Reproductive effects of nonylphenol in rats after gavage administration: a two-generation study

被引:143
作者
Nagao, T
Wada, K
Marumo, H
Yoshimura, S
Ono, H
机构
[1] Food & Drug Safety Ctr, Hatano Res Inst, Dept Reprod & Dev Biol, Kanagawa 2578523, Japan
[2] Food & Drug Safety Ctr, Hatano Res Inst, Dept Pathol, Kanagawa 2578523, Japan
关键词
nonylphenol; two-generation; reproduction; multigeneration;
D O I
10.1016/S0890-6238(01)00123-X
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The potential reproductive toxicity of nonylphenol (NP) was assessed in a two-generation reproductive toxicity study. Groups of 25 male and female Crj:CD (SD) IGS rats were given NP by gavage at levels of 2, 10, or 50 mg/kg, and 25 males and female; were given corn oil as controls. No adverse changes in clinical signs were observed in any rats throughout the study. Significant increases in the liver, kidney and pituitary gland weights in males. and decreases in thymus weight in males and in ovary weight in females were observed in the 50 mg/kg group. NP did not affect sperm characteristics or the estrous cycle at any dose administered. A significant increase in the TSH level was observed in males in the 50 mg/kg group. No adverse effects of NP on reproduction were found. At necropsy, no treatment-related alterations were observed in any organs including the reproductive tissues in any group. Histopathologic changes were found in the liver of male and female rats and kidneys of malts in the 50 mg/kg group. The viability of offspring from postnatal day 0 to 4 in the 50 mg/kg group was reduced as compared with that in the controls, although growth was not affected by NP administration. On postnatal day 22, an increase in the serum FSH level and decrease in T, level for males, and decreases in LH and TSH levels and an increase in T, levels for females were observed in the 50 mg/kg group. NP did not affect the timing of preputial separation, while vaginal opening was accelerated in the 50 mg/kg group. No adverse changes were found in behavior or learning in the offspring of NP-treated groups. There were no treatment-related changes in any reproductive parameter, including estrous cycle, mating. fertility, delivery, and lactation, except for significant decreases in the numbers of implantation sites and live pups, and a significant decrease in ovary weight in the 50 mg/kg group. Kidney and liver weight were increased in males in the 50 mg/kg group. Histopathologic examination revealed changes in the liver of males and females of the 50 mg/kg group. No treatment-related changes were observed in the sperm characteristics. Hormone data should be interpreted cautiously until the findings are repeated and confirmed by further studies. These results of NP suggested that the no observed adverse effect level (NOAEL) on reproductive capacity is 50 mg/kg/day or greater in parent animals, and 10 mg/kg/day in the next generation under the present experimental condition. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:293 / 315
页数:23
相关论文
共 42 条
[1]   BIOACCUMULATION OF THE LIPOPHILIC METABOLITES OF NONIONIC SURFACTANTS IN FRESH-WATER ORGANISMS [J].
AHEL, M ;
MCEVOY, J ;
GIGER, W .
ENVIRONMENTAL POLLUTION, 1993, 79 (03) :243-248
[2]  
Biel WC, 1940, PEDAGOG SEMIN J GEN, V56, P439
[3]   Chronic administration of the environmental pollutant 4-tert-octylphenol to adult male rats interferes with the secretion of luteinizing hormone, follicle-stimulating hormone, prolactin, and testosterone [J].
Blake, CA ;
Boockfor, FR .
BIOLOGY OF REPRODUCTION, 1997, 57 (02) :255-266
[4]   Chronic administration of 4-tert-octylphenol to adult male rats causes shrinkage of the testes and male accessory sex organs, disrupts spermatogenesis, and increases the incidence of sperm deformities [J].
Boockfor, FR ;
Blake, CA .
BIOLOGY OF REPRODUCTION, 1997, 57 (02) :267-277
[5]   CONGENITAL HYPOTHYROIDISM, AS STUDIED IN RATS - CRUCIAL ROLE OF MATERNAL THYROXINE BUT NOT OF 3,5,3'-TRIIODOTHYRONINE IN THE PROTECTION OF THE FETAL BRAIN [J].
CALVO, R ;
OBREGON, MJ ;
DEONA, CR ;
DELREY, FE ;
DEESCOBAR, GM .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (03) :889-899
[6]  
CAPEN CC, 1995, CASARETT DOULLS TOXI, P617
[7]   Toxicokinetics of p-tert-octylphenol in male Wistar rats [J].
Certa, H ;
Fedtke, N ;
Wiegand, HJ ;
Muller, AMF ;
Bolt, HM .
ARCHIVES OF TOXICOLOGY, 1996, 71 (1-2) :112-122
[8]   The effects of 4-nonylphenol in rats: A multigeneration reproduction study [J].
Chapin, RE ;
Delaney, J ;
Wang, YF ;
Lanning, L ;
Davis, B ;
Collins, B ;
Mintz, N ;
Wolfe, G .
TOXICOLOGICAL SCIENCES, 1999, 52 (01) :80-91
[9]   DETERMINATION OF ALKYLPHENOL ETHOXYLATES AND THEIR ACETIC-ACID DERIVATIVES IN DRINKING-WATER BY PARTICLE BEAM LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY [J].
CLARK, LB ;
ROSEN, RT ;
HARTMAN, TG ;
LOUIS, JB ;
SUFFET, IH ;
LIPPINCOTT, RL ;
ROSEN, JD .
INTERNATIONAL JOURNAL OF ENVIRONMENTAL ANALYTICAL CHEMISTRY, 1992, 47 (03) :167-180
[10]   DEVELOPMENTAL EFFECTS OF ENDOCRINE-DISRUPTING CHEMICALS IN WILDLIFE AND HUMANS [J].
COLBORN, T ;
SAAL, FSV ;
SOTO, AM .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1993, 101 (05) :378-384