Antinociceptive and Anti‐Inflammatory Effects of Ketamine and the Relationship to Its Antidepressant Action and GSK3 Inhibition

Ketamine (KET), a NMDA antagonist, exerts an antidepressant effect at subanaesthetic doses and possesses analgesic and anti‐inflammatory activities. We evaluated the involvement of KET antinociceptive and anti‐inflammatory effects with its antidepressant action. Male Swiss mice were subjected to for...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Basic & clinical pharmacology & toxicology 2016-12, Vol.119 (6), p.562-573
Hauptverfasser: Vale, Eduardo Mulato, Xavier, Cecília Coelho, Nogueira, Brenda Gomes, Campos, Bruna Caldas, Aquino, Pedro Everson Alexandre, Costa, Roberta Oliveira, Leal, Luzia Kalyne Almeida Moreira, Vasconcelos, Silvânia Maria Mendes, Neves, Kelly Rose Tavares, Barros Viana, Glauce Socorro
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 573
container_issue 6
container_start_page 562
container_title Basic & clinical pharmacology & toxicology
container_volume 119
creator Vale, Eduardo Mulato
Xavier, Cecília Coelho
Nogueira, Brenda Gomes
Campos, Bruna Caldas
Aquino, Pedro Everson Alexandre
Costa, Roberta Oliveira
Leal, Luzia Kalyne Almeida Moreira
Vasconcelos, Silvânia Maria Mendes
Neves, Kelly Rose Tavares
Barros Viana, Glauce Socorro
description Ketamine (KET), a NMDA antagonist, exerts an antidepressant effect at subanaesthetic doses and possesses analgesic and anti‐inflammatory activities. We evaluated the involvement of KET antinociceptive and anti‐inflammatory effects with its antidepressant action. Male Swiss mice were subjected to formalin, carrageenan‐induced paw oedema and forced swimming tests, for assessing antinociceptive, anti‐inflammatory and antidepressant effects. The treatment groups were as follows: control, KET (2, 5 and 10 mg/kg), lithium (LI: 5 mg/kg) and KET2 + LI5 combination. Immunohistochemistry analyses (TNF‐α, iNOS, COX‐2 and GSK3) in oedematous paws were performed. KET5 and KET10 reduced licking times in neurogenic (22 and 38%) and inflammatory (67 and 78%) phases of the formalin test, respectively, as related to controls. While LI5 inhibited the second phase by 24%, the licking time was inhibited by 26 and 59% in the KET2 + LI5 group (first and second phases). Furthermore, oedema volumes were reduced by 37 and 45% in the KET5 and KET10 groups, respectively. Oedema reductions were 29% in the LI5 group and 48% in the KET2 + LI5 group. In the forced swimming test, there were 23, 38 and 53% decreases in the immobility time in KET2, KET5 and KET10 groups, respectively. While LI5 caused no significant effect, decreases of 52% were observed with KET2 + LI5. KET also decreased TNF‐α, iNOS, COX‐2 and GSK3 immunostainings in oedematous paws, effects intensified with KET2 + LI5. We showed that KET presents antinociceptive and anti‐inflammatory effects associated with its antidepressant response. Furthermore, our results indicate the close involvement of GSK3 inhibition and blockade of inflammatory responses, in the antidepressant drug effect.
