We propose to study the effects of calcium on renal tubule epithelial transport using the technic of in vitro microperfusion, and the specific aims may be divided into two categories. Firstly, the modification of fluid and electrolyte transport processes by calcium will be studied in individual nephron segments. To determine the effect of altering ambient calcium, the calcium concentration will be varied in the perfusing or bathing solution or calcium will be replaced in these solutions with magnesium or manganese. Phosphate transport will be examined in proximal tubule segments from animals in which chronic hypercalcemia or hypocalcemia has been induced. Also to be studied is the effect of increasing cytosolic calcium with ionophores, and inhibitors of mitochondrial Ca-ATPase and the Na/Ca antiport at the basolateral membrane. The contribution of the Ca-calmodulin complex to transport processes will be examined by the use of its inhbitors. The studies in the second category will examine the role of changes in cytosolic calcium by various hormones and the effect this has on tubular transport. To determine if calcium entry is an important mechanism, calcium-channel blockers and low external calcium will be used to attenuate this entry. The role of membrane-bound calcium and calcium-stimulated C-kinase activity will be examined by the addition of lanthanum and phorbol esters, respectively, to the perfusing and/or bathing solutions. Finally, the role of intracellular organelles which store calcium and the extrusion of calcium at the basolateral membrane will be studied. Inhibitors of mitochondrial Ca-ATPase, endoplasmic reticulum calcium release, and the Na/Ca antiport will be used to study this aspect. These studies should provide a better understanding of the role of calcium on various transport processes in the mammalian nephron.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK037543-03
Application #
3236514
Study Section
General Medicine B Study Section (GMB)
Project Start
1986-09-01
Project End
1991-08-31
Budget Start
1988-09-01
Budget End
1989-08-31
Support Year
3
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Rouse, D; Leite, M; Suki, W N (1994) ATP inhibits the hydrosmotic effect of AVP in rabbit CCT: evidence for a nucleotide P2u receptor. Am J Physiol 267:F289-95
Gonzalez, J M; Dalmeida, W; Abramowitz, J et al. (1992) Evidence for a fourth rat isoform of the plasma membrane calcium pump in the kidney. Biochem Biophys Res Commun 184:387-93
Sugimura, K; Abramowitz, J; Tsukamoto, Y et al. (1992) Reconstitution and partial purification of calcium transport activity from rat kidney cortex. Am J Physiol 263:F192-200
Leite Jr, M; Rouse, D; Lederer, E et al. (1991) TMB-8 prevents the hydroosmotic response to ADH in rabbit cortical collecting tubules. Kidney Int 40:434-40
Rouse, D; Suki, W N (1990) Renal control of extracellular calcium. Kidney Int 38:700-8
Rouse, D; Williams, S; Suki, W N (1990) Clonidine inhibits fluid absorption in the rabbit proximal convoluted renal tubule. Kidney Int 38:80-5
Leite Jr, M; Suki, W N (1990) AVP and dDAVP in rabbit cortical collecting tubule: a comparative time-course study. Am J Physiol 258:R99-103
Guruprakash, G H; Krothapalli, R K; Rouse, D et al. (1988) The mechanism of hypercalciuria in streptozotocin-induced diabetic rats. Metabolism 37:306-11
Peraino, R A; Rouse, D; Suki, W N (1988) Calcifediol antagonizes PTH action on water and phosphate absorption in rabbit pars recta. Am J Physiol 254:F45-50
Edwards, G A; Crumb, C K; Suki, W N (1987) Renal handling of phosphate following release of ureteral obstruction. Miner Electrolyte Metab 13:377-84