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Synchronized Astrocytic Ca(2+) Responses in Neurovascular Coupling during Somatosensory Stimulation and for the Resting State

The role of astrocytes in neurovascular coupling (NVC) is unclear. Here, we applied a multimodality imaging approach to concomitantly measure synchronized neuronal or astrocytic Ca(2+) and hemodynamic changes in the mouse somatosensory cortex at rest and during sensory electrical stimulation. Striki...

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Autores principales: Gu, Xiaochun, Chen, Wei, Volkow, Nora D., Koretsky, Alan P., Du, Congwu, Pan, Yingtian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469112/
https://www.ncbi.nlm.nih.gov/pubmed/29949771
http://dx.doi.org/10.1016/j.celrep.2018.05.091
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author Gu, Xiaochun
Chen, Wei
Volkow, Nora D.
Koretsky, Alan P.
Du, Congwu
Pan, Yingtian
author_facet Gu, Xiaochun
Chen, Wei
Volkow, Nora D.
Koretsky, Alan P.
Du, Congwu
Pan, Yingtian
author_sort Gu, Xiaochun
collection PubMed
description The role of astrocytes in neurovascular coupling (NVC) is unclear. Here, we applied a multimodality imaging approach to concomitantly measure synchronized neuronal or astrocytic Ca(2+) and hemodynamic changes in the mouse somatosensory cortex at rest and during sensory electrical stimulation. Strikingly, we found that low-frequency stimulation (0.3–1 Hz), which consistently evokes fast neuronal Ca(2+) transients (6.0 ± 2.7 ms latency) that always precede vascular responses, does not always elicit astrocytic Ca(2+) transients (313 ± 65 ms latency). However, the magnitude of the hemodynamic response is increased when astrocytic transients occur, suggesting a facilitatory role of astrocytes in NVC. High-frequency stimulation (5–10 Hz) consistently evokes a large, delayed astrocytic Ca(2+) accumulation (3.48 ± 0.09 s latency) that is temporarily associated with vasoconstriction, suggesting a role for astrocytes in resetting NVC. At rest, neuronal, but not astrocytic, Ca(2+) fluctuations correlate with hemodynamic low-frequency oscillations. Taken together, these results support a role for astrocytes in modulating, but not triggering, NVC.
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spelling pubmed-74691122020-09-03 Synchronized Astrocytic Ca(2+) Responses in Neurovascular Coupling during Somatosensory Stimulation and for the Resting State Gu, Xiaochun Chen, Wei Volkow, Nora D. Koretsky, Alan P. Du, Congwu Pan, Yingtian Cell Rep Article The role of astrocytes in neurovascular coupling (NVC) is unclear. Here, we applied a multimodality imaging approach to concomitantly measure synchronized neuronal or astrocytic Ca(2+) and hemodynamic changes in the mouse somatosensory cortex at rest and during sensory electrical stimulation. Strikingly, we found that low-frequency stimulation (0.3–1 Hz), which consistently evokes fast neuronal Ca(2+) transients (6.0 ± 2.7 ms latency) that always precede vascular responses, does not always elicit astrocytic Ca(2+) transients (313 ± 65 ms latency). However, the magnitude of the hemodynamic response is increased when astrocytic transients occur, suggesting a facilitatory role of astrocytes in NVC. High-frequency stimulation (5–10 Hz) consistently evokes a large, delayed astrocytic Ca(2+) accumulation (3.48 ± 0.09 s latency) that is temporarily associated with vasoconstriction, suggesting a role for astrocytes in resetting NVC. At rest, neuronal, but not astrocytic, Ca(2+) fluctuations correlate with hemodynamic low-frequency oscillations. Taken together, these results support a role for astrocytes in modulating, but not triggering, NVC. 2018-06-26 /pmc/articles/PMC7469112/ /pubmed/29949771 http://dx.doi.org/10.1016/j.celrep.2018.05.091 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Gu, Xiaochun
Chen, Wei
Volkow, Nora D.
Koretsky, Alan P.
Du, Congwu
Pan, Yingtian
Synchronized Astrocytic Ca(2+) Responses in Neurovascular Coupling during Somatosensory Stimulation and for the Resting State
title Synchronized Astrocytic Ca(2+) Responses in Neurovascular Coupling during Somatosensory Stimulation and for the Resting State
title_full Synchronized Astrocytic Ca(2+) Responses in Neurovascular Coupling during Somatosensory Stimulation and for the Resting State
title_fullStr Synchronized Astrocytic Ca(2+) Responses in Neurovascular Coupling during Somatosensory Stimulation and for the Resting State
title_full_unstemmed Synchronized Astrocytic Ca(2+) Responses in Neurovascular Coupling during Somatosensory Stimulation and for the Resting State
title_short Synchronized Astrocytic Ca(2+) Responses in Neurovascular Coupling during Somatosensory Stimulation and for the Resting State
title_sort synchronized astrocytic ca(2+) responses in neurovascular coupling during somatosensory stimulation and for the resting state
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469112/
https://www.ncbi.nlm.nih.gov/pubmed/29949771
http://dx.doi.org/10.1016/j.celrep.2018.05.091
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