indexed in Scilit:
- In vivo evidence that cGMP is the second messenger for atrial natriuretic factor.Proceedings of the National Academy of Sciences, 1986
- Development and characterization of a radioimmunoassay to measure human tissue kallikrein in biological fluidsJournal of Endocrinology, 1984