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Amelioration of indole acetic acid-induced cytotoxicity in mice using zinc nanoparticles biosynthesized with Ochradenus arabicus leaf extract

The diversity of natural phytochemicals represents an unlimited source for discovery and development of new drugs. Ochradenus arabicus, (family: Resedaceae) a notable medicinal plant displays a high content of flavonoid glycosides. This study investigates a possible preventative role of zinc nanopar...

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Autores principales: Alanazi, Khalid Mashai, Al-kawmani, Ahmed Ali, Farah, Mohammad Abul, Hailan, Waleed Ali, Alsalme, Ali, Al-Zaqri, Nabil, Ajmal Ali, M., Almansob, Abobakr Mahmood
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626273/
https://www.ncbi.nlm.nih.gov/pubmed/34867022
http://dx.doi.org/10.1016/j.sjbs.2021.08.015
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author Alanazi, Khalid Mashai
Al-kawmani, Ahmed Ali
Farah, Mohammad Abul
Hailan, Waleed Ali
Alsalme, Ali
Al-Zaqri, Nabil
Ajmal Ali, M.
Almansob, Abobakr Mahmood
author_facet Alanazi, Khalid Mashai
Al-kawmani, Ahmed Ali
Farah, Mohammad Abul
Hailan, Waleed Ali
Alsalme, Ali
Al-Zaqri, Nabil
Ajmal Ali, M.
Almansob, Abobakr Mahmood
author_sort Alanazi, Khalid Mashai
collection PubMed
description The diversity of natural phytochemicals represents an unlimited source for discovery and development of new drugs. Ochradenus arabicus, (family: Resedaceae) a notable medicinal plant displays a high content of flavonoid glycosides. This study investigates a possible preventative role of zinc nanoparticles biosynthesized by O. arabicus leaf extracts (OAZnO NPs) in limiting genotoxicity and cytotoxicity caused by indole acetic acid (IAA) in laboratory mice. ZnO NPs were synthesized using O. arabicus leaf extracts and characterized with UV–visible spectroscopy, scanning electron microscopy (SEM) and X-Ray diffraction (XRD). The mice were randomly distributed into the following six groups: control, OAZnO NPs treated (10 mg/kg BW), IAA treated (50 mg/kg BW); simultaneous treatment, pre-treatment, and post-treatment. Reactive oxygen species (ROS), DNA damage, chromosome aberration, and apoptosis were analyzed as toxicity endpoints. IAA exposure significantly induced production of ROS, DNA damage, apoptosis, chromosome aberrations, and micronuclei. Pre-, post-, and simultaneous treatment with OAZnO NPs ameliorated the damage caused by IAA exposure. Exposure to OAZnO NPs alone caused no toxicity for any endpoint based on comparison to controls. This study demonstrated that IAA-induced cytotoxic damage in mice could be ameliorated by treatment with OAZnO NPs. These findings require additional verification in mechanistic and in vitro studies.
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spelling pubmed-86262732021-12-02 Amelioration of indole acetic acid-induced cytotoxicity in mice using zinc nanoparticles biosynthesized with Ochradenus arabicus leaf extract Alanazi, Khalid Mashai Al-kawmani, Ahmed Ali Farah, Mohammad Abul Hailan, Waleed Ali Alsalme, Ali Al-Zaqri, Nabil Ajmal Ali, M. Almansob, Abobakr Mahmood Saudi J Biol Sci Original Article The diversity of natural phytochemicals represents an unlimited source for discovery and development of new drugs. Ochradenus arabicus, (family: Resedaceae) a notable medicinal plant displays a high content of flavonoid glycosides. This study investigates a possible preventative role of zinc nanoparticles biosynthesized by O. arabicus leaf extracts (OAZnO NPs) in limiting genotoxicity and cytotoxicity caused by indole acetic acid (IAA) in laboratory mice. ZnO NPs were synthesized using O. arabicus leaf extracts and characterized with UV–visible spectroscopy, scanning electron microscopy (SEM) and X-Ray diffraction (XRD). The mice were randomly distributed into the following six groups: control, OAZnO NPs treated (10 mg/kg BW), IAA treated (50 mg/kg BW); simultaneous treatment, pre-treatment, and post-treatment. Reactive oxygen species (ROS), DNA damage, chromosome aberration, and apoptosis were analyzed as toxicity endpoints. IAA exposure significantly induced production of ROS, DNA damage, apoptosis, chromosome aberrations, and micronuclei. Pre-, post-, and simultaneous treatment with OAZnO NPs ameliorated the damage caused by IAA exposure. Exposure to OAZnO NPs alone caused no toxicity for any endpoint based on comparison to controls. This study demonstrated that IAA-induced cytotoxic damage in mice could be ameliorated by treatment with OAZnO NPs. These findings require additional verification in mechanistic and in vitro studies. Elsevier 2021-12 2021-08-11 /pmc/articles/PMC8626273/ /pubmed/34867022 http://dx.doi.org/10.1016/j.sjbs.2021.08.015 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Alanazi, Khalid Mashai
Al-kawmani, Ahmed Ali
Farah, Mohammad Abul
Hailan, Waleed Ali
Alsalme, Ali
Al-Zaqri, Nabil
Ajmal Ali, M.
Almansob, Abobakr Mahmood
Amelioration of indole acetic acid-induced cytotoxicity in mice using zinc nanoparticles biosynthesized with Ochradenus arabicus leaf extract
title Amelioration of indole acetic acid-induced cytotoxicity in mice using zinc nanoparticles biosynthesized with Ochradenus arabicus leaf extract
title_full Amelioration of indole acetic acid-induced cytotoxicity in mice using zinc nanoparticles biosynthesized with Ochradenus arabicus leaf extract
title_fullStr Amelioration of indole acetic acid-induced cytotoxicity in mice using zinc nanoparticles biosynthesized with Ochradenus arabicus leaf extract
title_full_unstemmed Amelioration of indole acetic acid-induced cytotoxicity in mice using zinc nanoparticles biosynthesized with Ochradenus arabicus leaf extract
title_short Amelioration of indole acetic acid-induced cytotoxicity in mice using zinc nanoparticles biosynthesized with Ochradenus arabicus leaf extract
title_sort amelioration of indole acetic acid-induced cytotoxicity in mice using zinc nanoparticles biosynthesized with ochradenus arabicus leaf extract
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626273/
https://www.ncbi.nlm.nih.gov/pubmed/34867022
http://dx.doi.org/10.1016/j.sjbs.2021.08.015
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