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The effect of CA1 administration of orexin-A on hippocampal expression of COX-2 and BDNF in a rat model of orofacial pain

ABSTRACT The neuropeptide orexin-A and its receptors are widely distributed in both hippocampal circuitry and pain transmission pathways. Objective: Involvement of the CA1 orexin 1 receptor (OX1R) on the modulation of orofacial pain and pain-induced changes in hippocampal expression of cyclooxygenas...

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Published in:Arquivos de neuro-psiquiatria 2018-09, Vol.76 (9), p.603-608
Main Authors: Kooshki, Razieh, Abbasnejad, Mehdi, Esmaeili-Mahani, Saeed, Raoof, Maryam
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creator Kooshki, Razieh
Abbasnejad, Mehdi
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Raoof, Maryam
description ABSTRACT The neuropeptide orexin-A and its receptors are widely distributed in both hippocampal circuitry and pain transmission pathways. Objective: Involvement of the CA1 orexin 1 receptor (OX1R) on the modulation of orofacial pain and pain-induced changes in hippocampal expression of cyclooxygenase-2 (COX-2) and brain-derived neurotrophic factor (BDNF) was investigated. Methods: Orofacial pain was induced by an intra-lip injection of capsaicin (100 μg). Reverse transcription polymerase chain reaction and immunoblot analysis were used to indicate changes in hippocampal BDNF and COX-2 expression, respectively. Results: Capsaicin induces a significant pain response, which is not affected by either orexin-A or SB-334867-A, an OX1R antagonist. However, an increased expression of COX-2 and decreased expression of BDNF was observed in the hippocampus of animals that received capsaicin or SB-334867-A (80 nM) plus capsaicin. Meanwhile, orexin-A (40 pM) attenuated the effects of capsaicin on the expression of COX-2 and BDNF. Conclusions: CA1 OX1R activation moderates capsaicin-induced neuronal inflammation and neurotrophic deficiency.
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Objective: Involvement of the CA1 orexin 1 receptor (OX1R) on the modulation of orofacial pain and pain-induced changes in hippocampal expression of cyclooxygenase-2 (COX-2) and brain-derived neurotrophic factor (BDNF) was investigated. Methods: Orofacial pain was induced by an intra-lip injection of capsaicin (100 μg). Reverse transcription polymerase chain reaction and immunoblot analysis were used to indicate changes in hippocampal BDNF and COX-2 expression, respectively. Results: Capsaicin induces a significant pain response, which is not affected by either orexin-A or SB-334867-A, an OX1R antagonist. However, an increased expression of COX-2 and decreased expression of BDNF was observed in the hippocampus of animals that received capsaicin or SB-334867-A (80 nM) plus capsaicin. Meanwhile, orexin-A (40 pM) attenuated the effects of capsaicin on the expression of COX-2 and BDNF. Conclusions: CA1 OX1R activation moderates capsaicin-induced neuronal inflammation and neurotrophic deficiency.</description><identifier>ISSN: 0004-282X</identifier><identifier>ISSN: 1678-4227</identifier><identifier>EISSN: 1678-4227</identifier><identifier>DOI: 10.1590/0004-282X20180099</identifier><identifier>PMID: 30365624</identifier><language>eng</language><publisher>Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil: Thieme Revinter Publicações Ltda</publisher><subject>Animals ; Benzoxazoles - pharmacology ; Brain-derived neurotrophic factor ; Brain-Derived Neurotrophic Factor - metabolism ; Capsaicin ; Cyclooxygenase 2 - metabolism ; Cyclooxygenase-2 ; Disease Models, Animal ; Facial Pain - metabolism ; Hippocampus ; Hippocampus - drug effects ; Hippocampus - metabolism ; Male ; Neurons - drug effects ; Neurons - metabolism ; NEUROSCIENCES ; Orexin Receptors - metabolism ; Orexins ; Orexins - pharmacology ; Orofacial pain ; Pain ; Polymerase chain reaction ; PSYCHIATRY ; Rats ; Rats, Wistar ; Reverse Transcriptase Polymerase Chain Reaction ; Reverse transcription ; Urea - analogs &amp; derivatives ; Urea - pharmacology</subject><ispartof>Arquivos de neuro-psiquiatria, 2018-09, Vol.76 (9), p.603-608</ispartof><rights>Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon.</rights><rights>Copyright Arquivos de Neuro-Psiquiatria Sep 2018</rights><rights>This work is licensed under a Creative Commons Attribution 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c544t-b3310cef4ad6b50545286f6a1befc15f2a99f7dbfcc56e88df8e7ffb0b96db0b3</citedby><cites>FETCH-LOGICAL-c544t-b3310cef4ad6b50545286f6a1befc15f2a99f7dbfcc56e88df8e7ffb0b96db0b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,24150,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30365624$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kooshki, Razieh</creatorcontrib><creatorcontrib>Abbasnejad, Mehdi</creatorcontrib><creatorcontrib>Esmaeili-Mahani, Saeed</creatorcontrib><creatorcontrib>Raoof, Maryam</creatorcontrib><title>The effect of CA1 administration of orexin-A on hippocampal expression of COX-2 and BDNF in a rat model of orofacial pain</title><title>Arquivos de neuro-psiquiatria</title><addtitle>Arq Neuropsiquiatr</addtitle><description>ABSTRACT The neuropeptide orexin-A and its receptors are widely distributed in both hippocampal circuitry and pain transmission pathways. Objective: Involvement of the CA1 orexin 1 receptor (OX1R) on the modulation of orofacial pain and pain-induced changes in hippocampal expression of cyclooxygenase-2 (COX-2) and brain-derived neurotrophic factor (BDNF) was investigated. Methods: Orofacial pain was induced by an intra-lip injection of capsaicin (100 μg). Reverse transcription polymerase chain reaction and immunoblot analysis were used to indicate changes in hippocampal BDNF and COX-2 expression, respectively. Results: Capsaicin induces a significant pain response, which is not affected by either orexin-A or SB-334867-A, an OX1R antagonist. However, an increased expression of COX-2 and decreased expression of BDNF was observed in the hippocampus of animals that received capsaicin or SB-334867-A (80 nM) plus capsaicin. Meanwhile, orexin-A (40 pM) attenuated the effects of capsaicin on the expression of COX-2 and BDNF. Conclusions: CA1 OX1R activation moderates capsaicin-induced neuronal inflammation and neurotrophic deficiency.