doi_str_mv 10.1111/bcpt.12637
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1844749029</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4265708351</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3577-22e9ca3a8cb27823f7d0c7b09a27f29ad7e86c2b948afcb915961c4899ab97233</originalsourceid><addsrcrecordid>eNp9kMFKwzAYgIMobk4vPoAEvAmdTdIuzXGOOcsGis5zSdOEZbRpbTJlN30Dn9EnsV3njuaS8PPl--ED4BL5Q9Sc21RUbojwiNAj0Ec0wB6NAnJ8eJOwB86sXfs-pgHyT0EPU8J8jMI--Bobp00ptJCV0-8ScpPBdvbz-R0blfOi4K6st3CqlBTOwlLBuXS80KZj3UrCZ5lzp0tjV7qCroRxw7WOTFa1tJYbB8eiBXY_Zi9zAmOz0qluZ-fgRPHcyov9PQCv99Pl5MFbPM7iyXjhCRJS6mEsmeCERyLFNMJE0cwXNPUZx1RhxjMqo5HAKQsirkTKUMhGSAQRYzxlFBMyANedt6rLt420LlmXm9o0KxMUBQENmiKsoW46StSltbVUSVXrgtfbBPlJWztpaye72g18tVdu0kJmB_QvbwOgDvjQudz-o0ruJk_LTvoLJ9OMFQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1844749029</pqid></control><display><type>article</type><title>Antinociceptive and Anti‐Inflammatory Effects of Ketamine and the Relationship to Its Antidepressant Action and GSK3 Inhibition</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Alma/SFX Local Collection</source><creator>Vale, Eduardo Mulato ; Xavier, Cecília Coelho ; Nogueira, Brenda Gomes ; Campos, Bruna Caldas ; Aquino, Pedro Everson Alexandre ; Costa, Roberta Oliveira ; Leal, Luzia Kalyne Almeida Moreira ; Vasconcelos, Silvânia Maria Mendes ; Neves, Kelly Rose Tavares ; Barros Viana, Glauce Socorro</creator><creatorcontrib>Vale, Eduardo Mulato ; Xavier, Cecília Coelho ; Nogueira, Brenda Gomes ; Campos, Bruna Caldas ; Aquino, Pedro Everson Alexandre ; Costa, Roberta Oliveira ; Leal, Luzia Kalyne Almeida Moreira ; Vasconcelos, Silvânia Maria Mendes ; Neves, Kelly Rose Tavares ; Barros Viana, Glauce Socorro</creatorcontrib><description>Ketamine (KET), a NMDA antagonist, exerts an antidepressant effect at subanaesthetic doses and possesses analgesic and anti‐inflammatory activities. We evaluated the involvement of KET antinociceptive and anti‐inflammatory effects with its antidepressant action. Male Swiss mice were subjected to formalin, carrageenan‐induced paw oedema and forced swimming tests, for assessing antinociceptive, anti‐inflammatory and antidepressant effects. The treatment groups were as follows: control, KET (2, 5 and 10 mg/kg), lithium (LI: 5 mg/kg) and KET2 + LI5 combination. Immunohistochemistry analyses (TNF‐α, iNOS, COX‐2 and GSK3) in oedematous paws were performed. KET5 and KET10 reduced licking times in neurogenic (22 and 38%) and inflammatory (67 and 78%) phases of the formalin test, respectively, as related to controls. While LI5 inhibited the second phase by 24%, the licking time was inhibited by 26 and 59% in the KET2 + LI5 group (first and second phases). Furthermore, oedema volumes were reduced by 37 and 45% in the KET5 and KET10 groups, respectively. Oedema reductions were 29% in the LI5 group and 48% in the KET2 + LI5 group. In the forced swimming test, there were 23, 38 and 53% decreases in the immobility time in KET2, KET5 and KET10 groups, respectively. While LI5 caused no significant effect, decreases of 52% were observed with KET2 + LI5. KET also decreased TNF‐α, iNOS, COX‐2 and GSK3 immunostainings in oedematous paws, effects intensified with KET2 + LI5. We showed that KET presents antinociceptive and anti‐inflammatory effects associated with its antidepressant response. Furthermore, our results indicate the close involvement of GSK3 inhibition and blockade of inflammatory responses, in the antidepressant drug effect.