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Chinese Journal of Industrial Hygiene and Occupational Diseases ; (12): 43-46, 2004.
Artigo em Chinês | WPRIM | ID: wpr-272046

RESUMO

<p><b>OBJECTIVE</b>To determine the effects of buthionine sulfoximine (BSO) and free radical scavenger, dimethyl sulfoxide (DMSO), on mutation frequency and the formation of 8-hydroxydeoxyganosine (8-OHdG) induced by crocidolite fibers in human-hamster hybrid (A(L)) cells.</p><p><b>METHODS</b>The cytotoxicity and mutagenicity were determined by the formation of colonies. 8-OHdG was examined by immunoperoxidase staining. Non-protein sulfhydryl (NPSH) compound was assayed by modified Tietze's method.</p><p><b>RESULTS</b>The level of NPSH in A(L) cell pretreated with 25 micro mol/L of BSO was decreased to 2 nmol/10(7) cells, only 5% of the control after 24 h. The mutation frequency of CD59 gene of A(L) cell in crocidolite alone treated group was 208 +/- 18 while that in BSO pretreated group (397 +/- 55) was about twice the former (P < 0.05). The mutation frequency of CD59 gene in the group treated with crocidolite and in the presence of DMSO (57 +/- 8) was 72.6% less than that in crocidolite alone treated group. Crocidolite fibers induced a dose-effect relationship in the formation of 8-OHdG in A(L) cells (y = 150 + 20x, r = 0.9621). The level of 8-OHdG in cells was 289 +/- 6 at the dose of 6 micro g/cm(2) crocidolite, which was about twice the control group (137 +/- 9). In the presence of DMSO, 8-OHdG level decreased to 170 +/- 3 at the same dose of crocidolite.</p><p><b>CONCLUSION</b>Free radicals are the important inducer of mutagenesis and DNA damage in A(L) cells caused by crocidolite, which has dose-effect relationship.</p>


Assuntos
Animais , Cricetinae , Humanos , Asbesto Crocidolita , Farmacologia , Butionina Sulfoximina , Farmacologia , Antígenos CD59 , Genética , DNA , Genética , Dano ao DNA , Desoxiguanosina , Metabolismo , Dimetil Sulfóxido , Farmacologia , Inibidores Enzimáticos , Farmacologia , Sequestradores de Radicais Livres , Farmacologia , Células Híbridas , Técnicas Imunoenzimáticas , Mutação
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