Program - Society of Toxicology
Program - Society of Toxicology
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