Developmental and Hepatic Gene Expression Changes in Chicken Embryos Exposed to p‐Tert‐Butylphenyl Diphenyl Phosphate and Isopropylphenyl Phosphate via Egg Injection
Organophosphate flame retardants (OPFRs) are used in a variety of products such as clear coats, resins, and plastics; however, research into their toxicological effects is limited. p‐Tert‐butylphenyl diphenyl phosphate (BPDP) and isopropylphenyl phosphate (IPPP) are two OPFRs that were prioritized f...
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description | Organophosphate flame retardants (OPFRs) are used in a variety of products such as clear coats, resins, and plastics; however, research into their toxicological effects is limited. p‐Tert‐butylphenyl diphenyl phosphate (BPDP) and isopropylphenyl phosphate (IPPP) are two OPFRs that were prioritized for whole‐animal toxicological studies based on observed effects in cultured avian hepatocytes in a previous study. The present study investigates the toxicity of BPDP and IPPP in chicken embryos at different developmental stages by evaluating morphological and gene expression endpoints. Chicken eggs were exposed via air cell injection to 0–250 μg/g (nominal) of either compound and then artificially incubated. At day 11 (midincubation), liver samples were collected for mRNA expression analysis; and at day 20 (1 day prehatch), morphological measurements and liver samples for transcriptomic evaluation were collected. At 250 μg/g, gallbladder size was significantly reduced for both compounds, head/bill length and tarsus length were significantly decreased, and liver somatic index was significantly increased following IPPP exposure only. No effects on mortality were observed up to the highest administered concentration for either chemical. Using a ToxChip polymerase chain reaction array, we report significant differences in hepatic gene expression for both compounds and time points; the most pronounced transcriptomic effects occurred at midincubation. Genes related to xenobiotic metabolism, bile acid/cholesterol regulation, and oxidative stress were significantly dysregulated. Given these changes observed throughout avian embryonic development, further research into the long‐term effects of BPDP and IPPP are warranted, especially as they pertain to liver cholestasis. Environ Toxicol Chem 2022;41:739–747. © 2021 Her Majesty the Queen in Right of Canada. Environmental Toxicology and Chemistry © 2021 SETAC. Reproduced with the permission of the Minister of Environment and Climate Change Canada. |
doi_str_mv | 10.1002/etc.5274 |
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The present study investigates the toxicity of BPDP and IPPP in chicken embryos at different developmental stages by evaluating morphological and gene expression endpoints. Chicken eggs were exposed via air cell injection to 0–250 μg/g (nominal) of either compound and then artificially incubated. At day 11 (midincubation), liver samples were collected for mRNA expression analysis; and at day 20 (1 day prehatch), morphological measurements and liver samples for transcriptomic evaluation were collected. At 250 μg/g, gallbladder size was significantly reduced for both compounds, head/bill length and tarsus length were significantly decreased, and liver somatic index was significantly increased following IPPP exposure only. No effects on mortality were observed up to the highest administered concentration for either chemical. Using a ToxChip polymerase chain reaction array, we report significant differences in hepatic gene expression for both compounds and time points; the most pronounced transcriptomic effects occurred at midincubation. Genes related to xenobiotic metabolism, bile acid/cholesterol regulation, and oxidative stress were significantly dysregulated. Given these changes observed throughout avian embryonic development, further research into the long‐term effects of BPDP and IPPP are warranted, especially as they pertain to liver cholestasis. Environ Toxicol Chem 2022;41:739–747. © 2021 Her Majesty the Queen in Right of Canada. Environmental Toxicology and Chemistry © 2021 SETAC. Reproduced with the permission of the Minister of Environment and Climate Change Canada.