Theories which account for renal medullary handling of solutes and water frequently neglect the role of the microcirculation. In contrast, recent studies revealed unique vasa recta transport properties as well as the existence of water channels and a facilitated urea transporter in the outer medullary descending vasa recta (OMDVR). The overall object of these studies is to obtain further information on the magnitude and regulation of those properties and to incorporate that information into models of medullary physiology. We will employ methods for in vivo microperfusion of inner medullary descending (IMDVR) and ascending vasa recta (IMAVR) and for in vitro microperfusion of OMDVR from rat vascular bundles to accomplish the following specific objectives. 1. To determine the pathways and mechanisms responsible for transport of water across OMDVR. The hypothesis that water is transported across OMDVR by paracellular and cellular pathways will be tested. Osmotic water permeability of these pathways will be measured. Experiments will verify and quantitate the role of water channels by examining Arrhenius activation energy, mercurial inhibition and quantitation of aquaporin CHIP by fluorescent ELISA. 2. To measure the permselectivity of descending and ascending vasa recta by measuring transport of labeled dextran probes. 3. To verify preliminary data that solute transport in OMDVR is regulated by the separate effects of pericyte constriction and modulation of the urea transporter. Hormonal actions of vasoconstrictors and vasopressin on urea and sodium transport will be examined. The effects of pre-existing diuretic state and osmolality on solute and water transport will also be determined. 4. To employ the measurements from aims 1-4 to complete a mathematical simulation of microvascular exchange in the renal medulla. The model will account for paracellular and cellular transport pathways and simulate exchange of middle molecular weight solutes and albumin.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK042495-09
Application #
2518295
Study Section
General Medicine B Study Section (GMB)
Project Start
1990-09-01
Project End
1999-08-31
Budget Start
1997-09-01
Budget End
1998-08-31
Support Year
9
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Maryland Baltimore
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
003255213
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Zhang, Zhong; Payne, Kristie; Pallone, Thomas L (2018) Adaptive responses of rat descending vasa recta to ischemia. Am J Physiol Renal Physiol 314:F373-F380
Zhang, Zhong; Payne, Kristie; Pallone, Thomas L (2016) Descending Vasa Recta Endothelial Membrane Potential Response Requires Pericyte Communication. PLoS One 11:e0154948
Palant, Carlos E; Chawla, Lakhmir S; Faselis, Charles et al. (2016) High serum creatinine nonlinearity: a renal vital sign? Am J Physiol Renal Physiol 311:F305-9
Pallone, Thomas L (2014) Complex vascular bundles, thick ascending limbs, and aquaporins: wringing out the outer medulla. Am J Physiol Renal Physiol 306:F505-6
Zhang, Zhong; Payne, Kristie; Pallone, Thomas L (2014) Syncytial communication in descending vasa recta includes myoendothelial coupling. Am J Physiol Renal Physiol 307:F41-52
Zhang, Zhong; Lin, Hai; Cao, Chunhua et al. (2014) Descending vasa recta endothelial cells and pericytes form mural syncytia. Am J Physiol Renal Physiol 306:F751-63
Zhang, Zhong; Payne, Kristie; Cao, Chunhua et al. (2013) Mural propagation of descending vasa recta responses to mechanical stimulation. Am J Physiol Renal Physiol 305:F286-94
Zhang, Zhong; Lin, Hai; Cao, Chunhua et al. (2010) Voltage-gated divalent currents in descending vasa recta pericytes. Am J Physiol Renal Physiol 299:F862-71