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Extract of Lillium candidum L. Can Modulate the Genotoxicity of the Antibiotic Zeocin

Lilium candidum L. extract (LE) is well known in folk medicine for the treatment of burns, ulcers, inflammations and for healing wounds. This work aims to clarify whether the genotoxic potential of the radiomimetic antibiotic zeocin (Zeo) could be modulated by LE. Our results indicate that LE exerts...

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Autores principales: Kopaskova, Marcela, Hadjo, Lina, Yankulova, Bisera, Jovtchev, Gabriele, Galova, Eliska, Sevcovicova, Andrea, Mucaji, Pavel, Miadokova, Eva, Bryant, Peter, Chankova, Stephka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268910/
https://www.ncbi.nlm.nih.gov/pubmed/22269865
http://dx.doi.org/10.3390/molecules17010080
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author Kopaskova, Marcela
Hadjo, Lina
Yankulova, Bisera
Jovtchev, Gabriele
Galova, Eliska
Sevcovicova, Andrea
Mucaji, Pavel
Miadokova, Eva
Bryant, Peter
Chankova, Stephka
author_facet Kopaskova, Marcela
Hadjo, Lina
Yankulova, Bisera
Jovtchev, Gabriele
Galova, Eliska
Sevcovicova, Andrea
Mucaji, Pavel
Miadokova, Eva
Bryant, Peter
Chankova, Stephka
author_sort Kopaskova, Marcela
collection PubMed
description Lilium candidum L. extract (LE) is well known in folk medicine for the treatment of burns, ulcers, inflammations and for healing wounds. This work aims to clarify whether the genotoxic potential of the radiomimetic antibiotic zeocin (Zeo) could be modulated by LE. Our results indicate that LE exerts no cytotoxic, DNA-damaging and clastogenic activity in in Chlamydomonas reinhardtii, Pisum sativum L. and Hordeum vulgare L. test systems over a broad concentration range. Weak but statistically significant clastogenic effects due to the induction of micronuclei and chromosome aberrations have been observed in H. vulgare L. after treatment with 200 and 300 μg/mL LE. To discriminate protective from adverse action of LE different experimental designs have been used. Our results demonstrate that the treatment with mixtures of LE and Zeo causes an increase in the level of DNA damage, micronuclei and “metaphases with chromatid aberrations” (MwA). Clear evidence has been also obtained indicating that pretreatment with LE given 4 h before the treatment with Zeo accelerates the rejoining kinetics of Zeo-induced DNA damage in P. sativum L. and C. reinhardtii, and can decrease clastogenic effect of Zeo measured as frequencies of micronuclei and MwA in H. vulgare L. Here, we show for the first time that LE can modulate the genotoxic effects of zeocin. The molecular mode of action strongly depends on the experimental design and varies from synergistic to protective effect (adaptive response–AR). Our results also revealed that LE-induced AR to zeocin involves up-regulation of DSB rejoining in C. reinhardtii and P. sativum L. cells.
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spelling pubmed-62689102018-12-11 Extract of Lillium candidum L. Can Modulate the Genotoxicity of the Antibiotic Zeocin Kopaskova, Marcela Hadjo, Lina Yankulova, Bisera Jovtchev, Gabriele Galova, Eliska Sevcovicova, Andrea Mucaji, Pavel Miadokova, Eva Bryant, Peter Chankova, Stephka Molecules Article Lilium candidum L. extract (LE) is well known in folk medicine for the treatment of burns, ulcers, inflammations and for healing wounds. This work aims to clarify whether the genotoxic potential of the radiomimetic antibiotic zeocin (Zeo) could be modulated by LE. Our results indicate that LE exerts no cytotoxic, DNA-damaging and clastogenic activity in in Chlamydomonas reinhardtii, Pisum sativum L. and Hordeum vulgare L. test systems over a broad concentration range. Weak but statistically significant clastogenic effects due to the induction of micronuclei and chromosome aberrations have been observed in H. vulgare L. after treatment with 200 and 300 μg/mL LE. To discriminate protective from adverse action of LE different experimental designs have been used. Our results demonstrate that the treatment with mixtures of LE and Zeo causes an increase in the level of DNA damage, micronuclei and “metaphases with chromatid aberrations” (MwA). Clear evidence has been also obtained indicating that pretreatment with LE given 4 h before the treatment with Zeo accelerates the rejoining kinetics of Zeo-induced DNA damage in P. sativum L. and C. reinhardtii, and can decrease clastogenic effect of Zeo measured as frequencies of micronuclei and MwA in H. vulgare L. Here, we show for the first time that LE can modulate the genotoxic effects of zeocin. The molecular mode of action strongly depends on the experimental design and varies from synergistic to protective effect (adaptive response–AR). Our results also revealed that LE-induced AR to zeocin involves up-regulation of DSB rejoining in C. reinhardtii and P. sativum L. cells. MDPI 2011-12-22 /pmc/articles/PMC6268910/ /pubmed/22269865 http://dx.doi.org/10.3390/molecules17010080 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Kopaskova, Marcela
Hadjo, Lina
Yankulova, Bisera
Jovtchev, Gabriele
Galova, Eliska
Sevcovicova, Andrea
Mucaji, Pavel
Miadokova, Eva
Bryant, Peter
Chankova, Stephka
Extract of Lillium candidum L. Can Modulate the Genotoxicity of the Antibiotic Zeocin
title Extract of Lillium candidum L. Can Modulate the Genotoxicity of the Antibiotic Zeocin
title_full Extract of Lillium candidum L. Can Modulate the Genotoxicity of the Antibiotic Zeocin
title_fullStr Extract of Lillium candidum L. Can Modulate the Genotoxicity of the Antibiotic Zeocin
title_full_unstemmed Extract of Lillium candidum L. Can Modulate the Genotoxicity of the Antibiotic Zeocin
title_short Extract of Lillium candidum L. Can Modulate the Genotoxicity of the Antibiotic Zeocin
title_sort extract of lillium candidum l. can modulate the genotoxicity of the antibiotic zeocin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268910/
https://www.ncbi.nlm.nih.gov/pubmed/22269865
http://dx.doi.org/10.3390/molecules17010080
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