</description><identifier>ISSN: 1742-7835</identifier><identifier>EISSN: 1742-7843</identifier><identifier>DOI: 10.1111/bcpt.12637</identifier><identifier>PMID: 27390215</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject><![CDATA[Analgesics - administration & dosage ; Analgesics - therapeutic use ; Animals ; Anti-Inflammatory Agents, Non-Steroidal - administration & dosage ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Antidepressive Agents - administration & dosage ; Antidepressive Agents - therapeutic use ; Behavior, Animal - drug effects ; Cyclooxygenase 2 - chemistry ; Cyclooxygenase 2 - metabolism ; Depression - metabolism ; Depression - pathology ; Depression - prevention & control ; Disease Models, Animal ; Dose-Response Relationship, Drug ; Drug Therapy, Combination ; Edema ; Excitatory Amino Acid Antagonists - administration & dosage ; Excitatory Amino Acid Antagonists - therapeutic use ; Glycogen Synthase Kinase 3 beta - antagonists & inhibitors ; Glycogen Synthase Kinase 3 beta - metabolism ; Immunohistochemistry ; Ketamine - administration & dosage ; Ketamine - therapeutic use ; Lithium - therapeutic use ; Male ; Mice ; Nitric Oxide Synthase Type II - antagonists & inhibitors ; Nitric Oxide Synthase Type II - metabolism ; Protein Kinase Inhibitors - administration & dosage ; Protein Kinase Inhibitors - therapeutic use ; Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors ; Receptors, N-Methyl-D-Aspartate - metabolism ; Rodents ; Subcutaneous Tissue - drug effects ; Subcutaneous Tissue - metabolism ; Subcutaneous Tissue - pathology ; Tumor Necrosis Factor-alpha - antagonists & inhibitors ; Tumor Necrosis Factor-alpha - metabolism]]></subject><ispartof>Basic &amp; clinical pharmacology &amp; toxicology, 2016-12, Vol.119 (6), p.562-573</ispartof><rights>2016 Nordic Association for the Publication of BCPT (former Nordic Pharmacological Society)</rights><rights>2016 Nordic Association for the Publication of BCPT (former Nordic Pharmacological Society).</rights><rights>Copyright © 2016 Nordic Association for the Publication of BCPT (former Nordic Pharmacological Society). Published by John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3577-22e9ca3a8cb27823f7d0c7b09a27f29ad7e86c2b948afcb915961c4899ab97233</citedby><cites>FETCH-LOGICAL-c3577-22e9ca3a8cb27823f7d0c7b09a27f29ad7e86c2b948afcb915961c4899ab97233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fbcpt.12637$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbcpt.12637$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27390215$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vale, Eduardo Mulato</creatorcontrib><creatorcontrib>Xavier, Cecília Coelho</creatorcontrib><creatorcontrib>Nogueira, Brenda Gomes</creatorcontrib><creatorcontrib>Campos, Bruna Caldas</creatorcontrib><creatorcontrib>Aquino, Pedro Everson Alexandre</creatorcontrib><creatorcontrib>Costa, Roberta Oliveira</creatorcontrib><creatorcontrib>Leal, Luzia Kalyne Almeida Moreira</creatorcontrib><creatorcontrib>Vasconcelos, Silvânia Maria Mendes</creatorcontrib><creatorcontrib>Neves, Kelly Rose Tavares</creatorcontrib><creatorcontrib>Barros Viana, Glauce Socorro</creatorcontrib><title>Antinociceptive and Anti‐Inflammatory Effects of Ketamine and the Relationship to Its Antidepressant Action and GSK3 Inhibition</title><title>Basic &amp; clinical pharmacology &amp; toxicology</title><addtitle>Basic Clin Pharmacol Toxicol</addtitle><description>Ketamine (KET), a NMDA antagonist, exerts an antidepressant effect at subanaesthetic doses and possesses analgesic and anti‐inflammatory activities. We evaluated the involvement of KET antinociceptive and anti‐inflammatory effects with its antidepressant action. Male Swiss mice were subjected to formalin, carrageenan‐induced paw oedema and forced swimming tests, for assessing antinociceptive, anti‐inflammatory and antidepressant effects. The treatment groups were as follows: control, KET (2, 5 and 10 mg/kg), lithium (LI: 5 mg/kg) and KET2 + LI5 combination. Immunohistochemistry analyses (TNF‐α, iNOS, COX‐2 and GSK3) in oedematous paws were performed. KET5 and KET10 reduced licking times in neurogenic (22 and 38%) and inflammatory (67 and 78%) phases of the formalin test, respectively, as related to controls. While LI5 inhibited the second phase by 24%, the licking time was inhibited by 26 and 59% in the KET2 + LI5 group (first and second phases). Furthermore, oedema volumes were reduced by 37 and 45% in the KET5 and KET10 groups, respectively. Oedema reductions were 29% in the LI5 group and 48% in the KET2 + LI5 group. In the forced swimming test, there were 23, 38 and 53% decreases in the immobility time in KET2, KET5 and KET10 groups, respectively. While LI5 caused no significant effect, decreases of 52% were observed with KET2 + LI5. KET also decreased TNF‐α, iNOS, COX‐2 and GSK3 immunostainings in oedematous paws, effects intensified with KET2 + LI5. We showed that KET presents antinociceptive and anti‐inflammatory effects associated with its antidepressant response. Furthermore, our results indicate the close involvement of GSK3 inhibition and blockade of inflammatory responses, in the antidepressant drug effect.