Because of the countercurrent arrangement of blood flow in the capillaries of the renal medulla, medullary tension is always low, and medullary cells, especially of the thick ascending limb (mTAL), are at special risk of hypoxic injury. We hypothesize that local mechanisms normally operate to feedback and down-regulate transport activity in these cells, in order to protect them from anoxic damage. We therefore intend to investigate autocrine and paracrine substances that may modulate transport of the mTAL. These include adenosine, prostaglandin E2, and other eicosanoids. The effects of these substances on respiration and transport by mTAL tubules and cells, their mechanism of action, and their local production and action in states of increased cellular transport or of hypoxia will be examined. As a counterpoint to these studies, we will investigate the effect of prostaglandins on another species of medullary tubule, the inner medullary collecting duct.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK018078-18
Application #
3225929
Study Section
General Medicine B Study Section (GMB)
Project Start
1974-09-01
Project End
1994-03-31
Budget Start
1991-04-15
Budget End
1992-03-31
Support Year
18
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02215
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Priatna, A; Epstein, F H; Spokes, K et al. (1999) Evaluation of changes in intrarenal oxygenation in rats using multiple gradient-recalled echo (mGRE) sequence. J Magn Reson Imaging 9:842-6
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Derman, M P; Chen, J Y; Spokes, K C et al. (1996) An 11-amino acid sequence from c-met initiates epithelial chemotaxis via phosphatidylinositol 3-kinase and phospholipase C. J Biol Chem 271:4251-5
Medina, R; Cantley, L; Spokes, K et al. (1996) Effect of water diuresis and water restriction on expression of HSPs-27, -60 and -70 in rat kidney. Kidney Int 50:1191-4

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