Increased cortical neuronal responses to NMDA and improved attentional set-shifting performance in rats following prebiotic (B-GOS®) ingestion
We have previously shown that prebiotics (dietary fibres that augment the growth of indigenous beneficial gut bacteria) such as Bimuno™ galacto-oligosaccharides (B-GOS®), increased N-methyl-D-aspartate (NMDA) receptor levels in the rat brain. The current investigation examined the functional correla...
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description | We have previously shown that prebiotics (dietary fibres that augment the growth of indigenous beneficial gut bacteria) such as Bimuno™ galacto-oligosaccharides (B-GOS®), increased N-methyl-D-aspartate (NMDA) receptor levels in the rat brain. The current investigation examined the functional correlates of these changes in B-GOS®-fed rats by measuring cortical neuronal responses to NMDA using in vivo NMDA micro-iontophoresis electrophysiology, and performance in the attentional set-shifting task. Adult male rats were supplemented with B-GOS® in the drinking water 3 weeks prior to in vivo iontophoresis or behavioural testing. Cortical neuronal responses to NMDA iontophoresis, were greater (+30%) in B-GOS® administered rats compared to non-supplemented controls. The intake of B-GOS® also partially hindered the reduction of NMDA responses by the glycine site antagonist, HA-966. In the attentional set-shifting task, B-GOS® -fed rats shifted from an intra-dimensional to an extra-dimensional set in fewer trials than controls, thereby indicating greater cognitive flexibility. An initial exploration into the mechanisms revealed that rats ingesting B-GOS® had increased levels of plasma acetate, and cortical GluN2B subunits and Acetyl Co-A Carboxylase mRNA. These changes were also observed in rats fed daily for 3 weeks with glyceryl triacetate, though unlike B-GOS®, cortical histone deacetylase (HDAC1, HDAC2) mRNAs were also increased which suggested an additional epigenetic action of direct acetate supplementation. Our data demonstrate that a pro-cognitive effect of B-GOS® intake in rats is associated with an increase in cortical NMDA receptor function, but the role of circulating acetate derived from gut bacterial fermentation of this prebiotic requires further investigation. |
doi_str_mv | 10.1016/j.euroneuro.2017.11.001 |
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The current investigation examined the functional correlates of these changes in B-GOS®-fed rats by measuring cortical neuronal responses to NMDA using in vivo NMDA micro-iontophoresis electrophysiology, and performance in the attentional set-shifting task. Adult male rats were supplemented with B-GOS® in the drinking water 3 weeks prior to in vivo iontophoresis or behavioural testing. Cortical neuronal responses to NMDA iontophoresis, were greater (+30%) in B-GOS® administered rats compared to non-supplemented controls. The intake of B-GOS® also partially hindered the reduction of NMDA responses by the glycine site antagonist, HA-966. In the attentional set-shifting task, B-GOS® -fed rats shifted from an intra-dimensional to an extra-dimensional set in fewer trials than controls, thereby indicating greater cognitive flexibility. An initial exploration into the mechanisms revealed that rats ingesting B-GOS® had increased levels of plasma acetate, and cortical GluN2B subunits and Acetyl Co-A Carboxylase mRNA. These changes were also observed in rats fed daily for 3 weeks with glyceryl triacetate, though unlike B-GOS®, cortical histone deacetylase (HDAC1, HDAC2) mRNAs were also increased which suggested an additional epigenetic action of direct acetate supplementation. Our data demonstrate that a pro-cognitive effect of B-GOS® intake in rats is associated with an increase in cortical NMDA receptor function, but the role of circulating acetate derived from gut bacterial fermentation of this prebiotic requires further investigation.