Reversibility of the chronic effects of di(2-ethylhexyl) phthalate

被引:22
作者
David, RM [1 ]
Moore, MR
Finney, DC
Guest, D
机构
[1] Eastman Kodak Co, Hlth & Environm Labs, Rochester, NY 14652 USA
[2] Covance Inc, Vienna, VA 22182 USA
[3] Eastman Chem Co, Kingsport, TN 37662 USA
关键词
DEHP; di(2-ethylhexyl) phthalate; kidney; liver; testes;
D O I
10.1080/01926230152500040
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Fischer-344 rats treated with 12,500 ppm (728 and 879 mg/kg/d for male and females, respectively) and B6C3F(1) mice treated with 6, 000 ppm (1,227 and 1,408 mg/kg/d, respectively) di(2-ethylhexyl) phthalate (DEHP) in the diet for 78 weeks were allowed to recover for an additional 26 weeks on control diet. Blood was analyzed at weeks 78 and 104 from 10 animals per sex per group; animals were sacrificed at weeks 79 and 105 for histopathologic examination. The results are compared with data from animals continuously exposed to these dietary levels for 104 weeks (10, 11). Body weights and food consumption were measured monthly. BUN, albumin, and globulin that were significantly different for rats exposed to DEHP throughout 104 weeks, were comparable to controls for the recovery group. Reversibility of chronic effects on erythrocyte count, hemoglobin, and hematocrit values was apparent only for female rats. Chronic exposure demonstrated effects on liver, kidney, and testes weights. All organ weight effects except for testes for the Recovery group of rats, and all organ weight effects for mice, were reversible. Pigmentation of Kupffer cells and renal tubules present in chronically treated rats were not observed for the Recovery group. Lesions in the testes and pituitary gland were not reversible in rats. This may be a reflection of the senescence of the hypothalamic-gonad axis in rats. Cessation of exposure for mice resulted in amelioration of effects in the kidneys, liver, and testes. The extent of reversibility suggests that many chronic effects may be associated with a metabolic phenomenon such as peroxisome proliferation, which also reverted to control levels after 26 weeks of recovery.
引用
收藏
页码:430 / 439
页数:10
相关论文
共 38 条
[1]   EFFECTS OF DI(2-ETHYLHEXYL) PHTHALATE ON THE GONADAL PATHOPHYSIOLOGY, SPERM MORPHOLOGY, AND REPRODUCTIVE-PERFORMANCE OF MALE-RATS [J].
AGARWAL, DK ;
EUSTIS, S ;
LAMB, JC ;
REEL, JR ;
KLUWE, WM .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1986, 65 :343-350
[2]   NEOPLASTIC LESIONS OF QUESTIONABLE SIGNIFICANCE TO HUMANS [J].
ALISON, RH ;
CAPEN, CC ;
PRENTICE, DE .
TOXICOLOGIC PATHOLOGY, 1994, 22 (02) :179-186
[3]   Differential expression of peroxisome proliferator-activated receptors (PPARs): Tissue distribution of PPAR-alpha, -beta, and -gamma in the adult rat [J].
Braissant, O ;
Foufelle, F ;
Scotto, C ;
Dauca, M ;
Wahli, W .
ENDOCRINOLOGY, 1996, 137 (01) :354-366
[4]   Retrospective evaluation of alpha 2u-globulin accumulation in male rat kidneys following high doses of diisononyl phthalate [J].
Caldwell, DJ ;
Eldridge, SR ;
Lington, AW ;
McKee, RH .
TOXICOLOGICAL SCIENCES, 1999, 51 (01) :153-160
[5]  
CASEY HW, 1978, PATHOLOGY LAB ANIMAL, P142
[6]   PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR)-GAMMA - ADIPOSE-PREDOMINANT EXPRESSION AND INDUCTION EARLY IN ADIPOCYTE DIFFERENTIATION [J].
CHAWLA, A ;
SCHWARZ, EJ ;
DIMACULANGAN, DD ;
LAZAR, MA .
ENDOCRINOLOGY, 1994, 135 (02) :798-800
[7]  
CURTO KA, 1983, THESIS W VIRGINIA U
[8]  
DAUGHTREY WC, 1994, NEUROBEHAVIORAL TOXI
[9]   Chronic peroxisome proliferation and hepatomegaly associated with the hepatocellular tumorigenesis of di(2-ethylhexyl)phthalate and the effects of recovery [J].
David, RM ;
Moore, MR ;
Cifone, MA ;
Finney, DC ;
Guest, D .
TOXICOLOGICAL SCIENCES, 1999, 50 (02) :195-205
[10]   Chronic toxicity of di(2-ethylhexyl)phthalate in rats [J].
David, RM ;
Moore, MR ;
Finney, DC ;
Guest, D .
TOXICOLOGICAL SCIENCES, 2000, 55 (02) :433-443