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...
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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 |
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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 & clinical pharmacology & 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 & 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 & clinical pharmacology & 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 & dosage</subject><subject>Analgesics - therapeutic use</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Antidepressive Agents - administration & 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 & 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 & dosage</subject><subject>Excitatory Amino Acid Antagonists - therapeutic use</subject><subject>Glycogen Synthase Kinase 3 beta - antagonists & inhibitors</subject><subject>Glycogen Synthase Kinase 3 beta - metabolism</subject><subject>Immunohistochemistry</subject><subject>Ketamine - administration & 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 & inhibitors</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Protein Kinase Inhibitors - administration & dosage</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Receptors, N-Methyl-D-Aspartate - antagonists & 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 & 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 & dosage</topic><topic>Analgesics - therapeutic use</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Antidepressive Agents - administration & 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 & 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 & dosage</topic><topic>Excitatory Amino Acid Antagonists - therapeutic use</topic><topic>Glycogen Synthase Kinase 3 beta - antagonists & inhibitors</topic><topic>Glycogen Synthase Kinase 3 beta - metabolism</topic><topic>Immunohistochemistry</topic><topic>Ketamine - administration & 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 & inhibitors</topic><topic>Nitric Oxide Synthase Type II - metabolism</topic><topic>Protein Kinase Inhibitors - administration & dosage</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Receptors, N-Methyl-D-Aspartate - antagonists & 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 & 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 & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Basic & clinical pharmacology & 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 & clinical pharmacology & 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> |
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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 |
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