</description><identifier>ISSN: 0924-977X</identifier><identifier>EISSN: 1873-7862</identifier><identifier>DOI: 10.1016/j.euroneuro.2017.11.001</identifier><identifier>PMID: 29174530</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Attention - physiology ; Cerebral Cortex - drug effects ; Cerebral Cortex - metabolism ; Cognition ; Dietary Supplements ; Electrophysiology ; Executive Function - physiology ; Glutamate ; Male ; Membrane Potentials - drug effects ; Membrane Potentials - physiology ; Microbiota ; N-Methylaspartate - metabolism ; Neurons - drug effects ; Neurons - metabolism ; Neurotransmitter Agents - pharmacology ; Prebiotics - administration & dosage ; Random Allocation ; Rats, Sprague-Dawley ; Short-chain fatty acid ; Triglycerides - administration & dosage</subject><ispartof>European neuropsychopharmacology, 2018-01, Vol.28 (1), p.211-224</ispartof><rights>2018 The Authors</rights><rights>Copyright © 2017 Elsevier B.V. and ECNP. All rights reserved.</rights><rights>2017 The Authors. Published by Elsevier B.V. 2017 Elsevier B.V. and ECNP</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-5bcb9552d8ce62482ceeb17d5a90cb90523f2fb7c8550470cc2d2c2c24a9d1e23</citedby><cites>FETCH-LOGICAL-c475t-5bcb9552d8ce62482ceeb17d5a90cb90523f2fb7c8550470cc2d2c2c24a9d1e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.euroneuro.2017.11.001$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,777,781,882,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29174530$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gronier, Benjamin</creatorcontrib><creatorcontrib>Savignac, Helene M.</creatorcontrib><creatorcontrib>Di Miceli, Mathieu</creatorcontrib><creatorcontrib>Idriss, Sherif M.</creatorcontrib><creatorcontrib>Tzortzis, George</creatorcontrib><creatorcontrib>Anthony, Daniel</creatorcontrib><creatorcontrib>Burnet, Philip W.J.</creatorcontrib><title>Increased cortical neuronal responses to NMDA and improved attentional set-shifting performance in rats following prebiotic (B-GOS®) ingestion</title><title>European neuropsychopharmacology</title><addtitle>Eur Neuropsychopharmacol</addtitle><description>We have previously shown that prebiotics (dietary fibres that augment the growth of indigenous beneficial gut bacteria) such as Bimuno™ galacto-oligosaccharides (B-GOS®), increased N-methyl-D-aspartate (NMDA) receptor levels in the rat brain. The current investigation examined the functional correlates of these changes in B-GOS®-fed rats by measuring cortical neuronal responses to NMDA using in vivo NMDA micro-iontophoresis electrophysiology, and performance in the attentional set-shifting task. Adult male rats were supplemented with B-GOS® in the drinking water 3 weeks prior to in vivo iontophoresis or behavioural testing. Cortical neuronal responses to NMDA iontophoresis, were greater (+30%) in B-GOS® administered rats compared to non-supplemented controls. The intake of B-GOS® also partially hindered the reduction of NMDA responses by the glycine site antagonist, HA-966. In the attentional set-shifting task, B-GOS® -fed rats shifted from an intra-dimensional to an extra-dimensional set in fewer trials than controls, thereby indicating greater cognitive flexibility. An initial exploration into the mechanisms revealed that rats ingesting B-GOS® had increased levels of plasma acetate, and cortical GluN2B subunits and Acetyl Co-A Carboxylase mRNA. These changes were also observed in rats fed daily for 3 weeks with glyceryl triacetate, though unlike B-GOS®, cortical histone deacetylase (HDAC1, HDAC2) mRNAs were also increased which suggested an additional epigenetic action of direct acetate supplementation. Our data demonstrate that a pro-cognitive effect of B-GOS® intake in rats is associated with an increase in cortical NMDA receptor function, but the role of circulating acetate derived from gut bacterial fermentation of this prebiotic requires further investigation.