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Immune system challenge improves recognition memory and reverses malaria-induced cognitive impairment in mice
The immune system plays a role in the maintenance of healthy neurocognitive function. Different patterns of immune response triggered by distinct stimuli may affect nervous functions through regulatory or deregulatory signals, depending on the properties of the exogenous immunogens. Here, we investi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295320/ https://www.ncbi.nlm.nih.gov/pubmed/34290279 http://dx.doi.org/10.1038/s41598-021-94167-8 |
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author | de Sousa, Luciana Pereira Ribeiro-Gomes, Flávia Lima de Almeida, Roberto Farina Souza, Tadeu Mello e Werneck, Guilherme Loureiro Souza, Diogo Onofre Daniel-Ribeiro, Cláudio Tadeu |
author_facet | de Sousa, Luciana Pereira Ribeiro-Gomes, Flávia Lima de Almeida, Roberto Farina Souza, Tadeu Mello e Werneck, Guilherme Loureiro Souza, Diogo Onofre Daniel-Ribeiro, Cláudio Tadeu |
author_sort | de Sousa, Luciana Pereira |
collection | PubMed |
description | The immune system plays a role in the maintenance of healthy neurocognitive function. Different patterns of immune response triggered by distinct stimuli may affect nervous functions through regulatory or deregulatory signals, depending on the properties of the exogenous immunogens. Here, we investigate the effect of immune stimulation on cognitive-behavioural parameters in healthy mice and its impact on cognitive sequelae resulting from non-severe experimental malaria. We show that immune modulation induced by a specific combination of immune stimuli that induce a type 2 immune response can enhance long-term recognition memory in healthy adult mice subjected to novel object recognition task (NORT) and reverse a lack of recognition ability in NORT and anxiety-like behaviour in a light/dark task that result from a single episode of mild Plasmodium berghei ANKA malaria. Our findings suggest a potential use of immunogens for boosting and recovering recognition memory that may be impaired by chronic and infectious diseases and by the effects of ageing. |
format | Online Article Text |
id | pubmed-8295320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82953202021-07-22 Immune system challenge improves recognition memory and reverses malaria-induced cognitive impairment in mice de Sousa, Luciana Pereira Ribeiro-Gomes, Flávia Lima de Almeida, Roberto Farina Souza, Tadeu Mello e Werneck, Guilherme Loureiro Souza, Diogo Onofre Daniel-Ribeiro, Cláudio Tadeu Sci Rep Article The immune system plays a role in the maintenance of healthy neurocognitive function. Different patterns of immune response triggered by distinct stimuli may affect nervous functions through regulatory or deregulatory signals, depending on the properties of the exogenous immunogens. Here, we investigate the effect of immune stimulation on cognitive-behavioural parameters in healthy mice and its impact on cognitive sequelae resulting from non-severe experimental malaria. We show that immune modulation induced by a specific combination of immune stimuli that induce a type 2 immune response can enhance long-term recognition memory in healthy adult mice subjected to novel object recognition task (NORT) and reverse a lack of recognition ability in NORT and anxiety-like behaviour in a light/dark task that result from a single episode of mild Plasmodium berghei ANKA malaria. Our findings suggest a potential use of immunogens for boosting and recovering recognition memory that may be impaired by chronic and infectious diseases and by the effects of ageing. Nature Publishing Group UK 2021-07-21 /pmc/articles/PMC8295320/ /pubmed/34290279 http://dx.doi.org/10.1038/s41598-021-94167-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article de Sousa, Luciana Pereira Ribeiro-Gomes, Flávia Lima de Almeida, Roberto Farina Souza, Tadeu Mello e Werneck, Guilherme Loureiro Souza, Diogo Onofre Daniel-Ribeiro, Cláudio Tadeu Immune system challenge improves recognition memory and reverses malaria-induced cognitive impairment in mice |
title | Immune system challenge improves recognition memory and reverses malaria-induced cognitive impairment in mice |
title_full | Immune system challenge improves recognition memory and reverses malaria-induced cognitive impairment in mice |
title_fullStr | Immune system challenge improves recognition memory and reverses malaria-induced cognitive impairment in mice |
title_full_unstemmed | Immune system challenge improves recognition memory and reverses malaria-induced cognitive impairment in mice |
title_short | Immune system challenge improves recognition memory and reverses malaria-induced cognitive impairment in mice |
title_sort | immune system challenge improves recognition memory and reverses malaria-induced cognitive impairment in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295320/ https://www.ncbi.nlm.nih.gov/pubmed/34290279 http://dx.doi.org/10.1038/s41598-021-94167-8 |
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