Rapid Reconfiguration of the Functional Connectome after Chemogenetic Locus Coeruleus Activation.
Animals
Anxiety
/ physiopathology
Clozapine
/ pharmacology
Connectome
Corpus Striatum
/ metabolism
Designer Drugs
/ pharmacology
Dopamine
/ metabolism
Exploratory Behavior
/ physiology
Functional Neuroimaging
Genes, fos
Locus Coeruleus
/ drug effects
Magnetic Resonance Imaging
Male
Mice
Mice, Transgenic
Nerve Net
/ physiology
Nerve Tissue Proteins
/ biosynthesis
Norepinephrine
/ metabolism
Proto-Oncogene Proteins c-fos
/ biosynthesis
Receptors, Adrenergic, alpha-1
/ biosynthesis
Receptors, Adrenergic, beta-1
/ biosynthesis
Receptors, Drug
/ physiology
Rotarod Performance Test
Up-Regulation
/ drug effects
DREADDs
anxiety
chemogenetics
functional connectivity
locus coeruleus
noradrenaline
resting-state functional magnetic resonance imaging
rs-fMRI
salience
stress
Journal
Neuron
ISSN: 1097-4199
Titre abrégé: Neuron
Pays: United States
ID NLM: 8809320
Informations de publication
Date de publication:
21 08 2019
21 08 2019
Historique:
received:
08
02
2019
revised:
15
04
2019
accepted:
21
05
2019
pubmed:
23
6
2019
medline:
29
10
2019
entrez:
23
6
2019
Statut:
ppublish
Résumé
The locus coeruleus (LC) supplies norepinephrine (NE) to the entire forebrain and regulates many fundamental brain functions. Studies in humans have suggested that strong LC activation might shift network connectivity to favor salience processing. To causally test this hypothesis, we use a mouse model to study the effect of LC stimulation on large-scale functional connectivity by combining chemogenetic activation of the LC with resting-state fMRI, an approach we term "chemo-connectomics." We show that LC activation rapidly interrupts ongoing behavior and strongly increases brain-wide connectivity, with the most profound effects in the salience and amygdala networks. Functional connectivity changes strongly correlate with transcript levels of alpha-1 and beta-1 adrenergic receptors across the brain, and functional network connectivity correlates with NE turnover within select brain regions. We propose that these changes in large-scale network connectivity are critical for optimizing neural processing in the context of increased vigilance and threat detection.
Identifiants
pubmed: 31227310
pii: S0896-6273(19)30487-8
doi: 10.1016/j.neuron.2019.05.034
pii:
doi:
Substances chimiques
Designer Drugs
0
Nerve Tissue Proteins
0
Proto-Oncogene Proteins c-fos
0
Receptors, Adrenergic, alpha-1
0
Receptors, Adrenergic, beta-1
0
Receptors, Drug
0
Clozapine
J60AR2IKIC
Dopamine
VTD58H1Z2X
Norepinephrine
X4W3ENH1CV
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
702-718.e5Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.