The ability to regulate glomerular filtration rate is essential for the normal functioning of kidneys. In recent years, it has become evident that significant alterations in the permeability of the glomerular wall and/or surface area available for ultrafiltration (i.e. the ultrafiltration coefficient) can occur in response to a wide variety of important hormones, nephrotoxic compounds, and other altered physiological states. At present, the glomerular cells and morphological changes which are responsible for these alterations in the ultrafiltration coefficient are very speculative or unknown. In the proposed investigations, in vitro and in vivo studies are designed to carefully evaluate the morphological responses of glomerular epithelial podocytes, the glomerular endothelium, and the glomerular mesothelial cells in situations which alter the ultrafiltration coefficient in Munich-Wistar rats. Particular attention will be paid to the roles that cytoplasmic contractile elements, cytoskeletal elements, calcium ions, and prostaglandins play in affecting ultrastructural changes in these cells. Together, it is believed that the above studies will provide important insights into the roles played by the different cell types which make up the kidney glomerulus in regulating flow of filtrate across the glomerular wall, the cell biological parameters which underlie ultrafiltration coefficient related morphological changes in these cells, and will help define the mechanisms of action of many important compounds and conditions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM031111-03
Application #
3152203
Study Section
Pathology A Study Section (PTHA)
Project Start
1983-06-01
Project End
1987-02-28
Budget Start
1985-06-01
Budget End
1987-02-28
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Georgetown University
Department
Type
School of Medicine & Dentistry
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Andrews, P M; Bates, S B (1987) Effects of dietary protein on uranyl-nitrate-induced acute renal failure. Nephron 45:296-301
Andrews, P M; Bates, S B (1987) Dietary protein as a risk factor in gentamicin nephrotoxicity. Ren Fail 10:153-9
Andrews, P M; Bates, S B (1987) Dietary protein prior to renal ischemia and postischemic kidney function. Kidney Int Suppl 22:S76-80
Andrews, P M; Bates, S B (1986) Dietary protein prior to renal ischemia dramatically affects postischemic kidney function. Kidney Int 30:299-303
Andrews, P M; Bates, S B (1985) Improving Euro-Collins flushing solution's ability to protect kidneys from normothermic ischemia. Miner Electrolyte Metab 11:309-13
Andrews, P M; Bates, S B (1985) Evaluation of a flushing solution designed to protect kidneys from in situ ischemia. Am J Kidney Dis 6:53-8
Andrews, P M; Bates, S B (1985) Dose-dependent movement of cationic molecules across the glomerular wall. Anat Rec 212:223-31