The primary objective of the proposed protocol is to more clearly define the mechanism(s) of urinary acidification by the direct determination of pH, pCO2, and total CO2 concentration in vivo in the accessible nephrons of the rat kidney utilizing standard cortical and papillary micropuncture techniques. In this series of studies, three specific areas will be investigated: (1) determination of the magnitude and direction of the disequilibrium pH in proximal and distal convoluted tubules, (2) contribution of luminal carbonic anhydrase to bicarbonate reabsorption in the in vivo perfused isolated proximal tubule, and (3) determination of pH, pCO2, and total CO2 concentration in the accessible segments of the renal papilla. These studies will utilize pH and pCO2 microelectrodes developed in our laboratory for application in rat micropuncture, as well as the microcalorimetric method of Vurek for determination of total CO2 concentration. These studies should allow differentiation between the two proposed mechanisms of bicarbonate reabsorption: 1) H+ secretion, or 2) primary HCO-3 reabsorption. In summary, the proposed studies will utilize microelectrode and microcalorimetric techniques in concern to evaluate acid-base homeostasis directly by application of cortical and papillary micropuncture and in vivo microperfusion techniques.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK030603-06
Application #
3229556
Study Section
General Medicine B Study Section (GMB)
Project Start
1981-07-01
Project End
1987-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
6
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Texas Medical Br Galveston
Department
Type
Schools of Medicine
DUNS #
041367053
City
Galveston
State
TX
Country
United States
Zip Code
77555
Fisher, Kimberly D; Codina, Juan; Petrovic, Snezana et al. (2012) Pyk2 regulates H+-ATPase-mediated proton secretion in the outer medullary collecting duct via an ERK1/2 signaling pathway. Am J Physiol Renal Physiol 303:F1353-62
Codina, Juan; Opyd, Timothy S; Powell, Zachary B et al. (2011) pH-dependent regulation of the ýý-subunit of H+-K+-ATPase (HKýý2). Am J Physiol Renal Physiol 301:F536-43
Codina, Juan; DuBose Jr, Thomas D (2006) Molecular regulation and physiology of the H+,K+ -ATPases in kidney. Semin Nephrol 26:345-51
Codina, Juan; Liu, Jingfang; Bleyer, Anthony J et al. (2006) Phosphorylation of S955 at the protein kinase A consensus promotes maturation of the alpha subunit of the colonic H+,K+ -ATPase. J Am Soc Nephrol 17:1833-40
Codina, Juan; Li, Jian; Dubose Jr, Thomas D (2005) CD63 interacts with the carboxy terminus of the colonic H+-K+-ATPase to decrease [corrected] plasma membrane localization and 86Rb+ uptake. Am J Physiol Cell Physiol 288:C1279-86
Li, Jian; Codina, Juan; Petroske, Elizabeth et al. (2004) The effect of beta-subunit assembly on function and localization of the colonic H+,K+-ATPase alpha-subunit. Kidney Int 66:1068-75
Codina, Juan; Li, Jian; Dubose Jr, Thomas D (2004) A carboxy-terminus motif of HKalpha2 is necessary for assembly and function. Kidney Int 66:2283-92
Li, Jian; Codina, Juan; Petroske, Elizabeth et al. (2004) The carboxy terminus of the colonic H(+), K(+)-ATPase alpha-subunit is required for stable beta subunit assembly and function. Kidney Int 65:1301-10
Codina, Juan; Li, Jian; Hong, Yan et al. (2002) The gamma-Na+,K+-ATPase subunit assembles selectively with alpha1/beta1-Na+,K+-ATPase but not with the colonic H+,K+-ATPase. Kidney Int 61:967-74
DuBose Jr, T D (2000) Molecular and pathophysiologic mechanisms of hyperkalemic metabolic acidosis. Trans Am Clin Climatol Assoc 111:122-33; discussion 133-4

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