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Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling

Advanced physiological aging is associated with impaired cognitive performance and the inability to induce long-term potentiation (LTP), an electrophysiological correlate of memory. Here, we demonstrate in the physiologically aged, senescent mouse brain that scanning ultrasound combined with microbu...

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Autores principales: Blackmore, Daniel G., Turpin, Fabrice, Palliyaguru, Tishila, Evans, Harrison T., Chicoteau, Antony, Lee, Wendy, Pelekanos, Matthew, Nguyen, Nghia, Song, Jae, Sullivan, Robert K. P., Sah, Pankaj, Bartlett, Perry F., Götz, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760044/
https://www.ncbi.nlm.nih.gov/pubmed/34040151
http://dx.doi.org/10.1038/s41380-021-01129-7
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author Blackmore, Daniel G.
Turpin, Fabrice
Palliyaguru, Tishila
Evans, Harrison T.
Chicoteau, Antony
Lee, Wendy
Pelekanos, Matthew
Nguyen, Nghia
Song, Jae
Sullivan, Robert K. P.
Sah, Pankaj
Bartlett, Perry F.
Götz, Jürgen
author_facet Blackmore, Daniel G.
Turpin, Fabrice
Palliyaguru, Tishila
Evans, Harrison T.
Chicoteau, Antony
Lee, Wendy
Pelekanos, Matthew
Nguyen, Nghia
Song, Jae
Sullivan, Robert K. P.
Sah, Pankaj
Bartlett, Perry F.
Götz, Jürgen
author_sort Blackmore, Daniel G.
collection PubMed
description Advanced physiological aging is associated with impaired cognitive performance and the inability to induce long-term potentiation (LTP), an electrophysiological correlate of memory. Here, we demonstrate in the physiologically aged, senescent mouse brain that scanning ultrasound combined with microbubbles (SUS(+MB)), by transiently opening the blood–brain barrier, fully restores LTP induction in the dentate gyrus of the hippocampus. Intriguingly, SUS treatment without microbubbles (SUS(only)), i.e., without the uptake of blood-borne factors, proved even more effective, not only restoring LTP, but also ameliorating the spatial learning deficits of the aged mice. This functional improvement is accompanied by an altered milieu of the aged hippocampus, including a lower density of perineuronal nets, increased neurogenesis, and synaptic signaling, which collectively results in improved spatial learning. We therefore conclude that therapeutic ultrasound is a non-invasive, pleiotropic modality that may enhance cognition in elderly humans.
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spelling pubmed-87600442022-01-26 Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling Blackmore, Daniel G. Turpin, Fabrice Palliyaguru, Tishila Evans, Harrison T. Chicoteau, Antony Lee, Wendy Pelekanos, Matthew Nguyen, Nghia Song, Jae Sullivan, Robert K. P. Sah, Pankaj Bartlett, Perry F. Götz, Jürgen Mol Psychiatry Article Advanced physiological aging is associated with impaired cognitive performance and the inability to induce long-term potentiation (LTP), an electrophysiological correlate of memory. Here, we demonstrate in the physiologically aged, senescent mouse brain that scanning ultrasound combined with microbubbles (SUS(+MB)), by transiently opening the blood–brain barrier, fully restores LTP induction in the dentate gyrus of the hippocampus. Intriguingly, SUS treatment without microbubbles (SUS(only)), i.e., without the uptake of blood-borne factors, proved even more effective, not only restoring LTP, but also ameliorating the spatial learning deficits of the aged mice. This functional improvement is accompanied by an altered milieu of the aged hippocampus, including a lower density of perineuronal nets, increased neurogenesis, and synaptic signaling, which collectively results in improved spatial learning. We therefore conclude that therapeutic ultrasound is a non-invasive, pleiotropic modality that may enhance cognition in elderly humans. Nature Publishing Group UK 2021-05-27 2021 /pmc/articles/PMC8760044/ /pubmed/34040151 http://dx.doi.org/10.1038/s41380-021-01129-7 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Blackmore, Daniel G.
Turpin, Fabrice
Palliyaguru, Tishila
Evans, Harrison T.
Chicoteau, Antony
Lee, Wendy
Pelekanos, Matthew
Nguyen, Nghia
Song, Jae
Sullivan, Robert K. P.
Sah, Pankaj
Bartlett, Perry F.
Götz, Jürgen
Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling
title Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling
title_full Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling
title_fullStr Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling
title_full_unstemmed Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling
title_short Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling
title_sort low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including nmdar signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760044/
https://www.ncbi.nlm.nih.gov/pubmed/34040151
http://dx.doi.org/10.1038/s41380-021-01129-7
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