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Title: Identification of cytochrome P4501A inducers in complex mixtures of polycyclic aromatic hydrocarbons

Conference ·
OSTI ID:320945
 [1]; ;  [2]
  1. Michigan State Univ., East Lansing, MI (United States)
  2. Univ. of Wisconsin, Stevens Point, WI (United States). Coll. of Natural Resources

An in vitro ethoxyresorufin O-deethylase (EROD) assay was used to study the ability of individual polycyclic aromatic hydrocarbons (PAHs) and mixtures of PAHs to induce Ah receptor (AhR) mediated cytochrome P4501A activity in PLHC-1 fish hepatoma cells. The purpose was to identify the most potent inducers from a set of thirteen separate PAHs and describe interactions occurring in complex mixtures of these PAHs. Where possible, potency was expressed in terms of 2,3,7,8 tetrachlorodibenzo-p-dioxin (TCDD) equivalents (TCDD-EQ) by normalizing the PAH results to a TCDD standard curve. The most potent inducers were benzo(k)fluoranthene > benzo(a)pyrene {approx} benzo(b)fluoranthene > chrysene {approx} benzo(a)anthracene. At equal concentrations, these PAHs yielded potencies of 1670, 940, 655, 255, and 185 pg TCDD-EQ/g, respectively. Analysis of various mixtures of the thirteen PAHs suggested that complex interactions may be occurring.

OSTI ID:
320945
Report Number(s):
CONF-9704249-; TRN: IM9910%%135
Resource Relation:
Conference: 7. symposium on toxicology and risk assessment: ultraviolet radiation and the environment, St. Louis, MO (United States), 7-9 Apr 1997; Other Information: PBD: 1998; Related Information: Is Part Of Environmental toxicology and risk assessment: Seventh volume; Little, E.E.; DeLonay, A.J. [eds.] [Geological Survey, Columbia, MO (United States)]; Greenberg, B.M. [ed.] [Univ. of Waterloo, Ontario (Canada). Dept. of Biology]; PB: 427 p.; ASTM special technical publication, Volume 1333
Country of Publication:
United States
Language:
English