Nitroimidazole derivatives: Non-randomness sister chromatid exchanges in human peripheral blood lymphocytes

Nitroimidazole derivatives exhibited genotoxic effect in different experimental conditions. This study focuses on an evaluation of possible genomic targets, at a chromosomal level, of two 5-nitroimidazoles (ornidazole and metronidazole) using the in vitro human peripheral blood culture as experiment...

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Autores principales: Martinez Montaño, Romari Alejandra, Mudry, Marta Dolores
Publicado: 2009
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0260437X_v29_n3_p248_Carballo
http://hdl.handle.net/20.500.12110/paper_0260437X_v29_n3_p248_Carballo
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spelling paper:paper_0260437X_v29_n3_p248_Carballo2023-06-08T15:22:14Z Nitroimidazole derivatives: Non-randomness sister chromatid exchanges in human peripheral blood lymphocytes Martinez Montaño, Romari Alejandra Mudry, Marta Dolores Biomarkers Chromosomal damage Genomic instability Genotoxicity Nitroimidazoles biological marker metronidazole nitroimidazole derivative ornidazole adult article blood culture cell proliferation chromosome chromosome band chromosome damage chromosome size controlled study cytotoxicity drug exposure female genome analysis genomic instability genotoxicity human human cell human experiment in vitro study male mitosis index normal human peripheral lymphocyte priority journal sister chromatid exchange Biological Markers Cell Division Cells, Cultured Chromosome Banding Dose-Response Relationship, Drug Female Humans Leukocytes, Mononuclear Male Metronidazole Mitotic Index Mutagenicity Tests Mutagens Nitroimidazoles Ornidazole Sister Chromatid Exchange Young Adult Nitroimidazole derivatives exhibited genotoxic effect in different experimental conditions. This study focuses on an evaluation of possible genomic targets, at a chromosomal level, of two 5-nitroimidazoles (ornidazole and metronidazole) using the in vitro human peripheral blood culture as experimental system. We observed that both derivatives showed a decrease in mitotic index (MI) (P < 0.001), an increase in sister chromatid exchanges (SCE) frequency (P < 0.001) and no modifications in cellular proliferation kinetics (CPK). As a null hypothesis we considered the assumption that larger chromosomes should harbor more SCE, which was viewed using a novel sequential G-band (400 band resolution)/SCE technique. The analysis showed highly significant chi square values (P < 0.001), indicating that SCE frequency per chromosome is not proportional to chromosome length. SCE could be considered an instability indicator due to the high correlation between SCEs in certain chromosomal bands and the exposure to nitroimidazole derivatives. Copyright © 2008 John Wiley & Sons, Ltd. Fil:Martinez, R.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Mudry, M.D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2009 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0260437X_v29_n3_p248_Carballo http://hdl.handle.net/20.500.12110/paper_0260437X_v29_n3_p248_Carballo
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Biomarkers
Chromosomal damage
Genomic instability
Genotoxicity
Nitroimidazoles
biological marker
metronidazole
nitroimidazole derivative
ornidazole
adult
article
blood culture
cell proliferation
chromosome
chromosome band
chromosome damage
chromosome size
controlled study
cytotoxicity
drug exposure
female
genome analysis
genomic instability
genotoxicity
human
human cell
human experiment
in vitro study
male
mitosis index
normal human
peripheral lymphocyte
priority journal
sister chromatid exchange
Biological Markers
Cell Division
Cells, Cultured
Chromosome Banding
Dose-Response Relationship, Drug
Female
Humans
Leukocytes, Mononuclear
Male
Metronidazole
Mitotic Index
Mutagenicity Tests
Mutagens
Nitroimidazoles
Ornidazole
Sister Chromatid Exchange
Young Adult
spellingShingle Biomarkers
Chromosomal damage
Genomic instability
Genotoxicity
Nitroimidazoles
biological marker
metronidazole
