TNF-α-Mediated RIPK1 Pathway Participates in the Development of Trigeminal Neuropathic Pain in Rats
Receptor-interacting serine/threonine-protein kinase 1 (RIPK1) participates in the regulation of cellular stress and inflammatory responses, but its function in neuropathic pain remains poorly understood. This study evaluated the role of RIPK1 in neuropathic pain following inferior alveolar nerve in...
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description | Receptor-interacting serine/threonine-protein kinase 1 (RIPK1) participates in the regulation of cellular stress and inflammatory responses, but its function in neuropathic pain remains poorly understood. This study evaluated the role of RIPK1 in neuropathic pain following inferior alveolar nerve injury. We developed a model using malpositioned dental implants in male Sprague Dawley rats. This model resulted in significant mechanical allodynia and upregulated RIPK1 expression in the trigeminal subnucleus caudalis (TSC). The intracisternal administration of Necrosatin-1 (Nec-1), an RIPK1 inhibitor, blocked the mechanical allodynia produced by inferior alveolar nerve injury The intracisternal administration of recombinant rat tumor necrosis factor-α (rrTNF-α) protein in naive rats produced mechanical allodynia and upregulated RIPK1 expression in the TSC. Moreover, an intracisternal pretreatment with Nec-1 inhibited the mechanical allodynia produced by rrTNF-α protein. Nerve injury caused elevated TNF-α concentration in the TSC and a TNF-α block had anti-allodynic effects, thereby attenuating RIPK1 expression in the TSC. Finally, double immunofluorescence analyses revealed the colocalization of TNF receptor and RIPK1 with astrocytes. Hence, we have identified that astroglial RIPK1, activated by the TNF-α pathway, is a central driver of neuropathic pain and that the TNF-α-mediated RIPK1 pathway is a potential therapeutic target for reducing neuropathic pain following nerve injury. |
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This study evaluated the role of RIPK1 in neuropathic pain following inferior alveolar nerve injury. We developed a model using malpositioned dental implants in male Sprague Dawley rats. This model resulted in significant mechanical allodynia and upregulated RIPK1 expression in the trigeminal subnucleus caudalis (TSC). The intracisternal administration of Necrosatin-1 (Nec-1), an RIPK1 inhibitor, blocked the mechanical allodynia produced by inferior alveolar nerve injury The intracisternal administration of recombinant rat tumor necrosis factor-α (rrTNF-α) protein in naive rats produced mechanical allodynia and upregulated RIPK1 expression in the TSC. Moreover, an intracisternal pretreatment with Nec-1 inhibited the mechanical allodynia produced by rrTNF-α protein. Nerve injury caused elevated TNF-α concentration in the TSC and a TNF-α block had anti-allodynic effects, thereby attenuating RIPK1 expression in the TSC. Finally, double immunofluorescence analyses revealed the colocalization of TNF receptor and RIPK1 with astrocytes. Hence, we have identified that astroglial RIPK1, activated by the TNF-α pathway, is a central driver of neuropathic pain and that the TNF-α-mediated RIPK1 pathway is a potential therapeutic target for reducing neuropathic pain following nerve injury.