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Comparison of tris(2‐ethylhexyl) phosphate and di(2‐ethylhexyl) phosphoric acid toxicities in a rat 28‐day oral exposure study

Tris(2‐ethylhexyl) phosphate (TEHP, CAS no. 78‐42‐2) is a plasticizer and a flame retardant, while di(2‐ethylhexyl) phosphoric acid (DEHPA, CAS no. 298‐07‐7) is an oil additive and extraction solvent. Publicly‐available information on repeated exposure to these two related organophosphate compounds...

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Autores principales: Pelletier, Guillaume, Rigden, Marc, Wang, Gen Sheng, Caldwell, Don, Siddique, Shabana, Leingartner, Karen, Kosarac, Ivana, Cakmak, Sabit, Kubwabo, Cariton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216891/
https://www.ncbi.nlm.nih.gov/pubmed/31884710
http://dx.doi.org/10.1002/jat.3930
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author Pelletier, Guillaume
Rigden, Marc
Wang, Gen Sheng
Caldwell, Don
Siddique, Shabana
Leingartner, Karen
Kosarac, Ivana
Cakmak, Sabit
Kubwabo, Cariton
author_facet Pelletier, Guillaume
Rigden, Marc
Wang, Gen Sheng
Caldwell, Don
Siddique, Shabana
Leingartner, Karen
Kosarac, Ivana
Cakmak, Sabit
Kubwabo, Cariton
author_sort Pelletier, Guillaume
collection PubMed
description Tris(2‐ethylhexyl) phosphate (TEHP, CAS no. 78‐42‐2) is a plasticizer and a flame retardant, while di(2‐ethylhexyl) phosphoric acid (DEHPA, CAS no. 298‐07‐7) is an oil additive and extraction solvent. Publicly‐available information on repeated exposure to these two related organophosphate compounds is fragmentary. Hence, adult male and female Fischer rats were exposed to TEHP (300, 1000 and 3000 mg/kg body weight [BW]/day) or DEHPA (20, 60 and 180 mg/kg BW/day) by gavage for 28 consecutive days, to assess and compare their toxicities. Although significantly impaired BW gains and evidence of TEHP enzymatic hydrolysis to DEHPA were observed only in males, exposures to the highest TEHP and DEHPA doses often resulted in similar alterations of hematology, serum clinical chemistry and liver enzymatic activities in both males and females. The squamous epithelial hyperplasia and hyperkeratosis observed in the non‐glandular forestomach of rats exposed to the middle and high DEHPA doses were most likely caused by the slightly corrosive nature of this chemical. Although tubular degeneration and spermatid retention were observed only in the testes of males exposed to the highest TEHP dose, numerous periodic acid‐Schiff stained crystalline inclusions were observed in testis interstitial cells at all TEHP dose levels. No‐observed‐adverse‐effect levels for TEHP and DEHPA are proposed, but the lower serum pituitary hormone levels resulting from TEHP and DEHPA exposures and the perturbations of testicular histology observed in TEHP‐treated males deserve further investigation. Improved characterization of the toxicity of flame retardants will contribute to better informed substitution choices for legacy flame retardants phased‐out over health concerns.
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spelling pubmed-72168912020-05-13 Comparison of tris(2‐ethylhexyl) phosphate and di(2‐ethylhexyl) phosphoric acid toxicities in a rat 28‐day oral exposure study Pelletier, Guillaume Rigden, Marc Wang, Gen Sheng Caldwell, Don Siddique, Shabana Leingartner, Karen Kosarac, Ivana Cakmak, Sabit Kubwabo, Cariton J Appl Toxicol Research Articles Tris(2‐ethylhexyl) phosphate (TEHP, CAS no. 78‐42‐2) is a plasticizer and a flame retardant, while di(2‐ethylhexyl) phosphoric acid (DEHPA, CAS no. 298‐07‐7) is an oil additive and extraction solvent. Publicly‐available information on repeated exposure to these two related organophosphate compounds is fragmentary. Hence, adult male and female Fischer rats were exposed to TEHP (300, 1000 and 3000 mg/kg body weight [BW]/day) or DEHPA (20, 60 and 180 mg/kg BW/day) by gavage for 28 consecutive days, to assess and compare their toxicities. Although significantly impaired BW gains and evidence of TEHP enzymatic hydrolysis to DEHPA were observed only in males, exposures to the highest TEHP and DEHPA doses often resulted in similar alterations of hematology, serum clinical chemistry and liver enzymatic activities in both males and females. The squamous epithelial hyperplasia and hyperkeratosis observed in the non‐glandular forestomach of rats exposed to the middle and high DEHPA doses were most likely caused by the slightly corrosive nature of this chemical. Although tubular degeneration and spermatid retention were observed only in the testes of males exposed to the highest TEHP dose, numerous periodic acid‐Schiff stained crystalline inclusions were observed in testis interstitial cells at all TEHP dose levels. No‐observed‐adverse‐effect levels for TEHP and DEHPA are proposed, but the lower serum pituitary hormone levels resulting from TEHP and DEHPA exposures and the perturbations of testicular histology observed in TEHP‐treated males deserve further investigation. Improved characterization of the toxicity of flame retardants will contribute to better informed substitution choices for legacy flame retardants phased‐out over health concerns. John Wiley and Sons Inc. 2019-12-29 2020-05 /pmc/articles/PMC7216891/ /pubmed/31884710 http://dx.doi.org/10.1002/jat.3930 Text en © 2019 Her Majesty the Queen in Right of Canada. Journal of Applied Toxicology published by John Wiley & Sons. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Pelletier, Guillaume
Rigden, Marc
Wang, Gen Sheng
Caldwell, Don
Siddique, Shabana
Leingartner, Karen
Kosarac, Ivana
Cakmak, Sabit
Kubwabo, Cariton
Comparison of tris(2‐ethylhexyl) phosphate and di(2‐ethylhexyl) phosphoric acid toxicities in a rat 28‐day oral exposure study
title Comparison of tris(2‐ethylhexyl) phosphate and di(2‐ethylhexyl) phosphoric acid toxicities in a rat 28‐day oral exposure study
title_full Comparison of tris(2‐ethylhexyl) phosphate and di(2‐ethylhexyl) phosphoric acid toxicities in a rat 28‐day oral exposure study
title_fullStr Comparison of tris(2‐ethylhexyl) phosphate and di(2‐ethylhexyl) phosphoric acid toxicities in a rat 28‐day oral exposure study
title_full_unstemmed Comparison of tris(2‐ethylhexyl) phosphate and di(2‐ethylhexyl) phosphoric acid toxicities in a rat 28‐day oral exposure study
title_short Comparison of tris(2‐ethylhexyl) phosphate and di(2‐ethylhexyl) phosphoric acid toxicities in a rat 28‐day oral exposure study
title_sort comparison of tris(2‐ethylhexyl) phosphate and di(2‐ethylhexyl) phosphoric acid toxicities in a rat 28‐day oral exposure study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216891/
https://www.ncbi.nlm.nih.gov/pubmed/31884710
http://dx.doi.org/10.1002/jat.3930
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