EVALUATION OF DEHP-PLASTICIZER TOXICITY MECHANISMS

Information

  • Research Project
  • 3438178
  • ApplicationId
    3438178
  • Core Project Number
    R15ES005118
  • Full Project Number
    1R15ES005118-01
  • Serial Number
    5118
  • FOA Number
  • Sub Project Id
  • Project Start Date
    4/7/1989 - 35 years ago
  • Project End Date
    12/31/1993 - 31 years ago
  • Program Officer Name
  • Budget Start Date
    4/7/1989 - 35 years ago
  • Budget End Date
    12/31/1993 - 31 years ago
  • Fiscal Year
    1989
  • Support Year
    1
  • Suffix
  • Award Notice Date
    4/3/1989 - 35 years ago

EVALUATION OF DEHP-PLASTICIZER TOXICITY MECHANISMS

Plasticizers have an important role in our life due to their physical properties, low cost, and wide applications-including lifesaving medical applications. Several questions need to be answered in order to evaluate their safety: 1) Is the hepato- carcinogenicity of DEHP in rats relevant to humans, considering the differences in metabolism of DEHP by these species? and 2) Are the toxicities associated with DEHP a function of the phthalate ester moiety or could other less toxic phthalate esters be substituted for DEHP? An understanding of the mechanism of toxicity of DEHP and its biotransformation should help answer these questions. DEHP, di-(2-ethylhexyl) phthalate, is the most commonly used plasticizer, a known peroxisome proliferator, and a suspected carcinogen. DEHP is leached from plastic by food and blood products, thus most of the U.S. population may be exposed to significant concentrations of this material. Rats and mice fed DEHP developed hepato carcinomas. Peroxisome proliferation has been associated with the development of carcinomas. The broad objective of the proposed research is to investigate the biotransformation and hepatotoxicity of DEHP. Specific studies will investigate the metabolism of DEHP in the rat, with emphasis on the role of cytochrome P-450-mediated omega and omega-1 oxidation, aldehyde dehydrogenase oxidations and peroxisomal beta- oxidation. The relationship between the metabolism of DEHP and hepatic peroxisome proliferation will be examined. The changes in in vivo toxicity will be related to changes in in vitro toxicity in an effort to elucidate the events leading to peroxisome proliferation. These studies may define potential sites for biochemical intervention to reduce the potential health risk.

IC Name
NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES
  • Activity
    R15
  • Administering IC
    ES
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    114
  • Ed Inst. Type
    SCHOOLS OF PHARMACY
  • Funding ICs
  • Funding Mechanism
  • Study Section
    TOX
  • Study Section Name
    Toxicology Study Section
  • Organization Name
    CAMPBELL UNIVERSITY
  • Organization Department
  • Organization DUNS
    075586057
  • Organization City
    BUIES CREEK
  • Organization State
    NC
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    27506
  • Organization District
    UNITED STATES