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Sample GSM442625 Query DataSets for GSM442625
Status Public on Aug 22, 2009
Title ButMorphine Rep 1
Sample type RNA
 
Source name Induction: butyrate-morphine. Challenge: morphine
Organism Mus musculus
Characteristics tissue: Striatum
age: 2 months
gender: male
Treatment protocol Behavioural sensitization: Locomotor sensitization induced by morphine was evaluated using a protocol divided into two phases: induction and challenge. The induction phase involved six trials on alternate days, one trial per day. On each one of these trials, mice received and injection of saline or sodium butyrate (300 mg/kg) immediatedly followed by a second injection of morphine (20 mg/kg). The challenge phases consisted of a single trial conducted 7 days after the last test of the induction phase. In this case, all animals received a single injection of morphine (20 mg/kg). Striatal RNA was extracted 1h after the morphine challenge in groups of four animals that received either saline (N=6) or morphine (N=3), or the sodium butyrate-morphine (N=3) co-treatment during the sensitization induction phase.
Growth protocol Two months-old Swiss-Albino male mice maintained in housing standard conditions.
Extracted molecule total RNA
Extraction protocol Mice striatal tissue was rapidly dissected from anterior 6mm coronal sections using a chilled acrylic mouse brain slicer matrix (Zivic Instruments) with 2 mm coronal section slice intervals, in RNAlater solution until further RNA extraction (Qiagen, Venlo, The Netherlands). Equal amounts of total RNA from four animals were pooled, processed and hybridized to Mouse Gene 1.0 ST genechips (Affymetrix, Santa Clara, CA). Three to six biological replicates of the microarray were prepared for each experimental group (saline-saline, N=6; saline-morphine, N=3; butyrate-morphine, N=3)..
Label biotin
Label protocol Following Affymetrix instructions
 
Hybridization protocol Following Affymetrix instructions
Scan protocol Following Affymetrix instructions
Description Gene expression data from striatal tissue
Data processing GeneSpring GX software (Agilent Technologies Inc) was used. Data were extracting using RMA16 algorithm and values were normalized by the median of controls. Data are represented as log2
 
Submission date Aug 20, 2009
Last update date Sep 16, 2019
Contact name Angel Barco
Organization name Instituto de Neurociencias (UMH-CSIC)
Street address Av. Santiago Ramón y Cajal
City Sant Joan d'Alacant
State/province Alicante
ZIP/Postal code 03550
Country Spain
 
Platform ID GPL6246
Series (1)
GSE17731 Selective boosting of transcriptional and behavioral responses to drugs of abuse by histone deacetylase inhibition

Data table header descriptions
ID_REF
VALUE RMA16 normalized (scaled) signal count data

Data table
ID_REF VALUE
10344614 -0.073679924
10344616 0.016777515
10344618 0.042047977
10344620 -0.046764374
10344622 -0.14373255
10344624 0.25762177
10344633 -0.059740067
10344637 0.044405937
10344653 0.12399006
10344658 0.1945095
10344674 -0.014543533
10344679 0.1337204
10344705 0.051360607
10344707 0.087301254
10344713 -0.049456596
10344715 -0.026194096
10344717 0.031178951
10344719 0.03920698
10344721 0.021634102
10344723 0.3246193

Total number of rows: 28815

Table truncated, full table size 584 Kbytes.




Supplementary file Size Download File type/resource
GSM442625.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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