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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 />

WEDNESDAY<br />

#1903 GENE EXPRESSION IN PORPHYRIA INDUCED<br />

BY 2, 3, 7, 8-TETRACHLORO-DIBENZO-P-<br />

DIOXIN IN SUSCEPTIBLE MICE. A. G. Smith, B.<br />

Clothier and R. Davies. MRC <strong>Toxicology</strong> Unit,<br />

University <strong>of</strong> Leicester, Leicester, United Kingdom.<br />

#1904 STRESS- AND INFLAMMATORY-RELATED<br />

MNRA INDUCTION IN HEPATOCYTES AND<br />

NON-PARENCHYMAL CELLS RESPONSE TO<br />

OXIDATIVE STIMULI. T. Yamamoto, H. Utsumi, N.<br />

Shimada and N. Tsutsui. Mitsubishi Pharmacology<br />

Corporation, Kisarazu, Chiba, Japan. Sponsor: J.<br />

Sugimoto.<br />

#1905 DEVELOPMENT OF PROTEIN MICROARRAY<br />

TECHNOLOGY TO FACILITATE<br />

IDENTIFICATION OF PROTEINS ISOLATED BY<br />

GEL FILTRATION AND ION-EXCHANGE<br />

CHROMATOGRAPHIES. H. Kim 1,2 , Y. Yuan 1 , D. J.<br />

Kaplan 1 , D. A. Putt 1 , Z. Li 1 and K. Fleischmann 1 .<br />

1 2 Detroit R&D, Inc., Detroit, MI and Institute <strong>of</strong><br />

Environmental Health Sciences, Wayne State<br />

University, Detroit, MI.<br />

#1906 HEPATIC GENE EXPRESSION PROFILES OF<br />

RATS EXPOSED TO<br />

PERFLUOROOCTANESULFONATE (PFOS) IN<br />

UTERO. J. A. Bjork 1 , J. M. Berthiaume 1 , C. Lau 2 , J. L.<br />

Butenh<strong>of</strong>f 3 and K. B. Wallace 1 . 1 Biochem. & Mol.<br />

Biology, Medical School, University <strong>of</strong> Minnesota,<br />

Duluth, MN, 2 Reproductive <strong>Toxicology</strong> Division,<br />

NHEERL, U.S. EPA, Research Triangle Park, NC and<br />

3 3M Company, St. Paul, MN.<br />

#1907 LIVER SLICE MODEL SYSTEM FOR BILIARY<br />

CELL EFFECTS: CHANGES IN CLINICAL<br />

CHEMISTRY PARAMETERS. H. P. Behrsing, C. Ip,<br />

L. Jimenez and C. A. Tyson. <strong>Toxicology</strong> Laboratory, SRI<br />

International, Menlo Park, CA.<br />

#1908 LIVER SLICE MODEL SYSTEM FOR BILIARY<br />

CELL EFFECTS: HISTOLOGICAL CHANGES. K.<br />

Amin, C. Ip, H. P. Behrsing and C. A. Tyson.<br />

<strong>Toxicology</strong> Laboratory, SRI International, Menlo Park,<br />

CA.<br />

#1909 IMPAIRED G1 TO S-PHASE SIGNALING<br />

EXPLAINS INHIBITED TISSUE REPAIR IN<br />

THIOACETAMIDE-TREATED TYPE 1 DIABETIC<br />

RATS. S. S. Devi and H. M. Mehendale. <strong>Toxicology</strong>,<br />

The University <strong>of</strong> Louisiana at Monroe, Monroe, LA.<br />

#1910 MOLECULAR MECHANISMS OF INHIBITED<br />

COMPENSATORY LIVER REPAIR UPON<br />

HEPATOTOXIC CHALLENGE IN TYPE 2<br />

DIABETIC RATS. S. P. Sawant 1 , A. V. Dnyanmote 1 , J.<br />

R. Latendresse 2 , A. Warbritton 2 and H. M. Mehendale 1 .<br />

1 The University <strong>of</strong> Louisiana at Monroe, Monroe, LA<br />

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

#1911 PPARβ-MEDIATED HEPATOTOXICITY IN A<br />

DIETARY MODEL OF NONALCOHOLIC<br />

STEATOHEPATITIS (NASH). M. A. Peraza, W.<br />

Shan, M. J. Kennett and J. M. Peters. Veterinary<br />

Sciences, Center for Molecular <strong>Toxicology</strong> and<br />

Carcinogenesis, The Pennsylvania State University,<br />

University Park, PA.<br />

#1912 INDUCTION OF CYTOTOXICITY IN PRIMARY<br />

RAT HEPATOCYTES AND HUMAN HEPG2<br />

