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Cholinergic and serotonergic modulations differentially affect large-scale functional networks in the mouse brain
Resting-state functional MRI (rsfMRI) is a widely implemented technique used to investigate large-scale topology in the human brain during health and disease. Studies in mice provide additional advantages, including the possibility to flexibly modulate the brain by pharmacological or genetic manipul...
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Published in: | Brain Structure and Function 2016-07, Vol.221 (6), p.3067-3079 |
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container_title | Brain Structure and Function |
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creator | Shah, Disha Blockx, Ines Keliris, Georgios A. Kara, Firat Jonckers, Elisabeth Verhoye, Marleen Van der Linden, Annemie |
description | Resting-state functional MRI (rsfMRI) is a widely implemented technique used to investigate large-scale topology in the human brain during health and disease. Studies in mice provide additional advantages, including the possibility to flexibly modulate the brain by pharmacological or genetic manipulations in combination with high-throughput functional connectivity (FC) investigations. Pharmacological modulations that target specific neurotransmitter systems, partly mimicking the effect of pathological events, could allow discriminating the effect of specific systems on functional network disruptions. The current study investigated the effect of cholinergic and serotonergic antagonists on large-scale brain networks in mice. The cholinergic system is involved in cognitive functions and is impaired in, e.g., Alzheimer’s disease, while the serotonergic system is involved in emotional and introspective functions and is impaired in, e.g., Alzheimer’s disease, depression and autism. Specific interest goes to the default-mode-network (DMN), which is studied extensively in humans and is affected in many neurological disorders. The results show that both cholinergic and serotonergic antagonists impaired the mouse DMN-like network similarly, except that cholinergic modulation additionally affected the retrosplenial cortex. This suggests that both neurotransmitter systems are involved in maintaining integrity of FC within the DMN-like network in mice. Cholinergic and serotonergic modulations also affected other functional networks, however, serotonergic modulation impaired the frontal and thalamus networks more extensively. In conclusion, this study demonstrates the utility of pharmacological rsfMRI in animal models to provide insights into the role of specific neurotransmitter systems on functional networks in neurological disorders. |
doi_str_mv | 10.1007/s00429-015-1087-7 |
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Studies in mice provide additional advantages, including the possibility to flexibly modulate the brain by pharmacological or genetic manipulations in combination with high-throughput functional connectivity (FC) investigations. Pharmacological modulations that target specific neurotransmitter systems, partly mimicking the effect of pathological events, could allow discriminating the effect of specific systems on functional network disruptions. The current study investigated the effect of cholinergic and serotonergic antagonists on large-scale brain networks in mice. The cholinergic system is involved in cognitive functions and is impaired in, e.g., Alzheimer’s disease, while the serotonergic system is involved in emotional and introspective functions and is impaired in, e.g., Alzheimer’s disease, depression and autism. Specific interest goes to the default-mode-network (DMN), which is studied extensively in humans and is affected in many neurological disorders. The results show that both cholinergic and serotonergic antagonists impaired the mouse DMN-like network similarly, except that cholinergic modulation additionally affected the retrosplenial cortex. This suggests that both neurotransmitter systems are involved in maintaining integrity of FC within the DMN-like network in mice. Cholinergic and serotonergic modulations also affected other functional networks, however, serotonergic modulation impaired the frontal and thalamus networks more extensively. In conclusion, this study demonstrates the utility of pharmacological rsfMRI in animal models to provide insights into the role of specific neurotransmitter systems on functional networks in neurological disorders.</description><identifier>ISSN: 1863-2653</identifier><identifier>EISSN: 1863-2661</identifier><identifier>EISSN: 0340-2061</identifier><identifier>DOI: 10.1007/s00429-015-1087-7</identifier><identifier>PMID: 26195064</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject><![CDATA[Acetylcholine - physiology ; Animals ; Biomedical and Life Sciences ; Biomedicine ; Brain ; Brain - drug effects ; Brain - physiology ; Brain Mapping ; Cell Biology ; Hypnotics and Sedatives - administration & dosage ; Magnetic Resonance Imaging ; Male ; Medetomidine - administration & dosage ; Mice ; Mice, Inbred C57BL ; Muscarinic Antagonists - administration & dosage ; Neural Pathways - drug effects ; Neural Pathways - physiology ; Neurology ; Neurosciences ; NMR ; Nuclear magnetic resonance ; Original Article ; Piperazines - administration & dosage ; Receptors, Muscarinic - physiology ; Receptors, Serotonin - physiology ; Rodents ; Scopolamine Hydrobromide - administration & dosage ; Serotonin - physiology ; Serotonin Antagonists - administration & dosage]]></subject><ispartof>Brain Structure and Function, 2016-07, Vol.221 (6), p.3067-3079</ispartof><rights>Springer-Verlag Berlin Heidelberg 2015</rights><rights>Springer-Verlag Berlin Heidelberg 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-a83165fe3603752221de220381793cfb38276db2d7d5e32629f8b3b6c959a9233</citedby><cites>FETCH-LOGICAL-c471t-a83165fe3603752221de220381793cfb38276db2d7d5e32629f8b3b6c959a9233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26195064$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shah, Disha</creatorcontrib><creatorcontrib>Blockx, Ines</creatorcontrib><creatorcontrib>Keliris, Georgios A.