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Series GSE58282 Query DataSets for GSE58282
Status Public on Jun 07, 2014
Title A Gpr120 Selective Agonist Improves Insulin Resistance and Chronic Inflammation
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary We report that a high affinity, selective, small molecule Gpr120 agonist (cpdA), exerts potent anti-inflammatory effects on macrophages in vitro, and in obese mice in vivo. Gpr120 agonist treatment of high fat diet (HFD)/obese mice causes improved glucose tolerance, decreased hyperinsulinemia, increased insulin sensitivity and decreased hepatic steatosis. This suggests that Gpr120 agonists could become new insulin sensitizing drugs for the treatment of Type 2 diabetes and other human insulin resistant states in the future.
 
Overall design Examination of effects of DHA and compound A on primary macrophages stimulated by LPS, 3 replicates for each condition
 
Contributor(s) Sasik R
Citation(s) 24997608
Submission date Jun 06, 2014
Last update date May 15, 2019
Contact name Roman Sasik
E-mail(s) rsasik@ucsd.edu
Phone 858-822-3966
Organization name UCSD
Department Center for Computational Biology and Bioinformatics
Street address 9500 Gilman Dr.
City La Jolla
State/province CA
ZIP/Postal code 92093
Country USA
 
Platforms (1)
GPL9185 Illumina Genome Analyzer (Mus musculus)
Samples (9)
GSM1405828 WT_DHA_LPS_1
GSM1405829 WT_DHA_LPS_2
GSM1405830 WT_DHA_LPS_3
Relations
BioProject PRJNA251891
SRA SRP043006

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE58282_wt_LPS_DHA_cpdA_norm.txt.gz 879.7 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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