Pregled bibliografske jedinice broj: 268005
Mercury chloride genotoxicity in human lymphocyte culture assessed by the alkaline comet assay
Mercury chloride genotoxicity in human lymphocyte culture assessed by the alkaline comet assay, 2006. str. 195-195 (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 268005 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Mercury chloride genotoxicity in human lymphocyte culture assessed by the alkaline comet assay
Autori
Milić, Mirta ; Rozgaj, Ružica ; Želježić, Davor ; Kabuša, Vilena
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Mjesto i datum
,
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
mercury chloride; alkaline comet assay; genotoxicity
Sažetak
Mercury is the most toxic of the heavy metals and exerts a variety of toxic effects in the body. Within the cell it can destroy the various components selectively or in total by releasing lysosomes, damaging DNA and by rupturing the cell membrane. Mercury from mercuric chloride binds to the sulfhydryl groups of the cell membrane and other proteins, causing increased membrane permeability and inhibition of ATPase-dependent transport. The genotoxicity of mercury chloride in this study was assessed by alkaline single-cell gel electrophoresis (the comet assay) in human peripheral blood lymphocytes. Four concentrations of metal salt dissolved in re-destilled water were used, 10, 50, 100 and 200 mM. Mitomicyn C (MMC) (0.5 mg/ml) was used as a positive control. An untreated control sample was also included in the experiment. Whole blood was exposed to HgCl2 for 24 and 48h at+370 C in CO2 incubator. All the samples were in duplicate. Three parameters were measured: tail length, tail moment, and tail intensity. The data were statistically analyzed by one-way ANOVA followed by Tukey post hoc test. P< 0.05 was assumed significant. After 24 h of exposure to mercury chloride tail length values in samples treated with 50 and 100 mM of HgCl2 were statistically different from the control sample. There were no significant differences neither in tail moment neither in tail intensity after 24 hours of exposure. In 48 h of exposure statistically significant differences in tail length were found between the positive control and all other samples, and non-treated control sample and the highest mercury chloride concentration (200 mM). For the tail intensity and tail moment only the positive control sample was significantly different from all other samples.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
0022019
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE