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Effects of iron oxide nanoparticles as T(2)-MRI contrast agents on reproductive system in male mice

Iron oxide nanoparticles (IONPs)-based contrast agents are widely used for T(2)-weighted magnetic resonance imaging (MRI) in clinical diagnosis, highlighting the necessity and importance to evaluate their potential systematic toxicities. Although a few previous studies have documented the toxicity c...

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Autores principales: Yang, Heyu, Wang, Hui, Wen, Chenghao, Bai, Shun, Wei, Pengfei, Xu, Bo, Xu, Yunjun, Liang, Chaozhao, Zhang, Yunjiao, Zhang, Guilong, Wen, Huiqin, Zhang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889634/
https://www.ncbi.nlm.nih.gov/pubmed/35236363
http://dx.doi.org/10.1186/s12951-022-01291-2
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author Yang, Heyu
Wang, Hui
Wen, Chenghao
Bai, Shun
Wei, Pengfei
Xu, Bo
Xu, Yunjun
Liang, Chaozhao
Zhang, Yunjiao
Zhang, Guilong
Wen, Huiqin
Zhang, Li
author_facet Yang, Heyu
Wang, Hui
Wen, Chenghao
Bai, Shun
Wei, Pengfei
Xu, Bo
Xu, Yunjun
Liang, Chaozhao
Zhang, Yunjiao
Zhang, Guilong
Wen, Huiqin
Zhang, Li
author_sort Yang, Heyu
collection PubMed
description Iron oxide nanoparticles (IONPs)-based contrast agents are widely used for T(2)-weighted magnetic resonance imaging (MRI) in clinical diagnosis, highlighting the necessity and importance to evaluate their potential systematic toxicities. Although a few previous studies have documented the toxicity concerns of IONPs to major organs, limited data are available on the potential reproductive toxicity caused by IONPs, especially when administrated via intravenous injection to mimic clinical use of MRI contrast agents. Our study aimed to determine whether exposure to IONPs would affect male reproductive system and cause other related health concerns in ICR mice. The mice were intravenously injected with different concentrations IONPs once followed by routine toxicity tests of major organs and a series of reproductive function-related analyses at different timepoints. As a result, most of the contrast agents were captured by reticuloendothelial system (RES) organs such as liver and spleen, while IONPs have not presented adverse effects on the normal function of these major organs. In contrast, although IONPs were not able to enter testis through the blood testicular barrier (BTB), and they have not obviously impaired the overall testicular function or altered the serum sex hormones levels, IONPs exposure could damage Sertoli cells in BTB especially at a relative high concentration. Moreover, IONPs administration led to a short-term reduction in the quantity and quality of sperms in a dose-dependent manner, which might be attributed to the increase of oxidative stress and apoptotic activity in epididymis. However, the semen parameters have gradually returned to the normal range within 14 days after the initial injection of IONPs. Collectively, these results demonstrated that IONPs could cause reversible damage to the reproductive system of male mice without affecting the main organs, providing new guidance for the clinical application of IONPs as T(2)-MRI contrast agents. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01291-2.
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spelling pubmed-88896342022-03-09 Effects of iron oxide nanoparticles as T(2)-MRI contrast agents on reproductive system in male mice Yang, Heyu Wang, Hui Wen, Chenghao Bai, Shun Wei, Pengfei Xu, Bo Xu, Yunjun Liang, Chaozhao Zhang, Yunjiao Zhang, Guilong Wen, Huiqin Zhang, Li J Nanobiotechnology Research Iron oxide nanoparticles (IONPs)-based contrast agents are widely used for T(2)-weighted magnetic resonance imaging (MRI) in clinical diagnosis, highlighting the necessity and importance to evaluate their potential systematic toxicities. Although a few previous studies have documented the toxicity concerns of IONPs to major organs, limited data are available on the potential reproductive toxicity caused by IONPs, especially when administrated via intravenous injection to mimic clinical use of MRI contrast agents. Our study aimed to determine whether exposure to IONPs would affect male reproductive system and cause other related health concerns in ICR mice. The mice were intravenously injected with different concentrations IONPs once followed by routine toxicity tests of major organs and a series of reproductive function-related analyses at different timepoints. As a result, most of the contrast agents were captured by reticuloendothelial system (RES) organs such as liver and spleen, while IONPs have not presented adverse effects on the normal function of these major organs. In contrast, although IONPs were not able to enter testis through the blood testicular barrier (BTB), and they have not obviously impaired the overall testicular function or altered the serum sex hormones levels, IONPs exposure could damage Sertoli cells in BTB especially at a relative high concentration. Moreover, IONPs administration led to a short-term reduction in the quantity and quality of sperms in a dose-dependent manner, which might be attributed to the increase of oxidative stress and apoptotic activity in epididymis. However, the semen parameters have gradually returned to the normal range within 14 days after the initial injection of IONPs. Collectively, these results demonstrated that IONPs could cause reversible damage to the reproductive system of male mice without affecting the main organs, providing new guidance for the clinical application of IONPs as T(2)-MRI contrast agents. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01291-2. BioMed Central 2022-03-02 /pmc/articles/PMC8889634/ /pubmed/35236363 http://dx.doi.org/10.1186/s12951-022-01291-2 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
Yang, Heyu
Wang, Hui
Wen, Chenghao
Bai, Shun
Wei, Pengfei
Xu, Bo
Xu, Yunjun
Liang, Chaozhao
Zhang, Yunjiao
Zhang, Guilong
Wen, Huiqin
Zhang, Li
Effects of iron oxide nanoparticles as T(2)-MRI contrast agents on reproductive system in male mice
title Effects of iron oxide nanoparticles as T(2)-MRI contrast agents on reproductive system in male mice
title_full Effects of iron oxide nanoparticles as T(2)-MRI contrast agents on reproductive system in male mice
title_fullStr Effects of iron oxide nanoparticles as T(2)-MRI contrast agents on reproductive system in male mice
title_full_unstemmed Effects of iron oxide nanoparticles as T(2)-MRI contrast agents on reproductive system in male mice
title_short Effects of iron oxide nanoparticles as T(2)-MRI contrast agents on reproductive system in male mice
title_sort effects of iron oxide nanoparticles as t(2)-mri contrast agents on reproductive system in male mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889634/
https://www.ncbi.nlm.nih.gov/pubmed/35236363
http://dx.doi.org/10.1186/s12951-022-01291-2
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