2017
Different DNA damage response of cis and trans isomers of commonly used UV filter after the exposure on adult human liver stem cells and human lymphoblastoid cells
SHARMA, Anežka, Katarína BÁNYIOVÁ, Pavel BABICA, Naouale EL YAMANI, Andrew Richard COLLINS et. al.Základní údaje
Originální název
Different DNA damage response of cis and trans isomers of commonly used UV filter after the exposure on adult human liver stem cells and human lymphoblastoid cells
Autoři
SHARMA, Anežka (203 Česká republika, domácí), Katarína BÁNYIOVÁ (703 Slovensko, domácí), Pavel BABICA (203 Česká republika), Naouale EL YAMANI (578 Norsko), Andrew Richard COLLINS (578 Norsko) a Pavel ČUPR (203 Česká republika, garant, domácí)
Vydání
Science of the Total Environment, AMSTERDAM, Elsevier Science BV, 2017, 0048-9697
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10511 Environmental sciences
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.610
Kód RIV
RIV/00216224:14310/17:00095509
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000401201800003
Klíčová slova anglicky
trans/cis-EHMC; Isomerization; Human risk assessment; Genotoxicity; Adult human liver stem cells; High-throughput comet assay
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 1. 4. 2018 09:34, Ing. Nicole Zrilić
Anotace
V originále
2-ethylhexyl 4-methoxycinnamate (EHMC), used in many categories of personal care products (PCPs), is one of the most discussed ultraviolet filters because of its endocrine-disrupting effects. EHMC is unstable in sunlight and can be transformed from trans-EHMC to emergent cis-EHMC. Toxicological studies are focusing only on transEHMC; thus the toxicological data for cis-EHMC are missing. In this study, the in vitro genotoxic effects of trans- and cis-EHMC on adult human liver stem cells HL1-hT1 and human-derived lymphoblastoid cells TK-6 using a high-throughput comet assay were studied. TK-6 cells treated with cis-EHMC showed a high level of DNA damage when compared to untreated cells in concentrations 1.56 to 25 mu g mL(-1). trans-EHMC showed genotoxicity after exposure to the two highest concentrations 12.5 and 25 mu g mL(-1). The increase in DNA damage on HL1-hT1 cells induced by cis-EHMC and transEHMC was detected at the concentration 25 pg mL-1. The No observed adverse effect level (NOAEL, mg kg lbw day I) was determined using a Quantitative in vitro to in vivo extrapolation (QIVIVE) approach: NOAEL(trans-EHMC) = 3.07, NOAEL(cis-EHMC) = 0.30 for TK-6 and NOAEL(trans-EHMC) = 26.46, NOAEL(cis-EHMC) = 20.36 for HL1-hT1. The hazard index (HI) was evaluated by comparing the reference dose (RID, mg kg(-1) bw day(-1)) obtained from our experimental data with the chronic daily intake (CDI) of the female population. Using comet assay experimental data with the more sensitive TK-6 cells, HIcis-EHMC was 7 times higher than HItrans-EHMC In terms of CDI, relative contributions were; dermal exposure route > oral > inhalation. According to our results we recommend the RfD(trans-EHMC) = 0.20 and RfD(cis-EHMC) = 0.02 for trans-EHMC and cis-EHMC, respectively, to use for human health risk assessment. The significant difference in trans-EHMC and cis-EHMC response points to the need for toxicological reevaluation and application reassessment of both isomers in PCPs.
Návaznosti
GA14-27941S, projekt VaV |
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LM2015051, projekt VaV |
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LO1214, projekt VaV |
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