Pregled bibliografske jedinice broj: 654
Micronucleus assay and mitotic activity : the methods for determinarion of recent vinyl chloride monomer exposure
Micronucleus assay and mitotic activity : the methods for determinarion of recent vinyl chloride monomer exposure // Abstracts of the 29th Annual Meeting of the Environmental Mutagen Society ; u: Environmental and Molecular Mutagenesis 31 (1998) (S29) 1-76, 1998. (poster, nije recenziran, sažetak, stručni)
CROSBI ID: 654 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Micronucleus assay and mitotic activity : the methods for determinarion of recent vinyl chloride monomer exposure
Autori
Fučić, Aleksandra ; Garaj-Vrhovac, Verica
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Abstracts of the 29th Annual Meeting of the Environmental Mutagen Society ; u: Environmental and Molecular Mutagenesis 31 (1998) (S29) 1-76
/ - , 1998
Skup
Environmental Mutagen Society Annual Meeting (29 ; 1998)
Mjesto i datum
,
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
micronuclei; mitotic activity; vinly chloride monomer; occupational exposure
Sažetak
In the absence of personal dosimeters for majority of chemical mutagens, biomonitoring should provide reliable data in order to determine period and severity of caused genome damage. According to our previous reports, micronucleus assay (MN) can serve as a suitable indicator of the period which elapsed after the last exposure to elevated concentrations of well known mutagen and carcinogen vinyl chloride (VCM). The aim of our study was to improve method for determination of the period which elapsed after last exposure by means of lymphocyte mitotic activity (MA). The study involved a group of 20 workers from VCM plant exposed to 1 ppm concentration with periodically increasing concentrations up to 70 ppm. The MN was performed on 72h cultures in which 3 microg/ml of Cyt-B was added. MA was analysed on lymphocyte cultures to which BrdU was added. Results show that distribution of MA differs significantly (M1 - 6 ; M2 - 12.5 ; M3 - 80.4) from control values (M1 - 7.9 ; M2 - 36.2 ; M3 - 53.8). Presented in percentages in case of recent VCM exposure and corellate with increased MN frequency or distribution of binucleated cells with more than 2 MN. In spite of different mechanisms of their origin after exposure MN and MA exhibit corresponding decrease of values and approach of control values. It could be therefore assumed that MA could serve as an additional parameter fot the evaluation of the time and dose effect in the monitoring of exposure to chemical mutagens.
Izvorni jezik
Engleski
Znanstvena područja
Javno zdravstvo i zdravstvena zaštita
POVEZANOST RADA
Projekti:
00220107
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb