A basic understanding of the cell, in health and disease, is essential if we are to understand more complex tissue and organ function. As a result of ion flux and electrical studies of osmotically perturbed Amphiuma erythrocytes, obligatorily coupled, electroneutral alkali metal/H exchange pathways have been identified as being responsible for volume regulation by that cell. Functionally similar pathways have been reported to participate in cell growth, intracellular pH regulation and epithelial fluid and electrolyte transport. By virtue of the central role played by alkali metal/H (particularly Na/H) exchange in a variety of physiologically important processes an increased understanding of the kinetics and control of the pathway is of interest to both clinical and basic scientists. The proposed studies of the activation, control and pharmacological sensitivity of alkali metal/H exchange using the Amphiuma red blood cells as a model system are therefore of general interest and biological importance. In addition to the above, studies intended to evaluate the contribution of electroneutral alkali metal transport to cell volume disturbances associated with ischemia and anoxia are proposed. These studies will be performed upon perfused rabbit heart and will employ pressure/volume measurements to evaluate volume distributions and NMR to evaluate changes in intracellular alkali metal ion content. The information gained in the red blood cell studies regarding the kinetics, control and pharmacology of Na/H exchange will be used on a predictive and interpretive basis in assessing the participation of that pathway in cardiac cell volume disturbances. To the extent that Na/H exchange contributes to volume disturbances associated with pathological conditions the information obtained in the red blood cell studies is clinically significant.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL021179-08
Application #
3336406
Study Section
Physiology Study Section (PHY)
Project Start
1978-04-01
Project End
1989-03-31
Budget Start
1985-04-01
Budget End
1986-03-31
Support Year
8
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California Davis
Department
Type
Schools of Medicine
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
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Nygaard, Eva B; Lagerstedt, Jens O; Bjerre, Gabriel et al. (2011) Structural modeling and electron paramagnetic resonance spectroscopy of the human Na+/H+ exchanger isoform 1, NHE1. J Biol Chem 286:634-48
Liu, Hong; Cala, Peter M; Anderson, Steve E (2010) Na/H exchange inhibition protects newborn heart from ischemia/reperfusion injury by limiting Na+-dependent Ca2+ overload. J Cardiovasc Pharmacol 55:227-33
Ortiz-Acevedo, Alejandro; Rigor, Robert R; Maldonado, Hector M et al. (2010) Coordinated control of volume regulatory Na+/H+ and K+/H+ exchange pathways in Amphiuma red blood cells. Am J Physiol Cell Physiol 298:C510-20
Ortiz-Acevedo, Alejandro; Rigor, Robert R; Maldonado, Hector M et al. (2008) Activation of Na+/H+ and K+/H+ exchange by calyculin A in Amphiuma tridactylum red blood cells: implications for the control of volume-induced ion flux activity. Am J Physiol Cell Physiol 295:C1316-25
Pedersen, Stine Falsig; Cala, Peter Michael (2004) Comparative biology of the ubiquitous Na+/H+ exchanger, NHE1: lessons from erythrocytes. J Exp Zool A Comp Exp Biol 301:569-78
Liu, H; Cala, P M; Anderson, S E (1998) Ischemic preconditioning: effects on pH, Na and Ca in newborn rabbit hearts during Ischemia/Reperfusion. J Mol Cell Cardiol 30:685-97
Liu, H; Cala, P M; Anderson, S E (1997) Ethylisopropylamiloride diminishes changes in intracellular Na, Ca and pH in ischemic newborn myocardium. J Mol Cell Cardiol 29:2077-86
Cala, P M; Maldonado, H M (1994) pH regulatory Na/H exchange by Amphiuma red blood cells. J Gen Physiol 103:1035-53
Maldonado, H M; Cala, P M (1994) Labeling of the Amphiuma erythrocyte K+/H+ exchanger with H2DIDS. Am J Physiol 267:C1002-12

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