• Something wrong with this record ?

Accumulation of chlorinated paraffins in adipocytes is determined by cellular lipid content and chlorination level

N. Vrzáčková, J. Tomáško, P. Svoboda, V. Škop, M. Melčová, J. Dudová, J. Zelenka, J. Pulkrabová, T. Ruml

. 2025 ; 99 (3) : 1117-1131. [pub] 20250110

Language English Country Germany

Document type Journal Article

Grant support
21-19437S Grantová Agentura České Republiky
CZ.02.2.69/0.0/0.0/19_073/0016928 European Science Foundation

Chlorinated paraffins (CPs) are environmental pollutants extensively used in industries. While the use of short-chain chlorinated paraffins (SCCPs) has been restricted since 2017, the use of medium-chain chlorinated paraffins (MCCPs) has risen as their replacement. Due to lipophilic character, it can be expected that CPs enter the cells; however, the in vitro accumulation potential of CPs remains poorly understood. In this study, we aimed to explore the ability of SCCPs and MCCPs to accumulate in fat cells. We utilized an in vitro model of mouse 3T3-L1 preadipocytes and adipocytes. Using gas chromatography coupled with high-resolution mass spectrometry operated in negative chemical ionization mode, we determined the intracellular amounts of CPs. These compounds accumulated at rates of 8.5 ± 0.1 μg/gcells/h for SCCPs and 7.8 ± 0.3 μg/gcells/h for MCCPs when an initial concentration of 120 ng/ml was present in the medium. This rate increased approximately tenfold when the concentration of CPs was raised to 1200 ng/ml. CPs content in adipocytes steadily increased over 5 days, whereas preadipocytes accumulated 15-20 times less CPs. This highlights the importance of cellular lipid content, which was about 12 times higher in adipocytes. Furthermore, we found that the level of chlorine content in the CPs molecules significantly influenced their accumulation. Our results demonstrate that MCCPs exhibit a similar accumulation potential to SCCPs, with lipid content playing a crucial role. As with SCCPs, restrictions on the use of MCCPs in industry should be considered to mitigate their environmental and health impacts.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc25009694
003      
CZ-PrNML
005      
20250429135018.0
007      
ta
008      
250415s2025 gw f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s00204-024-03956-3 $2 doi
035    __
$a (PubMed)39789331
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a gw
100    1_
$a Vrzáčková, Nikola $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Technická 3, 16000, Prague, Czech Republic $1 https://orcid.org/0000000291083053
245    10
$a Accumulation of chlorinated paraffins in adipocytes is determined by cellular lipid content and chlorination level / $c N. Vrzáčková, J. Tomáško, P. Svoboda, V. Škop, M. Melčová, J. Dudová, J. Zelenka, J. Pulkrabová, T. Ruml
520    9_
$a Chlorinated paraffins (CPs) are environmental pollutants extensively used in industries. While the use of short-chain chlorinated paraffins (SCCPs) has been restricted since 2017, the use of medium-chain chlorinated paraffins (MCCPs) has risen as their replacement. Due to lipophilic character, it can be expected that CPs enter the cells; however, the in vitro accumulation potential of CPs remains poorly understood. In this study, we aimed to explore the ability of SCCPs and MCCPs to accumulate in fat cells. We utilized an in vitro model of mouse 3T3-L1 preadipocytes and adipocytes. Using gas chromatography coupled with high-resolution mass spectrometry operated in negative chemical ionization mode, we determined the intracellular amounts of CPs. These compounds accumulated at rates of 8.5 ± 0.1 μg/gcells/h for SCCPs and 7.8 ± 0.3 μg/gcells/h for MCCPs when an initial concentration of 120 ng/ml was present in the medium. This rate increased approximately tenfold when the concentration of CPs was raised to 1200 ng/ml. CPs content in adipocytes steadily increased over 5 days, whereas preadipocytes accumulated 15-20 times less CPs. This highlights the importance of cellular lipid content, which was about 12 times higher in adipocytes. Furthermore, we found that the level of chlorine content in the CPs molecules significantly influenced their accumulation. Our results demonstrate that MCCPs exhibit a similar accumulation potential to SCCPs, with lipid content playing a crucial role. As with SCCPs, restrictions on the use of MCCPs in industry should be considered to mitigate their environmental and health impacts.
650    _2
$a zvířata $7 D000818
650    _2
$a myši $7 D051379
650    12
$a tukové buňky $x metabolismus $x účinky léků $7 D017667
650    12
$a buňky 3T3-L1 $7 D041721
650    12
$a halogenace $7 D054879
650    12
$a chlorované uhlovodíky $x metabolismus $x toxicita $7 D006843
650    12
$a parafín $7 D010232
650    _2
$a látky znečišťující životní prostředí $x toxicita $x metabolismus $7 D004785
650    _2
$a metabolismus lipidů $x účinky léků $7 D050356
650    _2
$a plynová chromatografie s hmotnostně spektrometrickou detekcí $7 D008401
655    _2
$a časopisecké články $7 D016428
700    1_
$a Tomáško, Jakub $u Department of Food Analysis and Nutrition, University of Chemistry and Technology, Technická 3, 16000, Prague, Czech Republic $1 https://orcid.org/0000000227382913
700    1_
$a Svoboda, Petr $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Technická 3, 16000, Prague, Czech Republic $1 https://orcid.org/0000000172974208 $7 jn20000710631
700    1_
$a Škop, Vojtěch $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Technická 3, 16000, Prague, Czech Republic $u Center for Experimental Medicine, Institute for Clinical and Experimental Medicine, Vídeňská 1958, 14021, Prague, Czech Republic $1 https://orcid.org/0000000246854429 $7 xx0121451
700    1_
$a Melčová, Magdalena $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Technická 3, 16000, Prague, Czech Republic $1 https://orcid.org/0000000200546113
700    1_
$a Dudová, Jana $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Technická 3, 16000, Prague, Czech Republic $u Center for Experimental Medicine, Institute for Clinical and Experimental Medicine, Vídeňská 1958, 14021, Prague, Czech Republic $1 https://orcid.org/0009000207652901
700    1_
$a Zelenka, Jaroslav $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Technická 3, 16000, Prague, Czech Republic $1 https://orcid.org/0000000181458037 $7 xx0190812
700    1_
$a Pulkrabová, Jana $u Department of Food Analysis and Nutrition, University of Chemistry and Technology, Technická 3, 16000, Prague, Czech Republic $1 https://orcid.org/0000000319654672
700    1_
$a Ruml, Tomáš $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Technická 3, 16000, Prague, Czech Republic. Tomas.Ruml@vscht.cz $1 https://orcid.org/0000000256984366 $7 nlk20030128618
773    0_
$w MED00009265 $t Archives of toxicology $x 1432-0738 $g Roč. 99, č. 3 (2025), s. 1117-1131
856    41
$u https://pubmed.ncbi.nlm.nih.gov/39789331 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20250415 $b ABA008
991    __
$a 20250429135014 $b ABA008
999    __
$a ok $b bmc $g 2311209 $s 1246775
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2025 $b 99 $c 3 $d 1117-1131 $e 20250110 $i 1432-0738 $m Archives of toxicology $n Arch Toxicol $x MED00009265
GRA    __
$a 21-19437S $p Grantová Agentura České Republiky
GRA    __
$a CZ.02.2.69/0.0/0.0/19_073/0016928 $p European Science Foundation
LZP    __
$a Pubmed-20250415

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...