Natriuretic responses to water immersion or acute volume expansion with isotonic saline are diminished in diabetic patients indicating a defect in renal function and volume regulation in these individuals. However, specific intrarenal mechanisms involved in the altered renal excretory response to volume expansion in diabetes remain unidentified. Recently, the P.I. has confirmed that diabetic rats demonstrate a blunted natriuresis and diuresis in response to acute volume expansion (VE). Furthermore, renal denervation only partially improves the renal excretory response in diabetic rats. These results suggest that part of the blunted natriuretic response to VE in diabetic rats is mediated by non-neural mechanisms, a major component of which is likely intrarenal origin. Thus, their overall hypothesis is the intrarenal factors which drive the excretory response to acute volume expansion and altered in diabetic rats. Two key intrarenal factors that dictate sodium excretion during acute VE are renal medullary blood flow (MBF) and renal interstitial hydrostatic pressure (RIHP). Furthermore, preliminary data suggest that influence of nitric oxide (NO), atrial natriuretic factor (ANF) and renal nerves on renal excretory function are altered in diabetic rats. Hence, the present proposal is designed to determine; first if MBF and RIHP responses to VE are altered in diabetic rats, second if a defective renal nitric oxide (NO) system contributes to the altered are altered in diabetic rats, second if a defective renal nitric oxide (NO) system contributes to the altered MBF and RIHP responses to acute VE in diabetic rats, third if intrarenal mechanisms (MBF and RIHP) involved in the excretory response to ANF are altered in diabetic rats, fourth if intrarenal mechanisms (MBF and RIHP) are involved in the altered neural component of the excretory response to VE in diabetic rats. Successful completion of the proposed studies will provide added insight into the intrarenal mechanisms that disrupt fluid and electrolyte balance during the early stage of diabetes. Once they understand and identify the basic intrarenal mechanisms that are involved in this phenomenon during the early phase of diabetes, the long term goal would be to develop better strategies to treat and manage these abnormalities which would alleviate subsequent renal damage and cardiovascular complications commonly observed in the diabetic state.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL048023-07
Application #
6537021
Study Section
Cardiovascular and Renal Study Section (CVB)
Program Officer
Rabadan-Diehl, Cristina
Project Start
1994-05-01
Project End
2004-04-30
Budget Start
2002-05-01
Budget End
2004-04-30
Support Year
7
Fiscal Year
2002
Total Cost
$170,725
Indirect Cost
Name
University of Nebraska Medical Center
Department
Physiology
Type
Schools of Medicine
DUNS #
City
Omaha
State
NE
Country
United States
Zip Code
68198
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Patel, K P; Zhang, K; Hein, M et al. (1997) Peripheral noradrenergic turnover in streptozotocin-induced diabetic rats. Diabetes Res Clin Pract 35:1-9
Patel, K P (1997) Neural regulation in experimental heart failure. Baillieres Clin Neurol 6:283-96
Patel, K P (1997) Volume reflex in diabetes. Cardiovasc Res 34:81-90
Patel, K P; Zhang, K (1996) Neurohumoral activation in heart failure: role of paraventricular nucleus. Clin Exp Pharmacol Physiol 23:722-6
Patel, K P; Zhang, P L (1995) Baroreflex function in streptozotocin (STZ) induced diabetic rats. Diabetes Res Clin Pract 27:1-9
Patel, K P; Zhang, P L (1994) Reduced renal sympathoinhibition in response to acute volume expansion in diabetic rats. Am J Physiol 267:R372-9