The specific aim of the present proposal is to use multiple different technical approaches to examine the central theme of regulation of salt, water, and acid base transport by various nephron segments. In vitro microperfusion, in vivo micropuncture, microelectrode, microenzymologic and NMR techniques will be utilized. The following specific aims can be enumerated: in vitro microperfusion studies have been designed to construct a model of H reabsorption in proximal and distal tubules by measuring intracellular pH, magnitude of hydrogen permeability and factors which regulate hydrogen transport. Additional studies are designed to examine hormonal regulation of salt transport across the proximal and distal tubules and to determine whether luminal pH influences transport of potassium. The micropuncture studies will determine whether pCO2 is elevated in the cortex of other species besides the rat and examine whether lack of capillary endothelial carbonic anhydrase participates in the maintenance of the high pCO2. Studies also are designed to examine hydrogen transport in chronic hyperparathyroidism and across the papillary collecting duct. Finally, studies will determine factors contributing to the concentrating defect seen in potassium deficiency. Our microelectrode section plans to develop new types of sodium and hydrogen sensitive microelectrodes to be used for microperfusion and micropuncture studies including intracellular punctures. The microenzymology studies are designed to determine the role of Na-K ATPase activity in transport of Na and K across the cortical collecting tubule and plans are outlined by which we hope to develop an ultra-microassay for hydrogen activated ATPase. Finally, the nuclear magnetic resonance studies will determine the effect of aldosterone on intracellular pH and phosphorylation potential of toad bladder epithelium.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM014677-16
Application #
3150924
Study Section
Physiology Study Section (PHY)
Project Start
1978-02-01
Project End
1988-01-31
Budget Start
1985-02-01
Budget End
1986-01-31
Support Year
16
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Cordova, H R; Kokko, J P; Marver, D (1989) Chronic indomethacin increases rabbit cortical collecting tubule Na+-K+-ATPase activity. Am J Physiol 256:F570-6
Baum, M; Hays, S R (1988) Phorbol myristate acetate and dioctanoylglycerol inhibit transport in rabbit proximal convoluted tubule. Am J Physiol 254:F9-14
de Zeeuw, D; Brater, D C; Jacobson, H R (1988) Micro-HPLC and transfer techniques for directly measuring drug (indomethacin) transport across the isolated perfused renal proximal straight tubule. J Pharmacol Methods 19:275-82
Stokols, M; Corona, S K; Pucacco, L R et al. (1987) Microelectrode of the Thomas type using a liquid membrane electrode. Anal Biochem 163:530-4
Baum, M (1987) Evidence that parallel Na+-H+ and Cl(-)-HCO3-(OH-) antiporters transport NaCl in the proximal tubule. Am J Physiol 252:F338-45
Baum, M (1987) Insulin stimulates volume absorption in the rabbit proximal convoluted tubule. J Clin Invest 79:1104-9
Kokko, J P (1987) The role of the collecting duct in urinary concentration. Kidney Int 31:606-10
Hays, S R; Baum, M; Kokko, J P (1987) Effects of protein kinase C activation on sodium, potassium, chloride, and total CO2 transport in the rabbit cortical collecting tubule. J Clin Invest 80:1561-70
Hays, S; Kokko, J P; Jacobson, H R (1986) Hormonal regulation of proton secretion in rabbit medullary collecting duct. J Clin Invest 78:1279-86
Breyer, M D; Kokko, J P; Jacobson, H R (1986) Regulation of net bicarbonate transport in rabbit cortical collecting tubule by peritubular pH, carbon dioxide tension, and bicarbonate concentration. J Clin Invest 77:1650-60

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