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Boron Oxide Nanoparticles Exhibit Minor, Species-Specific Acute Toxicity to North-Temperate and Amazonian Freshwater Fishes

Boron oxide nanoparticles (nB(2)O(3)) are manufactured for structural, propellant, and clinical applications and also form spontaneously through the degradation of bulk boron compounds. Bulk boron is not toxic to vertebrates but the distinctive properties of its nanostructured equivalent may alter i...

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Autores principales: MacCormack, Tyson J., Gormley, Patrick T., Khuong, B. Ninh, Adams, Olivia A., Braz-Mota, Susana, Duarte, Rafael M., Vogels, Christopher M., Tremblay, Luc, Val, Adalberto L., Almeida-Val, Vera M. F., Westcott, Stephen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8194395/
https://www.ncbi.nlm.nih.gov/pubmed/34124028
http://dx.doi.org/10.3389/fbioe.2021.689933
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author MacCormack, Tyson J.
Gormley, Patrick T.
Khuong, B. Ninh
Adams, Olivia A.
Braz-Mota, Susana
Duarte, Rafael M.
Vogels, Christopher M.
Tremblay, Luc
Val, Adalberto L.
Almeida-Val, Vera M. F.
Westcott, Stephen A.
author_facet MacCormack, Tyson J.
Gormley, Patrick T.
Khuong, B. Ninh
Adams, Olivia A.
Braz-Mota, Susana
Duarte, Rafael M.
Vogels, Christopher M.
Tremblay, Luc
Val, Adalberto L.
Almeida-Val, Vera M. F.
Westcott, Stephen A.
author_sort MacCormack, Tyson J.
collection PubMed
description Boron oxide nanoparticles (nB(2)O(3)) are manufactured for structural, propellant, and clinical applications and also form spontaneously through the degradation of bulk boron compounds. Bulk boron is not toxic to vertebrates but the distinctive properties of its nanostructured equivalent may alter its biocompatibility. Few studies have addressed this possibility, thus our goal was to gain an initial understanding of the potential acute toxicity of nB(2)O(3) to freshwater fish and we used a variety of model systems to achieve this. Bioactivity was investigated in rainbow trout (Oncorhynchus mykiss) hepatocytes and at the whole animal level in three other North and South American fish species using indicators of aerobic metabolism, behavior, oxidative stress, neurotoxicity, and ionoregulation. nB(2)O(3) reduced O. mykiss hepatocyte oxygen consumption (ṀO(2)) by 35% at high doses but whole animal ṀO(2) was not affected in any species. Spontaneous activity was assessed using ṀO(2) frequency distribution plots from live fish. nB(2)O(3) increased the frequency of high ṀO(2) events in the Amazonian fish Paracheirodon axelrodi, suggesting exposure enhanced spontaneous aerobic activity. ṀO(2) frequency distributions were not affected in the other species examined. Liver lactate accumulation and significant changes in cardiac acetylcholinesterase and gill Na(+)/K(+)-ATPase activity were noted in the north-temperate Fundulus diaphanus exposed to nB(2)O(3), but not in the Amazonian Apistogramma agassizii or P. axelrodi. nB(2)O(3) did not induce oxidative stress in any of the species studied. Overall, nB(2)O(3) exhibited modest, species-specific bioactivity but only at doses exceeding predicted environmental relevance. Chronic, low dose exposure studies are required for confirmation, but our data suggest that, like bulk boron, nB(2)O(3) is relatively non-toxic to aquatic vertebrates and thus represents a promising formulation for further development.
