The brominated flame retardant tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether) as well as hexabromocyclododecane lead to lipid disorders in mice

The brominated flame retardant tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether) (TBBPA-DBMPE) is a recommended substitute for hexabromocyclododecane (HBCD), a banned persistent organic pollutant, yet its potential toxicities remains largely unexplored. Here, we investigated the effects of...

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Veröffentlicht in:Environmental pollution (1987) 2024-01, Vol.341, p.122895-122895, Article 122895
Hauptverfasser: Chen, Xuan-Yue, Li, Yuan-Yuan, Lv, Lin, Xiong, Yi-Ming, Qin, Zhan-Fen
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container_start_page 122895
container_title Environmental pollution (1987)
container_volume 341
creator Chen, Xuan-Yue
Li, Yuan-Yuan
Lv, Lin
Xiong, Yi-Ming
Qin, Zhan-Fen
description The brominated flame retardant tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether) (TBBPA-DBMPE) is a recommended substitute for hexabromocyclododecane (HBCD), a banned persistent organic pollutant, yet its potential toxicities remains largely unexplored. Here, we investigated the effects of a long-term exposure to TBBPA-DBMPE at nominal doses of 50 and 1000 μg/kg/d on lipid homeostasis in CD-1 mice, in comparison with 50 μg/kg/d HBCD as a positive control. Male pups received chemical treatments through maternal administration via drinking water from postnatal day 0-21, followed by direct administration through drinking water after weaning. On the 23rd week after treatment, the oral lipid tolerance test revealed that low-dose TBBPA-DBMPE as well as HBCD affected lipid tolerance, although the fasting serum triglyceride (TG) levels were not altered. When chemical treatment was extended to the 32nd week, TBBPA-DBMPE-treated animals displayed adipocyte hypertrophy in both white adipose tissue (eWAT) and brown adipose tissue (BAT) and hepatic steatosis, which was largely consistent with the effects of HBCD. These findings indicate that like HBCD, TBBPA-DBMPE led to increased lipid load in mice. Interestingly, we also observed intestinal histological changes, coupled with increased expression of lipid absorption-related genes in both HBCD and TBBPA-DBMPE treatments, suggesting increased lipid absorption. This was supported by in vitro findings that both HBCD and TBBPA-DBMPE promoted lipid accumulation in IEC-6 cells under the stress of oleic acid for 6 h, implying that altered lipid absorption by the intestine may partly contributed to increased lipid load in mice. Overall, the effects of 50 μg/kg/d TBBPA-DBMPE in terms of some parameters were comparable with 50 μg/kg/d HBCD, suggesting that TBBPA-DBMPE may not be an ideal substitute of HBCD.
doi_str_mv 10.1016/j.envpol.2023.122895
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Here, we investigated the effects of a long-term exposure to TBBPA-DBMPE at nominal doses of 50 and 1000 μg/kg/d on lipid homeostasis in CD-1 mice, in comparison with 50 μg/kg/d HBCD as a positive control. Male pups received chemical treatments through maternal administration via drinking water from postnatal day 0-21, followed by direct administration through drinking water after weaning. On the 23rd week after treatment, the oral lipid tolerance test revealed that low-dose TBBPA-DBMPE as well as HBCD affected lipid tolerance, although the fasting serum triglyceride (TG) levels were not altered. When chemical treatment was extended to the 32nd week, TBBPA-DBMPE-treated animals displayed adipocyte hypertrophy in both white adipose tissue (eWAT) and brown adipose tissue (BAT) and hepatic steatosis, which was largely consistent with the effects of HBCD. These findings indicate that like HBCD, TBBPA-DBMPE led to increased lipid load in mice. 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Li, Yuan-Yuan ; Lv, Lin ; Xiong, Yi-Ming ; Qin, Zhan-Fen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c289t-259d32431f8dfab48971a8c5fe22f828f312a49c947e83c29a98b2de2ce7487e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>absorption</topic><topic>adipocytes</topic><topic>Animals</topic><topic>blood serum</topic><topic>brown adipose tissue</topic><topic>chemical treatment</topic><topic>chronic exposure</topic><topic>Drinking Water</topic><topic>Ether</topic><topic>Ethers</topic><topic>Ethyl Ethers</topic><topic>fatty liver</topic><topic>flame retardants</topic><topic>Flame Retardants - analysis</topic><topic>Flame Retardants - toxicity</topic><topic>hexabromocyclododecane</topic><topic>histology</topic><topic>homeostasis</topic><topic>Hydrocarbons, Brominated - analysis</topic><topic>Hydrocarbons, Brominated - toxicity</topic><topic>hypertrophy</topic><topic>intestines</topic><topic>Lipids</topic><topic>Male</topic><topic>males</topic><topic>Mice</topic><topic>oleic acid</topic><topic>persistent organic pollutants</topic><topic>pollution</topic><topic>Polybrominated Biphenyls - analysis</topic><topic>Polybrominated Biphenyls - toxicity</topic><topic>triacylglycerols</topic><topic>white adipose tissue</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Xuan-Yue</creatorcontrib><creatorcontrib>Li, Yuan-Yuan</creatorcontrib><creatorcontrib>Lv, Lin</creatorcontrib><creatorcontrib>Xiong, Yi-Ming</creatorcontrib><creatorcontrib>Qin, Zhan-Fen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Environmental pollution (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Xuan-Yue</au><au>Li, Yuan-Yuan</au><au>Lv, Lin</au><au>Xiong, Yi-Ming</au><au>Qin, Zhan-Fen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The brominated flame retardant tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether) as well as hexabromocyclododecane lead to lipid disorders in mice</atitle><jtitle>Environmental pollution (1987)</jtitle><addtitle>Environ Pollut</addtitle><date>2024-01-15</date><risdate>2024</risdate><volume>341</volume><spage>122895</spage><epage>122895</epage><pages>122895-122895</pages><artnum>122895</artnum><issn>0269-7491</issn><eissn>1873-6424</eissn><abstract>The brominated flame retardant tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether) (TBBPA-DBMPE) is a recommended substitute for hexabromocyclododecane (HBCD), a banned persistent organic pollutant, yet its potential toxicities remains largely unexplored. Here, we investigated the effects of a long-term exposure to TBBPA-DBMPE at nominal doses of 50 and 1000 μg/kg/d on lipid homeostasis in CD-1 mice, in comparison with 50 μg/kg/d HBCD as a positive control. Male pups received chemical treatments through maternal administration via drinking water from postnatal day 0-21, followed by direct administration through drinking water after weaning. On the 23rd week after treatment, the oral lipid tolerance test revealed that low-dose TBBPA-DBMPE as well as HBCD affected lipid tolerance, although the fasting serum triglyceride (TG) levels were not altered. When chemical treatment was extended to the 32nd week, TBBPA-DBMPE-treated animals displayed adipocyte hypertrophy in both white adipose tissue (eWAT) and brown adipose tissue (BAT) and hepatic steatosis, which was largely consistent with the effects of HBCD. These findings indicate that like HBCD, TBBPA-DBMPE led to increased lipid load in mice. Interestingly, we also observed intestinal histological changes, coupled with increased expression of lipid absorption-related genes in both HBCD and TBBPA-DBMPE treatments, suggesting increased lipid absorption. This was supported by in vitro findings that both HBCD and TBBPA-DBMPE promoted lipid accumulation in IEC-6 cells under the stress of oleic acid for 6 h, implying that altered lipid absorption by the intestine may partly contributed to increased lipid load in mice. Overall, the effects of 50 μg/kg/d TBBPA-DBMPE in terms of some parameters were comparable with 50 μg/kg/d HBCD, suggesting that TBBPA-DBMPE may not be an ideal substitute of HBCD.</abstract><cop>England</cop><pmid>37949162</pmid><doi>10.1016/j.envpol.2023.122895</doi><tpages>1</tpages></addata></record>
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identifier ISSN: 0269-7491
ispartof Environmental pollution (1987), 2024-01, Vol.341, p.122895-122895, Article 122895
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source MEDLINE; Elsevier ScienceDirect Journals
subjects absorption
adipocytes
Animals
blood serum
brown adipose tissue
chemical treatment
chronic exposure
Drinking Water
Ether
Ethers
Ethyl Ethers
fatty liver
flame retardants
Flame Retardants - analysis
Flame Retardants - toxicity
hexabromocyclododecane
histology
homeostasis
Hydrocarbons, Brominated - analysis
Hydrocarbons, Brominated - toxicity
hypertrophy
intestines
Lipids
Male
males
Mice
oleic acid
persistent organic pollutants
pollution
Polybrominated Biphenyls - analysis
Polybrominated Biphenyls - toxicity
triacylglycerols
white adipose tissue
title The brominated flame retardant tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether) as well as hexabromocyclododecane lead to lipid disorders in mice
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