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Assessment of the Toxicity of Aluminum Oxide and Its Nanoparticles in the Bone Marrow and Liver of Male Mice: Ameliorative Efficacy of Curcumin Nanoparticles
[Image: see text] The potential influence of nanoparticles (NPs) on the liver and bone marrow has received attention. The aim of this work was to evaluate the effect of nanocurcumin on the oxidative stress, apoptosis, and toxicity induced by Al(2)O(3) and its NPs. The experimental animals (n = 72 mi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088947/ https://www.ncbi.nlm.nih.gov/pubmed/35559158 http://dx.doi.org/10.1021/acsomega.2c00195 |
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author | Alghriany, Alshaimaa A. I. Omar, Hossam EL-din M. Mahmoud, Amera M. Atia, Mona M. |
author_facet | Alghriany, Alshaimaa A. I. Omar, Hossam EL-din M. Mahmoud, Amera M. Atia, Mona M. |
author_sort | Alghriany, Alshaimaa A. I. |
collection | PubMed |
description | [Image: see text] The potential influence of nanoparticles (NPs) on the liver and bone marrow has received attention. The aim of this work was to evaluate the effect of nanocurcumin on the oxidative stress, apoptosis, and toxicity induced by Al(2)O(3) and its NPs. The experimental animals (n = 72 mice) were divided into the following groups: group I, as a control; groups II and III, as aluminum oxide and its NPs (6 mg/kg); group IV, as aluminum oxide + nanocurcumin (Al(2)O(3) + N-Cur, 20 mg/kg); and group V, as aluminum oxide NPs + nanocurcumin (Al(2)O(3)-NP + N.Cur., 20 mg/kg). Al(2)O(3) and its NP groups significantly increased p53, Nrf2 levels, and the white blood cell count. They also decreased the Hsp70 level, antitrypsin, immunoglobulin G, and the red blood cell count. In addition, they significantly decreased the total and differential bone marrow cell counts and the maturation index ratio (MIR). Nanocurcumin (N.Cur.) reverted the previous proteins, blood parameters, total bone marrow cell count, and the MIR as M/E, I/Mg, MMI, I/Me, and EMI to normal. Furthermore, N.Cur. prevented apoptosis and reduced the histopathological score and collagen fiber percentage caused by Al(2)O(3) and its NPs in the liver. Nanotechnology was used to increase the therapeutic efficiency of curcumin against the harmful effects of oxidative stress associated with Al(2)O(3) NPs. |
format | Online Article Text |
id | pubmed-9088947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90889472022-05-11 Assessment of the Toxicity of Aluminum Oxide and Its Nanoparticles in the Bone Marrow and Liver of Male Mice: Ameliorative Efficacy of Curcumin Nanoparticles Alghriany, Alshaimaa A. I. Omar, Hossam EL-din M. Mahmoud, Amera M. Atia, Mona M. ACS Omega [Image: see text] The potential influence of nanoparticles (NPs) on the liver and bone marrow has received attention. The aim of this work was to evaluate the effect of nanocurcumin on the oxidative stress, apoptosis, and toxicity induced by Al(2)O(3) and its NPs. The experimental animals (n = 72 mice) were divided into the following groups: group I, as a control; groups II and III, as aluminum oxide and its NPs (6 mg/kg); group IV, as aluminum oxide + nanocurcumin (Al(2)O(3) + N-Cur, 20 mg/kg); and group V, as aluminum oxide NPs + nanocurcumin (Al(2)O(3)-NP + N.Cur., 20 mg/kg). Al(2)O(3) and its NP groups significantly increased p53, Nrf2 levels, and the white blood cell count. They also decreased the Hsp70 level, antitrypsin, immunoglobulin G, and the red blood cell count. In addition, they significantly decreased the total and differential bone marrow cell counts and the maturation index ratio (MIR). Nanocurcumin (N.Cur.) reverted the previous proteins, blood parameters, total bone marrow cell count, and the MIR as M/E, I/Mg, MMI, I/Me, and EMI to normal. Furthermore, N.Cur. prevented apoptosis and reduced the histopathological score and collagen fiber percentage caused by Al(2)O(3) and its NPs in the liver. Nanotechnology was used to increase the therapeutic efficiency of curcumin against the harmful effects of oxidative stress associated with Al(2)O(3) NPs. American Chemical Society 2022-04-14 /pmc/articles/PMC9088947/ /pubmed/35559158 http://dx.doi.org/10.1021/acsomega.2c00195 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Alghriany, Alshaimaa A. I. Omar, Hossam EL-din M. Mahmoud, Amera M. Atia, Mona M. Assessment of the Toxicity of Aluminum Oxide and Its Nanoparticles in the Bone Marrow and Liver of Male Mice: Ameliorative Efficacy of Curcumin Nanoparticles |
title | Assessment of the Toxicity of Aluminum Oxide and Its
Nanoparticles in the Bone Marrow and Liver of Male Mice: Ameliorative
Efficacy of Curcumin Nanoparticles |
title_full | Assessment of the Toxicity of Aluminum Oxide and Its
Nanoparticles in the Bone Marrow and Liver of Male Mice: Ameliorative
Efficacy of Curcumin Nanoparticles |
title_fullStr | Assessment of the Toxicity of Aluminum Oxide and Its
Nanoparticles in the Bone Marrow and Liver of Male Mice: Ameliorative
Efficacy of Curcumin Nanoparticles |
title_full_unstemmed | Assessment of the Toxicity of Aluminum Oxide and Its
Nanoparticles in the Bone Marrow and Liver of Male Mice: Ameliorative
Efficacy of Curcumin Nanoparticles |
title_short | Assessment of the Toxicity of Aluminum Oxide and Its
Nanoparticles in the Bone Marrow and Liver of Male Mice: Ameliorative
Efficacy of Curcumin Nanoparticles |
title_sort | assessment of the toxicity of aluminum oxide and its
nanoparticles in the bone marrow and liver of male mice: ameliorative
efficacy of curcumin nanoparticles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088947/ https://www.ncbi.nlm.nih.gov/pubmed/35559158 http://dx.doi.org/10.1021/acsomega.2c00195 |
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