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OLS Field Name OLS Field Data
Main Title Effects of 7,12-Dimethylbenz(a)anthracene on Immune Function and Mixed-Function Oxygenase Activity in the European Starling.
Author Trust, K. A. ; Fairbrother, A. ; Hooper, M. J. ;
CORP Author Corvallis Environmental Research Lab., OR. ;Clemson Univ., SC. Inst. of Wildlife and Environmental Toxicology.;National Inst. of Environmental Health Sciences, Research Triangle Park, NC.
Publisher c1994
Year Published 1994
Report Number EPA/600/J-94/302; NIEHS-ES04696;
Stock Number PB94-190568
Additional Subjects Cellular immunity ; Mixed function oxygenases ; Toxicity ; Reprints ; Liver ; Phagocytosis ; Lymphocyte transformation ; Hemagglutination tests ; Antibody formation ; European starlings ; Sturnus vulgaris ; Anthracene/7-12-dimethylbenz(a)
Holdings
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Status
NTIS  PB94-190568 Most EPA libraries have a fiche copy filed under the call number shown. Check with individual libraries about paper copy. 11/11/1994
Collation 12p
Abstract
Immune function and hepatic MFO activity were examined in adult and nestling starlings administered a synthetic PAH, 7,12-dimethylbenz(a)anthracene (DMBA). Methods used to examine the starling immune system included immunopathology, macrophage phagocytosis, lymphocyte blastogenesis to concanavalin A, and hemagglutination of sheep erythrocytes (SRBC). Concomitant investigations of MFO activity were conducted in starlings exposed to DMBA. Ethoxyresorufin O-dealkylase (EROD) and pentoxyresorufin O-depentylase (PROD) were used as indicators of hepatic MFO activity. Changes in MFO activity were compared to chemically altered immune responses following DMBA exposure. Subcutaneous exposure of adult starlings to 125 mg/kg DMBA resulted in suppression of lymphocyte blastogenesis and antibody production to SRBC. EROD and PROD activity were increased 2.8- and 3.4-fold, respectively. Lymphocyte blastogenesis was impaired in adult starlings orally exposed to 125 mg/kg DMBA. The immune system of nestling starlings exposed orally to 100 mg/kg DMBA was altered, as evidenced by decreased phagocytic ability of macrophages and inhibition of lymphocyte blastogenesis. Oral exposure to DMBA did not induce MFO activity in starlings of either age class. Effects of DMBA on immune function and MFO activity in starlings varied with the age of birds and route and length of chemical exposure.