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Analgesic effect of electroacupuncture on inflammatory pain in the rat model of collagen-induced arthritis: Mediation by cholinergic and serotonergic receptors
The analgesic effect and its mechanism of electroacupuncture (EA) on inflammatory pain, especially in the rat model of collagen-induced arthritis (CIA), have not yet been studied. This study was designed to investigate the analgesic effect and its cholinergic and serotonergic mechanism of EA in the...
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Published in: | Brain research 2005-09, Vol.1057 (1), p.181-185 |
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description | The analgesic effect and its mechanism of electroacupuncture (EA) on inflammatory pain, especially in the rat model of collagen-induced arthritis (CIA), have not yet been studied. This study was designed to investigate the analgesic effect and its cholinergic and serotonergic mechanism of EA in the CIA rat model. To induce CIA, male Sprague–Dawley rats were immunized with bovine type II collagen emulsified in Freund's incomplete adjuvant, followed by a booster injection 14 days later. The analgesic effect was evaluated by tail flick latency (TFL). After induction of arthritis, the inflammatory pain threshold decreased as time passed and there was no big change of the pain threshold after 3 weeks. Three weeks after the first immunization, low frequency EA stimulation (2 Hz, 0.07 mA, 0.3 ms) delivered to Zusanli (ST
36) for 30 min showed the analgesic effect. Also, the analgesic effect of EA was blocked by pretreatment with atropine (muscarinic cholinergic receptor antagonist, 1 mg/kg i.p.), spiroxatrine (5-HT1a receptor antagonist, 1 mg/kg i.p.), and ondansetron (5-HT3 receptor antagonist, 0.5 mg/kg i.p.), but not by pretreatment with ketanserin (5-HT2 receptor antagonist, 1 mg/kg i.p.). These results suggest that low frequency EA can relieve inflammatory pain in CIA and the analgesic effect of EA can be mediated by muscarinic cholinergic receptor, 5-HT1a and 5-HT3 receptors, but not by 5-HT2 receptor. |
doi_str_mv | 10.1016/j.brainres.2005.07.014 |
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36) for 30 min showed the analgesic effect. Also, the analgesic effect of EA was blocked by pretreatment with atropine (muscarinic cholinergic receptor antagonist, 1 mg/kg i.p.), spiroxatrine (5-HT1a receptor antagonist, 1 mg/kg i.p.), and ondansetron (5-HT3 receptor antagonist, 0.5 mg/kg i.p.), but not by pretreatment with ketanserin (5-HT2 receptor antagonist, 1 mg/kg i.p.). These results suggest that low frequency EA can relieve inflammatory pain in CIA and the analgesic effect of EA can be mediated by muscarinic cholinergic receptor, 5-HT1a and 5-HT3 receptors, but not by 5-HT2 receptor.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2005.07.014</identifier><identifier>PMID: 16139820</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Acupuncture Points ; Analgesics ; Analysis of Variance ; Animals ; Arthritis, Experimental - therapy ; Atropine ; Biological and medical sciences ; Cholinesterase Inhibitors - administration & dosage ; Collagen-induced arthritis ; Dioxanes - administration & dosage ; Disease Models, Animal ; Diseases of the osteoarticular system ; Drug Interactions ; Electroacupuncture ; Inflammation - complications ; Inflammation - therapy ; Ketanserin ; Male ; Medical sciences ; Miscellaneous ; Miscellaneous. Osteoarticular involvement in other diseases ; Neostigmine - administration & dosage ; Neuropharmacology ; Ondansetron ; Pain - etiology ; Pain Management ; Pain Measurement - methods ; Pain Threshold - physiology ; Pharmacology. Drug treatments ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; Rats ; Rats, Sprague-Dawley ; Reaction Time - physiology ; Serotonin Antagonists - administration & dosage ; Spiro Compounds - administration & dosage ; Spiroxatrine ; Time Factors</subject><ispartof>Brain research, 2005-09, Vol.1057 (1), p.181-185</ispartof><rights>2005 Elsevier B.V.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-e0914d8a1e264bdf01162b772d1da468db59a5f36572e0dce8fbcfae852f114c3</citedby><cites>FETCH-LOGICAL-c427t-e0914d8a1e264bdf01162b772d1da468db59a5f36572e0dce8fbcfae852f114c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17143534$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16139820$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baek, Yong Hyeon</creatorcontrib><creatorcontrib>Choi, Do Young</creatorcontrib><creatorcontrib>Yang, Hyung In</creatorcontrib><creatorcontrib>Park, Dong Suk</creatorcontrib><title>Analgesic effect of electroacupuncture on inflammatory pain in the rat model of collagen-induced arthritis: Mediation by cholinergic and serotonergic receptors</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>The analgesic