</description><subject>Animals</subject><subject>Benzoxazoles - pharmacology</subject><subject>Brain-derived neurotrophic factor</subject><subject>Brain-Derived Neurotrophic Factor - metabolism</subject><subject>Capsaicin</subject><subject>Cyclooxygenase 2 - metabolism</subject><subject>Cyclooxygenase-2</subject><subject>Disease Models, Animal</subject><subject>Facial Pain - metabolism</subject><subject>Hippocampus</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Male</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>NEUROSCIENCES</subject><subject>Orexin Receptors - metabolism</subject><subject>Orexins</subject><subject>Orexins - pharmacology</subject><subject>Orofacial pain</subject><subject>Pain</subject><subject>Polymerase chain reaction</subject><subject>PSYCHIATRY</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Reverse transcription</subject><subject>Urea - analogs &amp; 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Abbasnejad, Mehdi ; Esmaeili-Mahani, Saeed ; Raoof, Maryam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c544t-b3310cef4ad6b50545286f6a1befc15f2a99f7dbfcc56e88df8e7ffb0b96db0b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Benzoxazoles - pharmacology</topic><topic>Brain-derived neurotrophic factor</topic><topic>Brain-Derived Neurotrophic Factor - metabolism</topic><topic>Capsaicin</topic><topic>Cyclooxygenase 2 - metabolism</topic><topic>Cyclooxygenase-2</topic><topic>Disease Models, Animal</topic><topic>Facial Pain - metabolism</topic><topic>Hippocampus</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>Male</topic><topic>Neurons - drug effects</topic><topic>Neurons - metabolism</topic><topic>NEUROSCIENCES</topic><topic>Orexin Receptors - metabolism</topic><topic>Orexins</topic><topic>Orexins - pharmacology</topic><topic>Orofacial pain</topic><topic>Pain</topic><topic>Polymerase chain reaction</topic><topic>PSYCHIATRY</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Reverse transcription</topic><topic>Urea - analogs &amp; derivatives</topic><topic>Urea - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kooshki, Razieh</creatorcontrib><creatorcontrib>Abbasnejad, Mehdi</creatorcontrib><creatorcontrib>Esmaeili-Mahani, Saeed</creatorcontrib><creatorcontrib>Raoof, Maryam</creatorcontrib><collection>Thieme_OA刊</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>SciELO</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Arquivos de neuro-psiquiatria</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kooshki, Razieh</au><au>Abbasnejad, Mehdi</au><au>Esmaeili-Mahani, Saeed</au><au>Raoof, Maryam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of CA1 administration of orexin-A on hippocampal expression of COX-2 and BDNF in a rat model of orofacial pain</atitle><jtitle>Arquivos de neuro-psiquiatria</jtitle><addtitle>Arq Neuropsiquiatr</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>76</volume><issue>9</issue><spage>603</spage><epage>608</epage><pages>603-608</pages><issn>0004-282X</issn><issn>1678-4227</issn><eissn>1678-4227</eissn><abstract>ABSTRACT The neuropeptide orexin-A and its receptors are widely distributed in both hippocampal circuitry and pain transmission pathways. Objective: Involvement of the CA1 orexin 1 receptor (OX1R) on the modulation of orofacial pain and pain-induced changes in hippocampal expression of cyclooxygenase-2 (COX-2) and brain-derived neurotrophic factor (BDNF) was investigated. Methods: Orofacial pain was induced by an intra-lip injection of capsaicin (100 μg). Reverse transcription polymerase chain reaction and immunoblot analysis were used to indicate changes in hippocampal BDNF and COX-2 expression, respectively. Results: Capsaicin induces a significant pain response, which is not affected by either orexin-A or SB-334867-A, an OX1R antagonist. However, an increased expression of COX-2 and decreased expression of BDNF was observed in the hippocampus of animals that received capsaicin or SB-334867-A (80 nM) plus capsaicin. Meanwhile, orexin-A (40 pM) attenuated the effects of capsaicin on the expression of COX-2 and BDNF. 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identifier ISSN: 0004-282X
ispartof Arquivos de neuro-psiquiatria, 2018-09, Vol.76 (9), p.603-608
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1678-4227
language eng
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source SciELO Brazil
subjects Animals
Benzoxazoles - pharmacology
Brain-derived neurotrophic factor
Brain-Derived Neurotrophic Factor - metabolism
Capsaicin
Cyclooxygenase 2 - metabolism
Cyclooxygenase-2
Disease Models, Animal
Facial Pain - metabolism
Hippocampus
Hippocampus - drug effects
Hippocampus - metabolism
Male
Neurons - drug effects
Neurons - metabolism
NEUROSCIENCES
Orexin Receptors - metabolism
Orexins
Orexins - pharmacology
Orofacial pain
Pain
Polymerase chain reaction
PSYCHIATRY
Rats
Rats, Wistar
Reverse Transcriptase Polymerase Chain Reaction
Reverse transcription
Urea - analogs & derivatives
Urea - pharmacology
title The effect of CA1 administration of orexin-A on hippocampal expression of COX-2 and BDNF in a rat model of orofacial pain
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