</description><subject>Analgesics - administration &amp; dosage</subject><subject>Analgesics - therapeutic use</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration &amp; dosage</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Antidepressive Agents - administration &amp; dosage</subject><subject>Antidepressive Agents - therapeutic use</subject><subject>Behavior, Animal - drug effects</subject><subject>Cyclooxygenase 2 - chemistry</subject><subject>Cyclooxygenase 2 - metabolism</subject><subject>Depression - metabolism</subject><subject>Depression - pathology</subject><subject>Depression - prevention &amp; control</subject><subject>Disease Models, Animal</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Therapy, Combination</subject><subject>Edema</subject><subject>Excitatory Amino Acid Antagonists - administration &amp; dosage</subject><subject>Excitatory Amino Acid Antagonists - therapeutic use</subject><subject>Glycogen Synthase Kinase 3 beta - antagonists &amp; inhibitors</subject><subject>Glycogen Synthase Kinase 3 beta - metabolism</subject><subject>Immunohistochemistry</subject><subject>Ketamine - administration &amp; dosage</subject><subject>Ketamine - therapeutic use</subject><subject>Lithium - therapeutic use</subject><subject>Male</subject><subject>Mice</subject><subject>Nitric Oxide Synthase Type II - antagonists &amp; inhibitors</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Protein Kinase Inhibitors - administration &amp; dosage</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Receptors, N-Methyl-D-Aspartate - antagonists &amp; inhibitors</subject><subject>Receptors, N-Methyl-D-Aspartate - metabolism</subject><subject>Rodents</subject><subject>Subcutaneous Tissue - drug effects</subject><subject>Subcutaneous Tissue - metabolism</subject><subject>Subcutaneous Tissue - pathology</subject><subject>Tumor Necrosis Factor-alpha - antagonists &amp; inhibitors</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>1742-7835</issn><issn>1742-7843</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFKwzAYgIMobk4vPoAEvAmdTdIuzXGOOcsGis5zSdOEZbRpbTJlN30Dn9EnsV3njuaS8PPl--ED4BL5Q9Sc21RUbojwiNAj0Ec0wB6NAnJ8eJOwB86sXfs-pgHyT0EPU8J8jMI--Bobp00ptJCV0-8ScpPBdvbz-R0blfOi4K6st3CqlBTOwlLBuXS80KZj3UrCZ5lzp0tjV7qCroRxw7WOTFa1tJYbB8eiBXY_Zi9zAmOz0qluZ-fgRPHcyov9PQCv99Pl5MFbPM7iyXjhCRJS6mEsmeCERyLFNMJE0cwXNPUZx1RhxjMqo5HAKQsirkTKUMhGSAQRYzxlFBMyANedt6rLt420LlmXm9o0KxMUBQENmiKsoW46StSltbVUSVXrgtfbBPlJWztpaye72g18tVdu0kJmB_QvbwOgDvjQudz-o0ruJk_LTvoLJ9OMFQ</recordid><startdate>201612</startdate><enddate>201612</enddate><creator>Vale, Eduardo Mulato</creator><creator>Xavier, Cecília Coelho</creator><creator>Nogueira, Brenda Gomes</creator><creator>Campos, Bruna Caldas</creator><creator>Aquino, Pedro Everson Alexandre</creator><creator>Costa, Roberta Oliveira</creator><creator>Leal, Luzia Kalyne Almeida Moreira</creator><creator>Vasconcelos, Silvânia Maria Mendes</creator><creator>Neves, Kelly Rose Tavares</creator><creator>Barros Viana, Glauce Socorro</creator><general>Wiley Subscription Services, Inc</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>7QP</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>201612</creationdate><title>Antinociceptive and Anti‐Inflammatory Effects of Ketamine and the Relationship to Its Antidepressant Action and GSK3 Inhibition</title><author>Vale, Eduardo Mulato ; Xavier, Cecília Coelho ; Nogueira, Brenda Gomes ; Campos, Bruna Caldas ; Aquino, Pedro Everson