Effects of calcium on the vasopressin-sensitive cAMP metabolism in medullary tubules
- 1 December 1985
- journal article
- research article
- Published by American Physiological Society in American Journal of Physiology-Renal Physiology
- Vol. 249 (6), F956-F966
- https://doi.org/10.1152/ajprenal.1985.249.6.f956
Abstract
The modulatory effect of Ca on [Arg8]vasopressin-dependent (AVP) cAMP metabolism was studied in medullary collecting tubules (MCT) and medullary ascending limbs (MAL) microdissected from rat kidney. In MCT segments incubated in vitro with AVP, the accumulation of cAMP was enhanced (.DELTA. +59%) when Ca was omitted from the incubation medium compared with a medium with 2 mM of ionized calcium (Ca2+). Ionophore A23187 caused a decrease in AVP-stimulated cAMP accumulation in MCT in the presence of 2 mM Ca2+ but not in a Ca2+-free medium. Diltiazem and verapamil enhanced the AVP-stimulated cAMP accumulation in MCT; PTH had no detectable effect. A23187 caused a dose-dependent inhibition of cAMP accumulation stimulated by AVP with forskolin in both MCT and in MAL. However, in MAL the A23187 concentration needed for half-maximum inhibition (6.3 .times. 10-6 M) was higher than for MCT (3.9 .times. 10-7 M). The maximum inhibition in MAL (-65%) was less than in MCT (-97%). In the presence of 3-isobutyl-1-methylxanthine, AVP stimulated cAMP accumulation was inhibited by A23187 in MCT (-45%) but not in MAL. Naproxen or ibuprofen did not relieve the inhibitory action of A23187 in MCT. Added Ca2+ inhibited the AVP-stimulated adenylate cyclase in MCT and MAL (half-maximum .simeq. 5 .times. 10-4 M Ca2+) and stimulated cAMP phosphodiesterase (cAMP-PDIE) in both MCT and in MAL (half-maximum .simeq. 9 .times. 10-5 Ca2+). Incubation of MCT and MAL with A23187 decreased (-50%) the content of ATP. Results suggest that increased influx of extracellular Ca2+ inhibits the AVP-stiumulated cAMP accumulation in MCT and to a much lesser degree in MAL. Decreased cAMP accumulation in MCT is probably due to both stimulation of cAMP-PDIE and the inhibition of adenylate cyclase, whereas in MAL it is due to stimulation of cAMP-PDIE. The results suggest that Ca2+ influx exhibits a negative modulatory effect on AVP-dependent cAMP metabolism mainly in MCT.This publication has 8 references indexed in Scilit:
- Pathogenesis of nephrogenic diabetes insipidus due to chronic administration of lithium in rats.Journal of Clinical Investigation, 1985
- Chlorpropamide action on renal concentrating mechanism in rats with hypothalamic diabetes insipidus.Journal of Clinical Investigation, 1983
- Hydroosmotic response of collecting tubules to ADH or cAMP at reduced peritubular sodiumAmerican Journal of Physiology-Renal Physiology, 1982
- Effects of calcium on ADH action in the cortical collecting tubule perfused in vitroAmerican Journal of Physiology-Renal Physiology, 1982
- Cytosolic free calcium levels in rabbit proximal kidney tubulesAmerican Journal of Physiology-Cell Physiology, 1982
- ADH-sensitive cAMP system in papillary collecting duct: effect of osmolality and PGE2American Journal of Physiology-Renal Physiology, 1981
- Intracellular calcium as a modulator of transepithelial permeability to water in frog urinary bladder.The Journal of cell biology, 1978
- Effects of ionophore A23187 on base-line and vasopressin-stimulated sodium transport in the toad bladder.Journal of Clinical Investigation, 1977