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Studies on the genotoxicity of molybdenum salts in human cells in vitro and in mice in vivo

โœ Scribed by Nina Titenko-Holland; Jianhua Shao; Luoping Zhang; Liqiang Xi; Hailong Ngo; Nong Shang; Martyn T. Smith


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
164 KB
Volume
32
Category
Article
ISSN
0893-6692

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โœฆ Synopsis


Molybdenum is an essential element in plants and observed. Based on the results of a toxicity study of animals as a cofactor for enzymes. Molybdenum sodium molybdate, two doses, 200 and 400 mg/ trioxide is used in metallurgical processes, in cos-kg, were assessed in the bone marrow MN assay metics as a pigment, and in contact lens solution, in mice (two i.p. injections 24 and 48 hr prior to yet limited information is available on molybdenum euthanasia). A modest but statistically significant ingenotoxicity. In the present study the micronucleus crease in MN frequency in polychromatic erythro-(MN) assay in human lymphocytes and mouse bone cytes was observed (P รต 0.05). The same treatment marrow and the dominant lethal assay in mice were protocol was used to analyze dominant lethality. A used to assess the genotoxic effects of molybdenum dose-dependent increase in postimplantation loss salts in vitro and in vivo. Two salts of molybdenum represented mostly by early resorptions was obwere tested in whole blood cultures. Ammonium mo-served the first week after treatment (P ร… 0.003). lybdate was more potent than sodium molybdate in These preliminary data suggest that sodium molybcausing a dose-dependent decrease in viability and date induces dominant lethality at the postmeiotic replicative index and an increase in MN formation stage of spermatogenesis. Overall, molybdenum in binucleated lymphocytes (P รต 0.001). A dose -salts produced moderately positive results both in vitro response in both kinetochore-positive MN (caused in human cells and in vivo in mice. Environ. Mol. Mutaby chromosome lagging) and kinetochore-negative gen. 32: 251-259, 1998 แญง


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