Cargando…

In vivo Detection of Macromolecule Free Radicals in Mouse Sepsis-Associated Encephalopathy Using a New MRI and Immunospin Trapping Strategy

INTRODUCTION: Free radicals in oxidative stress are known to play a pathogenic role in sepsis. A major clinical challenge associated with sepsis is sepsis-associated encephalopathy (SAE). The rapid increase of free radicals in the brain promotes SAE progression. Here, macromolecule free radicals in...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Hanrui, Ma, Chengyong, Xu, Huayan, Zhang, Huan, Xu, Rong, Zhang, Kun, Sun, Ran, Li, Kuan, Wu, Qihong, Wen, Lingyi, Zhang, Lizhi, Guo, Yingkun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444031/
https://www.ncbi.nlm.nih.gov/pubmed/36072961
http://dx.doi.org/10.2147/IJN.S378726
_version_ 1784783124666777600
author Liu, Hanrui
Ma, Chengyong
Xu, Huayan
Zhang, Huan
Xu, Rong
Zhang, Kun
Sun, Ran
Li, Kuan
Wu, Qihong
Wen, Lingyi
Zhang, Lizhi
Guo, Yingkun
author_facet Liu, Hanrui
Ma, Chengyong
Xu, Huayan
Zhang, Huan
Xu, Rong
Zhang, Kun
Sun, Ran
Li, Kuan
Wu, Qihong
Wen, Lingyi
Zhang, Lizhi
Guo, Yingkun
author_sort Liu, Hanrui
collection PubMed
description INTRODUCTION: Free radicals in oxidative stress are known to play a pathogenic role in sepsis. A major clinical challenge associated with sepsis is sepsis-associated encephalopathy (SAE). The rapid increase of free radicals in the brain promotes SAE progression. Here, macromolecule free radicals in the mouse brain were uniquely detected by immunospin trapping (IST) and magnetic resonance imaging (MRI). METHODS: The new strategy uses spin trapping agent DEPMPO-biotin to capture macromolecule free radicals in lesions and form biotin-DEPMPO-radical adducts. Then, a targeting MRI probe, avidin-BSA@Gd-ESIO, was used to detect the radical adducts through the highly specific binding of avidin and biotin. The avidin-BSA@Gd-ESIO probe was synthesized and systematically characterized. The detection capability of the new strategy was evaluated in vitro and in vivo using a confocal microscope and a 7T MRI, respectively. RESULTS: In reactive oxygen species (ROS)–induced microglial cells, the accumulation of the avidin-BSA@Gd-ESIO probe in the DEPMPO-biotin-treated group was significantly higher than that of control groups. In vivo MRI T1 signal intensities were significantly higher within the hippocampus, striatum, and medial cortex of the brain in mice with a mild or severe degree of sepsis compared with the sham control group. Histological analysis validated that the distribution of the avidin-BSA@Gd-ESIO probe in brain tissue slices was consistent with the MRI images. The fluorescence signals of ROS and avidin-BSA@Gd-ESIO probe were overlapped and visualized using immunofluorescent staining. By evaluating the T1 signal changes over time in different areas of the brain, we estimated the optimal MRI detection time to be 30 minutes after the probe administration. DISCUSSION: This method can be applied specifically to assess the level of macromolecular free radicals in vivo in a simple and stable manner, providing a pathway for a more comprehensive understanding of the role of free radicals in SAE.