</description><identifier>ISSN: 0730-7268</identifier><identifier>EISSN: 1552-8618</identifier><identifier>DOI: 10.1002/etc.5274</identifier><identifier>PMID: 34913512</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Animals ; Avian toxicity ; Chick Embryo ; Chickens ; Chickens - metabolism ; Cholestasis ; Cholesterol ; Climate change ; Developmental stages ; Eggs ; Embryogenesis ; Embryonic growth stage ; Embryos ; Evaluation ; Exposure ; Female ; Flame retardants ; Flame Retardants - metabolism ; Flame Retardants - toxicity ; Gallbladder ; Gene expression ; Hepatocytes ; Injection ; Isopropylphenyl phosphate ; Lipid metabolism ; Liver ; Liver - metabolism ; Morphology ; Organophosphates ; Organophosphates - toxicity ; Oxidative stress ; Phosphates ; Polymerase chain reaction ; p‐Tert‐butylphenyl diphenyl phosphate ; Quantitative polymerase chain reaction ; Resins ; Toxicity ; Toxicity testing ; Toxicology ; Transcriptome ; Transcriptomics</subject><ispartof>Environmental toxicology and chemistry, 2022-03, Vol.41 (3), p.739-747</ispartof><rights>2021 Her Majesty the Queen in Right of Canada. © 2021 SETAC. 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The present study investigates the toxicity of BPDP and IPPP in chicken embryos at different developmental stages by evaluating morphological and gene expression endpoints. Chicken eggs were exposed via air cell injection to 0–250 μg/g (nominal) of either compound and then artificially incubated. At day 11 (midincubation), liver samples were collected for mRNA expression analysis; and at day 20 (1 day prehatch), morphological measurements and liver samples for transcriptomic evaluation were collected. At 250 μg/g, gallbladder size was significantly reduced for both compounds, head/bill length and tarsus length were significantly decreased, and liver somatic index was significantly increased following IPPP exposure only. No effects on mortality were observed up to the highest administered concentration for either chemical. Using a ToxChip polymerase chain reaction array, we report significant differences in hepatic gene expression for both compounds and time points; the most pronounced transcriptomic effects occurred at midincubation. Genes related to xenobiotic metabolism, bile acid/cholesterol regulation, and oxidative stress were significantly dysregulated. Given these changes observed throughout avian embryonic development, further research into the long‐term effects of BPDP and IPPP are warranted, especially as they pertain to liver cholestasis. Environ Toxicol Chem 2022;41:739–747. © 2021 Her Majesty the Queen in Right of Canada. Environmental Toxicology and Chemistry © 2021 SETAC. Reproduced with the permission of the Minister of Environment and Climate Change Canada.</description><subject>Animals</subject><subject>Avian toxicity</subject><subject>Chick Embryo</subject><subject>Chickens</subject><subject>Chickens - metabolism</subject><subject>Cholestasis</subject><subject>Cholesterol</subject><subject>Climate change</subject><subject>Developmental stages</subject><subject>Eggs</subject><subject>Embryogenesis</subject><subject>Embryonic growth stage</subject><subject>Embryos</subject><subject>Evaluation</subject><subject>Exposure</subject><subject>Female</subject><subject>Flame retardants</subject><subject>Flame Retardants - metabolism</subject><subject>Flame Retardants - toxicity</subject><subject>Gallbladder</subject><subject>Gene expression</subject><subject>Hepatocytes</subject><subject>Injection</subject><subject>Isopropylphenyl phosphate</subject><subject>Lipid metabolism</subject><subject>Liver</subject><subject>Liver - metabolism</subject><subject>Morphology</subject><subject>Organophosphates</subject><subject>Organophosphates - toxicity</subject><subject>Oxidative stress</subject><subject>Phosphates</subject><subject>Polymerase chain reaction</subject><subject>p‐Tert‐butylphenyl diphenyl phosphate</subject><subject>Quantitative polymerase chain reaction</subject><subject>Resins</subject><subject>Toxicity</subject><subject>Toxicity