Alexandre ; Costa, Roberta Oliveira ; Leal, Luzia Kalyne Almeida Moreira ; Vasconcelos, Silvânia Maria Mendes ; Neves, Kelly Rose Tavares ; Barros Viana, Glauce Socorro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3577-22e9ca3a8cb27823f7d0c7b09a27f29ad7e86c2b948afcb915961c4899ab97233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Analgesics - administration &amp; dosage</topic><topic>Analgesics - therapeutic use</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - administration &amp; dosage</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Antidepressive Agents - administration &amp; dosage</topic><topic>Antidepressive Agents - therapeutic use</topic><topic>Behavior, Animal - drug effects</topic><topic>Cyclooxygenase 2 - chemistry</topic><topic>Cyclooxygenase 2 - metabolism</topic><topic>Depression - metabolism</topic><topic>Depression - pathology</topic><topic>Depression - prevention &amp; control</topic><topic>Disease Models, Animal</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Therapy, Combination</topic><topic>Edema</topic><topic>Excitatory Amino Acid Antagonists - administration &amp; dosage</topic><topic>Excitatory Amino Acid Antagonists - therapeutic use</topic><topic>Glycogen Synthase Kinase 3 beta - antagonists &amp; inhibitors</topic><topic>Glycogen Synthase Kinase 3 beta - metabolism</topic><topic>Immunohistochemistry</topic><topic>Ketamine - administration &amp; dosage</topic><topic>Ketamine - therapeutic use</topic><topic>Lithium - therapeutic use</topic><topic>Male</topic><topic>Mice</topic><topic>Nitric Oxide Synthase Type II - antagonists &amp; inhibitors</topic><topic>Nitric Oxide Synthase Type II - metabolism</topic><topic>Protein Kinase Inhibitors - administration &amp; dosage</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Receptors, N-Methyl-D-Aspartate - antagonists &amp; inhibitors</topic><topic>Receptors, N-Methyl-D-Aspartate - metabolism</topic><topic>Rodents</topic><topic>Subcutaneous Tissue - drug effects</topic><topic>Subcutaneous Tissue - metabolism</topic><topic>Subcutaneous Tissue - pathology</topic><topic>Tumor Necrosis Factor-alpha - antagonists &amp; inhibitors</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vale, Eduardo Mulato</creatorcontrib><creatorcontrib>Xavier, Cecília Coelho</creatorcontrib><creatorcontrib>Nogueira, Brenda Gomes</creatorcontrib><creatorcontrib>Campos, Bruna Caldas</creatorcontrib><creatorcontrib>Aquino, Pedro Everson Alexandre</creatorcontrib><creatorcontrib>Costa, Roberta Oliveira</creatorcontrib><creatorcontrib>Leal, Luzia Kalyne Almeida Moreira</creatorcontrib><creatorcontrib>Vasconcelos, Silvânia Maria Mendes</creatorcontrib><creatorcontrib>Neves, Kelly Rose Tavares</creatorcontrib><creatorcontrib>Barros Viana, Glauce Socorro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Basic &amp; clinical pharmacology &amp; toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vale, Eduardo Mulato</au><au>Xavier, Cecília Coelho</au><au>Nogueira, Brenda Gomes</au><au>Campos, Bruna Caldas</au><au>Aquino, Pedro Everson Alexandre</au><au>Costa, Roberta Oliveira</au><au>Leal, Luzia Kalyne Almeida Moreira</au><au>Vasconcelos, Silvânia Maria Mendes</au><au>Neves, Kelly Rose Tavares</au><au>Barros Viana, Glauce Socorro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antinociceptive and Anti‐Inflammatory Effects of Ketamine and the Relationship to Its Antidepressant Action and GSK3 Inhibition</atitle><jtitle>Basic &amp; clinical pharmacology &amp; toxicology</jtitle><addtitle>Basic Clin Pharmacol Toxicol</addtitle><date>2016-12</date><risdate>2016</risdate><volume>119</volume><issue>6</issue><spage>562</spage><epage>573</epage><pages>562-573</pages><issn>1742-7835</issn><eissn>1742-7843</eissn><abstract>Ketamine (KET), a NMDA antagonist, exerts an antidepressant effect at subanaesthetic doses and possesses analgesic and anti‐inflammatory activities. We evaluated the involvement of KET antinociceptive and anti‐inflammatory effects with its antidepressant action. Male Swiss mice were subjected