format Online
Article
Text
id pubmed-9444031
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-94440312022-09-06 In vivo Detection of Macromolecule Free Radicals in Mouse Sepsis-Associated Encephalopathy Using a New MRI and Immunospin Trapping Strategy Liu, Hanrui Ma, Chengyong Xu, Huayan Zhang, Huan Xu, Rong Zhang, Kun Sun, Ran Li, Kuan Wu, Qihong Wen, Lingyi Zhang, Lizhi Guo, Yingkun Int J Nanomedicine Original Research INTRODUCTION: Free radicals in oxidative stress are known to play a pathogenic role in sepsis. A major clinical challenge associated with sepsis is sepsis-associated encephalopathy (SAE). The rapid increase of free radicals in the brain promotes SAE progression. Here, macromolecule free radicals in the mouse brain were uniquely detected by immunospin trapping (IST) and magnetic resonance imaging (MRI). METHODS: The new strategy uses spin trapping agent DEPMPO-biotin to capture macromolecule free radicals in lesions and form biotin-DEPMPO-radical adducts. Then, a targeting MRI probe, avidin-BSA@Gd-ESIO, was used to detect the radical adducts through the highly specific binding of avidin and biotin. The avidin-BSA@Gd-ESIO probe was synthesized and systematically characterized. The detection capability of the new strategy was evaluated in vitro and in vivo using a confocal microscope and a 7T MRI, respectively. RESULTS: In reactive oxygen species (ROS)–induced microglial cells, the accumulation of the avidin-BSA@Gd-ESIO probe in the DEPMPO-biotin-treated group was significantly higher than that of control groups. In vivo MRI T1 signal intensities were significantly higher within the hippocampus, striatum, and medial cortex of the brain in mice with a mild or severe degree of sepsis compared with the sham control group. Histological analysis validated that the distribution of the avidin-BSA@Gd-ESIO probe in brain tissue slices was consistent with the MRI images. The fluorescence signals of ROS and avidin-BSA@Gd-ESIO probe were overlapped and visualized using immunofluorescent staining. By evaluating the T1 signal changes over time in different areas of the brain, we estimated the optimal MRI detection time to be 30 minutes after the probe administration. DISCUSSION: This method can be applied specifically to assess the level of macromolecular free radicals in vivo in a simple and stable manner, providing a pathway for a more comprehensive understanding of the role of free radicals in SAE. Dove 2022-09-01 /pmc/articles/PMC9444031/ /pubmed/36072961 http://dx.doi.org/10.2147/IJN.S378726 Text en © 2022 Liu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Liu, Hanrui
Ma, Chengyong
Xu, Huayan
Zhang, Huan
Xu, Rong
Zhang, Kun
Sun, Ran
Li, Kuan
Wu, Qihong
Wen, Lingyi
Zhang, Lizhi
Guo, Yingkun
In vivo Detection of Macromolecule Free Radicals in Mouse Sepsis-Associated Encephalopathy Using a New MRI and Immunospin Trapping Strategy
title In vivo Detection of Macromolecule Free Radicals in Mouse Sepsis-Associated Encephalopathy Using a New MRI and Immunospin Trapping Strategy
title_full In vivo Detection of Macromolecule Free Radicals in Mouse Sepsis-Associated Encephalopathy Using a New MRI and Immunospin Trapping Strategy
title_fullStr In vivo Detection of Macromolecule Free Radicals in Mouse Sepsis-Associated Encephalopathy Using a New MRI and Immunospin Trapping Strategy
title_full_unstemmed In vivo Detection of Macromolecule Free Radicals in Mouse Sepsis-Associated Encephalopathy Using a New MRI and Immunospin Trapping Strategy
title_short In vivo Detection of Macromolecule Free Radicals in Mouse Sepsis-Associated Encephalopathy Using a New MRI and Immunospin Trapping Strategy
title_sort in vivo detection of macromolecule free radicals in mouse sepsis-associated encephalopathy using a new mri and immunospin trapping strategy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444031/
https://www.ncbi.nlm.nih.gov/pubmed/36072961
http://dx.doi.org/10.2147/IJN.S378726
work_keys_str_mv AT liuhanrui invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT machengyong invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT xuhuayan invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT zhanghuan invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT xurong invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT zhangkun invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT sunran invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT likuan invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT wuqihong invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT wenlingyi invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT zhanglizhi invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy
AT guoyingkun invivodetectionofmacromoleculefreeradicalsinmousesepsisassociatedencephalopathyusinganewmriandimmunospintrappingstrategy