Chronic administration of leptin increases arterial pressure through renal sympathetic activation. Renal denervation substantially attenuates obesity induced hypertension.The ability of leptin to increase renal sympathetic nerve activity (SNA)and arterial pressure is preserved in two murine models of obesity despite resistance to the appetite suppressant action of leptin suggesting that leptin could contribute to hypertension in obesity despite resistance to its appetite suppressant actions. The focus of this project is on the hypothalamic molecular leptin signaling pathways mediating selective leptin actions and specifically renal SNA and arterial pressure versus appetite suppressant responses. We have demonstrated that the renal SNA responses to leptin are mediated through PI3 kinase. In contrast, based on preliminary studies, we will test the hypothesis that hypothalamic STAT3 and MAP, while mediating appetite suppressant effectsof leptin, are not involved in leptin induced increases in renal SNA and arterial pressure. Thus, disrupting leptin induced STAT3 or MAP kinase signaling would attenuate the appetite suppressant actions of leptin while preserving the renal SNA and arterial pressure responses. Based on this hypothesis, resistance to the effects of leptin on STATS and MAPK signaling in obesity could promote obesity induced hypertension. We will combine two complementary approaches to evaluate the role of STATS and MAP kinase on renal SNA and arterial pressure responses to leptin: 1) study of obese mouse models with gene targeted disruption of Shp 2 that mediates leptin induced MAP kinase activation or of leptin STATS signaling; and 2) study of mice with conditional """"""""floxed"""""""" alleles allowing site specific deletion of STATS, MAP kinase or the leptin receptor using targeted viral microinjections of Cre recombinase into the arcuate nucleus. A distinctive strength of this project is a constellation of highly interactive investigators who can assure the successful application of a combination of robust cardiovascular, neurophysiologic and genetic strategies to advance understanding of the role of leptin signaling pathways in regulation of renal SNA and arterial pressure. Insight into mechanisms of leptin actions on the sympathetic nervous system and arterial pressure should shed insight into cardiovascular complications of obesity.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL084207-02
Application #
7700577
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
Project End
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
2
Fiscal Year
2008
Total Cost
$569,543
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Pellegrinelli, Vanessa; Peirce, Vivian J; Howard, Laura et al. (2018) Adipocyte-secreted BMP8b mediates adrenergic-induced remodeling of the neuro-vascular network in adipose tissue. Nat Commun 9:4974
Peng, Hua; Jensen, Dane D; Li, Wencheng et al. (2018) Overexpression of the neuronal human (pro)renin receptor mediates angiotensin II-independent blood pressure regulation in the central nervous system. Am J Physiol Heart Circ Physiol 314:H580-H592
Bell, Balyssa B; Harlan, Shannon M; Morgan, Donald A et al. (2018) Differential contribution of POMC and AgRP neurons to the regulation of regional autonomic nerve activity by leptin. Mol Metab 8:1-12
Sandgren, Jeremy A; Deng, Guorui; Linggonegoro, Danny W et al. (2018) Arginine vasopressin infusion is sufficient to model clinical features of preeclampsia in mice. JCI Insight 3:
Yoon, Young-Sil; Tsai, Wen-Wei; Van de Velde, Sam et al. (2018) cAMP-inducible coactivator CRTC3 attenuates brown adipose tissue thermogenesis. Proc Natl Acad Sci U S A 115:E5289-E5297
Imai, Yumi; Fink, Brian D; Promes, Joseph A et al. (2018) Effect of a mitochondrial-targeted coenzyme Q analog on pancreatic ?-cell function and energetics in high fat fed obese mice. Pharmacol Res Perspect 6:e00393
Morselli, Lisa L; Claflin, Kristin E; Cui, Huxing et al. (2018) Control of Energy Expenditure by AgRP Neurons of the Arcuate Nucleus: Neurocircuitry, Signaling Pathways, and Angiotensin. Curr Hypertens Rep 20:25
Nair, Anand R; Agbor, Larry N; Mukohda, Masashi et al. (2018) Interference With Endothelial PPAR (Peroxisome Proliferator-Activated Receptor)-? Causes Accelerated Cerebral Vascular Dysfunction in Response to Endogenous Renin-Angiotensin System Activation. Hypertension 72:1227-1235
Seoane-Collazo, Patricia; Roa, Juan; Rial-Pensado, Eva et al. (2018) SF1-Specific AMPK?1 Deletion Protects Against Diet-Induced Obesity. Diabetes 67:2213-2226
Schmidt, Eric A; Despas, Fabien; Pavy-Le Traon, Anne et al. (2018) Intracranial Pressure Is a Determinant of Sympathetic Activity. Front Physiol 9:11

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