Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2006-12-12
pubmed:abstractText
Different degrees of a toxic response between and within the various lobes of the liver have been observed in rodents following treatment with acetaminophen. This study was designed to compare 2 sampling methods of the rat liver for gene-expression analysis. Ten male Fischer 344/N rats, 12-14 weeks of age, were treated with vehicle (0.5% aqueous ethyl cellulose) or acetaminophen (APAP, 1500 mg/kg) and sacrificed 24 hours following dose administration. Two representative sections were collected from the left liver lobe, stained with hematoxylin and eosin (H&E), and evaluated independently by 2 pathologists. The central core of the left lobe was cubed and frozen. Five random cubes were conserved, while the remaining left lobe core was pulverized. From each of the 10 animals, 2 random cubes and 2 samples from the homogeneous, pulverized samples were prepared for microarray analysis. Histopathologic evaluation revealed a variable response of centrilobular necrosis within the left lobe. Multiple methods used to analyze the microarray data indicated that sampling technique was not a major contributor to the variability observed in the gene expression data; however, only the powdered samples clustered for all animals, even those with disparate histopathologic results. Additionally, a powdered sample provided the advantages of a homogenous sample pool and the ability to use sample aliquots for other analyses to include proteomics, metabonomics, and other molecular techniques.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-1122260, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-11568368, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-12454641, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-15084756, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-15209406, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-15800033, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-15805062, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-15814895, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-15846362, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-15924886, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-16005536, http://linkedlifedata.com/resource/pubmed/commentcorrection/17162537-2868806
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0192-6233
pubmed:author
pubmed:issnType
Print
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
795-801
pubmed:dateRevised
2011-9-15
pubmed:meshHeading
pubmed-meshheading:17162537-Acetaminophen, pubmed-meshheading:17162537-Analgesics, Non-Narcotic, pubmed-meshheading:17162537-Analysis of Variance, pubmed-meshheading:17162537-Animals, pubmed-meshheading:17162537-Cluster Analysis, pubmed-meshheading:17162537-Gene Expression Profiling, pubmed-meshheading:17162537-Gene Expression Regulation, pubmed-meshheading:17162537-Liver, pubmed-meshheading:17162537-Male, pubmed-meshheading:17162537-Oligonucleotide Array Sequence Analysis, pubmed-meshheading:17162537-Principal Component Analysis, pubmed-meshheading:17162537-Rats, pubmed-meshheading:17162537-Rats, Inbred F344, pubmed-meshheading:17162537-Reproducibility of Results, pubmed-meshheading:17162537-Selection Bias, pubmed-meshheading:17162537-Specimen Handling, pubmed-meshheading:17162537-Toxicogenetics
pubmed:year
2006
pubmed:articleTitle
Optimal sampling of rat liver tissue for toxicogenomic studies.
pubmed:affiliation
Laboratory of Experimental Pathology, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA. foley1@niehs.nih.gov
pubmed:publicationType
Journal Article, Comparative Study