nitroimidazole derivative
ornidazole
adult
article
blood culture
cell proliferation
chromosome
chromosome band
chromosome damage
chromosome size
controlled study
cytotoxicity
drug exposure
female
genome analysis
genomic instability
genotoxicity
human
human cell
human experiment
in vitro study
male
mitosis index
normal human
peripheral lymphocyte
priority journal
sister chromatid exchange
Biological Markers
Cell Division
Cells, Cultured
Chromosome Banding
Dose-Response Relationship, Drug
Female
Humans
Leukocytes, Mononuclear
Male
Metronidazole
Mitotic Index
Mutagenicity Tests
Mutagens
Nitroimidazoles
Ornidazole
Sister Chromatid Exchange
Young Adult
Martinez Montaño, Romari Alejandra
Mudry, Marta Dolores
Nitroimidazole derivatives: Non-randomness sister chromatid exchanges in human peripheral blood lymphocytes
topic_facet Biomarkers
Chromosomal damage
Genomic instability
Genotoxicity
Nitroimidazoles
biological marker
metronidazole
nitroimidazole derivative
ornidazole
adult
article
blood culture
cell proliferation
chromosome
chromosome band
chromosome damage
chromosome size
controlled study
cytotoxicity
drug exposure
female
genome analysis
genomic instability
genotoxicity
human
human cell
human experiment
in vitro study
male
mitosis index
normal human
peripheral lymphocyte
priority journal
sister chromatid exchange
Biological Markers
Cell Division
Cells, Cultured
Chromosome Banding
Dose-Response Relationship, Drug
Female
Humans
Leukocytes, Mononuclear
Male
Metronidazole
Mitotic Index
Mutagenicity Tests
Mutagens
Nitroimidazoles
Ornidazole
Sister Chromatid Exchange
Young Adult
description Nitroimidazole derivatives exhibited genotoxic effect in different experimental conditions. This study focuses on an evaluation of possible genomic targets, at a chromosomal level, of two 5-nitroimidazoles (ornidazole and metronidazole) using the in vitro human peripheral blood culture as experimental system. We observed that both derivatives showed a decrease in mitotic index (MI) (P < 0.001), an increase in sister chromatid exchanges (SCE) frequency (P < 0.001) and no modifications in cellular proliferation kinetics (CPK). As a null hypothesis we considered the assumption that larger chromosomes should harbor more SCE, which was viewed using a novel sequential G-band (400 band resolution)/SCE technique. The analysis showed highly significant chi square values (P < 0.001), indicating that SCE frequency per chromosome is not proportional to chromosome length. SCE could be considered an instability indicator due to the high correlation between SCEs in certain chromosomal bands and the exposure to nitroimidazole derivatives. Copyright © 2008 John Wiley & Sons, Ltd.
author Martinez Montaño, Romari Alejandra
Mudry, Marta Dolores
author_facet Martinez Montaño, Romari Alejandra
Mudry, Marta Dolores
author_sort Martinez Montaño, Romari Alejandra
title Nitroimidazole derivatives: Non-randomness sister chromatid exchanges in human peripheral blood lymphocytes
title_short Nitroimidazole derivatives: Non-randomness sister chromatid exchanges in human peripheral blood lymphocytes
title_full Nitroimidazole derivatives: Non-randomness sister chromatid exchanges in human peripheral blood lymphocytes
title_fullStr Nitroimidazole derivatives: Non-randomness sister chromatid exchanges in human peripheral blood lymphocytes
title_full_unstemmed Nitroimidazole derivatives: Non-randomness sister chromatid exchanges in human peripheral blood lymphocytes
title_sort nitroimidazole derivatives: non-randomness sister chromatid exchanges in human peripheral blood lymphocytes
publishDate 2009
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0260437X_v29_n3_p248_Carballo
http://hdl.handle.net/20.500.12110/paper_0260437X_v29_n3_p248_Carballo
work_keys_str_mv AT martinezmontanoromarialejandra nitroimidazolederivativesnonrandomnesssisterchromatidexchangesinhumanperipheralbloodlymphocytes
AT mudrymartadolores nitroimidazolederivativesnonrandomnesssisterchromatidexchangesinhumanperipheralbloodlymphocytes
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