Literature DB >> 14713547

Follicular epithelial cell hypertrophy induced by chronic oral administration of 2,3,7,8-tetrachlorodibenzo-p-dioxin in female Harlan Sprague-Dawley rats.

Yoshiro Tani1, Robert R Maronpot, Julie F Foley, Joseph K Haseman, Nigel J Walker, Abraham Nyska.   

Abstract

2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) affects the thyroid morphologically and/or functionally in adult animals. Recently, the National Toxicology Program conducted a 2-year gavage study of TCDD in female Harlan Sprague-Dawley rats. The only treatment-related alterations found in thyroid follicles were decreased luminal size and increased height of the follicular epithelial cells, without prominent protrusion into the lumen. The present study elucidated the nature of these follicular lesions. Thyroid glands of 10 rats each from the control, high (100 ng/kg/day)-dose, and stop-study (100 ng/kg/day, 30 weeks; vehicle to study termination) groups in the 2-year study were evaluated microscopically. Twenty randomly selected follicles were measured morphometrically in each animal. TCDD treatment significantly decreased the mean ratio of luminal/epithelial areas and increased the mean sectional epithelial height of the high-dose group compared to controls. Thyroid sections were immunostained with antibody against minichromosome maintenance (MCM) proteins, a novel cell-cycle biomarker. The MCM labeling index of the high-dose group was significantly higher than that of the control; however, the TUNEL labeling index was also higher in the high-dose group than the control. All data from the stop group were comparable to those from controls. These results indicate that the follicular cell response was hypertrophic and reversible. This information should contribute to diagnosis of nonneoplastic thyroid follicular lesions in rats.

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Year:  2004        PMID: 14713547     DOI: 10.1080/01926230490260952

Source DB:  PubMed          Journal:  Toxicol Pathol        ISSN: 0192-6233            Impact factor:   1.902


  5 in total

1.  Comparison of chronic toxicity and carcinogenicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in 2-year bioassays in female Sprague-Dawley rats.

Authors:  Nigel J Walker; Michael E Wyde; Lawrence J Fischer; Abraham Nyska; John R Bucher
Journal:  Mol Nutr Food Res       Date:  2006-10       Impact factor: 5.914

Review 2.  A review of species differences in the control of, and response to, chemical-induced thyroid hormone perturbations leading to thyroid cancer.

Authors:  John R Foster; Helen Tinwell; Stephanie Melching-Kollmuss
Journal:  Arch Toxicol       Date:  2021-01-05       Impact factor: 5.153

Review 3.  A critical comparison of murine pathology and epidemiological data of TCDD, PCB126, and PeCDF.

Authors:  Katsuhiko Yoshizawa; Allison Heatherly; David E Malarkey; Nigel J Walker; Abraham Nyska
Journal:  Toxicol Pathol       Date:  2007-12       Impact factor: 1.902

4.  Pulmonary lesions in female Harlan Sprague-Dawley rats following two-year oral treatment with dioxin-like compounds.

Authors:  Nigel J Walker; Katsuhiko Yoshizawa; Rodney A Miller; Amy E Brix; Donald M Sells; Micheal P Jokinen; Michael E Wyde; Michael Easterling; Abraham Nyska
Journal:  Toxicol Pathol       Date:  2007-12       Impact factor: 1.902

5.  Inflammatory and chloracne-like skin lesions in B6C3F1 mice exposed to 3,3',4,4'-tetrachloroazobenzene for 2 years.

Authors:  Yuval Ramot; Abraham Nyska; Warren Lieuallen; Alex Maly; Gordon Flake; Grace E Kissling; Amy Brix; David E Malarkey; Michelle J Hooth
Journal:  Toxicology       Date:  2009-09-06       Impact factor: 4.221

  5 in total

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