CELLS BY SELECTED PPARγ AGONISTS. L.<br />

Guo 1 , L. Muskhelishvili 2 , E. Blann 1 , S. Dial 1 , E.<br />

Hermann 3 and Y. Dragan 1 . 1 Systems <strong>Toxicology</strong>,<br />

National Center for Toxicolological Research, Jefferson,<br />

AR, 2 Molecular Pathology Branch, Charles River<br />

Laboratories at NCTR, Jefferson, AR and 3 Center for<br />

Drug Evaluation and Research, Jefferson, AR.<br />

#1913 INDUCTION OF EARLY FIBROGENESIS IN<br />

PRECISION-CUT HUMAN AND RAT LIVER<br />

SLICES AFTER CARBON TETRACHLORIDE<br />

TOXICITY. M. van de Bovenkamp 1 , G. M.<br />

Groothuis 1 , A. L. Draaisma 1 , M. T. Merema 1 , D. K.<br />

Meijer 1 , S. L. Friedman 2 and P. Olinga 1 .<br />

1 Pharmacokinetics and Drug Delivery, University <strong>of</strong><br />

Groningen, Groningen, Netherlands and 2 Division <strong>of</strong><br />

Liver Diseases, Mount Sinai School <strong>of</strong> Medicine, New<br />

York. Sponsor: A. Vickers.<br />

#1914 HUMAN LIVER AND KIDNEY SLICE VIABILITY<br />

IS EXTENDED AND PATHWAYS OF FIBROSIS<br />

ARE CHARACTERIZED. A. E. Vickers 1 , R. L.<br />

Fisher 2 and P. Olinga 3 . 1 Safety Evaluation, Allergan,<br />

Inc., Irvine, CA, 2 Vitron Inc., Tucson, AZ and<br />

3 Department Pharmacokinetics & Drug Delivery,<br />

University Groningen, Groningen, Netherlands.<br />

#1915 THE EFFECT OF THE PPARα AGONIST WY-14,<br />

643 ON MITOCHONDRIAL MEMBRANE<br />

POTENTIAL IN HUMAN AND RODENT LIVER<br />

CELL LINES. S. Barnes 1 , S. E. Boldt 2 , A. K.<br />

Hubbard 1 , J. Singh 2 and D. E. Amacher 2 . 1 Department<br />

<strong>of</strong> Pharmaceutical Sciences, University <strong>of</strong> Connecticut,<br />

Storrs, CT and 2 Drug Safety Evaluation, Pfizer Inc.,<br />

Groton, CT.<br />

#1916 IN SITU QUANTITATIVE EVALUATION OF<br />

PEROXISOMAL PROLIFERATION IN THE NON-<br />

HUMAN PRIMATE LIVER VIA LASER<br />

SCANNING CYTOMETRY (LSC). L. A. Obert 1 , V.<br />

Kostrubsky 1 , C. Okerberg 1 , J. Wijsman 1 , E. Urda 1 , J.<br />

Hanson 1 , K. Toy 1 , W. Collard 1 , W. Maier 1 , R. Bell 1 , L.<br />

Zwick 2 , S. Frantz 2 , R. Dunstan 1 and R. Adler 1 .<br />

1 2 WWSS, Pfizer Inc., Ann Arbor, MI and MPI<br />

Research, Mattawan, MI.<br />

#1917 COMPARISON OF ALDEHYDE<br />

DEHYDROGENASE (ALDH) ACTIVITY IN THE<br />

LIVER AND LUNG. M. Yoon 1,2 , M. C. Madden 2 and<br />

H. A. Barton 2 . 1 NRC, The National Academies,<br />

Washington, DC and 2 NHEERL, U.S. EPA, Research<br />

Triangle Park, NC.<br />

#1918 ETHANOL HAS BIPHASIC EFFECTS ON<br />

EXPRESSION OF STEROL REGULATORY<br />

ELEMENT BINDING PROTEIN-1 (SREBP-1) IN<br />

RAT FGC-4 HEPATOMA CELLS WITH<br />

INHIBITION AT HIGH DOSES RESULTING IN<br />

INDUCTION OF ADH CLASS I. L. He 1,3 , M. J.<br />

Ronis 2,3 , F. A. Simmen 1,3 and T. M. Badger 1,3 .<br />

1 Physiology & Biophysics, University <strong>of</strong> Arkansas for<br />

Medical Sciences, Little Rock, AR, 2 Pharmacology &<br />

<strong>Toxicology</strong>, University <strong>of</strong> Arkansas for Medical<br />

Sciences, Little Rock, AR and 3 Arkansas Children’s<br />

Nutrition Center, Little Rock, AR.<br />

194<br />

SOT’s 44 th Annual Meeting

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