Chronic toxicity and carcinogenic evaluation of diisononyl phthalate in rats

被引:62
作者
Lington, AW
Bird, MG
Plutnick, RT
Stubblefield, WA
Scala, RA
机构
[1] Exxon Biomedical Sciences, Inc., East Millstone
[2] Exxon Biomedical Sciences, Inc., East Millstone, NJ 08875-2350, Mettlers Road
[3] ENSR Consulting and Engineering, Fort Collins, CO 80621
[4] Rehobeth Beach, DE 19971-3023
来源
FUNDAMENTAL AND APPLIED TOXICOLOGY | 1997年 / 36卷 / 01期
关键词
D O I
10.1006/faat.1997.2286
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Groups of 110 Fischer 344 rats/sex were fed diisononyl phthalate (DINP) at dietary levels of 0, 0.03, 0.3, and 0.6 wt% for periods up to 2 years. Interim sacrifices of 10 predesignated rats/sex/dose were at 6, 12, and 18 months with surviving animals sacrificed at 24 months. At study termination, survival was in excess of 60% for every group. At the mid or high dose, the following biological effects were noted: slight decreases in food consumption and body weight; slight increase in mortality; a dose-related increase in relative organ weights of liver and kidney; and some slight effects on urinalysis, hematologic, and clinical chemistry parameters. No peroxisome induction was observed in livers of treated rats compared with controls. No clear treatment-related nonneoplastic or neoplastic lesions were found. However, mononuclear cell leukemia (MNCL) and changes known to be associated with an increased incidence of MNCL were seen in the mid-dose and high-dose groups. A literature review suggests that MNCL is a common finding in aging F344 rats and that this increased incidence in rats treated with DINE is not relevant to man. A clear no-observed-effect level was demonstrated for all biological end points at a dietary level of 0.03 wt% or approximately 17 mg/kg/day of (C) 1997 Society of Toxicology.
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页码:79 / 89
页数:11
相关论文
共 66 条
[61]  
SWAEN GJV, 1987, PATHOLOGY TUMORS LAB, V1, P187
[62]  
TARONE RE, 1975, BIOMETRIKA, V62, P679
[63]  
THURMAN JD, 1994, TOXICOL PATHOL, V23, P1
[64]   ANALYSIS OF STUDIES RELATED TO TUMORIGENICITY INDUCED BY HYDROQUINONE [J].
WHYSNER, J ;
VERNA, L ;
ENGLISH, JC ;
WILLIAMS, GM .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1995, 21 (01) :158-176
[65]   CHRONIC TOXICITY AND CARCINOGENICITY STUDIES OF OLESTRA IN FISCHER 344 RATS [J].
WOOD, FE ;
TIERNEY, WJ ;
KNEZEVICH, AL ;
BOLTE, HF ;
MAURER, JK ;
BRUCE, RD .
FOOD AND CHEMICAL TOXICOLOGY, 1991, 29 (04) :223-230
[66]   MUTAGENICITY TESTING OF DI(2-ETHYLHEXYL)PHTHALATE AND RELATED CHEMICALS IN SALMONELLA [J].
ZEIGER, E ;
HAWORTH, S ;
MORTELMANS, K ;
SPECK, W .
ENVIRONMENTAL MUTAGENESIS, 1985, 7 (02) :213-232