The action of the posterior pituitary hormone vasopressin to increase water permeability of the apical surface of renal collecting tubular cells is critical in the maintenance of normal body water balance. Clarification of the mechanism of the hydro-osmotic effect of vasopressin is the long-range goal of the applicant. As a step toward this goal, the present studies will examine the role of the calcium ion and calcium binding proteins in modulating the water permeability effect of vasopressin. Rabbit collecting tubules, perfused in vitro, will be used to determine the effect of altering collecting tubular cell calcium and calmodulin activities on water permeability response to vasopressin. The effect of vasopressin on net water flux and hydraulic conductivity in the presence and absence of calcium ion, calcium ionophores and inhibitors of cellular calcium uptake and calmodulin will be measured. To characterize any observed effects, both diffusional and osmotic water permeabilities as well as electrical potential difference across the tubule will be measured. Two additional types of studies will be performed to elucidate a potential role for cyclic necleotides in any observed effect: (1) perfused collecting tubule studies utilizing pharmacologic probes which manipulate renal collecting tubular cell content of cyclic nucleotides (for example, forskolin, diterpene compound which directly activates the catalytic unit of adenylate cyclase) and (2) collecting tubular biochemical assays for adenylate cyclase and phosphodiesterase. The proposed studies combine physiologic, pharmacologic, and biochemical approaches to clarify the role of the calcium ion and calcium-activated proteins in mediating the effect of vasopressin to increase collecting tubular cell apical water permeability. These studies should help clarify the mechanism of action of vasopressin in the mammalian nephron. These studies have health-related implications in view of the importance of the wather retaining effect of vasopressin in maintenance of normal tonicity and volume of body fluids.

Project Start
1984-07-01
Project End
1987-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Type
Schools of Medicine
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Dillingham, M A; Anderson, R J (1989) Mechanism of neuropeptide Y inhibition of vasopressin action in rat cortical collecting tubule. Am J Physiol 256:F408-13
Dillingham, M A; Anderson, R J (1988) Cyclic guanosine monophosphate increases hydraulic conductivity in rabbit and rat CCT. Am J Physiol 255:F841-6
Dillingham, M A; Better, O S; Anderson, R J (1988) Sodium taurocholate increases hydraulic conductivity in rabbit collecting tubule. Kidney Int 33:782-6
Dillingham, M A; Dixon, B S; Anderson, R J (1987) Calcium modulates vasopressin effect in rabbit cortical collecting tubule. Am J Physiol 252:F115-21
Dillingham, M A; Dixon, B S; Kim, J K et al. (1986) Effect of trifluoperazine on rabbit cortical collecting tubular response to vasopressin. J Physiol 372:41-50
Wilson, P D; Dixon, B S; Dillingham, M A et al. (1986) Pertussis toxin prevents homologous desensitization of adenylate cyclase in cultured renal epithelial cells. J Biol Chem 261:1503-6
Dillingham, M A; Anderson, R J (1986) Inhibition of vasopressin action by atrial natriuretic factor. Science 231:1572-3
Dillingham, M A; Anderson, R J (1985) Purinergic regulation of basal and arginine vasopressin-stimulated hydraulic conductivity in rabbit cortical collecting tubule. J Membr Biol 88:277-81