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Therapeutic Methods and Therapies TCIM
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1.
Mutat Res ; 488(2): 93-118, 2001 May.
Article in English | MEDLINE | ID: mdl-11344039

ABSTRACT

From a literature survey, 117 chemicals are tabulated that have been assayed in 179 assays for their clastogenic effects in Pisum. Of the 117 chemicals that have been assayed, 65 are reported at giving a positive reaction (i.e. causing chromosome aberrations), 30 positive with a dose response, five borderline positive. Seventeen chemicals gave a negative response. Eighty-one percent of the chemicals gave a definite positive response. A c-mitotic effect was detected from treatment with 17 chemicals. In addition to the above tabulation of chemicals, 39 chemicals have been reported with an antimitotic effect. Thirteen assays have been recorded for five types of radiation, which with the exception of ultrasound reacted positively. The results of assays with 38 chemicals and/or radiations in combined treatments, as well as 15 chemicals and three types of radiations that induce somatic mutations are tabulated. The Pisum sativum (2n=14) bioassay has been shown to be a very good plant bioassay for assessing chromosome damage both in mitosis and meiosis for somatic mutations induced by chemicals, radiations, and environmental pollutants. For some chemicals, the Pisum assay is not as sensitive in assessing clastogenicity as the Allium assay, although this should be considered in relative terms. Pisum fulvum (2n=14) has been used in clastogenic studies also, but to a much lesser extent.


Subject(s)
Chromosome Aberrations , Fabaceae/drug effects , Fabaceae/genetics , Mutagens/toxicity , Plants, Medicinal , Biological Assay , Carcinogens/toxicity , Chromosomes/drug effects , Chromosomes/genetics , DNA, Plant/genetics , Environmental Monitoring , Environmental Pollutants/toxicity , Humans , Meiosis , Mitosis , Mutagenicity Tests , Mutation , Pisum sativum/drug effects , Pisum sativum/genetics , Ploidies
2.
Mutat Res ; 310(2): 169-73, 1994 Oct 16.
Article in English | MEDLINE | ID: mdl-7523889

ABSTRACT

Under the sponsorship of the International Programme on Chemical Safety (IPCS), 17 laboratories from diverse regions of the world participated in evaluating the utility of four plant bioassays for detecting genetic hazards of environmental chemicals. The bioassays included in this collaborative study were: Arabidopsis thaliana embryo and chlorophyll assay and Tradescantia stamen hair assay, Tradescantia paludosa micronucleus assay and Vicia faba root tip assay. Four to six laboratories participated in the performance of each of the bioassays. All laboratories participating in a particular bioassay were supplied with uniform plant material as well as standardized protocol. Five direct acting water soluble test chemicals, i.e. maleic hydrazide, methyl nitrosourea, ethyl methanesulfonate, sodium azide and azidoglycerol, were selected for this study. The study was designed to be completed in three phases. Ethyl methanesulfonate was used as a positive control and has already been reported earlier (Sandhu et al., 1991). The data from the remaining four chemicals used for the evaluation of four plant test systems in the first phase of the collaborative study are reported in this issue.


Subject(s)
Environmental Monitoring/methods , Mutagenicity Tests/methods , Mutagens/analysis , Plants/genetics , Arabidopsis/genetics , Biological Assay/methods , Chromosome Aberrations , Fabaceae/genetics , International Cooperation , Micronucleus Tests , Plants, Medicinal , Research Design
3.
Mutat Res ; 310(2): 257-63, 1994 Oct 16.
Article in English | MEDLINE | ID: mdl-7523896

ABSTRACT

In the first phase of a collaborative study by the International Programme on Chemical Safety (IPCS), four coded chemicals, i.e. azidoglycerol (AG, 3-azido-1,2-propanediol), methyl nitrosourea (MNU), sodium azide (NaN3) and maleic hydrazide (MH), and ethyl methanesulfonate (EMS) as a positive control were tested in four plant bioassays, namely the Arabidopsis embryo and chlorophyll mutation assay, the Tradescantia stamen hair assay (Trad-SH assay), the Tradescantia micronucleus assay (Trad-MCN), and the Vicia faba root tip assay. Seventeen laboratories from diverse regions of the world participated with four to six laboratories each using one plant assay. For the Arabidopsis assay, laboratories were in agreement with MNU and AG giving positive responses and NaN3 giving a negative response. With the exception of one laboratory which reported MH as weakly mutagenic, no mutagenic response was reported for MH by the other laboratories. For the Vicia faba assay, all laboratories reported a positive response for MNU, AG, and MH, whereas two of the six laboratories reported a negative response for NaN3. For the Trad-SH assay, MH was reported as giving a positive response and a positive response was also observed for MNU with the exception of one laboratory. NaN3, which exhibited a relatively high degree of toxicity, elicited a positive response in three of the five laboratories. AG was found positive in only one of the two laboratories which tested this chemical. For the Trad-MCN assay, MNU and MH were reported as positive by all laboratories, while four out of five laboratories reported NaN3 to be positive. Only one of three laboratories reported AG to be positive. The major sources of variability were identified and considered to be in the same range as found in similar studies on other test systems. Recommendations were made for minor changes in methodology and for initiating the second phase of this study.


Subject(s)
Environmental Monitoring/methods , Mutagenicity Tests/methods , Mutagens/analysis , Plants/genetics , Arabidopsis/genetics , Biological Assay/methods , Chromosome Aberrations , Fabaceae/genetics , International Cooperation , Micronucleus Tests , Plants, Medicinal , Reproducibility of Results
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