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spelling pubmed-81943952021-06-12 Boron Oxide Nanoparticles Exhibit Minor, Species-Specific Acute Toxicity to North-Temperate and Amazonian Freshwater Fishes MacCormack, Tyson J. Gormley, Patrick T. Khuong, B. Ninh Adams, Olivia A. Braz-Mota, Susana Duarte, Rafael M. Vogels, Christopher M. Tremblay, Luc Val, Adalberto L. Almeida-Val, Vera M. F. Westcott, Stephen A. Front Bioeng Biotechnol Bioengineering and Biotechnology Boron oxide nanoparticles (nB(2)O(3)) are manufactured for structural, propellant, and clinical applications and also form spontaneously through the degradation of bulk boron compounds. Bulk boron is not toxic to vertebrates but the distinctive properties of its nanostructured equivalent may alter its biocompatibility. Few studies have addressed this possibility, thus our goal was to gain an initial understanding of the potential acute toxicity of nB(2)O(3) to freshwater fish and we used a variety of model systems to achieve this. Bioactivity was investigated in rainbow trout (Oncorhynchus mykiss) hepatocytes and at the whole animal level in three other North and South American fish species using indicators of aerobic metabolism, behavior, oxidative stress, neurotoxicity, and ionoregulation. nB(2)O(3) reduced O. mykiss hepatocyte oxygen consumption (ṀO(2)) by 35% at high doses but whole animal ṀO(2) was not affected in any species. Spontaneous activity was assessed using ṀO(2) frequency distribution plots from live fish. nB(2)O(3) increased the frequency of high ṀO(2) events in the Amazonian fish Paracheirodon axelrodi, suggesting exposure enhanced spontaneous aerobic activity. ṀO(2) frequency distributions were not affected in the other species examined. Liver lactate accumulation and significant changes in cardiac acetylcholinesterase and gill Na(+)/K(+)-ATPase activity were noted in the north-temperate Fundulus diaphanus exposed to nB(2)O(3), but not in the Amazonian Apistogramma agassizii or P. axelrodi. nB(2)O(3) did not induce oxidative stress in any of the species studied. Overall, nB(2)O(3) exhibited modest, species-specific bioactivity but only at doses exceeding predicted environmental relevance. Chronic, low dose exposure studies are required for confirmation, but our data suggest that, like bulk boron, nB(2)O(3) is relatively non-toxic to aquatic vertebrates and thus represents a promising formulation for further development. Frontiers Media S.A. 2021-05-28 /pmc/articles/PMC8194395/ /pubmed/34124028 http://dx.doi.org/10.3389/fbioe.2021.689933 Text en Copyright © 2021 MacCormack, Gormley, Khuong, Adams, Braz-Mota, Duarte, Vogels, Tremblay, Val, Almeida-Val and Westcott. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
MacCormack, Tyson J.
Gormley, Patrick T.
Khuong, B. Ninh
Adams, Olivia A.
Braz-Mota, Susana
Duarte, Rafael M.
Vogels, Christopher M.
Tremblay, Luc
Val, Adalberto L.
Almeida-Val, Vera M. F.
Westcott, Stephen A.
Boron Oxide Nanoparticles Exhibit Minor, Species-Specific Acute Toxicity to North-Temperate and Amazonian Freshwater Fishes
title Boron Oxide Nanoparticles Exhibit Minor, Species-Specific Acute Toxicity to North-Temperate and Amazonian Freshwater Fishes
title_full Boron Oxide Nanoparticles Exhibit Minor, Species-Specific Acute Toxicity to North-Temperate and Amazonian Freshwater Fishes
title_fullStr Boron Oxide Nanoparticles Exhibit Minor, Species-Specific Acute Toxicity to North-Temperate and Amazonian Freshwater Fishes
title_full_unstemmed Boron Oxide Nanoparticles Exhibit Minor, Species-Specific Acute Toxicity to North-Temperate and Amazonian Freshwater Fishes
title_short Boron Oxide Nanoparticles Exhibit Minor, Species-Specific Acute Toxicity to North-Temperate and Amazonian Freshwater Fishes
title_sort boron oxide nanoparticles exhibit minor, species-specific acute toxicity to north-temperate and amazonian freshwater fishes
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8194395/
https://www.ncbi.nlm.nih.gov/pubmed/34124028
http://dx.doi.org/10.3389/fbioe.2021.689933
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