Cargando…

The neural basis of resting-state fMRI functional connectivity in fronto-limbic circuits revealed by chemogenetic manipulation

Measures of fMRI resting-state functional connectivity (rs-FC) are an essential tool for basic and clinical investigations of fronto-limbic circuits. Understanding the relationship between rs-FC and neural activity in these circuits is therefore vital. Here we introduced inhibitory designer receptor...

Descripción completa

Detalles Bibliográficos
Autores principales: Elorette, Catherine, Fujimoto, Atsushi, Stoll, Frederic M., Fujimoto, Satoka H., Fleysher, Lazar, Bienkowska, Niranjana, Russ, Brian E., Rudebeck, Peter H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515745/
https://www.ncbi.nlm.nih.gov/pubmed/37745436
http://dx.doi.org/10.1101/2023.06.21.545778
_version_ 1785109012063191040
author Elorette, Catherine
Fujimoto, Atsushi
Stoll, Frederic M.
Fujimoto, Satoka H.
Fleysher, Lazar
Bienkowska, Niranjana
Russ, Brian E.
Rudebeck, Peter H.
author_facet Elorette, Catherine
Fujimoto, Atsushi
Stoll, Frederic M.
Fujimoto, Satoka H.
Fleysher, Lazar
Bienkowska, Niranjana
Russ, Brian E.
Rudebeck, Peter H.
author_sort Elorette, Catherine
collection PubMed
description Measures of fMRI resting-state functional connectivity (rs-FC) are an essential tool for basic and clinical investigations of fronto-limbic circuits. Understanding the relationship between rs-FC and neural activity in these circuits is therefore vital. Here we introduced inhibitory designer receptors exclusively activated by designer drugs (DREADDs) into the macaque amygdala and activated them with a highly selective and potent DREADD agonist, deschloroclozapine. We evaluated the causal effect of activating the DREADD receptors on rs-FC and neural activity within circuits connecting amygdala and frontal cortex. Interestingly, activating the inhibitory DREADD increased rs-FC between amygdala and ventrolateral prefrontal cortex. Neurophysiological recordings revealed that the DREADD-induced increase in fMRI rs-FC was associated with increased local field potential coherency in the alpha band (6.5–14.5Hz) between amygdala and ventrolateral prefrontal cortex. Thus, our multi-disciplinary approach reveals the specific signature of neuronal activity that underlies rs-FC in fronto-limbic circuits.
format Online
Article
Text
id pubmed-10515745
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-105157452023-09-23 The neural basis of resting-state fMRI functional connectivity in fronto-limbic circuits revealed by chemogenetic manipulation Elorette, Catherine Fujimoto, Atsushi Stoll, Frederic M. Fujimoto, Satoka H. Fleysher, Lazar Bienkowska, Niranjana Russ, Brian E. Rudebeck, Peter H. bioRxiv Article Measures of fMRI resting-state functional connectivity (rs-FC) are an essential tool for basic and clinical investigations of fronto-limbic circuits. Understanding the relationship between rs-FC and neural activity in these circuits is therefore vital. Here we introduced inhibitory designer receptors exclusively activated by designer drugs (DREADDs) into the macaque amygdala and activated them with a highly selective and potent DREADD agonist, deschloroclozapine. We evaluated the causal effect of activating the DREADD receptors on rs-FC and neural activity within circuits connecting amygdala and frontal cortex. Interestingly, activating the inhibitory DREADD increased rs-FC between amygdala and ventrolateral prefrontal cortex. Neurophysiological recordings revealed that the DREADD-induced increase in fMRI rs-FC was associated with increased local field potential coherency in the alpha band (6.5–14.5Hz) between amygdala and ventrolateral prefrontal cortex. Thus, our multi-disciplinary approach reveals the specific signature of neuronal activity that underlies rs-FC in fronto-limbic circuits. Cold Spring Harbor Laboratory 2023-09-15 /pmc/articles/PMC10515745/ /pubmed/37745436 http://dx.doi.org/10.1101/2023.06.21.545778 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Elorette, Catherine
Fujimoto, Atsushi
Stoll, Frederic M.
Fujimoto, Satoka H.
Fleysher, Lazar
Bienkowska, Niranjana
Russ, Brian E.
Rudebeck, Peter H.
The neural basis of resting-state fMRI functional connectivity in fronto-limbic circuits revealed by chemogenetic manipulation
title The neural basis of resting-state fMRI functional connectivity in fronto-limbic circuits revealed by chemogenetic manipulation
title_full The neural basis of resting-state fMRI functional connectivity in fronto-limbic circuits revealed by chemogenetic manipulation
title_fullStr The neural basis of resting-state fMRI functional connectivity in fronto-limbic circuits revealed by chemogenetic manipulation
title_full_unstemmed The neural basis of resting-state fMRI functional connectivity in fronto-limbic circuits revealed by chemogenetic manipulation
title_short The neural basis of resting-state fMRI functional connectivity in fronto-limbic circuits revealed by chemogenetic manipulation
title_sort neural basis of resting-state fmri functional connectivity in fronto-limbic circuits revealed by chemogenetic manipulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515745/
https://www.ncbi.nlm.nih.gov/pubmed/37745436
http://dx.doi.org/10.1101/2023.06.21.545778
work_keys_str_mv AT elorettecatherine theneuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT fujimotoatsushi theneuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT stollfredericm theneuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT fujimotosatokah theneuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT fleysherlazar theneuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT bienkowskaniranjana theneuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT russbriane theneuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT rudebeckpeterh theneuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT elorettecatherine neuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT fujimotoatsushi neuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT stollfredericm neuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT fujimotosatokah neuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT fleysherlazar neuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT bienkowskaniranjana neuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT russbriane neuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation
AT rudebeckpeterh neuralbasisofrestingstatefmrifunctionalconnectivityinfrontolimbiccircuitsrevealedbychemogeneticmanipulation