This program began 14 years ago to explore the renal and vascular mechanisms involved in the long-term control of arterial pressure. Based on a number of important new observations, we have currently focused our studies on three important interactive controllers of renal and peripheral vascular tone and arterial pressure, i.e. nitric oxide (NO), 20- hydroxyeicotetraenoic acid (HETE) and angiotensin II (ANGII). Project 1 examines the hypothesis that stimulation of NO production in the renal medulla is critical for the maintenance of blood flow to this region and for maintenance of normal levels of arterial pressure in response to elevations in intrarenal ANGII or norepinephrine. Project 2 examines the influence of sodium intake on the expression of nitric oxide synthase (NOS) isoforms in the renal medulla and the role that each of these isoforms plays in the regulation of renal tubular and vascular function in the portion of the kidney. Project 3 examines a new NO signal transduction pathway whereby inhibition of 20-HETE production in the renal vasculature mediates the activation of K/+ channels and the vasodilation responses to NO. Project 4 tests the hypothesis that the P4504A2 enzymes serves as an """"""""oxygen sensor"""""""" whereby increases in tissue PO/2 stimulate the local production of 20-HETE leading to arterial constriction and autoregulation of blood flow. Project 5 explores the hypothesis that reduction of ANGII during periods of high salt intake mediates rare-faction of skeletal muscle microvessels. Based of evidence that ANGII alters expression of both NO and 20-HETE taken together, these five projects provide an important link between sodium homeostasis, the regulation of renal and peripheral vascular tone, and the long-term control of arterial pressure. This Program builds upon unique interdisciplinary and collaborative strengths and each project takes advantage of current molecular biochemical technologies in conjunction with state of the art integrative studies at the organ level and long-term studies in conscious animals. Successful completion of this work should enhance understanding of the biochemical and molecular basis of these mechanisms in the control of sodium and water excretion, renal and peripheral vascular function, and the long-term control of arterial pressure.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
2P01HL029587-16
Application #
2455585
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
1992-03-01
Project End
2003-02-28
Budget Start
1998-03-10
Budget End
1999-02-28
Support Year
16
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Medical College of Wisconsin
Department
Physiology
Type
Schools of Medicine
DUNS #
073134603
City
Milwaukee
State
WI
Country
United States
Zip Code
53226
Fan, Fan; Roman, Richard J (2017) Effect of Cytochrome P450 Metabolites of Arachidonic Acid in Nephrology. J Am Soc Nephrol 28:2845-2855
Fan, Fan; Pabbidi, Mallikarjuna R; Ge, Ying et al. (2017) Knockdown of Add3 impairs the myogenic response of renal afferent arterioles and middle cerebral arteries. Am J Physiol Renal Physiol 312:F971-F981
Rudemiller, Nathan P; Mattson, David L (2015) Candidate genes for hypertension: insights from the Dahl S rat. Am J Physiol Renal Physiol 309:F993-5
Cowley Jr, Allen W; Abe, Michiaki; Mori, Takefumi et al. (2015) Reactive oxygen species as important determinants of medullary flow, sodium excretion, and hypertension. Am J Physiol Renal Physiol 308:F179-97
Neuner, Sarah M; Wilmott, Lynda A; Hope, Kevin A et al. (2015) TRPC3 channels critically regulate hippocampal excitability and contextual fear memory. Behav Brain Res 281:69-77
Rudemiller, Nathan; Lund, Hayley; Jacob, Howard J et al. (2014) CD247 modulates blood pressure by altering T-lymphocyte infiltration in the kidney. Hypertension 63:559-64
He, Xiaofeng; Liu, Yong; Usa, Kristie et al. (2014) Ultrastructure of mitochondria and the endoplasmic reticulum in renal tubules of Dahl salt-sensitive rats. Am J Physiol Renal Physiol 306:F1190-7
Lakshmikanthan, Sribalaji; Zieba, Bartosz J; Ge, Zhi-Dong et al. (2014) Rap1b in smooth muscle and endothelium is required for maintenance of vascular tone and normal blood pressure. Arterioscler Thromb Vasc Biol 34:1486-94
Liu, Yong; Liu, Pengyuan; Yang, Chun et al. (2014) Base-resolution maps of 5-methylcytosine and 5-hydroxymethylcytosine in Dahl S rats: effect of salt and genomic sequence. Hypertension 63:827-38
Fan, Fan; Sun, Cheng-Wen; Maier, Kristopher G et al. (2013) 20-Hydroxyeicosatetraenoic acid contributes to the inhibition of K+ channel activity and vasoconstrictor response to angiotensin II in rat renal microvessels. PLoS One 8:e82482

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