Literature DB >> 2373295

Characterization of the peak period of sensitivity for the induction of hydronephrosis in C57BL/6N mice following exposure to 2,3,7, 8-tetrachlorodibenzo-p-dioxin.

L A Couture1, M W Harris, L S Birnbaum.   

Abstract

2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is an extremely potent teratogen in mice. Hydronephrosis and cleft palate are the most sensitive measures of teratogenicity in mice following exposure to TCDD and other structurally related polyhalogenated aromatic hydrocarbons. Despite a relatively long half-life, investigators have identified a critical window for the induction of cleft palate in C57BL/6N mice. To characterize the critical period for renal teratogenesis, pregnant C57BL/6N mice were treated once by gavage with 0-24 micrograms TCDD/kg body wt on Gestation Day (GD) 6, 8, 10, 12, or 14. All dams were killed on GD 18, and the fetuses were examined for the presence of hydronephrosis and cleft palate. Maternal liver-to-body weight ratios were significantly elevated above controls on all days, while maternal weight gain was unaffected. Fetal mortality was increased relative to controls only at 24 micrograms TCDD/kg on GD 6. There was no significant difference in fetal body weights between control and TCDD-treated fetuses. The incidence of cleft palate increased in a dose-related fashion from GD 6 to GD 12, and identification of GD 12 as the critical window for induction of clefting of the hard palate was confirmed. Hydronephrosis was observed at all dose levels, regardless of exposure day, and the incidence was close to 100% at 3 micrograms TCDD/kg and higher doses on GD 12 and earlier. At all doses on GD 14, both the incidence and severity of hydronephrosis were decreased relative to all other days. There was a dose-related increase in the severity of the renal lesion on each day, but between GD 6 and 12 severity was constant. Thus, while palatal sensitivity to TCDD increased with gestational age between GD 6 and 12, there was no difference among these days in development of hydronephrosis. The data suggest, however, that on GD 14 the urinary tract may be less sensitive to TCDD.

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Year:  1990        PMID: 2373295     DOI: 10.1016/0272-0590(90)90171-f

Source DB:  PubMed          Journal:  Fundam Appl Toxicol        ISSN: 0272-0590


  10 in total

1.  Paternal exposure to Agent Orange and spina bifida: a meta-analysis.

Authors:  Anh Duc Ngo; Richard Taylor; Christine L Roberts
Journal:  Eur J Epidemiol       Date:  2009-11-06       Impact factor: 8.082

2.  Perinatal 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure sensitizes offspring to angiotensin II-induced hypertension.

Authors:  Andrea C Aragon; M Beth Goens; Eleanor Carbett; Mary K Walker
Journal:  Cardiovasc Toxicol       Date:  2008-08-01       Impact factor: 3.231

3.  Effects of short-term exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin on microRNA expression in zebrafish embryos.

Authors:  Matthew J Jenny; Neelakanteswar Aluru; Mark E Hahn
Journal:  Toxicol Appl Pharmacol       Date:  2012-08-18       Impact factor: 4.219

4.  Predominant role of cytosolic phospholipase A2α in dioxin-induced neonatal hydronephrosis in mice.

Authors:  Wataru Yoshioka; Tatsuya Kawaguchi; Nozomi Fujisawa; Keiko Aida-Yasuoka; Takao Shimizu; Fumio Matsumura; Chiharu Tohyama
Journal:  Sci Rep       Date:  2014-02-10       Impact factor: 4.379

5.  Perinatal DDT Exposure Induces Hypertension and Cardiac Hypertrophy in Adult Mice.

Authors:  Michele A La Merrill; Sunjay Sethi; Ludovic Benard; Erin Moshier; Borje Haraldsson; Christoph Buettner
Journal:  Environ Health Perspect       Date:  2016-06-21       Impact factor: 9.031

6.  Roles of cytosolic phospholipase A2α in reproductive and systemic toxicities in 2,3,7,8-tetrachlorodibenzo-p-dioxin-exposed mice.

Authors:  Nozomi Fujisawa; Wataru Yoshioka; Hiroyuki Yanagisawa; Chiharu Tohyama
Journal:  Arch Toxicol       Date:  2017-10-17       Impact factor: 5.153

Review 7.  Mechanisms of Developmental Toxicity of Dioxins and Related Compounds.

Authors:  Wataru Yoshioka; Chiharu Tohyama
Journal:  Int J Mol Sci       Date:  2019-01-31       Impact factor: 5.923

8.  Histological and Immunohistochemical Studies to Determine the Mechanism of Cleft Palate Induction after Palatal Fusion in Mice Exposed to TCDD.

Authors:  Chisato Sakuma; Hideto Imura; Tomohiro Yamada; Azumi Hirata; Yayoi Ikeda; Masaaki Ito; Nagato Natsume
Journal:  Int J Mol Sci       Date:  2022-02-13       Impact factor: 5.923

9.  Dioxin-dependent and dioxin-independent gene batteries: comparison of liver and kidney in AHR-null mice.

Authors:  Paul C Boutros; Kirsten A Bielefeld; Raimo Pohjanvirta; Patricia A Harper
Journal:  Toxicol Sci       Date:  2009-09-16       Impact factor: 4.849

10.  Developmental effects of dioxins.

Authors:  L S Birnbaum
Journal:  Environ Health Perspect       Date:  1995-10       Impact factor: 9.031

  10 in total

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