Phenotyping of the glutathione S-transferase M1 polymorphism in Zimbabweans and the effects of chloroquine on blood glutathione S-transferases M1 and A
Identifieur interne : 002873 ( Main/Exploration ); précédent : 002872; suivant : 002874Phenotyping of the glutathione S-transferase M1 polymorphism in Zimbabweans and the effects of chloroquine on blood glutathione S-transferases M1 and A
Auteurs : Stanley Mukanganyama [Zimbabwe] ; Collen M. Masimirembwa [Zimbabwe] ; Yogeshkumar S. Naik [Zimbabwe] ; Julia A. Hasler [Zimbabwe]Source :
- Clinica Chimica Acta [ 0009-8981 ] ; 1997.
English descriptors
- Teeft :
- Absorbance, Absorbance value, Absorbance values, Acta, Biochem, Biochem pharmacol, Chimica, Chloroquine, Chloroquine phosphate, Chloroquine treatment, Clinica, Clinica chimica acta, Discordant results, Elisa, Frequency distribution, Genotype, Genotyping, Glutathione, Gsta, Gsta levels, Gstm1, Gsts, Hepatic, Hepatocellular, Hepatocellular damage, Mukanganyama, Phenotype, Phenotyping, Positive control, Prophylactic, Serum gsta, Therapeutic dose, Therapeutic doses, Zimbabwean, Zimbabwean population.
Abstract
Abstract: The frequency of the null allele phenotype of glutathione S-transferase (GST) M1 was investigated in 114 Zimbabweans and results for a subset of 63 subsets were compared with genotyping by PCR. In addition, the effect of the antimalarial chloroquine on blood levels of GSTM1 and GSTA in 19 subjects was studied. Quantification of GSTs was by enzyme linked immunosorbent assays (ELISA). Thirty percent of the subjects were of the GSTM1 null phenotype. Comparison of results of phenotyping by ELISA and genotyping by PCR showed that 16% of samples were in discordance; unknown mutations in the GSTM1 gene in the Zimbabwean population may explain this observation. Chloroquine decreased levels of blood GSTM1 and GSTA by 50% or more. In populations treated with chloroquine, these decreases in GST activities might lead to compromised ability to detoxify xenobiotics, could confound GSTM1 phenotyping and might invalidate use of GSTA as an indicator of liver damage.
Url:
DOI: 10.1016/S0009-8981(97)00104-6
Affiliations:
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Le document en format XML
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<term>Biochem</term>
<term>Biochem pharmacol</term>
<term>Chimica</term>
<term>Chloroquine</term>
<term>Chloroquine phosphate</term>
<term>Chloroquine treatment</term>
<term>Clinica</term>
<term>Clinica chimica acta</term>
<term>Discordant results</term>
<term>Elisa</term>
<term>Frequency distribution</term>
<term>Genotype</term>
<term>Genotyping</term>
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<term>Gsta</term>
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<term>Gstm1</term>
<term>Gsts</term>
<term>Hepatic</term>
<term>Hepatocellular</term>
<term>Hepatocellular damage</term>
<term>Mukanganyama</term>
<term>Phenotype</term>
<term>Phenotyping</term>
<term>Positive control</term>
<term>Prophylactic</term>
<term>Serum gsta</term>
<term>Therapeutic dose</term>
<term>Therapeutic doses</term>
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<term>Zimbabwean population</term>
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<front><div type="abstract" xml:lang="en">Abstract: The frequency of the null allele phenotype of glutathione S-transferase (GST) M1 was investigated in 114 Zimbabweans and results for a subset of 63 subsets were compared with genotyping by PCR. In addition, the effect of the antimalarial chloroquine on blood levels of GSTM1 and GSTA in 19 subjects was studied. Quantification of GSTs was by enzyme linked immunosorbent assays (ELISA). Thirty percent of the subjects were of the GSTM1 null phenotype. Comparison of results of phenotyping by ELISA and genotyping by PCR showed that 16% of samples were in discordance; unknown mutations in the GSTM1 gene in the Zimbabwean population may explain this observation. Chloroquine decreased levels of blood GSTM1 and GSTA by 50% or more. In populations treated with chloroquine, these decreases in GST activities might lead to compromised ability to detoxify xenobiotics, could confound GSTM1 phenotyping and might invalidate use of GSTA as an indicator of liver damage.</div>
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