Inter strand crosslinks in DNA induced in vivo by percutaneous application of sulphur mustard to rats and mice
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60162694%3AG44__%2F18%3A43889569" target="_blank" >RIV/60162694:G44__/18:43889569 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00179906:_____/18:10377868
Výsledek na webu
<a href="https://www.sciencedirect.com/science/article/pii/S1383571818300822?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S1383571818300822?via%3Dihub</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.mrgentox.2018.06.014" target="_blank" >10.1016/j.mrgentox.2018.06.014</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Inter strand crosslinks in DNA induced in vivo by percutaneous application of sulphur mustard to rats and mice
Popis výsledku v původním jazyce
Inter-strand crosslinks (ICL) in the DNA are regarded to be the main toxic lesions induced by sulphur mustard (SM). We have followed the induction of ICL in the DNA of different organs of Wistar rats and Balb/c or NMRI mice by the percutaneous application of SM using the modified (reverse) comet assay. Significant amounts of ICL were found in Balb/C lymphocytes, in bone marrow and liver cells after the dose of 80 mg/kg. A dose-dependent amount of ICL was induced in rats, with efficient induction in lymphocytes and spleen cells already after 5 mg SM/kg, indicating a higher susceptibility of rats to the DNA-damaging effect of SM compared with mice. A significant induction of ICL in other tested tissues (liver, bone marrow, colon epithelium) was seen at the dose of 20 mg/kg. The induced ICL were removed from the DNA during 48 h except for rats at the dose of 80 mg/kg. In fact, we observed that ICL are almost completely repaired in tissues of rats receiving high lethal doses. Results suggest that the unhooking of ICL, which we followed with the comet assay, may lead to the formation of another toxic DNA lesion during the repair process.
Název v anglickém jazyce
Inter strand crosslinks in DNA induced in vivo by percutaneous application of sulphur mustard to rats and mice
Popis výsledku anglicky
Inter-strand crosslinks (ICL) in the DNA are regarded to be the main toxic lesions induced by sulphur mustard (SM). We have followed the induction of ICL in the DNA of different organs of Wistar rats and Balb/c or NMRI mice by the percutaneous application of SM using the modified (reverse) comet assay. Significant amounts of ICL were found in Balb/C lymphocytes, in bone marrow and liver cells after the dose of 80 mg/kg. A dose-dependent amount of ICL was induced in rats, with efficient induction in lymphocytes and spleen cells already after 5 mg SM/kg, indicating a higher susceptibility of rats to the DNA-damaging effect of SM compared with mice. A significant induction of ICL in other tested tissues (liver, bone marrow, colon epithelium) was seen at the dose of 20 mg/kg. The induced ICL were removed from the DNA during 48 h except for rats at the dose of 80 mg/kg. In fact, we observed that ICL are almost completely repaired in tissues of rats receiving high lethal doses. Results suggest that the unhooking of ICL, which we followed with the comet assay, may lead to the formation of another toxic DNA lesion during the repair process.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30108 - Toxicology
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Mutation Research-Genetic Toxicology and Environmental Mutagenesis
ISSN
1383-5718
e-ISSN
—
Svazek periodika
832
Číslo periodika v rámci svazku
Aug
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
6
Strana od-do
35-40
Kód UT WoS článku
000441855400005
EID výsledku v databázi Scopus
2-s2.0-85048761832