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms23010506</identifier><identifier>PMID: 35008931</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Alveoli ; Animals ; Antibodies ; Astrocytes ; Astrocytes - metabolism ; Cellular stress response ; Dental implants ; Dental prosthetics ; Disease Models, Animal ; Gene Expression Regulation ; Hyperalgesia - genetics ; Hyperalgesia - metabolism ; Immunofluorescence ; Inflammation ; Injury prevention ; Kinases ; Localization ; Male ; Neuralgia ; Pain ; Pain perception ; Protein kinase ; Proteins ; Rats ; Rats, Sprague-Dawley ; Receptor-Interacting Protein Serine-Threonine Kinases - genetics ; Receptor-Interacting Protein Serine-Threonine Kinases - metabolism ; Signal Transduction ; Spinal cord ; Spinal trigeminal nucleus ; Therapeutic targets ; Trigeminal Neuralgia - genetics ; Trigeminal Neuralgia - metabolism ; Tumor necrosis factor receptors ; Tumor Necrosis Factor-alpha - metabolism ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α</subject><ispartof>International journal of molecular sciences, 2022-01, Vol.23 (1), p.506</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-c63d9e33180b8e7651d67c8dfd5c6d332c0c39db9043402053fba00a25e9f4273</citedby><cites>FETCH-LOGICAL-c412t-c63d9e33180b8e7651d67c8dfd5c6d332c0c39db9043402053fba00a25e9f4273</cites><orcidid>0000-0002-5570-2371</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745573/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745573/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35008931$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Son, Jo Young</creatorcontrib><creatorcontrib>Ju, Jin Sook</creatorcontrib><creatorcontrib>Kim, Yu Mi</creatorcontrib><creatorcontrib>Ahn, Dong Kuk</creatorcontrib><title>TNF-α-Mediated RIPK1 Pathway Participates in the Development of Trigeminal Neuropathic Pain in Rats</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Receptor-interacting serine/threonine-protein kinase 1 (RIPK1) participates in the regulation of cellular stress and inflammatory responses, but its function in neuropathic pain remains poorly understood. This study evaluated the role of RIPK1 in neuropathic pain following inferior alveolar nerve injury. We developed a model using malpositioned dental implants in male Sprague Dawley rats. This model resulted in significant mechanical allodynia and upregulated RIPK1 expression in the trigeminal subnucleus caudalis (TSC). The intracisternal administration of Necrosatin-1 (Nec-1), an RIPK1 inhibitor, blocked the mechanical allodynia produced by inferior alveolar nerve injury The intracisternal administration of recombinant rat tumor necrosis factor-α (rrTNF-α) protein in naive rats produced mechanical allodynia and upregulated RIPK1 expression in the TSC. Moreover, an intracisternal pretreatment with Nec-1 inhibited the mechanical allodynia produced by rrTNF-α protein. Nerve injury caused elevated TNF-α concentration in the TSC and a TNF-α block had anti-allodynic effects, thereby attenuating RIPK1 expression in the TSC. Finally, double immunofluorescence analyses revealed the colocalization of TNF receptor and RIPK1 with astrocytes. Hence, we have identified that astroglial RIPK1, activated by the TNF-α pathway, is a central driver of neuropathic pain and that the TNF-α-mediated RIPK1 pathway is a potential therapeutic target for reducing neuropathic pain following nerve injury.</description><subject>Alveoli</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Astrocytes</subject><subject>Astrocytes - metabolism</subject><subject>Cellular stress response</subject><subject>Dental implants</subject><subject>Dental prosthetics</subject><subject>Disease Models, Animal</subject><subject>Gene Expression Regulation</subject><subject>Hyperalgesia - genetics</subject><subject>Hyperalgesia - metabolism</subject><subject>Immunofluorescence</subject><subject>Inflammation</subject><subject>Injury prevention</subject><subject>Kinases</subject><subject>Localization</subject><subject>Male</subject><subject>Neuralgia</subject><subject>Pain</subject><subject>Pain perception</subject><subject>Protein kinase</subject><subject>Proteins</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor-Interacting Protein Serine-Threonine Kinases - genetics</subject><subject>Receptor-Interacting Protein Serine-Threonine