Cargando…

Simultaneous CMOS-Based Imaging of Calcium Signaling of the Central Amygdala and the Dorsal Raphe Nucleus During Nociception in Freely Moving Mice

Fluorescence imaging devices have been indispensable in elucidating the workings of the brain in living animals, including unrestrained, active ones. Various devices are available, each with their own strengths and weaknesses in terms of many factors. We have developed CMOS-based needle-type imaging...

Descripción completa

Detalles Bibliográficos
Autores principales: Rebusi, Romeo, Olorocisimo, Joshua Philippe, Briones, Jeric, Ohta, Yasumi, Haruta, Makito, Takehara, Hironari, Tashiro, Hiroyuki, Sasagawa, Kiyotaka, Ohta, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202083/
https://www.ncbi.nlm.nih.gov/pubmed/34135728
http://dx.doi.org/10.3389/fnins.2021.667708
_version_ 1783707914237640704
author Rebusi, Romeo
Olorocisimo, Joshua Philippe
Briones, Jeric
Ohta, Yasumi
Haruta, Makito
Takehara, Hironari
Tashiro, Hiroyuki
Sasagawa, Kiyotaka
Ohta, Jun
author_facet Rebusi, Romeo
Olorocisimo, Joshua Philippe
Briones, Jeric
Ohta, Yasumi
Haruta, Makito
Takehara, Hironari
Tashiro, Hiroyuki
Sasagawa, Kiyotaka
Ohta, Jun
author_sort Rebusi, Romeo
collection PubMed
description Fluorescence imaging devices have been indispensable in elucidating the workings of the brain in living animals, including unrestrained, active ones. Various devices are available, each with their own strengths and weaknesses in terms of many factors. We have developed CMOS-based needle-type imaging devices that are small and lightweight enough to be doubly implanted in freely moving mice. The design also allowed angled implantations to avoid critical areas. We demonstrated the utility of the devices by using them on GCaMP6 mice in a formalin test experiment. Simultaneous implantations to the capsular-lateral central amygdala (CeLC) and dorsal raphe nucleus (DRN) were proven to be safe and did not hinder the execution of the study. Analysis of the collected calcium signaling data, supported by behavior data, showed increased activity in both regions as a result of pain stimulation. Thus, we have successfully demonstrated the various advantages of the device in its application in the pain experiment.
format Online
Article
Text
id pubmed-8202083
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-82020832021-06-15 Simultaneous CMOS-Based Imaging of Calcium Signaling of the Central Amygdala and the Dorsal Raphe Nucleus During Nociception in Freely Moving Mice Rebusi, Romeo Olorocisimo, Joshua Philippe Briones, Jeric Ohta, Yasumi Haruta, Makito Takehara, Hironari Tashiro, Hiroyuki Sasagawa, Kiyotaka Ohta, Jun Front Neurosci Neuroscience Fluorescence imaging devices have been indispensable in elucidating the workings of the brain in living animals, including unrestrained, active ones. Various devices are available, each with their own strengths and weaknesses in terms of many factors. We have developed CMOS-based needle-type imaging devices that are small and lightweight enough to be doubly implanted in freely moving mice. The design also allowed angled implantations to avoid critical areas. We demonstrated the utility of the devices by using them on GCaMP6 mice in a formalin test experiment. Simultaneous implantations to the capsular-lateral central amygdala (CeLC) and dorsal raphe nucleus (DRN) were proven to be safe and did not hinder the execution of the study. Analysis of the collected calcium signaling data, supported by behavior data, showed increased activity in both regions as a result of pain stimulation. Thus, we have successfully demonstrated the various advantages of the device in its application in the pain experiment. Frontiers Media S.A. 2021-05-21 /pmc/articles/PMC8202083/ /pubmed/34135728 http://dx.doi.org/10.3389/fnins.2021.667708 Text en Copyright © 2021 Rebusi, Olorocisimo, Briones, Ohta, Haruta, Takehara, Tashiro, Sasagawa and Ohta. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Rebusi, Romeo
Olorocisimo, Joshua Philippe
Briones, Jeric
Ohta, Yasumi
Haruta, Makito
Takehara, Hironari
Tashiro, Hiroyuki
Sasagawa, Kiyotaka
Ohta, Jun
Simultaneous CMOS-Based Imaging of Calcium Signaling of the Central Amygdala and the Dorsal Raphe Nucleus During Nociception in Freely Moving Mice
title Simultaneous CMOS-Based Imaging of Calcium Signaling of the Central Amygdala and the Dorsal Raphe Nucleus During Nociception in Freely Moving Mice
title_full Simultaneous CMOS-Based Imaging of Calcium Signaling of the Central Amygdala and the Dorsal Raphe Nucleus During Nociception in Freely Moving Mice
title_fullStr Simultaneous CMOS-Based Imaging of Calcium Signaling of the Central Amygdala and the Dorsal Raphe Nucleus During Nociception in Freely Moving Mice
title_full_unstemmed Simultaneous CMOS-Based Imaging of Calcium Signaling of the Central Amygdala and the Dorsal Raphe Nucleus During Nociception in Freely Moving Mice
title_short Simultaneous CMOS-Based Imaging of Calcium Signaling of the Central Amygdala and the Dorsal Raphe Nucleus During Nociception in Freely Moving Mice
title_sort simultaneous cmos-based imaging of calcium signaling of the central amygdala and the dorsal raphe nucleus during nociception in freely moving mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202083/
https://www.ncbi.nlm.nih.gov/pubmed/34135728
http://dx.doi.org/10.3389/fnins.2021.667708
work_keys_str_mv AT rebusiromeo simultaneouscmosbasedimagingofcalciumsignalingofthecentralamygdalaandthedorsalraphenucleusduringnociceptioninfreelymovingmice
AT olorocisimojoshuaphilippe simultaneouscmosbasedimagingofcalciumsignalingofthecentralamygdalaandthedorsalraphenucleusduringnociceptioninfreelymovingmice
AT brionesjeric simultaneouscmosbasedimagingofcalciumsignalingofthecentralamygdalaandthedorsalraphenucleusduringnociceptioninfreelymovingmice
AT ohtayasumi simultaneouscmosbasedimagingofcalciumsignalingofthecentralamygdalaandthedorsalraphenucleusduringnociceptioninfreelymovingmice
AT harutamakito simultaneouscmosbasedimagingofcalciumsignalingofthecentralamygdalaandthedorsalraphenucleusduringnociceptioninfreelymovingmice
AT takeharahironari simultaneouscmosbasedimagingofcalciumsignalingofthecentralamygdalaandthedorsalraphenucleusduringnociceptioninfreelymovingmice
AT tashirohiroyuki simultaneouscmosbasedimagingofcalciumsignalingofthecentralamygdalaandthedorsalraphenucleusduringnociceptioninfreelymovingmice
AT sasagawakiyotaka simultaneouscmosbasedimagingofcalciumsignalingofthecentralamygdalaandthedorsalraphenucleusduringnociceptioninfreelymovingmice
AT ohtajun simultaneouscmosbasedimagingofcalciumsignalingofthecentralamygdalaandthedorsalraphenucleusduringnociceptioninfreelymovingmice