Cargando…

Effects of chemical forms of gadolinium on the spleen in mice after single intravenous administration

Gadolinium-based contrast agents (GBCAs) are widely used to improve tissue contrast during magnetic resonance imaging. Exposure to GBCAs can result in gadolinium deposition within human tissues and has become a clinical concern because of the potential toxic effects of free gadolinium (Gd(3+)). Here...

Descripción completa

Detalles Bibliográficos
Autores principales: Nakamura, Ryosuke, Takanezawa, Yasukazu, Ohshiro, Yuka, Uraguchi, Shimpei, Kiyono, Masako
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8808065/
https://www.ncbi.nlm.nih.gov/pubmed/35128083
http://dx.doi.org/10.1016/j.bbrep.2022.101217
_version_ 1784643805764386816
author Nakamura, Ryosuke
Takanezawa, Yasukazu
Ohshiro, Yuka
Uraguchi, Shimpei
Kiyono, Masako
author_facet Nakamura, Ryosuke
Takanezawa, Yasukazu
Ohshiro, Yuka
Uraguchi, Shimpei
Kiyono, Masako
author_sort Nakamura, Ryosuke
collection PubMed
description Gadolinium-based contrast agents (GBCAs) are widely used to improve tissue contrast during magnetic resonance imaging. Exposure to GBCAs can result in gadolinium deposition within human tissues and has become a clinical concern because of the potential toxic effects of free gadolinium (Gd(3+)). Here, we report the impact of a single administration of GBCAs (Omniscan and Gadovist), and Gd(3+) on mouse tissues. Five-week-old male BALB/c mice were injected intravenously with GBCAs or Gd(3+). Seven days after injection, relatively high levels of gadolinium were detected in the spleen (118.87 nmol/g tissue), liver (83.00 nmol/g tissue), skin (48.56 nmol/g tissue), and kidneys (25.59 nmol/g tissue) of the Gd(NO(3))(3) (high dose: 0.165 mmol/kg) group; in the bones (11.12 nmol/g tissue), kidneys (7.49 nmol/g tissue), teeth (teeth: 6.18 nmol/g tissue), and skin (2.43 nmol/g tissue) of the Omniscan (high dose: 1.654 mmol/kg) group and in the kidneys (16.36 nmol/g tissue) and skin (4.88 nmol/g tissue) of the Gadovist (high dose: 3.308 mmol/kg) group. Enlargement of the spleen was observed in the Gd(3+) group (p < 0.05), but not in the Omniscan or Gadovist groups. Gd(3+) caused iron accumulation around the white pulp of the spleen, suggesting that enlargement of the spleen is, at least in part, associated with Gd(3+) and/or iron accumulation. Our results may help elucidate the relative risks of different types of gadolinium agents, the mechanisms involved, and even recognition of potential toxic effects of GBCAs.
format Online
Article
Text
id pubmed-8808065
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-88080652022-02-04 Effects of chemical forms of gadolinium on the spleen in mice after single intravenous administration Nakamura, Ryosuke Takanezawa, Yasukazu Ohshiro, Yuka Uraguchi, Shimpei Kiyono, Masako Biochem Biophys Rep Research Article Gadolinium-based contrast agents (GBCAs) are widely used to improve tissue contrast during magnetic resonance imaging. Exposure to GBCAs can result in gadolinium deposition within human tissues and has become a clinical concern because of the potential toxic effects of free gadolinium (Gd(3+)). Here, we report the impact of a single administration of GBCAs (Omniscan and Gadovist), and Gd(3+) on mouse tissues. Five-week-old male BALB/c mice were injected intravenously with GBCAs or Gd(3+). Seven days after injection, relatively high levels of gadolinium were detected in the spleen (118.87 nmol/g tissue), liver (83.00 nmol/g tissue), skin (48.56 nmol/g tissue), and kidneys (25.59 nmol/g tissue) of the Gd(NO(3))(3) (high dose: 0.165 mmol/kg) group; in the bones (11.12 nmol/g tissue), kidneys (7.49 nmol/g tissue), teeth (teeth: 6.18 nmol/g tissue), and skin (2.43 nmol/g tissue) of the Omniscan (high dose: 1.654 mmol/kg) group and in the kidneys (16.36 nmol/g tissue) and skin (4.88 nmol/g tissue) of the Gadovist (high dose: 3.308 mmol/kg) group. Enlargement of the spleen was observed in the Gd(3+) group (p < 0.05), but not in the Omniscan or Gadovist groups. Gd(3+) caused iron accumulation around the white pulp of the spleen, suggesting that enlargement of the spleen is, at least in part, associated with Gd(3+) and/or iron accumulation. Our results may help elucidate the relative risks of different types of gadolinium agents, the mechanisms involved, and even recognition of potential toxic effects of GBCAs. Elsevier 2022-01-28 /pmc/articles/PMC8808065/ /pubmed/35128083 http://dx.doi.org/10.1016/j.bbrep.2022.101217 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Nakamura, Ryosuke
Takanezawa, Yasukazu
Ohshiro, Yuka
Uraguchi, Shimpei
Kiyono, Masako
Effects of chemical forms of gadolinium on the spleen in mice after single intravenous administration
title Effects of chemical forms of gadolinium on the spleen in mice after single intravenous administration
title_full Effects of chemical forms of gadolinium on the spleen in mice after single intravenous administration
title_fullStr Effects of chemical forms of gadolinium on the spleen in mice after single intravenous administration
title_full_unstemmed Effects of chemical forms of gadolinium on the spleen in mice after single intravenous administration
title_short Effects of chemical forms of gadolinium on the spleen in mice after single intravenous administration
title_sort effects of chemical forms of gadolinium on the spleen in mice after single intravenous administration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8808065/
https://www.ncbi.nlm.nih.gov/pubmed/35128083
http://dx.doi.org/10.1016/j.bbrep.2022.101217
work_keys_str_mv AT nakamuraryosuke effectsofchemicalformsofgadoliniumonthespleeninmiceaftersingleintravenousadministration
AT takanezawayasukazu effectsofchemicalformsofgadoliniumonthespleeninmiceaftersingleintravenousadministration
AT ohshiroyuka effectsofchemicalformsofgadoliniumonthespleeninmiceaftersingleintravenousadministration
AT uraguchishimpei effectsofchemicalformsofgadoliniumonthespleeninmiceaftersingleintravenousadministration
AT kiyonomasako effectsofchemicalformsofgadoliniumonthespleeninmiceaftersingleintravenousadministration