to formalin, carrageenan‐induced paw oedema and forced swimming tests, for assessing antinociceptive, anti‐inflammatory and antidepressant effects. The treatment groups were as follows: control, KET (2, 5 and 10 mg/kg), lithium (LI: 5 mg/kg) and KET2 + LI5 combination. Immunohistochemistry analyses (TNF‐α, iNOS, COX‐2 and GSK3) in oedematous paws were performed. KET5 and KET10 reduced licking times in neurogenic (22 and 38%) and inflammatory (67 and 78%) phases of the formalin test, respectively, as related to controls. While LI5 inhibited the second phase by 24%, the licking time was inhibited by 26 and 59% in the KET2 + LI5 group (first and second phases). Furthermore, oedema volumes were reduced by 37 and 45% in the KET5 and KET10 groups, respectively. Oedema reductions were 29% in the LI5 group and 48% in the KET2 + LI5 group. In the forced swimming test, there were 23, 38 and 53% decreases in the immobility time in KET2, KET5 and KET10 groups, respectively. While LI5 caused no significant effect, decreases of 52% were observed with KET2 + LI5. KET also decreased TNF‐α, iNOS, COX‐2 and GSK3 immunostainings in oedematous paws, effects intensified with KET2 + LI5. We showed that KET presents antinociceptive and anti‐inflammatory effects associated with its antidepressant response. Furthermore, our results indicate the close involvement of GSK3 inhibition and blockade of inflammatory responses, in the antidepressant drug effect.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27390215</pmid><doi>10.1111/bcpt.12637</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1742-7835
ispartof Basic & clinical pharmacology & toxicology, 2016-12, Vol.119 (6), p.562-573
issn 1742-7835
1742-7843
language eng
recordid cdi_proquest_journals_1844749029
source MEDLINE; Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection
subjects Analgesics - administration & dosage
Analgesics - therapeutic use
Animals
Anti-Inflammatory Agents, Non-Steroidal - administration & dosage
Anti-Inflammatory Agents, Non-Steroidal - therapeutic use
Antidepressive Agents - administration & dosage
Antidepressive Agents - therapeutic use
Behavior, Animal - drug effects
Cyclooxygenase 2 - chemistry
Cyclooxygenase 2 - metabolism
Depression - metabolism
Depression - pathology
Depression - prevention & control
Disease Models, Animal
Dose-Response Relationship, Drug
Drug Therapy, Combination
Edema
Excitatory Amino Acid Antagonists - administration & dosage
Excitatory Amino Acid Antagonists - therapeutic use
Glycogen Synthase Kinase 3 beta - antagonists & inhibitors
Glycogen Synthase Kinase 3 beta - metabolism
Immunohistochemistry
Ketamine - administration & dosage
Ketamine - therapeutic use
Lithium - therapeutic use
Male
Mice
Nitric Oxide Synthase Type II - antagonists & inhibitors
Nitric Oxide Synthase Type II - metabolism
Protein Kinase Inhibitors - administration & dosage
Protein Kinase Inhibitors - therapeutic use
Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
Receptors, N-Methyl-D-Aspartate - metabolism
Rodents
Subcutaneous Tissue - drug effects
Subcutaneous Tissue - metabolism
Subcutaneous Tissue - pathology
Tumor Necrosis Factor-alpha - antagonists & inhibitors
Tumor Necrosis Factor-alpha - metabolism
title Antinociceptive and Anti‐Inflammatory Effects of Ketamine and the Relationship to Its Antidepressant Action and GSK3 Inhibition
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T23%3A31%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antinociceptive%20and%20Anti%E2%80%90Inflammatory%20Effects%20of%20Ketamine%20and%20the%20Relationship%20to%20Its%20Antidepressant%20Action%20and%20GSK3%20Inhibition&rft.jtitle=Basic%20&%20clinical%20pharmacology%20&%20toxicology&rft.au=Vale,%20Eduardo%20Mulato&rft.date=2016-12&rft.volume=119&rft.issue=6&rft.spage=562&rft.epage=573&rft.pages=562-573&rft.issn=1742-7835&rft.eissn=1742-7843&rft_id=info:doi/10.1111/bcpt.12637&rft_dat=%3Cproquest_cross%3E4265708351%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1844749029&rft_id=info:pmid/27390215&rfr_iscdi=true