Nitric oxide (NO) deficiency occurs in chronic kidney disease (CKD) irrespective of the primary cause and contributes to the cardiovascular complications and progression of CKD. There are many reasons for NO deficiency in CKD;1 major factor is accumulation of the endogenous NOS inhibitor, asymmetric dimethylarginine, ADMA, due partly to a failure of the hydrolyzing enzymes dimethylarginine dimethylamino-hydrolases (DDAHs). The kidney is a major site of DDAH activity. Another cause is loss of NO synthase (NOS) protein and activity and our work suggests that in kidney the neuronal (n)NOS is a primary target and that several isoforms are present and altered by CKD. We propose in vivo and in vitro studies in 2 separate models of CKD, the 5/6 renal mass ablation/infarction (A/I) and chronic puromycin aminonucleoside nephrosis (PAN) models to determine the pattern of change of the different NOS and DDAH enzymes in the kidney and how this contributes to the progression of CKD and development of hypertension. Both DDAH and NOS protein abundance and activity are severely compromised by oxidative stress, which is high in CKD and we will use apocyanin to inhibit oxidant production and dietary manipulation to enhance oxidative stress as methods of changing DDAH and NOS activity. Nephron number is a major determinant of progression of CKD and development of hypertension and we will determine how reductions in nephron number impact on the renal NOS and DDAH enzymes. By using our newly developed method of selective kidney transfection with genes of interest we will manipulate the local intrarenal NOS and DDAH enzymes to determine the role of different nNOS (and other NOS) isoforms and the 2 DDAH isoforms in progression of CKD. We will conduct in vivo functional studies in the conscious rat as well as glomerular micropuncture using anesthetized preparations. We will also conduct a range of in vitro studies to determine enzyme location, abundance and activity. Studies will be in the Sprague Dawley rat a strain vulnerable to CKD and hypertension and in the Wistar Furth which is protected from multiple types of CKD and hypertension to gain insights into mechanisms of progression. The incidence of CKD is rapidly increasing in the US and these patients also have a very high rate of cardiovascular morbidity and mortality, which is clearly linked to NO deficiency. These proposed studies will determine the role of the renal NO system in the progression of CKD and its cardiovascular complications which will lead to new therapeutic approaches.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK056843-08
Application #
7760042
Study Section
Special Emphasis Panel (ZRG1-RUS-B (02))
Program Officer
Ketchum, Christian J
Project Start
1999-12-01
Project End
2012-08-31
Budget Start
2010-02-01
Budget End
2012-08-31
Support Year
8
Fiscal Year
2010
Total Cost
$287,947
Indirect Cost
Name
University of Florida
Department
Physiology
Type
Schools of Medicine
DUNS #
969663814
City
Gainesville
State
FL
Country
United States
Zip Code
32611
West, Crystal A; Verlander, Jill W; Wall, Susan M et al. (2015) The chloride-bicarbonate exchanger pendrin is increased in the kidney of the pregnant rat. Exp Physiol 100:1177-86
Cunningham Jr, Mark W; West, Crystal A; Wen, Xuerong et al. (2015) Pregnant rats treated with a high-fat/prooxidant Western diet with ANG II and TNF-? are resistant to elevations in blood pressure and renal oxidative stress. Am J Physiol Regul Integr Comp Physiol 308:R945-56
West, Crystal A; McDonough, Alicia A; Masilamani, Shyama M E et al. (2015) Renal NCC is unchanged in the midpregnant rat and decreased in the late pregnant rat despite avid renal Na+ retention. Am J Physiol Renal Physiol 309:F63-70
Sasser, Jennifer M; Cunningham Jr, Mark W; Baylis, Chris (2014) Serelaxin reduces oxidative stress and asymmetric dimethylarginine in angiotensin II-induced hypertension. Am J Physiol Renal Physiol 307:F1355-62
Cunningham Jr, Mark W; Sasser, Jennifer M; West, Crystal A et al. (2013) Renal nitric oxide synthase and antioxidant preservation in Cyp1a1-Ren-2 transgenic rats with inducible malignant hypertension. Am J Hypertens 26:1242-9
West, Crystal A; Shaw, Stefan; Sasser, Jennifer M et al. (2013) Chronic vasodilation increases renal medullary PDE5A and *-ENaC through independent renin-angiotensin-aldosterone system pathways. Am J Physiol Regul Integr Comp Physiol 305:R1133-40
Cunningham Jr, Mark W; Sasser, Jennifer M; West, Crystal A et al. (2013) Renal redox response to normal pregnancy in the rat. Am J Physiol Regul Integr Comp Physiol 304:R443-9
Moningka, Natasha C; Cunningham Jr, Mark W; Sterling, Myrline et al. (2013) Effects of voluntary wheel running on the kidney at baseline and after ischaemia-reperfusion-induced acute kidney injury: a strain difference comparison. J Physiol 591:1313-24
Baylis, Chris (2012) Sexual dimorphism: the aging kidney, involvement of nitric oxide deficiency, and angiotensin II overactivity. J Gerontol A Biol Sci Med Sci 67:1365-72
Banki, Nora F; Ver, Agota; Wagner, Laszlo J et al. (2012) Aldosterone antagonists in monotherapy are protective against streptozotocin-induced diabetic nephropathy in rats. PLoS One 7:e39938

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