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Optimal Sampling of Rat Liver Tissue for Toxicogenomic Studies

Overview
Journal Toxicol Pathol
Publisher Sage Publications
Date 2006 Dec 13
PMID 17162537
Citations 6
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Abstract

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.

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References
1.
Rao G, Morris R, Seely J . Beneficial effects of NTP-2000 diet on growth, survival, and kidney and heart diseases of Fischer 344 rats in chronic studies. Toxicol Sci. 2001; 63(2):245-55. DOI: 10.1093/toxsci/63.2.245. View

2.
Bammler T, Beyer R, Bhattacharya S, Boorman G, Boyles A, Bradford B . Standardizing global gene expression analysis between laboratories and across platforms. Nat Methods. 2005; 2(5):351-6. DOI: 10.1038/nmeth754. View

3.
Irwin R, Parker J, Lobenhofer E, Burka L, Blackshear P, Vallant M . Transcriptional profiling of the left and median liver lobes of male f344/n rats following exposure to acetaminophen. Toxicol Pathol. 2005; 33(1):111-7. DOI: 10.1080/01926230590522257. View

4.
Richardson F, Boucheron J, Dyroff M, Popp J, Swenberg J . Biochemical and morphologic studies of heterogeneous lobe responses in hepatocarcinogenesis. Carcinogenesis. 1986; 7(2):247-51. DOI: 10.1093/carcin/7.2.247. View

5.
McLean A, DAY P . The effect of diet on the toxicity of paracetamol and the safety of paracetamol-methionine mixtures. Biochem Pharmacol. 1975; 24(1):37-42. DOI: 10.1016/0006-2952(75)90310-x. View