Retrospective evaluation of alpha 2u-globulin accumulation in male rat kidneys following high doses of diisononyl phthalate

Citation
Dj. Caldwell et al., Retrospective evaluation of alpha 2u-globulin accumulation in male rat kidneys following high doses of diisononyl phthalate, TOXICOL SCI, 51(1), 1999, pp. 153-160
Citations number
31
Categorie Soggetti
Pharmacology & Toxicology
Journal title
TOXICOLOGICAL SCIENCES
ISSN journal
10966080 → ACNP
Volume
51
Issue
1
Year of publication
1999
Pages
153 - 160
Database
ISI
SICI code
1096-6080(199909)51:1<153:REOA2A>2.0.ZU;2-9
Abstract
Diisononyl phthalate (DINP), a widely used plasticizer, has been evaluated in two chronic studies in rats and one in mice. In the early 1980s, Exxon f ound no carcinogenic potential at the estimated maximum tolerated dose (MTD ) of 0.6% (307 mg/kg/day for male rats) administered in the diet of rats fo r 2 years. A recent study conducted at dietary levels up to 1.2% DINP (733 mg/kg/d for male rats) reported kidney tumors in male rats at the high trea tment level, but not in female rats nor mice of either sex. Because these t umors occurred only in male rats, and only at high doses, the male rat-spec ific alpha 2u-globulin (alpha 2UG) mechanism of action was investigated. Te chnological advances in immunohistochemical staining and computerized image analysis techniques permitted measuring the accumulation of alpha 2UG in a rchived kidneys from the earlier Exxon study. Using archived tissue obtaine d at the la-month interim sacrifice, we identified a dose-dependent accumul ation of alpha 2UG in specific regions of male rat kidneys only. An increas e in cell proliferation was confirmed by immunohistochemical detection of p roliferating-cell nuclear antigen (PCNA) and was confined to the areas of a lpha 2UG accumulation. H and E-stained sections revealed tubular epithelial hypertrophy and regeneration, consistent with the immunohistopathology fin dings. These findings are consistent with the alpha 2UG mechanism of tumori genesis, which is not regarded as relevant for humans. Thus, exposure to DI NP produced a dose-dependent alpha 2UG accumulation in male rat kidneys, si gnificant at a dietary level of 0.6% and a likely mechanism for the kidney tumors seen only in male rats administered higher dietary levels of DINP.