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1.
Appl Radiat Isot ; 54(3): 497-507, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11214887

ABSTRACT

The examination of gamma-ray spectrometric data of the Missikat area was found to be useful in locating areas worth exploring for uranium occurrence. The statistical treatment of these data shows that the uranium threshold level is 13 ppm. Such a value represents indirectly the presence of uranium mineralization and identifies anomalous areas on the eU contour map in the northern border of the Missikat-Ria El Gerra granitic plutons. This area should be of prime concern in uranium exploration of these plutons. The interpretation of the variation in the eU/eTh ratio with eU and eTh suggests that uranium redistribution has occurred within the Missikat-Ria El Gerra granitic plutons. Uranium may be reconcentrated in silicification, sericitization and kaolinization alterations which are geologically evident. eU, eTh and their ratio eU/eTh for the Missikat-Ria El Gerra granites exhibit a lognormal distribution which is in agreement with the general distribution of trace elements, whereas the K content tends towards a normal distribution.

2.
Electrophoresis ; 20(6): 1195-203, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10380759

ABSTRACT

Single-strand conformation polymorphism (SSCP) is one of the most commonly used methods for searching for unknown base changes (mutations). In order to characterize systematically the effects of important physical parameters on the sensitivity and specificity of SSCP, we used the DNA toolbox constructed as described in the companion paper [2]. Using this set of DNA molecules as polymerase chain reaction (PCR) templates, amplicons of various lengths with the same base, mutated to all other bases, were generated. The behavior of these constructs in manual and automated SSCP was analyzed as a function of the size, overall base content of the fragment, nature and location of the base change, and the temperature and pH of electrophoresis. Our results demonstrate that all of these variables interact to determine the rate of detection of single-base changes, with the GC content being the predominant determinant of detection sensitivity.


Subject(s)
DNA/analysis , Mutation , Polymerase Chain Reaction/methods , Polymorphism, Single-Stranded Conformational , Evaluation Studies as Topic
3.
Toxicology ; 128(1): 9-16, 1998 Jun 26.
Article in English | MEDLINE | ID: mdl-9704901

ABSTRACT

DNA damage and the formation of stable carcinogen-DNA adducts are considered critical events in the initiation of the carcinogenic process. This study was carried out to assess whether exposure of plastics industry workers to the vinyl chloride monomer (VCM) for different periods of time would cause DNA damage, using the single-cell gel electrophoresis (SCGE) technique. Levels of DNA damage was assessed by both extent of DNA migration and numbers of DNA damaged spots in the peripheral blood lymphocytes from 32 plastics workers with different periods of exposure to VCM; they were evaluated by comparison with a group of non-exposed individuals. It was found that plastics workers who were exposed to VCM for different periods of time showed significantly increased levels of DNA damage compared with the non-exposed subjects. There was a significant correlation between the severity of DNA damage and duration of exposure. However, no significant correlation was found between the age of all subjects and DNA damage. Concentrations of VCM in the air inside the factory were found to be significantly higher than values in non-exposed areas, despite being lower than the threshold limit value (TLV). Our results encourage the application of SCGE as a sensitive, simple, fast and useful technique in the regular health screening of workers occupationally exposed to VCM (even at concentrations below the TLV) to assess the possibility of any DNA damage.


Subject(s)
Carcinogens/toxicity , Chemical Industry , DNA Damage/drug effects , Lymphocytes/drug effects , Occupational Exposure/adverse effects , Plastics , Vinyl Chloride/toxicity , Adult , Air/analysis , Carcinogens/analysis , Electrophoresis, Polyacrylamide Gel , Humans , Male , Middle Aged , Occupational Exposure/analysis , Time Factors , Vinyl Chloride/analysis
4.
Toxicology ; 125(1): 45-52, 1998 Jan 16.
Article in English | MEDLINE | ID: mdl-9585099

ABSTRACT

The mutagenic potential of carbamazepine (CBZ) therapy has been evaluated both in vivo and in vitro. Analysis of chromosome aberrations (CA), sister chromatid exchanges (SCEs), mitotic and proliferation indices (PRI) were performed. The in vivo study was carried out on 30 patients with idiopathic epilepsy end undergoing treatment with CBZ for different periods starting from 6 months up to 15 years. Plasma CBZ levels were also determined for each patient. The results showed that the total CA and SCEs were significantly increased in CBZ-treated patients. There was no significant correlation between CA and either duration of treatment or the plasma CBZ levels for each patient. The mitotic and proliferation indices were found to be slightly but non-significantly decreased compared to control values. On the other hand, in vitro analysis showed a significant dose-dependent increase in CA and SCEs in human lymphocyte cultures treated with CBZ (4-12 microg/ml). The mitotic and proliferation indices were also found to be decreased but only significantly in case of high doses of CBZ (12 microg/ml). Pretreatment of human lymphocytes with melatonin (0.5 mM) exhibited a significant decrease in the frequencies of CBZ-induced CA and SCEs as compared with non-treated cultures. The depressed mitotic and proliferation indices were also found to be improved in cultures pretreated with melatonin. In conclusion, these observations suggest that CBZ monotherapy may lead to chromosome damaging effects (genotoxic) and the use of melatonin as anti-mutagenic agent for human protection against CBZ-induced chromosome damage should be considered.


Subject(s)
Anticonvulsants/toxicity , Carbamazepine/toxicity , Lymphocytes/drug effects , Melatonin/pharmacology , Mutagenicity Tests , Adult , Anticonvulsants/antagonists & inhibitors , Anticonvulsants/blood , Carbamazepine/antagonists & inhibitors , Carbamazepine/blood , Chromosome Aberrations , Female , Humans , Lymphocytes/ultrastructure , Male , Sister Chromatid Exchange
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