testing</subject><subject>Toxicology</subject><subject>Transcriptome</subject><subject>Transcriptomics</subject><issn>0730-7268</issn><issn>1552-8618</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1u2zAQhYkiQe2mBXKCgEA22cghKVE_y9R2bQMBmkWyFihqbMuRSYakk2iXI_QavVZPUip23FUBAjMEP7zHmYfQOSUjSgi7Bi9HnGXJJzSknLMoT2l-goYki0mUsTQfoC_ObQihaVEUn9EgTgoac8qG6PcEnqHVZgvKixYLVeM5GOEbiWegAE9fjQXnGq3weC3UChxu-raRj6DwdFvZTrue0g5q7DU2f95-3YP1oXzf-a41a1BdiyfNoblba2fWwsO718JpY7U5Yv9enxuBp6sVXqgNSB_8v6LTpWgdfDvUM_TwY3o_nke3P2eL8c1tJMNUSVSApFCLWPCE5RmvK1os6zwtuIjrNAEg-ZJVjAvJWCHDoeFS98uIaVZBnsRn6HKvGz72tAPny43eWRUsS5bGLONplqSButpT0mrnLCxLY5utsF1JSdlnUoZMyj6TgF4cBHfVFuoj-BFCAKI98NK00P1XqAzMu-Bf_A6aTg</recordid><startdate>202203</startdate><enddate>202203</enddate><creator>Nguyen, Phuoc Tyler T.‐T.</creator><creator>Pagé‐Larivière, Florence</creator><creator>Williams, Kim</creator><creator>O'Brien, Jason</creator><creator>Crump, Doug</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><orcidid>https://orcid.org/0000-0003-2915-4989</orcidid><orcidid>https://orcid.org/0000-0001-8683-8012</orcidid></search><sort><creationdate>202203</creationdate><title>Developmental and Hepatic Gene Expression Changes in Chicken Embryos Exposed to p‐Tert‐Butylphenyl Diphenyl Phosphate and Isopropylphenyl Phosphate via Egg Injection</title><author>Nguyen, Phuoc Tyler T.‐T. ; 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however, research into their toxicological effects is limited. p‐Tert‐butylphenyl diphenyl phosphate (BPDP) and isopropylphenyl phosphate (IPPP) are two OPFRs that were prioritized for whole‐animal toxicological studies based on observed effects in cultured avian hepatocytes in a previous study. The present study investigates the toxicity of BPDP and IPPP in chicken embryos at different developmental stages by evaluating morphological and gene expression endpoints. Chicken eggs were exposed via air cell injection to 0–250 μg/g (nominal) of either compound and then artificially incubated. At day 11 (midincubation), liver samples were collected for mRNA expression analysis; and at day 20 (1 day prehatch), morphological measurements and liver samples for transcriptomic evaluation were collected. At 250 μg/g, gallbladder size was significantly reduced for both compounds, head/bill length and tarsus length were significantly decreased, and liver somatic index was significantly increased following IPPP exposure only. No effects on mortality were observed up to the highest administered concentration for either chemical. Using a ToxChip polymerase chain reaction array, we report significant differences in hepatic gene expression for both compounds and time points; the most pronounced transcriptomic effects occurred at midincubation. Genes related to xenobiotic metabolism, bile acid/cholesterol regulation, and oxidative stress were significantly dysregulated. Given these changes observed throughout avian embryonic development, further research into the long‐term effects of BPDP and IPPP are warranted, especially as they pertain to liver cholestasis. Environ Toxicol Chem 2022;41:739–747. © 2021 Her Majesty the Queen in Right of Canada. Environmental Toxicology and Chemistry © 2021 SETAC. 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subjects | Animals Avian toxicity Chick Embryo Chickens Chickens - metabolism Cholestasis Cholesterol Climate change Developmental stages Eggs Embryogenesis Embryonic growth stage Embryos Evaluation Exposure Female Flame retardants Flame Retardants - metabolism Flame Retardants - toxicity Gallbladder Gene expression Hepatocytes Injection Isopropylphenyl phosphate Lipid metabolism Liver Liver - metabolism Morphology Organophosphates Organophosphates - toxicity Oxidative stress Phosphates Polymerase chain reaction p‐Tert‐butylphenyl diphenyl phosphate Quantitative polymerase chain reaction Resins Toxicity Toxicity testing Toxicology Transcriptome Transcriptomics |
title | Developmental and Hepatic Gene Expression Changes in Chicken Embryos Exposed to p‐Tert‐Butylphenyl Diphenyl Phosphate and Isopropylphenyl Phosphate via Egg Injection |
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