Literature DB >> 21432160

Maternal exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin and the body burden in offspring of long-evans rats.

Junzo Yonemoto1, Tutomu Ichiki, Teiji Takei, Chiharu Tohyama.   

Abstract

OBJECTIVES: In utero and lactational exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) results in a wide variety of developmental effects in pups at doses much lower than those causing overt toxicity in adult animals. We investigated the relationship between tissue concentrations of TCDD in dams and fetuses and developmental effects on pups.
MATERIALS AND METHODS: Pregnant Long-Evans rats were given TCDD at a single oral dose of 12.5, 50, 200, or 800 ng of TCDD or [(3)H]-TCDD/kg bw on gestation day (GD) 15. Dams were sacrificed on GD16 and GD21, and the tissue concentrations of TCDD were measured in dams and fetuses. Pups were sacrificed on postnatal day (PND) 49 and PND63 for males and PND70 for females, and the reproductive effects and tissue concentrations of TCDD were determined.
RESULTS: The sex ratio (male/female) on GD21 was significantly reduced at 50 ng TCDD/kg and at 12.5 and 50 ng TCDD/kg at birth, but not at other doses. Delayed puberty was observed in males at 200 ng TCDD/kg and in males and females at 800 ng TCDD/kg. Anogenital distance, testis weight, epididymal sperm count, sperm motility, and ejaculated sperm count were not affected. Estrous cyclicity was not different from that of the control in any treatment group. A dose-dependent decrease in weight of seminal vesicle and prostate on PND49 was observed. Prostate weight was significantly decreased at 800 ng TCDD/kg. At this dose, maternal body burden and TCDD concentration in fetuses were 290 pg TCDD/g and 52 pg TCDD/g on GD16, respectively. Reduced prostate weight is a sensitive and commonly observed endpoint so that the body burdens of dams and fetuses at the LOAEL of this endpoint could be served as the basis for establishing TDI for dioxins.

Entities:  

Keywords:  TCDD; body burden; fetus; in utero and lactational exposure; male reproduction

Year:  2005        PMID: 21432160      PMCID: PMC2723627          DOI: 10.1265/ehpm.10.21

Source DB:  PubMed          Journal:  Environ Health Prev Med        ISSN: 1342-078X            Impact factor:   3.674


  25 in total

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Authors:  J J Diliberto; D E Burgin; L S Birnbaum
Journal:  Toxicol Appl Pharmacol       Date:  1999-08-15       Impact factor: 4.219

2.  In utero exposure to low doses of 2,3,7,8-tetrachlorodibenzo-p-dioxin alters reproductive development of female Long Evans hooded rat offspring.

Authors:  L E Gray; C Wolf; P Mann; J S Ostby
Journal:  Toxicol Appl Pharmacol       Date:  1997-10       Impact factor: 4.219

3.  In utero and lactational exposure of male rats to 2,3,7,8-tetrachlorodibenzo-p-dioxin. 3. Effects on spermatogenesis and reproductive capability.

Authors:  T A Mably; D L Bjerke; R W Moore; A Gendron-Fitzpatrick; R E Peterson
Journal:  Toxicol Appl Pharmacol       Date:  1992-05       Impact factor: 4.219

4.  Dioxins: WHO's tolerable daily intake (TDI) revisited.

Authors:  F X van Leeuwen; M Feeley; D Schrenk; J C Larsen; W Farland; M Younes
Journal:  Chemosphere       Date:  2000 May-Jun       Impact factor: 7.086

5.  Prostate enlargement in mice due to fetal exposure to low doses of estradiol or diethylstilbestrol and opposite effects at high doses.

Authors:  F S vom Saal; B G Timms; M M Montano; P Palanza; K A Thayer; S C Nagel; M D Dhar; V K Ganjam; S Parmigiani; W V Welshons
Journal:  Proc Natl Acad Sci U S A       Date:  1997-03-04       Impact factor: 11.205

Review 6.  The effects of dioxin on reproduction and development.

Authors:  J Yonemoto
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7.  Pattern of male reproductive system effects after in utero and lactational 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure in three differentially TCDD-sensitive rat lines.

Authors:  Ulla Simanainen; Tapio Haavisto; Jouni T Tuomisto; Jorma Paranko; Jorma Toppari; Jouko Tuomisto; Richard E Peterson; Matti Viluksela
Journal:  Toxicol Sci       Date:  2004-04-14       Impact factor: 4.849

8.  In utero and lactational exposure of the male rat to 2,3,7,8-tetrachlorodibenzo-p-dioxin impairs prostate development. 1. Effects on gene expression.

Authors:  B L Roman; R E Peterson
Journal:  Toxicol Appl Pharmacol       Date:  1998-06       Impact factor: 4.219

9.  Effects of aryl hydrocarbon receptor null mutation and in utero and lactational 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure on prostate and seminal vesicle development in C57BL/6 mice.

Authors:  Tien-Min Lin; Kinarm Ko; Robert W Moore; Ulla Simanainen; Terry D Oberley; Richard E Peterson
Journal:  Toxicol Sci       Date:  2002-08       Impact factor: 4.849

10.  Altered operant responding for motor reinforcement and the determination of benchmark doses following perinatal exposure to low-level 2,3,7,8-tetrachlorodibenzo-p-dioxin.

Authors:  V P Markowski; G Zareba; S Stern; C Cox; B Weiss
Journal:  Environ Health Perspect       Date:  2001-06       Impact factor: 9.031

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Journal:  Endocr Rev       Date:  2012-03-14       Impact factor: 19.871

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Review 3.  Dioxin-induced changes in epididymal sperm count and spermatogenesis.

Authors:  Warren G Foster; Serena Maharaj-Briceño; Daniel G Cyr
Journal:  Environ Health Perspect       Date:  2010-04       Impact factor: 9.031

4.  Animal Toxicology Studies on the Male Reproductive Effects of 2,3,7,8-Tetrachlorodibenzo-p-Dioxin: Data Analysis and Health Effects Evaluation.

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