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Program - Society of Toxicology

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44 th Annual Meeting<br />

and ToxExpo<br />

<strong>Program</strong> Description<br />

MONDAY<br />

#58 11:10 THE TRANSCRIPTIONAL RESPONSE TO A<br />

PEROXISOME PROLIFERATOR-ACTIVATED<br />

RECEPTOR ALPHA AGONIST INCLUDES<br />

INCREASED EXPRESSION OF PROTEOME<br />

MAINTENANCE GENES. S. P. Anderson 1 , P.<br />

Howroyd 2,3 , J. Liu 4 , X. Qian 4 , R. Bahnemann 5 , C.<br />

Swanson 3 , M. Kwak 6 , T. W. Kensler 6 and J. C.<br />

Corton 7,3 . 1 GSK, Research Triangle Park, NC, 2 EPL,<br />

Research Triangle Park, NC, 3 CIIT, Research Triangle<br />

Park, NC, 4 NCI at NIEHS, Research Triangle Park, NC,<br />

5 6 BASF, Ludwigshafen, Germany, Johns Hopkins<br />

University, Baltimore, MD and 7 ToxicoGenomics,<br />

Chapel Hill, NC.<br />

#59 11:30 ROLE OF PPARALPHA IN CALORIC<br />

RESTRICTION EFFECTS IN THE MOUSE<br />

LIVER. J. C. Corton 1,4 , U. Apte 2 , S. P. Anderson 3 , P.<br />

Limaye 2 , L. Yoon 3 , J. Latendresse 5 , J. Everitt 4 , K. A.<br />

Voss 6 , C. Kimbrough 3 , J. S. Wong 7 , S. S. Gill 7 , R. A.<br />

Chandraratna 8 , M. Kwak 9 , T. W. Kensler 9 , T. M.<br />

Stulnig 10 , K. R. Steffensen 10 , J. Gustafsson 10 and H. M.<br />

Mehendale 2 . 1 ToxicoGenomics, Chapel Hill, NC,<br />

2 3 University <strong>of</strong> Louisiana, Monroe, LA, GSK, Research<br />

Triangle Park, NC, 4 CIIT, Research Triangle Park, NC,<br />

5 6 7 PAI, Jefferson, AR, USDA, Athens, GA, University<br />

<strong>of</strong> California, Riverside, CA, 8 Allergan, Irvine, CA,<br />

9 Johns Hopkins University, Baltimore, MD and<br />

10 Karolinska Institute, Huddinge, Sweden.<br />

Monday Morning, March 7<br />

9:30 AM to 12:30 PM<br />

Exhibit Hall<br />

POSTER SESSION: LIVER I<br />

Chairperson(s): Hartmut Jaeschke, University <strong>of</strong> Arizona, Tucson, AZ.<br />

