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Expression profile of cytokines and chemokines in a mouse high-altitude cerebral edema model

INTRODUCTION: High-altitude cerebral edema (HACE) is considered to be the end-stage of acute mountain sickness (AMS); however, its pathophysiological mechanism remains unknown. Increasing evidences support that inflammation is an important risk factor for the occurrence of HACE. Including our publis...

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Autores principales: Shi, Zibi, Jiang, Xiufang, Geng, Yanan, Yue, Xiangpei, Gao, Jiayue, Cheng, Xiang, Zhao, Ming, Zhu, Lingling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192805/
https://www.ncbi.nlm.nih.gov/pubmed/37188519
http://dx.doi.org/10.1177/03946320231177189
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author Shi, Zibi
Jiang, Xiufang
Geng, Yanan
Yue, Xiangpei
Gao, Jiayue
Cheng, Xiang
Zhao, Ming
Zhu, Lingling
author_facet Shi, Zibi
Jiang, Xiufang
Geng, Yanan
Yue, Xiangpei
Gao, Jiayue
Cheng, Xiang
Zhao, Ming
Zhu, Lingling
author_sort Shi, Zibi
collection PubMed
description INTRODUCTION: High-altitude cerebral edema (HACE) is considered to be the end-stage of acute mountain sickness (AMS); however, its pathophysiological mechanism remains unknown. Increasing evidences support that inflammation is an important risk factor for the occurrence of HACE. Including our published papers, previous studies demonstrated that the levels of IL-6, IL-1β, and TNF-α in both serum and hippocampus were increased in the mouse HACE model induced by LPS stimulation combined with hypobaric hypoxia exposure; however, the expression profile of other cytokines and chemokines remains unknown. OBJECTIVE: This study was to analyze the expression profile of cytokines and chemokines in the HACE model. METHODS: The mouse HACE model was established by LPS stimulation combined with hypobaric hypoxia exposure (LH). The mice were divided into the normoxic group, LH-6 h group, LH-1 d group, and LH-7 d group. Brain water content (BWC) was determined using the wet/dry weight ratio. The levels of 30 cytokines and chemokines in the serum and hippocampal tissue were detected using LiquiChip. The mRNA expression of cytokines and chemokines in hippocampal tissue were determined by q-PCR. RESULTS: In the current study, we found that the brain water content was increased after the combinational treatment of LPS and hypobaric hypoxia. The results of LiquiChip showed that, in the serum and hippocampal tissue, most factors in all 30 cytokines and chemokines were dramatically upregulated at 6 h, and then declined at the 1st d and 7th d. Among these factors, G-CSF, M-CSF, MCP-1, KC, MIG, Eotaxin, Rantes, IP10, IL-6, MIP-2, and MIP-1β were all increased in both serum and hippocampal tissue at 6 h. In addition, the results of q-PCR showed the mRNA levels of G-CSF, MCP-1, KC, MIG, Eotaxin, Rantes, IP10, IL-6, MIP-2, and MIP-1β in hippocampal tissue were dramatically upregulated at 6 h. CONCLUSION: This study showed that the dynamic expression profile of 30 cytokines and chemokines in a mouse HACE model induced by LPS plus hypobaric hypoxia. The levels of G-CSF, MCP-1, KC, MIG, Eotaxin, Rantes, IP10, IL-6, MIP-2, and MIP-1β in both serum and hippocampus were significantly increased at 6 h, which may be involved in the occurrence and development of HACE.
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spelling pubmed-101928052023-05-19 Expression profile of cytokines and chemokines in a mouse high-altitude cerebral edema model Shi, Zibi Jiang, Xiufang Geng, Yanan Yue, Xiangpei Gao, Jiayue Cheng, Xiang Zhao, Ming Zhu, Lingling Int J Immunopathol Pharmacol Original Research Article INTRODUCTION: High-altitude cerebral edema (HACE) is considered to be the end-stage of acute mountain sickness (AMS); however, its pathophysiological mechanism remains unknown. Increasing evidences support that inflammation is an important risk factor for the occurrence of HACE. Including our published papers, previous studies demonstrated that the levels of IL-6, IL-1β, and TNF-α in both serum and hippocampus were increased in the mouse HACE model induced by LPS stimulation combined with hypobaric hypoxia exposure; however, the expression profile of other cytokines and chemokines remains unknown. OBJECTIVE: This study was to analyze the expression profile of cytokines and chemokines in the HACE model. METHODS: The mouse HACE model was established by LPS stimulation combined with hypobaric hypoxia exposure (LH). The mice were divided into the normoxic group, LH-6 h group, LH-1 d group, and LH-7 d group. Brain water content (BWC) was determined using the wet/dry weight ratio. The levels of 30 cytokines and chemokines in the serum and hippocampal tissue were detected using LiquiChip. The mRNA expression of cytokines and chemokines in hippocampal tissue were determined by q-PCR. RESULTS: In the current study, we found that the brain water content was increased after the combinational treatment of LPS and hypobaric hypoxia. The results of LiquiChip showed that, in the serum and hippocampal tissue, most factors in all 30 cytokines and chemokines were dramatically upregulated at 6 h, and then declined at the 1st d and 7th d. Among these factors, G-CSF, M-CSF, MCP-1, KC, MIG, Eotaxin, Rantes, IP10, IL-6, MIP-2, and MIP-1β were all increased in both serum and hippocampal tissue at 6 h. In addition, the results of q-PCR showed the mRNA levels of G-CSF, MCP-1, KC, MIG, Eotaxin, Rantes, IP10, IL-6, MIP-2, and MIP-1β in hippocampal tissue were dramatically upregulated at 6 h. CONCLUSION: This study showed that the dynamic expression profile of 30 cytokines and chemokines in a mouse HACE model induced by LPS plus hypobaric hypoxia. The levels of G-CSF, MCP-1, KC, MIG, Eotaxin, Rantes, IP10, IL-6, MIP-2, and MIP-1β in both serum and hippocampus were significantly increased at 6 h, which may be involved in the occurrence and development of HACE. SAGE Publications 2023-05-15 /pmc/articles/PMC10192805/ /pubmed/37188519 http://dx.doi.org/10.1177/03946320231177189 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Article
Shi, Zibi
Jiang, Xiufang
Geng, Yanan
Yue, Xiangpei
Gao, Jiayue
Cheng, Xiang
Zhao, Ming
Zhu, Lingling
Expression profile of cytokines and chemokines in a mouse high-altitude cerebral edema model
title Expression profile of cytokines and chemokines in a mouse high-altitude cerebral edema model
title_full Expression profile of cytokines and chemokines in a mouse high-altitude cerebral edema model
title_fullStr Expression profile of cytokines and chemokines in a mouse high-altitude cerebral edema model
title_full_unstemmed Expression profile of cytokines and chemokines in a mouse high-altitude cerebral edema model
title_short Expression profile of cytokines and chemokines in a mouse high-altitude cerebral edema model
title_sort expression profile of cytokines and chemokines in a mouse high-altitude cerebral edema model
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192805/
https://www.ncbi.nlm.nih.gov/pubmed/37188519
http://dx.doi.org/10.1177/03946320231177189
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