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β-Glucan alleviates goal-directed behavioral deficits in mice infected with Toxoplasma gondii

BACKGROUND: Toxoplasma gondii (T. gondii) is a neuroinvasive parasite causing neuroinflammation, which in turn is associated with a higher risk for several psycho-behavioral disorders. There is an urgent need to identify drugs capable of improving cognitive deficits induced by T. gondii infection. β...

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Autores principales: Cui, Zeyu, Gong, Yuying, Luo, Xiaotong, Zheng, Niuyi, Tan, Shimin, Liu, Shuxi, Li, Youwei, Wang, Qingling, Sun, Fenfen, Hu, Minmin, Pan, Wei, Yang, Xiaoying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926625/
https://www.ncbi.nlm.nih.gov/pubmed/36782332
http://dx.doi.org/10.1186/s13071-023-05686-4
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author Cui, Zeyu
Gong, Yuying
Luo, Xiaotong
Zheng, Niuyi
Tan, Shimin
Liu, Shuxi
Li, Youwei
Wang, Qingling
Sun, Fenfen
Hu, Minmin
Pan, Wei
Yang, Xiaoying
author_facet Cui, Zeyu
Gong, Yuying
Luo, Xiaotong
Zheng, Niuyi
Tan, Shimin
Liu, Shuxi
Li, Youwei
Wang, Qingling
Sun, Fenfen
Hu, Minmin
Pan, Wei
Yang, Xiaoying
author_sort Cui, Zeyu
collection PubMed
description BACKGROUND: Toxoplasma gondii (T. gondii) is a neuroinvasive parasite causing neuroinflammation, which in turn is associated with a higher risk for several psycho-behavioral disorders. There is an urgent need to identify drugs capable of improving cognitive deficits induced by T. gondii infection. β-Glucan, an active ingredient in mushrooms, could significantly enhance immunity. However, the effects of β-glucan against neuroinflammation and cognitive decline induced by T. gondii infection remain unknown. The present study aimed to investigate the neuroprotective effect of β-glucan on goal-directed behavior of mice chronically infected by T. gondii Wh6 strain. METHODS: A mice model of chronic T. gondii Wh6 infection was established by infecting mice by oral gavage with 10 cysts of T. gondii Wh6. Intraperitoneal injection of β-glucan was manipulated 2 weeks before T. gondii infection. Performance of the infected mice on the Y-maze test and temporal order memory (TOM) test was used to assess the goal-directed behavior. Golgi-Cox staining, transmission electron microscopy, immunofluorescence, real-time PCR and western blot assays were used to detect prefrontal cortex-associated pathological change and neuroinflammation. RESULTS: The administration of β-glucan significantly prevented T. gondii Wh6-induced goal-directed behavioral impairment as assessed behaviorally by the Y-maze test and TOM test. In the prefrontal cortex, β-glucan was able to counter T. gondii Wh6-induced degeneration of neurites, impairment of synaptic ultrastructure and decrease of pre- and postsynaptic protein levels. Also, β-glucan significantly prevented the hyperactivation of pro-inflammatory microglia and astrocytes, as well as the upregulation of proinflammatory cytokines caused by chronic T. gondii Wh6 infection. CONCLUSIONS: This study revealed that β-glucan prevents goal-directed behavioral impairment induced by chronic T. gondii infection in mice. These findings suggest that β-glucan may be an effective drug candidate to prevent T. gondii-associated psycho-behavioral disorders including goal-directed behavioral injury. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-99266252023-02-15 β-Glucan alleviates goal-directed behavioral deficits in mice infected with Toxoplasma gondii Cui, Zeyu Gong, Yuying Luo, Xiaotong Zheng, Niuyi Tan, Shimin Liu, Shuxi Li, Youwei Wang, Qingling Sun, Fenfen Hu, Minmin Pan, Wei Yang, Xiaoying Parasit Vectors Research BACKGROUND: Toxoplasma gondii (T. gondii) is a neuroinvasive parasite causing neuroinflammation, which in turn is associated with a higher risk for several psycho-behavioral disorders. There is an urgent need to identify drugs capable of improving cognitive deficits induced by T. gondii infection. β-Glucan, an active ingredient in mushrooms, could significantly enhance immunity. However, the effects of β-glucan against neuroinflammation and cognitive decline induced by T. gondii infection remain unknown. The present study aimed to investigate the neuroprotective effect of β-glucan on goal-directed behavior of mice chronically infected by T. gondii Wh6 strain. METHODS: A mice model of chronic T. gondii Wh6 infection was established by infecting mice by oral gavage with 10 cysts of T. gondii Wh6. Intraperitoneal injection of β-glucan was manipulated 2 weeks before T. gondii infection. Performance of the infected mice on the Y-maze test and temporal order memory (TOM) test was used to assess the goal-directed behavior. Golgi-Cox staining, transmission electron microscopy, immunofluorescence, real-time PCR and western blot assays were used to detect prefrontal cortex-associated pathological change and neuroinflammation. RESULTS: The administration of β-glucan significantly prevented T. gondii Wh6-induced goal-directed behavioral impairment as assessed behaviorally by the Y-maze test and TOM test. In the prefrontal cortex, β-glucan was able to counter T. gondii Wh6-induced degeneration of neurites, impairment of synaptic ultrastructure and decrease of pre- and postsynaptic protein levels. Also, β-glucan significantly prevented the hyperactivation of pro-inflammatory microglia and astrocytes, as well as the upregulation of proinflammatory cytokines caused by chronic T. gondii Wh6 infection. CONCLUSIONS: This study revealed that β-glucan prevents goal-directed behavioral impairment induced by chronic T. gondii infection in mice. These findings suggest that β-glucan may be an effective drug candidate to prevent T. gondii-associated psycho-behavioral disorders including goal-directed behavioral injury. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2023-02-13 /pmc/articles/PMC9926625/ /pubmed/36782332 http://dx.doi.org/10.1186/s13071-023-05686-4 Text en © The Author(s) 2023 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
Cui, Zeyu
Gong, Yuying
Luo, Xiaotong
Zheng, Niuyi
Tan, Shimin
Liu, Shuxi
Li, Youwei
Wang, Qingling
Sun, Fenfen
Hu, Minmin
Pan, Wei
Yang, Xiaoying
β-Glucan alleviates goal-directed behavioral deficits in mice infected with Toxoplasma gondii
title β-Glucan alleviates goal-directed behavioral deficits in mice infected with Toxoplasma gondii
title_full β-Glucan alleviates goal-directed behavioral deficits in mice infected with Toxoplasma gondii
title_fullStr β-Glucan alleviates goal-directed behavioral deficits in mice infected with Toxoplasma gondii
title_full_unstemmed β-Glucan alleviates goal-directed behavioral deficits in mice infected with Toxoplasma gondii
title_short β-Glucan alleviates goal-directed behavioral deficits in mice infected with Toxoplasma gondii
title_sort β-glucan alleviates goal-directed behavioral deficits in mice infected with toxoplasma gondii
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926625/
https://www.ncbi.nlm.nih.gov/pubmed/36782332
http://dx.doi.org/10.1186/s13071-023-05686-4
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