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Developmental exposure to silver nanoparticles leads to long term gut dysbiosis and neurobehavioral alterations

Due to their antimicrobial properties, silver nanoparticles (AgNPs) are used in a wide range of consumer products that includes topical wound dressings, coatings for biomedical devices, and food-packaging to extend the shelf-life. Despite their beneficial antimicrobial effects, developmental exposur...

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Autores principales: Lyu, Zhen, Ghoshdastidar, Shreya, Rekha, Karamkolly R., Suresh, Dhananjay, Mao, Jiude, Bivens, Nathan, Kannan, Raghuraman, Joshi, Trupti, Rosenfeld, Cheryl S., Upendran, Anandhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985313/
https://www.ncbi.nlm.nih.gov/pubmed/33753813
http://dx.doi.org/10.1038/s41598-021-85919-7
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author Lyu, Zhen
Ghoshdastidar, Shreya
Rekha, Karamkolly R.
Suresh, Dhananjay
Mao, Jiude
Bivens, Nathan
Kannan, Raghuraman
Joshi, Trupti
Rosenfeld, Cheryl S.
Upendran, Anandhi
author_facet Lyu, Zhen
Ghoshdastidar, Shreya
Rekha, Karamkolly R.
Suresh, Dhananjay
Mao, Jiude
Bivens, Nathan
Kannan, Raghuraman
Joshi, Trupti
Rosenfeld, Cheryl S.
Upendran, Anandhi
author_sort Lyu, Zhen
collection PubMed
description Due to their antimicrobial properties, silver nanoparticles (AgNPs) are used in a wide range of consumer products that includes topical wound dressings, coatings for biomedical devices, and food-packaging to extend the shelf-life. Despite their beneficial antimicrobial effects, developmental exposure to such AgNPs may lead to gut dysbiosis and long-term health consequences in exposed offspring. AgNPs can cross the placenta and blood–brain-barrier to translocate in the brain of offspring. The underlying hypothesis tested in the current study was that developmental exposure of male and female mice to AgNPs disrupts the microbiome–gut–brain axis. To examine for such effects, C57BL6 female mice were exposed orally to AgNPs at a dose of 3 mg/kg BW or vehicle control 2 weeks prior to breeding and throughout gestation. Male and female offspring were tested in various mazes that measure different behavioral domains, and the gut microbial profiles were surveyed from 30 through 120 days of age. Our study results suggest that developmental exposure results in increased likelihood of engaging in repetitive behaviors and reductions in resident microglial cells. Echo-MRI results indicate increased body fat in offspring exposed to AgNPs exhibit. Coprobacillus spp., Mucispirillum spp., and Bifidobacterium spp. were reduced, while Prevotella spp., Bacillus spp., Planococcaceae, Staphylococcus spp., Enterococcus spp., and Ruminococcus spp. were increased in those developmentally exposed to NPs. These bacterial changes were linked to behavioral and metabolic alterations. In conclusion, developmental exposure of AgNPs results in long term gut dysbiosis, body fat increase and neurobehavioral alterations in offspring.
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spelling pubmed-79853132021-03-25 Developmental exposure to silver nanoparticles leads to long term gut dysbiosis and neurobehavioral alterations Lyu, Zhen Ghoshdastidar, Shreya Rekha, Karamkolly R. Suresh, Dhananjay Mao, Jiude Bivens, Nathan Kannan, Raghuraman Joshi, Trupti Rosenfeld, Cheryl S. Upendran, Anandhi Sci Rep Article Due to their antimicrobial properties, silver nanoparticles (AgNPs) are used in a wide range of consumer products that includes topical wound dressings, coatings for biomedical devices, and food-packaging to extend the shelf-life. Despite their beneficial antimicrobial effects, developmental exposure to such AgNPs may lead to gut dysbiosis and long-term health consequences in exposed offspring. AgNPs can cross the placenta and blood–brain-barrier to translocate in the brain of offspring. The underlying hypothesis tested in the current study was that developmental exposure of male and female mice to AgNPs disrupts the microbiome–gut–brain axis. To examine for such effects, C57BL6 female mice were exposed orally to AgNPs at a dose of 3 mg/kg BW or vehicle control 2 weeks prior to breeding and throughout gestation. Male and female offspring were tested in various mazes that measure different behavioral domains, and the gut microbial profiles were surveyed from 30 through 120 days of age. Our study results suggest that developmental exposure results in increased likelihood of engaging in repetitive behaviors and reductions in resident microglial cells. Echo-MRI results indicate increased body fat in offspring exposed to AgNPs exhibit. Coprobacillus spp., Mucispirillum spp., and Bifidobacterium spp. were reduced, while Prevotella spp., Bacillus spp., Planococcaceae, Staphylococcus spp., Enterococcus spp., and Ruminococcus spp. were increased in those developmentally exposed to NPs. These bacterial changes were linked to behavioral and metabolic alterations. In conclusion, developmental exposure of AgNPs results in long term gut dysbiosis, body fat increase and neurobehavioral alterations in offspring. Nature Publishing Group UK 2021-03-22 /pmc/articles/PMC7985313/ /pubmed/33753813 http://dx.doi.org/10.1038/s41598-021-85919-7 Text en © The Author(s) 2021 Open Access This 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/.
spellingShingle Article
Lyu, Zhen
Ghoshdastidar, Shreya
Rekha, Karamkolly R.
Suresh, Dhananjay
Mao, Jiude
Bivens, Nathan
Kannan, Raghuraman
Joshi, Trupti
Rosenfeld, Cheryl S.
Upendran, Anandhi
Developmental exposure to silver nanoparticles leads to long term gut dysbiosis and neurobehavioral alterations
title Developmental exposure to silver nanoparticles leads to long term gut dysbiosis and neurobehavioral alterations
title_full Developmental exposure to silver nanoparticles leads to long term gut dysbiosis and neurobehavioral alterations
title_fullStr Developmental exposure to silver nanoparticles leads to long term gut dysbiosis and neurobehavioral alterations
title_full_unstemmed Developmental exposure to silver nanoparticles leads to long term gut dysbiosis and neurobehavioral alterations
title_short Developmental exposure to silver nanoparticles leads to long term gut dysbiosis and neurobehavioral alterations
title_sort developmental exposure to silver nanoparticles leads to long term gut dysbiosis and neurobehavioral alterations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985313/
https://www.ncbi.nlm.nih.gov/pubmed/33753813
http://dx.doi.org/10.1038/s41598-021-85919-7
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