</creatorcontrib><creatorcontrib>Kara, Firat</creatorcontrib><creatorcontrib>Jonckers, Elisabeth</creatorcontrib><creatorcontrib>Verhoye, Marleen</creatorcontrib><creatorcontrib>Van der Linden, Annemie</creatorcontrib><title>Cholinergic and serotonergic modulations differentially affect large-scale functional networks in the mouse brain</title><title>Brain Structure and Function</title><addtitle>Brain Struct Funct</addtitle><addtitle>Brain Struct Funct</addtitle><description>Resting-state functional MRI (rsfMRI) is a widely implemented technique used to investigate large-scale topology in the human brain during health and disease. 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The results show that both cholinergic and serotonergic antagonists impaired the mouse DMN-like network similarly, except that cholinergic modulation additionally affected the retrosplenial cortex. This suggests that both neurotransmitter systems are involved in maintaining integrity of FC within the DMN-like network in mice. Cholinergic and serotonergic modulations also affected other functional networks, however, serotonergic modulation impaired the frontal and thalamus networks more extensively. In conclusion, this study demonstrates the utility of pharmacological rsfMRI in animal models to provide insights into the role of specific neurotransmitter systems on functional networks in neurological disorders.</description><subject>Acetylcholine - physiology</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain</subject><subject>Brain - drug effects</subject><subject>Brain - physiology</subject><subject>Brain Mapping</subject><subject>Cell Biology</subject><subject>Hypnotics and Sedatives - administration & dosage</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medetomidine - administration & dosage</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Muscarinic Antagonists - administration & dosage</subject><subject>Neural Pathways - drug effects</subject><subject>Neural Pathways - physiology</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Original Article</subject><subject>Piperazines - administration & dosage</subject><subject>Receptors, Muscarinic - physiology</subject><subject>Receptors, Serotonin - physiology</subject><subject>Rodents</subject><subject>Scopolamine Hydrobromide - administration & dosage</subject><subject>Serotonin - physiology</subject><subject>Serotonin Antagonists - administration & dosage</subject><issn>1863-2653</issn><issn>1863-2661</issn><issn>0340-2061</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkU1rHSEUhqWkNB_tD-imCNl0M60f49eyXJImEOimXYvjnLkx9WqiM5T8-3iZm1AKJSuPnsfXIw9CHyn5QglRXyshPTMdoaKjRKtOvUEnVEveMSnp0Ust-DE6rfWOEGE0Ne_QMZPUCCL7E_Swuc0xJCjb4LFLI65Q8pwPB7s8LtHNIaeKxzBNUCDNwcX4iF3b-RlHV7bQVe8i4GlJfs-6iBPMf3L5XXFIeL6FFrRUwENxIb1HbycXK3w4rGfo1-XFz81Vd_Pj-_Xm203ne0XnzmlOpZiAS8KVYIzRERgjXFNluJ8GrpmS48BGNQrgTDIz6YEP0hthnGGcn6HPa-59yQ8L1NnuQvUQo0vQprFUEy11L4l6HVXGCKEpEQ09_we9y0tpX14pznRPdKPoSvmSay0w2fsSdq48WkrsXp1d1dmmzu7V2f0Qnw7Jy7CD8eXGs6sGsBWorZW2UP56-r-pT37yo9o</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Shah, Disha</creator><creator>Blockx, Ines</creator><creator>Keliris, Georgios A.</creator><creator>Kara, Firat</creator><creator>Jonckers, Elisabeth</creator><creator>Verhoye, Marleen</creator><creator>Van der Linden, Annemie</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20160701</creationdate><title>Cholinergic and serotonergic modulations differentially affect large-scale functional networks in the mouse brain</title><author>Shah, Disha ; Blockx, Ines ; Keliris, Georgios A. ; Kara, Firat ; Jonckers, Elisabeth ; Verhoye, Marleen ; Van der Linden, Annemie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-a83165fe3603752221de220381793cfb38276db2d7d5e32629f8b3b6c959a9233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acetylcholine - 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subjects | Acetylcholine - physiology Animals Biomedical and Life Sciences Biomedicine Brain Brain - drug effects Brain - physiology Brain Mapping Cell Biology Hypnotics and Sedatives - administration & dosage Magnetic Resonance Imaging Male Medetomidine - administration & dosage Mice Mice, Inbred C57BL Muscarinic Antagonists - administration & dosage Neural Pathways - drug effects Neural Pathways - physiology Neurology Neurosciences NMR Nuclear magnetic resonance Original Article Piperazines - administration & dosage Receptors, Muscarinic - physiology Receptors, Serotonin - physiology Rodents Scopolamine Hydrobromide - administration & dosage Serotonin - physiology Serotonin Antagonists - administration & dosage |
title | Cholinergic and serotonergic modulations differentially affect large-scale functional networks in the mouse brain |
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