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Oral administration of TiO(2) nanoparticles during early life impacts cardiac and neurobehavioral performance and metabolite profile in an age- and sex-related manner

BACKGROUND: Nanoparticles (NPs) are increasingly incorporated in everyday products. To investigate the effects of early life exposure to orally ingested TiO(2) NP, male and female Sprague–Dawley rat pups received four consecutive daily doses of 10 mg/kg body weight TiO(2) NP (diameter: 21 ± 5 nm) or...

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Autores principales: Mortensen, Ninell P., Pathmasiri, Wimal, Snyder, Rodney W., Caffaro, Maria Moreno, Watson, Scott L., Patel, Purvi R., Beeravalli, Lakshmi, Prattipati, Sharmista, Aravamudhan, Shyam, Sumner, Susan J., Fennell, Timothy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728993/
https://www.ncbi.nlm.nih.gov/pubmed/34986857
http://dx.doi.org/10.1186/s12989-021-00444-9
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author Mortensen, Ninell P.
Pathmasiri, Wimal
Snyder, Rodney W.
Caffaro, Maria Moreno
Watson, Scott L.
Patel, Purvi R.
Beeravalli, Lakshmi
Prattipati, Sharmista
Aravamudhan, Shyam
Sumner, Susan J.
Fennell, Timothy R.
author_facet Mortensen, Ninell P.
Pathmasiri, Wimal
Snyder, Rodney W.
Caffaro, Maria Moreno
Watson, Scott L.
Patel, Purvi R.
Beeravalli, Lakshmi
Prattipati, Sharmista
Aravamudhan, Shyam
Sumner, Susan J.
Fennell, Timothy R.
author_sort Mortensen, Ninell P.
collection PubMed
description BACKGROUND: Nanoparticles (NPs) are increasingly incorporated in everyday products. To investigate the effects of early life exposure to orally ingested TiO(2) NP, male and female Sprague–Dawley rat pups received four consecutive daily doses of 10 mg/kg body weight TiO(2) NP (diameter: 21 ± 5 nm) or vehicle control (water) by gavage at three different pre-weaning ages: postnatal day (PND) 2–5, PND 7–10, or PND 17–20. Cardiac assessment and basic neurobehavioral tests (locomotor activity, rotarod, and acoustic startle) were conducted on PND 20. Pups were sacrificed at PND 21. Select tissues were collected, weighed, processed for neurotransmitter and metabolomics analyses. RESULTS: Heart rate was found to be significantly decreased in female pups when dosed between PND 7–10 and PND 17–20. Females dosed between PND 2–5 showed decrease acoustic startle response and when dosed between PND 7–10 showed decreased performance in the rotarod test and increased locomotor activity. Male pups dosed between PND 17–20 showed decreased locomotor activity. The concentrations of neurotransmitters and related metabolites in brain tissue and the metabolomic profile of plasma were impacted by TiO(2) NP administration for all dose groups. Metabolomic pathways perturbed by TiO(2) NP administration included pathways involved in amino acid and lipid metabolism. CONCLUSION: Oral administration of TiO(2) NP to rat pups impacted basic cardiac and neurobehavioral performance, neurotransmitters and related metabolites concentrations in brain tissue, and the biochemical profiles of plasma. The findings suggested that female pups were more likely to experience adverse outcome following early life exposure to oral TiO(2) NP than male pups. Collectively the data from this exploratory study suggest oral administration of TiO(2) NP cause adverse biological effects in an age- and sex-related manner, emphasizing the need to understand the short- and long-term effects of early life exposure to TiO(2) NP. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12989-021-00444-9.
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spelling pubmed-87289932022-01-06 Oral administration of TiO(2) nanoparticles during early life impacts cardiac and neurobehavioral performance and metabolite profile in an age- and sex-related manner Mortensen, Ninell P. Pathmasiri, Wimal Snyder, Rodney W. Caffaro, Maria Moreno Watson, Scott L. Patel, Purvi R. Beeravalli, Lakshmi Prattipati, Sharmista Aravamudhan, Shyam Sumner, Susan J. Fennell, Timothy R. Part Fibre Toxicol Research BACKGROUND: Nanoparticles (NPs) are increasingly incorporated in everyday products. To investigate the effects of early life exposure to orally ingested TiO(2) NP, male and female Sprague–Dawley rat pups received four consecutive daily doses of 10 mg/kg body weight TiO(2) NP (diameter: 21 ± 5 nm) or vehicle control (water) by gavage at three different pre-weaning ages: postnatal day (PND) 2–5, PND 7–10, or PND 17–20. Cardiac assessment and basic neurobehavioral tests (locomotor activity, rotarod, and acoustic startle) were conducted on PND 20. Pups were sacrificed at PND 21. Select tissues were collected, weighed, processed for neurotransmitter and metabolomics analyses. RESULTS: Heart rate was found to be significantly decreased in female pups when dosed between PND 7–10 and PND 17–20. Females dosed between PND 2–5 showed decrease acoustic startle response and when dosed between PND 7–10 showed decreased performance in the rotarod test and increased locomotor activity. Male pups dosed between PND 17–20 showed decreased locomotor activity. The concentrations of neurotransmitters and related metabolites in brain tissue and the metabolomic profile of plasma were impacted by TiO(2) NP administration for all dose groups. Metabolomic pathways perturbed by TiO(2) NP administration included pathways involved in amino acid and lipid metabolism. CONCLUSION: Oral administration of TiO(2) NP to rat pups impacted basic cardiac and neurobehavioral performance, neurotransmitters and related metabolites concentrations in brain tissue, and the biochemical profiles of plasma. The findings suggested that female pups were more likely to experience adverse outcome following early life exposure to oral TiO(2) NP than male pups. Collectively the data from this exploratory study suggest oral administration of TiO(2) NP cause adverse biological effects in an age- and sex-related manner, emphasizing the need to understand the short- and long-term effects of early life exposure to TiO(2) NP. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12989-021-00444-9. BioMed Central 2022-01-05 /pmc/articles/PMC8728993/ /pubmed/34986857 http://dx.doi.org/10.1186/s12989-021-00444-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Mortensen, Ninell P.
Pathmasiri, Wimal
Snyder, Rodney W.
Caffaro, Maria Moreno
Watson, Scott L.
Patel, Purvi R.
Beeravalli, Lakshmi
Prattipati, Sharmista
Aravamudhan, Shyam
Sumner, Susan J.
Fennell, Timothy R.
Oral administration of TiO(2) nanoparticles during early life impacts cardiac and neurobehavioral performance and metabolite profile in an age- and sex-related manner
title Oral administration of TiO(2) nanoparticles during early life impacts cardiac and neurobehavioral performance and metabolite profile in an age- and sex-related manner
title_full Oral administration of TiO(2) nanoparticles during early life impacts cardiac and neurobehavioral performance and metabolite profile in an age- and sex-related manner
title_fullStr Oral administration of TiO(2) nanoparticles during early life impacts cardiac and neurobehavioral performance and metabolite profile in an age- and sex-related manner
title_full_unstemmed Oral administration of TiO(2) nanoparticles during early life impacts cardiac and neurobehavioral performance and metabolite profile in an age- and sex-related manner
title_short Oral administration of TiO(2) nanoparticles during early life impacts cardiac and neurobehavioral performance and metabolite profile in an age- and sex-related manner
title_sort oral administration of tio(2) nanoparticles during early life impacts cardiac and neurobehavioral performance and metabolite profile in an age- and sex-related manner
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728993/
https://www.ncbi.nlm.nih.gov/pubmed/34986857
http://dx.doi.org/10.1186/s12989-021-00444-9
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