Displayed: 9:30 AM–12:30 PM<br />

Attended: 9:30 AM–11:00 AM<br />

#60 TOXICOGENETIC ANALYSIS OF<br />

SUSCEPTIBILITY TO ACETAMINOPHEN-<br />

INDUCED LIVER INJURY. A. Hege 1 , C. Lodestro 3 ,<br />

D. Lee 3 , L. D. Balletta 3 , B. U. Bradford 2 , A. Maki 2 , R.<br />

Tennant 4 , M. A. Bogue 5 , K. Paigen 5 , D. W. Threadgill 1,3<br />

and I. Rusyn 1,2 . 1 Curriculum in <strong>Toxicology</strong>, UNC,<br />

Chapel Hill, NC, 2 Department <strong>of</strong> Environmental<br />

Sciences and Engineering, UNC, Chapel Hill, NC,<br />

3 Department <strong>of</strong> Genetics, UNC, Chapel Hill, NC,<br />

4 5 NIEHS, Research Triangle Park, NC and The Jackson<br />

Laboratory, Bar Harbor, ME.<br />

#61 PARACETAMOL TOXICITY IN RATS<br />

PRETREATED WITH CYTOCHROME P450 OR<br />

GLUTATHIONE INHIBITORS USING AN<br />

INTEGRATED GENOMICS APPROACH. M. F.<br />

DeCrist<strong>of</strong>aro 1 , D. Bodian 1 , E. Perentes 2 , I. M.<br />

Nicholls 2 , P. End 2 , J. Harleman 2 , S. Chibout 3 , F.<br />

Staedtler 3 and H. Firat 3 . 1 Biomarker Development,<br />

Novartis Pharmaceuticals Corporation, East Hanover,<br />

NY, 2 Preclinical Safety, Novartis Pharmacology AG,<br />

Basel, Switzerland and 3 Biomarker Development,<br />

Novartis Pharmacology AG, Basel, Switzerland.<br />

#62 DECREASED ACETAMINOPHEN AND<br />

BROMOBENZENE-INDUCED<br />

HEPATOTOXICITY AND LETHALITY IN TYPE 2<br />

DIABETIC MICE. M. S. Mitra 1 , S. P. Sawant 1 , A. V.<br />

Dnyanmote 1 , J. R. Latendresse 2 , A. Warbritton 2 and H.<br />

M. Mehendale 1 . 1 University <strong>of</strong> Louisiana at Monroe,<br />

Monroe, LA and 2 NCTR, Jefferson, AR.<br />

#63 ROLE OF POLY(ADP-RIBOSE) POLYMERASE<br />

(PARP) ACTIVATION IN ACETAMINOPHEN-<br />

INDUCED LIVER CELL NECROSIS IN MICE. C.<br />

Cover 1 , P. Fickert 2 , T. Knight 1 , A. Fuchsbichler 2 , M.<br />

Trauner 2 and H. Jaeschke 1 . 1 Liver Research Institute,<br />

University <strong>of</strong> Arizona, Tucson, AZ and 2 Department <strong>of</strong><br />

Medicine, Medical University <strong>of</strong> Graz, Graz, Austria.<br />

#64 PROTEOMIC ANALYSIS OF WHOLE LIVER<br />

AND SUBCELLULAR FRACTIONS FOLLOWING<br />

ACETAMINOPHEN-INDUCED<br />

HEPATOTOXICITY IN MALE RATS. M. E. Bruno 1 ,<br />

B. A. Wetmore 1 , J. H. Madenspacher 1 , R. Pieper 1 , A. M.<br />

McGrath 2 , C. L. Gatlin 2 , A. J. Makusky 2 , M. Zhao 2 , J.<br />

Zhou 2 , J. Taylor 2 , S. Steiner 2 , J. M. Fostel 1 , M. D.<br />

Waters 1 , R. W. Tennant 1 , K. B. Tomer 1 and B. A.<br />

Merrick 1 . 1 National Ctr Toxicogenomics, NIEHS,<br />

Research Triangle Pk, NC and 2 Proteomics Division,<br />

Large Scale Biology Corporation, Germantown, MD.<br />

#65 ROLE OF THE XENOBIOTIC RECEPTOR PXR<br />

IN ACETAMINOPHEN HEPATOTOXICITY. K. K.<br />

Wolf 2 , S. G. Wood 1 , B. W. Walton-Strong 3 , K. Yasuda 7 ,<br />

L. Lan 7 , P. R. Sinclair 1,3,2 , S. A. Wrighton 4 , E. H.<br />

Jeffery 5 , R. M. Evans 6 , E. G. Schuetz 7 and J. F.<br />

Sinclair 1,3,2 . 1 Veterans Administration Medical Center,<br />

White River Junction, VT, 2 Pharmacology and<br />

<strong>Toxicology</strong>, Dartmouth Medical School, Hanover, NH,<br />

3 Biochemistry, Dartmouth Medical School, Hanover,<br />

NH, 4 Department <strong>of</strong> Drug Disposition, Lilly Research<br />

Laboratories, Indianapolis, IN, 5 Department <strong>of</strong> Food<br />

Science and Human Nutrition, University <strong>of</strong> Illinois,<br />

Urbana, IL, 6 Howard Hughes Medical Institute, Gene<br />

Expression Laboratory, The Salk Institute for Biological<br />

Studies, La Jolla, CA and 7 Department <strong>of</strong><br />

Pharmaceutical Sciences, St. Jude Children’s Research<br />

Hospital, Memphis, TN.<br />

#66 THE EFFECT OF S-ADENOSYL-L-METHIONINE<br />

(SAME)ON MITOCHONDRIAL GLUTATHIONE<br />

AND PROTEIN CARBONYLS FOLLOWING<br />

ACETAMINOPHEN (APAP) TREATMENT IN<br />

MICE. M. Terneus, K. Kiningham and M. Valentovic.<br />

Pharmacology, Marshall University School <strong>of</strong> Medicine,<br />

Huntington, WV.<br />

#67 EVIDENCE SUGGESTING A ROLE FOR<br />

NAD(P)H:QUINONE OXIDOREDUCTASE 1 IN<br />

THE PROTECTION AGAINST<br />

ACETAMINOPHEN HEPATOTOXICITY BY<br />

CLOFIBRATE TREATMENT. J. S. M<strong>of</strong>fit 1 , L. M.<br />

Aleksunes 1 , A. M. Slitt 2 , M. Kardas 1 , C. D. Klaassen 2<br />

and J. E. Manautou 1 . 1 Department <strong>of</strong> Pharmaceutical<br />

Sciences, University <strong>of</strong> Connecticut, Storrs, CT and<br />

2 Department <strong>of</strong> Pharmacology, <strong>Toxicology</strong> and<br />

Therapeutics, University <strong>of</strong> Kansas Medical Center,<br />

Kansas City, KS.<br />

54<br />

SOT’s 44 th Annual Meeting

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