see

PubMedCrossRef 9. Valentine BA, Blue JT, Shelley SM, Cooper BJ: Increased serum alanine aminotransferase activity associated with muscle necrosis in the dog. J Vet selleck compound Intern Med 1990, 4:140–143.PubMedCrossRef 10. Lameire N, Van Biesen W, Vanholder R: Acute renal failure. Lancet 2005,365(9457):417–430.PubMed 11. Bruss M, Homann J, Molderings GJ: Dysferlinopathy as an extrahepatic cause for the elevation of serum transaminases. Med Klin (Munich) 2004, 99:326–329.CrossRef 12. Apostolov I, Minkov N, Koycheva M, Isterkov M, Abadjyev M, Ondeva V, Trendafilova T: Acute changes of serum markers for tissue

damage after ESWL of kidney stones. Int Urol Nephrol 1991, 23:215–220.PubMedCrossRef 13. Ambu R, Crisponi G, Sciot R, Van Eyken P, Parodo G, Iannelli S, Marongiu F, Silvagni R, Nurchi V, Costa V, Faac G, Desmet VJ: Uneven hepatic iron and phosphorus distribution in beta-thalassemia. J Hepatol 1995, 23:544–549.PubMedCrossRef 14. Haywood S: The non-random distribution of copper within

the liver of rats. Br J Nutr 1981, 45:295–300.PubMedCrossRef PRIMA-1MET mouse 15. Irwin RD, Boorman GA, Cunningham ML, Heinloth AN, Malarkey DE, Paules RS: Application of EX 527 research buy toxicogenomics to Toxicology: Basic Concepts in the Analysis of Microarray Data. Toxicol Pathol 2004,32(Supplement 1):72–83.PubMedCrossRef 16. Heinloth AN, Irwin RD, Boorman GA, Nettesheim P, Fannin RD, Sieber SO, Snell ML, Tucker CJ, Li L, Travlos GS, Vansant G, Blackshear PE, Tennant RW, Cunningham ML: Gene expression profiling of rat livers reveals indicators of potential adverse effects. Toxicol Sci 2004, 80:193–202.PubMedCrossRef Competing interests The authors declare that they have no competing interests. Authors’ contributions CF, GJS and WE have made substantial contributions to conception and design of the study, MB performed the experiments during

a research rotation (part of her DVM program), FS carried out the clinical pathology out tests and implemented the techniques for detection of liver enzymes in tissues, DT carried out the histology and implemented the immunohistochemical techniques, BJ assisted in implementation of toxicogenomics and interpreting data and AHY contributed to carry out toxicogenomics. CF coordinated the study and drafted the manuscript. All authors read and approved the manuscript content.”
“Background The isolated perfused rat liver (IPRL) is a well characterised model which is commonly used to study the biology and pathobiology of the liver in various experimental settings [1–3]. IPRL has a wide range of applications, including ischemia-reperfusion [4], biochemistry [5], pharmacology [6] and immunology [7]. Previous and ongoing studies in our laboratory have used this model to examine the hepatotoxicity of kava [8]. Liver lobe biopsies during IPRL enable temporal profiles of treatments to be observed in each liver. Lobe biopsy techniques have been described using microsurgical techniques in live rats [9, 10], and in perfused rat livers post hepatectomy [11].

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