Dr. Carolyn Ecelbarger, Ph.D. who has trained as both a nutritionist and a renal physiologist is in a unique position to bridge the gap between these fields. Her long-term career goals include investigating how nutritional factors affects renal function and especially how this relates to expression and regulation of salt and water transporters of the kidney. The mentored Research Career Award (KO1) will provide the proposed mentee, Dr. Ecelbarger, with the opportunity to broaden her training in physiology, under the guidance and expertise of Dr. Joseph Verbalis (proposed mentor), at Georgetown University. During her post-doctoral training at the National Institutes of Health in Dr. Mark Knepper's laboratory, her research focussed mainly on understanding those proteins which are important in the urinary concentrating mechanism, including the renal aquaporins and the Na- K-2Cl cotransporter. A key project of Dr. Ecelbarger's, done in collaboration with Dr. Verbalis' laboratory, involved assessing the role of aquaporin expression in the physiological phenomenon of vasopressin escape. Patients with this disorder initially retain water and become hyponatremic. However, if water loading continues, eventually they begin to excrete larger volumes of fairly dilute urine, despite the high circulating levels of vasopressin. This process of """"""""vasopressin escape"""""""" has puzzled renal physiologists for decades, although little is actually understood about the mechanisms involved. In a rat model, Ecelbarger et al. were able to show dramatic down-regulation of aquaporin-2 protein, a critical protein in water homeostasis. Naturesis is another physiologic component of vasopressin escape of which little is understood. Thus, the specific aims of the proposal are summarized as follows: (1) to evaluate changes in renal expression and cellular distribution of sodium transporters during physiologic """"""""escape"""""""" from the antidiuretic action of vasopressin; (2) to investigate signaling events involved in regulation of aquaporin-2 expression in models of vasopressin escape and chronic vasopressin exposure and (3) to assess the impact of long-term parenteral nutrition (TPN) on the expression and regulation of renal salt and water transporters. The main hypothesis is that direct regulation of expression and cellular distribution of several critical kidney tubule salt and water transporters is the means by which overall salt and water homeostasis is maintained in the body, despite physiological perturbations such as changes in blood vasopressin levels. The study proposals are briefly outlined for each specific aim, respectively; (1) to evaluate the time course of vasopressin escape with regard to expression and regulation of critical sodium transporters along the kidney tubule by immunoblotting and immunohistochemistry; (2) to utilize a variety of biochemical and immunolological approaches in order to assess important regulatory events in the V2-receptor/adenylyl-cyclase signaling cascade and determine how they relate to aquaporin-2 abundance; (3) to assess the effects of total parenteral nutrition on renal function, measures of renal hemodynamics, and expression and regulation of salt and water transporters in a rat model of TPN.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Scientist Development Award - Research & Training (K01)
Project #
1K01DK002672-01
Application #
2840956
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Rankin, Tracy L
Project Start
1999-06-21
Project End
2002-03-31
Budget Start
1999-06-21
Budget End
2000-03-31
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Georgetown University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Song, Jian; Knepper, Mark A; Hu, Xinqun et al. (2004) Rosiglitazone activates renal sodium- and water-reabsorptive pathways and lowers blood pressure in normal rats. J Pharmacol Exp Ther 308:426-33
Song, Jian; Knepper, Mark A; Verbalis, Joseph G et al. (2003) Increased renal ENaC subunit and sodium transporter abundances in streptozotocin-induced type 1 diabetes. Am J Physiol Renal Physiol 285:F1125-37
Bickel, Crystal A; Knepper, Mark A; Verbalis, Joseph G et al. (2002) Dysregulation of renal salt and water transport proteins in diabetic Zucker rats. Kidney Int 61:2099-110
Bickel, C A; Verbalis, J G; Knepper, M A et al. (2001) Increased renal Na-K-ATPase, NCC, and beta-ENaC abundance in obese Zucker rats. Am J Physiol Renal Physiol 281:F639-48
Ecelbarger, C A; Knepper, M A; Verbalis, J G (2001) Increased abundance of distal sodium transporters in rat kidney during vasopressin escape. J Am Soc Nephrol 12:207-17
Ecelbarger, C A; Sands, J M; Doran, J J et al. (2001) Expression of salt and urea transporters in rat kidney during cisplatin-induced polyuria. Kidney Int 60:2274-82
Ecelbarger, C A; Kim, G H; Knepper, M A et al. (2001) Regulation of potassium channel Kir 1.1 (ROMK) abundance in the thick ascending limb of Henle's loop. J Am Soc Nephrol 12:10-8
Ecelbarger, C A; Kim, G H; Terris, J et al. (2000) Vasopressin-mediated regulation of epithelial sodium channel abundance in rat kidney. Am J Physiol Renal Physiol 279:F46-53