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In vitro evaluation of the cytotoxicity and genotoxicity of resorcylidene aminoguanidine in human diploid cells B-HNF-1
Ján Vojtaššák, Milan Blaško Sr, Ľuboš Danišovič, Jozef Čársky, Mária Ďuríková, Vanda Repiská, Iveta Waczulíková, Daniel Böhmer
Language English Country Czech Republic
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
ProQuest Central
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
- MeSH
- Cell Line MeSH
- Cytotoxins pharmacology chemistry MeSH
- Diploidy MeSH
- Fibroblasts cytology physiology drug effects MeSH
- Guanidines pharmacology chemistry toxicity MeSH
- Infant MeSH
- Humans MeSH
- Micronucleus Tests MeSH
- Molecular Structure MeSH
- Mutagens pharmacology chemistry MeSH
- Cell Shape drug effects MeSH
- Dose-Response Relationship, Drug MeSH
- Check Tag
- Infant MeSH
- Humans MeSH
- Male MeSH
RAG belongs to appropriate inhibitors of protein glycation, i.e. formation of advanced glycation end products, which are thought to be responsible for some complications of DM, including neuropathy, angiopathy, retinopathy and nephropathy. In the present study authors have evaluated the genotoxic effect of RAG on the cell culture of human neonatal fibroblasts (B-HNF-1) in regard to its potential clinical application as inhibitor of advanced glycation end products in relationships to the pathogenesis of chronic diabetic complications. The direct contact cytotoxicity assay and micronucleus test were performed. The results showed that RAG in the concentration range of 1 x 10-4 to 1 x 10-6 mol.l-1 did not induce any changes in the morphology of exposed B-HNF-1 cells. The frequency of micronuclei was not significantly increased as well. The inhibitive effect of resorcylidene aminoguanidine was directly proportional to its concentration. It can be concluded that RAG at the selected concentrations has an inhibitive effect on proliferation of the treated cells and, at the same time, does not display any genotoxic effects on B-HNF-1 cells.
Lit.: 34
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- $a In vitro evaluation of the cytotoxicity and genotoxicity of resorcylidene aminoguanidine in human diploid cells B-HNF-1 / $c Ján Vojtaššák, Milan Blaško Sr, Ľuboš Danišovič, Jozef Čársky, Mária Ďuríková, Vanda Repiská, Iveta Waczulíková, Daniel Böhmer
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- $a Institute of Medical Biology and Genetics, Biochemistry and Clinical Biochemistry, Faculty of Medicine, Comenius University, Bratislava
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- $a Lit.: 34
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- $a RAG belongs to appropriate inhibitors of protein glycation, i.e. formation of advanced glycation end products, which are thought to be responsible for some complications of DM, including neuropathy, angiopathy, retinopathy and nephropathy. In the present study authors have evaluated the genotoxic effect of RAG on the cell culture of human neonatal fibroblasts (B-HNF-1) in regard to its potential clinical application as inhibitor of advanced glycation end products in relationships to the pathogenesis of chronic diabetic complications. The direct contact cytotoxicity assay and micronucleus test were performed. The results showed that RAG in the concentration range of 1 x 10-4 to 1 x 10-6 mol.l-1 did not induce any changes in the morphology of exposed B-HNF-1 cells. The frequency of micronuclei was not significantly increased as well. The inhibitive effect of resorcylidene aminoguanidine was directly proportional to its concentration. It can be concluded that RAG at the selected concentrations has an inhibitive effect on proliferation of the treated cells and, at the same time, does not display any genotoxic effects on B-HNF-1 cells.
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