Abstract
This investigation reports genotoxic effects of sodium fluoride (NaF) at 17, 34, and 51 ?M for 72 hr and induction of sister chromatid exchanges (SCEs) and related changes, together with ameliorative effects by melatonin and amla, in human peripheral blood lymphocyte cell cultures. The cell cycle proliferative index (CCPI) significantly decreased with increasing F concentration. SCEs, average generation time (AGT), and population doubling time (PDT) also significantly increased with F exposure. Treatment with the antioxidants melatonin and amla, separately or in combination with the highest level NaF-treated group, showed a detectable but non- significant increase in CCPI and a decrease in SCEs, AGT, and PDT, comparable to levels in control cultures. The results indicate substantial amelioration of F genotoxicity in lymphocyte cells by melatonin, amla, and their combination.
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Is fluoride a mutagen?
Recent studies suggest that fluoride may be genotoxic. While the concentration of fluoride in artificially fluoridated water (1 mg Fl-1) is generally considered to be "safe", levels of fluoride present in a number of widely used dental health products, such as fluoride-containing toothpaste, appear to be potentially mutagenic. Since fluoride
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Genotoxic evaluation of chronic fluoride exposure: micronucleus and sperm morphology studies
The purpose of this study was to investigate the genotoxic effects of chronic fluoride exposure on mammalian cells in vivo by use of the mouse bone-marrow micronucleus test and the sperm morphology methodology. Mice of genotype B6C3F1 were obtained at weaning and maintained on a low-fluoride diet (less than 0.2
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Sodium fluoride-induced morphological and neoplastic transformation, chromosome aberrations, sister chromatid exchanges, and unscheduled DNA synthesis in cultured syrian hamster embryo cells
The effects of exposure of early-passage Syrian hamster embryo cells in culture to sodium fluoride have been studied with respect to induction of morphological and neoplastic transformation, chromosome aberrations, sister chromatid exchanges, and unscheduled DNA synthesis. Exposure of Syrian hamster embryo cells to NaF concentrations between 75 and 125 micrograms/ml
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The effects of sodium fluoride and iodacetamide on mutation induction by x-irradiation in mature spermatoza of drosophila
The effect of two inhibitors of glycolysis, NaF and iodacetamide on the production of recessive lethal mutations by X-rays in mature Drosophila sperm has been investigated. Pre-treatment with NaF resulted in a consistent and highly significant increase of the mutation frequency. This effect is thought to result from interference with
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The effect of fluorine and lead ions on the chromosomes of human leucocytes in vitro
Human leukocytes in the cultures in vitro were exposed to the action of Pb and F ions at the concentrations of 10-3 M and 10-5 M for Pb and 3.15 x 10-3 M, 3.15 x 10-4 M, 3.15 x 10-5 M for F. Both factors caused structural and quantitative aberrations
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A Critique of Gelberg's Study on Fluoride/Osteosarcoma in New York
The case-control study by Gelberg, published first as a PhD dissertation and then later in two peer-reviewed journals, may represent the most substantive study on fluoride/osteosarcoma previous to Bassin’s 2001 analysis. In assessing Gelberg’s data, we were at first struck by the existence of several notable errors in both the thesis and papers. While these errors do raise questions about the study, our primary concern with Gelberg’s work relates to the methods she used to analyze her data.
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Micronucleus and Sister Chromatid Exchange Frequency in Endemic Fluorosis
The rise of sister chromatid exchange (SCE) and micronucleus (MN) in the peripheral blood lymphocytes of the fluorine-intoxicated patients indicates that fluorine is a mutagenic agent which can cause DNA and chromosomal damage.
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Fluoride & Osteosarcoma: A Timeline
Several human epidemiological studies have found an association between fluoride in drinking water and the occurrence of osteosarcoma (bone cancer) in young males. These studies are consistent with the National Toxicology Program's (NTP) cancer bioassay which found that fluoride-treated male rats had an dose-dependent increase in osteosarcoma. Although a number of studies have failed to detect an association between fluoride and osteosarcoma, none of these studies have measured the risk of fluoride at specific windows in time, which based on recent results, is the critical question with respect to fluoride and osteosarcoma.
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Fluoride's Mutagenicity: In vivo Studies
Consistent with dozens of in vitro studies, a number of in vivo studies, in both humans and animals, have found evidence of fluoride-induced genetic damage. In particular, research on humans exposed to high levels of fluoride have found increased levels of "sister chromatid exchange" (SCE). As noted in one study: "In
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NTP Bioassay on Fluoride/Cancer (1990)
In 1977, the U.S. Congress requested that animal studies be conducted to determine if fluoride can cause cancer. The result of the Congressional request was an extensive animal study conducted in the 1980s by the National Toxicology Program (NTP) and published in 1990. The main finding of NTP's study was a dose-dependent increase in osteosarcoma (bone cancer) among the fluoride-treated male rats.
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