</description><subject>Animals</subject><subject>Attention - physiology</subject><subject>Cerebral Cortex - drug effects</subject><subject>Cerebral Cortex - metabolism</subject><subject>Cognition</subject><subject>Dietary Supplements</subject><subject>Electrophysiology</subject><subject>Executive Function - physiology</subject><subject>Glutamate</subject><subject>Male</subject><subject>Membrane Potentials - drug effects</subject><subject>Membrane Potentials - physiology</subject><subject>Microbiota</subject><subject>N-Methylaspartate - metabolism</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Neurotransmitter Agents - pharmacology</subject><subject>Prebiotics - administration & dosage</subject><subject>Random Allocation</subject><subject>Rats, Sprague-Dawley</subject><subject>Short-chain fatty acid</subject><subject>Triglycerides - administration & dosage</subject><issn>0924-977X</issn><issn>1873-7862</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhi0EotvCK4CP5ZBgO3EcX5CWUkqlQg-AxM1ynMnWq8RebO8inoI34SF4MpzdsoITsmSPNN_8M54foeeUlJTQ5uW6hG3wbr5KRqgoKS0JoQ_QgraiKkTbsIdoQSSrCynElxN0GuM6A7yq5GN0wiQVNa_IAv24diaAjtBj40OyRo94L-tyECBuvIsQcfL4w_s3S6xdj-20CX6XC3RK4JLdoxFSEe_skKxb4Q2EwYdJOwPYOhx0injw4-i_7bMBOutzK3z-uri6_fjr54tMrSDOUk_Qo0GPEZ7ev2fo89vLTxfvipvbq-uL5U1hasFTwTvTSc5Z3xpoWN0yA9BR0XMtSc4QzqqBDZ0wLeekFsQY1jOTT61lT4FVZ-jVQXez7SboTf5I0KPaBDvp8F15bdW_GWfv1MrvFG-5YI3MAuf3AsF_3ebh1WSjgXHUDvw2KiobKVnTsBkVB9QEH2OA4diGEjXbqdbqaKea7VSUquxWrnz295THuj_-ZWB5ACDvamchqGgs5L33NoBJqvf2v01-AxlEu2k</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Gronier, Benjamin</creator><creator>Savignac, Helene M.</creator><creator>Di Miceli, Mathieu</creator><creator>Idriss, Sherif M.</creator><creator>Tzortzis, George</creator><creator>Anthony, Daniel</creator><creator>Burnet, Philip W.J.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>201801</creationdate><title>Increased cortical neuronal responses to NMDA and improved attentional set-shifting performance in rats following prebiotic (B-GOS®) ingestion</title><author>Gronier, Benjamin ; 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The current investigation examined the functional correlates of these changes in B-GOS®-fed rats by measuring cortical neuronal responses to NMDA using in vivo NMDA micro-iontophoresis electrophysiology, and performance in the attentional set-shifting task. Adult male rats were supplemented with B-GOS® in the drinking water 3 weeks prior to in vivo iontophoresis or behavioural testing. Cortical neuronal responses to NMDA iontophoresis, were greater (+30%) in B-GOS® administered rats compared to non-supplemented controls. The intake of B-GOS® also partially hindered the reduction of NMDA responses by the glycine site antagonist, HA-966. In the attentional set-shifting task, B-GOS® -fed rats shifted from an intra-dimensional to an extra-dimensional set in fewer trials than controls, thereby indicating greater cognitive flexibility. An initial exploration into the mechanisms revealed that rats ingesting B-GOS® had increased levels of plasma acetate, and cortical GluN2B subunits and Acetyl Co-A Carboxylase mRNA. These changes were also observed in rats fed daily for 3 weeks with glyceryl triacetate, though unlike B-GOS®, cortical histone deacetylase (HDAC1, HDAC2) mRNAs were also increased which suggested an additional epigenetic action of direct acetate supplementation. Our data demonstrate that a pro-cognitive effect of B-GOS® intake in rats is associated with an increase in cortical NMDA receptor function, but the role of circulating acetate derived from gut bacterial fermentation of this prebiotic requires further investigation.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>29174530</pmid><doi>10.1016/j.euroneuro.2017.11.001</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Attention - physiology Cerebral Cortex - drug effects Cerebral Cortex - metabolism Cognition Dietary Supplements Electrophysiology Executive Function - physiology Glutamate Male Membrane Potentials - drug effects Membrane Potentials - physiology Microbiota N-Methylaspartate - metabolism Neurons - drug effects Neurons - metabolism Neurotransmitter Agents - pharmacology Prebiotics - administration & dosage Random Allocation Rats, Sprague-Dawley Short-chain fatty acid Triglycerides - administration & dosage |
title | Increased cortical neuronal responses to NMDA and improved attentional set-shifting performance in rats following prebiotic (B-GOS®) ingestion |
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