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Multisensory Stimulation Reverses Memory Impairment in Adrβ(3)KO Male Mice

Norepinephrine plays an important role in modulating memory through its beta-adrenergic receptors (Adrβ: β(1), β(2) and β(3)). Here, we hypothesized that multisensory stimulation would reverse memory impairment caused by the inactivation of Adrβ(3) (Adrβ(3)KO) with consequent inhibition of sustained...

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Autores principales: Ravache, Thaís T., Batistuzzo, Alice, Nunes, Gabriela G., Gomez, Thiago G. B., Lorena, Fernanda B., Do Nascimento, Bruna P. P., Bernardi, Maria Martha, Lima, Eduarda R. R., Martins, Daniel O., Campos, Ana Carolina P., Pagano, Rosana L., Ribeiro, Miriam O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10342067/
https://www.ncbi.nlm.nih.gov/pubmed/37445699
http://dx.doi.org/10.3390/ijms241310522
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author Ravache, Thaís T.
Batistuzzo, Alice
Nunes, Gabriela G.
Gomez, Thiago G. B.
Lorena, Fernanda B.
Do Nascimento, Bruna P. P.
Bernardi, Maria Martha
Lima, Eduarda R. R.
Martins, Daniel O.
Campos, Ana Carolina P.
Pagano, Rosana L.
Ribeiro, Miriam O.
author_facet Ravache, Thaís T.
Batistuzzo, Alice
Nunes, Gabriela G.
Gomez, Thiago G. B.
Lorena, Fernanda B.
Do Nascimento, Bruna P. P.
Bernardi, Maria Martha
Lima, Eduarda R. R.
Martins, Daniel O.
Campos, Ana Carolina P.
Pagano, Rosana L.
Ribeiro, Miriam O.
author_sort Ravache, Thaís T.
collection PubMed
description Norepinephrine plays an important role in modulating memory through its beta-adrenergic receptors (Adrβ: β(1), β(2) and β(3)). Here, we hypothesized that multisensory stimulation would reverse memory impairment caused by the inactivation of Adrβ(3) (Adrβ(3)KO) with consequent inhibition of sustained glial-mediated inflammation. To test this, 21- and 86-day-old Adrβ(3)KO mice were exposed to an 8-week multisensory stimulation (MS) protocol that comprised gustatory and olfactory stimuli of positive and negative valence; intellectual challenges to reach food; the use of hidden objects; and the presentation of food in ways that prompted foraging, which was followed by analysis of GFAP, Iba-1 and EAAT2 protein expression in the hippocampus (HC) and amygdala (AMY). The MS protocol reduced GFAP and Iba-1 expression in the HC of young mice but not in older mice. While this protocol restored memory impairment when applied to Adrβ(3)KO animals immediately after weaning, it had no effect when applied to adult animals. In fact, we observed that aging worsened the memory of Adrβ(3)KO mice. In the AMY of Adrβ3KO older mice, we observed an increase in GFAP and EAAT2 expression when compared to wild-type (WT) mice that MS was unable to reduce. These results suggest that a richer and more diverse environment helps to correct memory impairment when applied immediately after weaning in Adrβ(3)KO animals and indicates that the control of neuroinflammation mediates this response.
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spelling pubmed-103420672023-07-14 Multisensory Stimulation Reverses Memory Impairment in Adrβ(3)KO Male Mice Ravache, Thaís T. Batistuzzo, Alice Nunes, Gabriela G. Gomez, Thiago G. B. Lorena, Fernanda B. Do Nascimento, Bruna P. P. Bernardi, Maria Martha Lima, Eduarda R. R. Martins, Daniel O. Campos, Ana Carolina P. Pagano, Rosana L. Ribeiro, Miriam O. Int J Mol Sci Article Norepinephrine plays an important role in modulating memory through its beta-adrenergic receptors (Adrβ: β(1), β(2) and β(3)). Here, we hypothesized that multisensory stimulation would reverse memory impairment caused by the inactivation of Adrβ(3) (Adrβ(3)KO) with consequent inhibition of sustained glial-mediated inflammation. To test this, 21- and 86-day-old Adrβ(3)KO mice were exposed to an 8-week multisensory stimulation (MS) protocol that comprised gustatory and olfactory stimuli of positive and negative valence; intellectual challenges to reach food; the use of hidden objects; and the presentation of food in ways that prompted foraging, which was followed by analysis of GFAP, Iba-1 and EAAT2 protein expression in the hippocampus (HC) and amygdala (AMY). The MS protocol reduced GFAP and Iba-1 expression in the HC of young mice but not in older mice. While this protocol restored memory impairment when applied to Adrβ(3)KO animals immediately after weaning, it had no effect when applied to adult animals. In fact, we observed that aging worsened the memory of Adrβ(3)KO mice. In the AMY of Adrβ3KO older mice, we observed an increase in GFAP and EAAT2 expression when compared to wild-type (WT) mice that MS was unable to reduce. These results suggest that a richer and more diverse environment helps to correct memory impairment when applied immediately after weaning in Adrβ(3)KO animals and indicates that the control of neuroinflammation mediates this response. MDPI 2023-06-23 /pmc/articles/PMC10342067/ /pubmed/37445699 http://dx.doi.org/10.3390/ijms241310522 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ravache, Thaís T.
Batistuzzo, Alice
Nunes, Gabriela G.
Gomez, Thiago G. B.
Lorena, Fernanda B.
Do Nascimento, Bruna P. P.
Bernardi, Maria Martha
Lima, Eduarda R. R.
Martins, Daniel O.
Campos, Ana Carolina P.
Pagano, Rosana L.
Ribeiro, Miriam O.
Multisensory Stimulation Reverses Memory Impairment in Adrβ(3)KO Male Mice
title Multisensory Stimulation Reverses Memory Impairment in Adrβ(3)KO Male Mice
title_full Multisensory Stimulation Reverses Memory Impairment in Adrβ(3)KO Male Mice
title_fullStr Multisensory Stimulation Reverses Memory Impairment in Adrβ(3)KO Male Mice
title_full_unstemmed Multisensory Stimulation Reverses Memory Impairment in Adrβ(3)KO Male Mice
title_short Multisensory Stimulation Reverses Memory Impairment in Adrβ(3)KO Male Mice
title_sort multisensory stimulation reverses memory impairment in adrβ(3)ko male mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10342067/
https://www.ncbi.nlm.nih.gov/pubmed/37445699
http://dx.doi.org/10.3390/ijms241310522
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