Detailed Information on Publication Record
2020
The effects of nano-sized PbO on biomarkers of membrane disruption and DNA damage in a sub-chronic inhalation study on mice
BLÁHOVÁ, Lucie, Zuzana NOVÁKOVÁ, Zbyněk VEČEŘA, Lucie VRLÍKOVÁ, Bohumil DOČEKAL et. al.Basic information
Original name
The effects of nano-sized PbO on biomarkers of membrane disruption and DNA damage in a sub-chronic inhalation study on mice
Authors
BLÁHOVÁ, Lucie (203 Czech Republic, belonging to the institution), Zuzana NOVÁKOVÁ (203 Czech Republic, belonging to the institution), Zbyněk VEČEŘA (203 Czech Republic), Lucie VRLÍKOVÁ (203 Czech Republic), Bohumil DOČEKAL (203 Czech Republic), Jana DUMKOVÁ (203 Czech Republic, belonging to the institution), Kamil KRUMAL (203 Czech Republic), Pavel MIKUSKA (203 Czech Republic), Marcela BUCHTOVÁ (203 Czech Republic, belonging to the institution), Aleš HAMPL (203 Czech Republic, belonging to the institution), Klára HILSCHEROVÁ (203 Czech Republic, belonging to the institution) and Luděk BLÁHA (203 Czech Republic, guarantor, belonging to the institution)
Edition
NANOTOXICOLOGY, ABINGDON, TAYLOR & FRANCIS LTD, 2020, 1743-5390
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30108 Toxicology
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 5.913
RIV identification code
RIV/00216224:14310/20:00115464
Organization unit
Faculty of Science
UT WoS
000496628900001
Keywords in English
Oxidative damage; lead; nanoparticle; 8-OHdG; TBARS; 8-isoPGF2(alpha); 8-isoPGE isoprostanes; LC-MS; MS; lipid peroxidation; inhalation
Tags
International impact, Reviewed
Změněno: 13/2/2023 17:26, Mgr. Michaela Hylsová, Ph.D.
Abstract
V originále
Although the production of engineered nanoparticles increases our knowledge of toxicity and mechanisms of bioactivity during relevant exposures is lacking. In the present study mice were exposed to PbO nanoparticles (PbONP; 192.5 mu g/m(3); 1.93 x 10(6) particles/cm(3)) for 2, 5 and 13 weeks through continuous inhalation. The analyses addressed Pb and PbONP distribution in organs (lung, liver, kidney, brain) using electrothermal atomic absorption spectrometry and transmission electron microscopy, as well as histopathology and analyses of oxidative stress biomarkers. New LC-MS/MS methods were validated for biomarkers of lipid damage F2-isoprostanes (8-iso-prostaglandins F2-alpha and E-2) and hydroxylated deoxoguanosine (8-OHdG, marker of DNA oxidation). Commonly studied malondialdehyde was also measured as TBARS by HPLC-DAD. The study revealed fast blood transport and distribution of Pb from the lung to the kidney and liver. A different Pb accumulation trend was observed in the brain, suggesting transfer of NP along the nasal nerve to the olfactory bulbs. Long-term inhalation of PbONP caused lipid peroxidation in animal brains (increased levels of TBARS and both isoprostanes). Membrane lipid damage was also detected in the kidney after shorter exposures, but not in the liver or lung. On the contrary, longer exposures to PbONP increased levels of 8-OHdG in the lung and temporarily increased lung weight after 2 and 5 weeks of exposure. The histopathological changes observed mainly in the lung and liver indicated inflammation and general toxicity responses. The present long-term inhalation study indicates risks of PbONP to both human health and the environment.
Links
EF16_013/0001761, research and development project |
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LM2015051, research and development project |
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