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Series GSE5488 Query DataSets for GSE5488
Status Public on Aug 09, 2007
Title Salt Induced Hypertensive Disease Results in Over Expression of Matricellular Genes in Cerebral Arteries
Organism Rattus norvegicus
Experiment type Expression profiling by array
Summary The Dahl salt-sensitive (S) rat model develops chronic hypertensive disease when fed a high salt diet that ultimately results in renal and heart failure, as well as prevalent cerebrovascular pathologies. Phenotypic changes in the cerebral vasculature are preceded by changes in gene expression, and evidence supports a role for extracellular signal-regulated kinase 1/2 (ERK1/2) in vascular cell proliferation, yet little is known regarding ERK1/2 –regulated gene transcription in cerebrovascular smooth muscle during hypertension. Findings presented here support the hypothesis that salt-induced hypertensive disease results in upregulation of ERK1/2 activity and ERK1/2-regulated genes that promote remodeling in cerebral resistance arteries. Dahl S rats were fed either a 0.4% NaCl (low salt, LS) or 8% NaCl (high salt, HS) diet until evidence of left ventricular dysfunction. Gene expression profiling using oligonucleotide array analysis detected a significant fold-change of 1.5 or greater in 133 out of 15,923 genes examined. Mitogen-activated protein kinase (MAPK)-regulated genes were overrepresented and provided a link to genes involved in proliferation and extracellular matrix signaling including plasminogen activator inhibitor I (PAI-1), osteopontin (OPN) and junB. These data suggests that salt induced hypertensive disease promotes hyperplasia and changes in matricellular genes that are likely important in vascular remodeling.
Keywords: Normotensive vs. Hypertensive Disease
 
Overall design Analysis was based on a comparison between the Low Salt and High Salt groups. Arteries from 3 animals were pooled for each sample, thus there were 9 animals/group. Analysis of significance amongst all genes as well as prospective hypotheses correlating to disease were performed.
 
Contributor(s) Rose P, Tighe S, Toth MJ, Wellman TL, Bond J, Lewinter MM, Lounsbury KM
Citation(s) 18156195
Submission date Aug 09, 2006
Last update date Mar 03, 2017
Contact name Karen M. Lounsbury
E-mail(s) karen.lounsbury@uvm.edu
Phone 802-656-1319
Fax 802-656-4523
Organization name University of Vermont
Department Pharmacology
Street address 89 Beaumont Avenue
City Burlington
State/province VT
ZIP/Postal code 05405
Country USA
 
Platforms (1)
GPL341 [RAE230A] Affymetrix Rat Expression 230A Array
Samples (6)
GSM126432 Dahl_Cerebral_Artery_low.salt.1
GSM126473 Dahl_Cerebral_Artery_low.salt.2
GSM126474 Dahl_Cerebral_Artery_low.salt.3
Relations
BioProject PRJNA96125

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