Kinases - metabolism</subject><subject>Signal Transduction</subject><subject>Spinal cord</subject><subject>Spinal trigeminal nucleus</subject><subject>Therapeutic targets</subject><subject>Trigeminal Neuralgia - genetics</subject><subject>Trigeminal Neuralgia - metabolism</subject><subject>Tumor necrosis factor receptors</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkcFu1DAQhi1ERUvhxhlF4sKB0LEndpILEioUqpZSVcvZ8tqTrldJvLWToj4WL8IzYbSl2iKNNCPNN79m5mfsFYf3iC0c-fWQBAIHCeoJO-CVECWAqp_u1PvseUprAIFCts_YPkqApkV-wNzi4qT8_av8Rs6biVxxdXp5xotLM61-mruc4-St3-RWKvxYTCsqPtEt9WEz0DgVoSsW0V_T4EfTFxc0x5DZlbd5MuM5rsyUXrC9zvSJXt7nQ_bj5PPi-Gt5_v3L6fHH89JWXEylVehaQuQNLBuqleRO1bZxnZNWOURhwWLrli1UWIEAid3SABghqe0qUeMh-7DV3czLgZzNG0bT6030g4l3OhivH3dGv9LX4VY3dSVljVng7b1ADDczpUkPPlnqezNSmJMWijctKF5BRt_8h67DHPMXtpTAplZVpt5tKRtDSpG6h2U46L_26V37Mv5694AH-J9f-Af6NpYY</recordid><startdate>20220103</startdate><enddate>20220103</enddate><creator>Son, Jo Young</creator><creator>Ju, Jin Sook</creator><creator>Kim, Yu Mi</creator><creator>Ahn, Dong Kuk</creator><general>MDPI AG</general><general>MDPI</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5570-2371</orcidid></search><sort><creationdate>20220103</creationdate><title>TNF-α-Mediated RIPK1 Pathway Participates in the Development of Trigeminal Neuropathic Pain in Rats</title><author>Son, Jo Young ; 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This study evaluated the role of RIPK1 in neuropathic pain following inferior alveolar nerve injury. We developed a model using malpositioned dental implants in male Sprague Dawley rats. This model resulted in significant mechanical allodynia and upregulated RIPK1 expression in the trigeminal subnucleus caudalis (TSC). The intracisternal administration of Necrosatin-1 (Nec-1), an RIPK1 inhibitor, blocked the mechanical allodynia produced by inferior alveolar nerve injury The intracisternal administration of recombinant rat tumor necrosis factor-α (rrTNF-α) protein in naive rats produced mechanical allodynia and upregulated RIPK1 expression in the TSC. Moreover, an intracisternal pretreatment with Nec-1 inhibited the mechanical allodynia produced by rrTNF-α protein. Nerve injury caused elevated TNF-α concentration in the TSC and a TNF-α block had anti-allodynic effects, thereby attenuating RIPK1 expression in the TSC. Finally, double immunofluorescence analyses revealed the colocalization of TNF receptor and RIPK1 with astrocytes. Hence, we have identified that astroglial RIPK1, activated by the TNF-α pathway, is a central driver of neuropathic pain and that the TNF-α-mediated RIPK1 pathway is a potential therapeutic target for reducing neuropathic pain following nerve injury.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35008931</pmid><doi>10.3390/ijms23010506</doi><orcidid>https://orcid.org/0000-0002-5570-2371</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alveoli Animals Antibodies Astrocytes Astrocytes - metabolism Cellular stress response Dental implants Dental prosthetics Disease Models, Animal Gene Expression Regulation Hyperalgesia - genetics Hyperalgesia - metabolism Immunofluorescence Inflammation Injury prevention Kinases Localization Male Neuralgia Pain Pain perception Protein kinase Proteins Rats Rats, Sprague-Dawley Receptor-Interacting Protein Serine-Threonine Kinases - genetics Receptor-Interacting Protein Serine-Threonine Kinases - metabolism Signal Transduction Spinal cord Spinal trigeminal nucleus Therapeutic targets Trigeminal Neuralgia - genetics Trigeminal Neuralgia - metabolism Tumor necrosis factor receptors Tumor Necrosis Factor-alpha - metabolism Tumor necrosis factor-TNF Tumor necrosis factor-α |
title | TNF-α-Mediated RIPK1 Pathway Participates in the Development of Trigeminal Neuropathic Pain in Rats |
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