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Sample GSM2122827 Query DataSets for GSM2122827
Status Public on Feb 02, 2017
Title Liver_PO_Clamp_rep3
Sample type RNA
 
Source name Liver tissue derived from C57BL/6NTac mice treated with palm oil and undergoing a hyperinsulinemic-euglycemic clamp
Organism Mus musculus
Characteristics strain/background: C57BL/6NTac
genotype/variation: WT
age: 14 weeks
gender: male
tissue: liver
treatment: palm oil
hyperinsulinemic-euglycemic clamp: yes
Treatment protocol As described in the paper. Briefly, mice were fasted for 10 h and were given 2 g/kg BM of PO (Landkrone, Germany) or water (VCL) per gavage. Lateral tail vein blood samples were obtained prior to treatment and 2 hours after. 6 hours after treatment, mice were euthanized with isoflurane and a vena cava-blood sample was collected, centrifuged at 4 °C, and plasma aliquots were immediately frozen in liquid nitrogen. Liver was dissected and immediately snap frozen in liquid nitrogen. For mice undergoing an hyperinsulinemic-euglycemic clamp, a permanent jugular vein catheter was placed in male C57BL/6NTac mice, while under ketamine/xylazine-anesthesia. 6-7 days later, mice were fasted for 10 hours, then received 2g/ kg BM PO or VCL via gavage. 6 hours later, unrestrained, conscious mice underwent euglycemic hyperinsulinemic clamp.
After 110 minutes of primed-continuous [3-3H]glucose infusion (1.85 kBq/min), a blood sample was collected to determine plasma insulin, glucose and [3-3H] glucose concentrations for calculating basal EGP. A [3-3H]glucose infusion (3.7 kBq/min) containing insulin (15 pmol/kg·min-1; HumulinR, Lilly, USA) was started. Blood glucose concentrations were measured every 10 minutes and target glycemia established by adjusting the GIR. At minute 120, 2-deoxy-D-[1-14C]glucose (370 kBq) was injected IV, to assess rates of tissue specific glucose uptake (Rg). Mice were euthanized by means of an IV ketamine/ xylazine injection. Liver was collected, immediately snap-frozen in liquid nitrogen, and stored at -80°C.
Growth protocol Animals housed under spf conditions.
Extracted molecule total RNA
Extraction protocol miRNeasy Mini (Qiagen) including DNase treatment.
Label biotin
Label protocol Ovation PicoSL WTA System V2 and Encore Biotin Module (Nugen).
 
Hybridization protocol According to the Affymetrix expression protocol (HWS kit).
Scan protocol According to the Affymetrix expression protocol, Scanner 3000 7G.
Description PO_CL_19
Gene expression data from liver tissue derived from C57BL/6NTac mice treated with palm oil and undergoing a hyperinsulinemic-euglycemic clamp.
Data processing RMA probeset summary with standard settings of the Affymetrix Expression Console software (v.1.3.0.187) including median polish and Sketch-Quantile normalisation.
 
Submission date Apr 13, 2016
Last update date Feb 03, 2017
Contact name Johannes Beckers
E-mail(s) johannes.beckers@helmholtz-munich.de
Organization name Helmholtz Zentrum Muenchen
Department Institute of Experimental Genetics
Street address Ingolstaedter Landstr. 1
City Neuherberg
ZIP/Postal code 85764
Country Germany
 
Platform ID GPL17400
Series (1)
GSE80259 Acute dietary fat intake initiates alterations in energy metabolism and insulin resistance

Data table header descriptions
ID_REF
VALUE RMA signal intensity (log2)

Data table
ID_REF VALUE
17294688 0.894
17299443 1.123
17458587 0.862
17458626 1.097
17526550 4.372
17536984 3.724
17227861 1.168
17278715 1.538
17211524 5.242
17216299 1.370
17216751 3.537
17222788 2.420
17239003 0.453
17245661 2.293
17249481 5.363
17274027 1.533
17283291 8.927
17285672 2.061
17286421 1.023
17287294 1.191

Total number of rows: 41345

Table truncated, full table size 605 Kbytes.




Supplementary file Size Download File type/resource
GSM2122827_PO_CL_19.CEL.gz 4.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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