effect and its mechanism of electroacupuncture (EA) on inflammatory pain, especially in the rat model of collagen-induced arthritis (CIA), have not yet been studied. This study was designed to investigate the analgesic effect and its cholinergic and serotonergic mechanism of EA in the CIA rat model. To induce CIA, male Sprague–Dawley rats were immunized with bovine type II collagen emulsified in Freund's incomplete adjuvant, followed by a booster injection 14 days later. The analgesic effect was evaluated by tail flick latency (TFL). After induction of arthritis, the inflammatory pain threshold decreased as time passed and there was no big change of the pain threshold after 3 weeks. Three weeks after the first immunization, low frequency EA stimulation (2 Hz, 0.07 mA, 0.3 ms) delivered to Zusanli (ST
36) for 30 min showed the analgesic effect. Also, the analgesic effect of EA was blocked by pretreatment with atropine (muscarinic cholinergic receptor antagonist, 1 mg/kg i.p.), spiroxatrine (5-HT1a receptor antagonist, 1 mg/kg i.p.), and ondansetron (5-HT3 receptor antagonist, 0.5 mg/kg i.p.), but not by pretreatment with ketanserin (5-HT2 receptor antagonist, 1 mg/kg i.p.). These results suggest that low frequency EA can relieve inflammatory pain in CIA and the analgesic effect of EA can be mediated by muscarinic cholinergic receptor, 5-HT1a and 5-HT3 receptors, but not by 5-HT2 receptor.</description><subject>Acupuncture Points</subject><subject>Analgesics</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Arthritis, Experimental - therapy</subject><subject>Atropine</subject><subject>Biological and medical sciences</subject><subject>Cholinesterase Inhibitors - administration & dosage</subject><subject>Collagen-induced arthritis</subject><subject>Dioxanes - administration & dosage</subject><subject>Disease Models, Animal</subject><subject>Diseases of the osteoarticular system</subject><subject>Drug Interactions</subject><subject>Electroacupuncture</subject><subject>Inflammation - complications</subject><subject>Inflammation - therapy</subject><subject>Ketanserin</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Miscellaneous. Osteoarticular involvement in other diseases</subject><subject>Neostigmine - administration & dosage</subject><subject>Neuropharmacology</subject><subject>Ondansetron</subject><subject>Pain - etiology</subject><subject>Pain Management</subject><subject>Pain Measurement - methods</subject><subject>Pain Threshold - physiology</subject><subject>Pharmacology. Drug treatments</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reaction Time - physiology</subject><subject>Serotonin Antagonists - administration & dosage</subject><subject>Spiro Compounds - administration & dosage</subject><subject>Spiroxatrine</subject><subject>Time Factors</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFUcuOFCEUJUbj9Iz-woSN7qoE6u3KyUQdkzFudE1uwaWbThWUQE3SX-OvSqfLzNIVcHMel3MIueWs5Iy3H47lGMC6gLEUjDUl60rG6xdkx_tOFK2o2UuyY4y1RT8M1RW5jvGYn1U1sNfkire8GnrBduTPnYNpj9EqisagStQbilO-BA9qXVan0hqQeketMxPMMyQfTnTJ5nlC0wFpgERnr3E6c5WfJtijK6zTq0JNIaRDsMnGj_Q7agvJZq3xRNXBT9Zh2GdrcJpGDD75bRBQ4ZKN4hvyysAU8e123pBfXz7_vH8oHn98_XZ_91ioWnSpQDbwWvfAUbT1qA3jvBVj1wnNNdRtr8dmgMZUbdMJZFphb0ZlAPtGGM5rVd2Q9xfdJfjfK8YkZxsV5r849GuUvKuGWvRNBrYXoAo-xoBGLsHOEE6SM3muRh7lv2rkuRrJOpmrycTbzWEdZ9TPtK2LDHi3ASAqmEwAp2x8xnVZpKnOQp8uOMx5PFkMMiqLLmdtc2xJam__t8tfwSm0-g</recordid><startdate>20050928</startdate><enddate>20050928</enddate><creator>Baek, Yong Hyeon</creator><creator>Choi, Do Young</creator><creator>Yang, Hyung In</creator><creator>Park, Dong Suk</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</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>7TK</scope></search><sort><creationdate>20050928</creationdate><title>Analgesic effect of electroacupuncture on inflammatory pain in the rat model of collagen-induced arthritis: Mediation by cholinergic and serotonergic receptors</title><author>Baek, Yong Hyeon ; Choi, Do Young ; Yang, Hyung In ; Park, Dong Suk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-e0914d8a1e264bdf01162b772d1da468db59a5f36572e0dce8fbcfae852f114c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acupuncture Points</topic><topic>Analgesics</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Arthritis, Experimental - therapy</topic><topic>Atropine</topic><topic>Biological and medical sciences</topic><topic>Cholinesterase Inhibitors - administration & dosage</topic><topic>Collagen-induced arthritis</topic><topic>Dioxanes - administration & dosage</topic><topic>Disease Models, Animal</topic><topic>Diseases of the osteoarticular system</topic><topic>Drug Interactions</topic><topic>Electroacupuncture</topic><topic>Inflammation - complications</topic><topic>Inflammation - therapy</topic><topic>Ketanserin</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Miscellaneous</topic><topic>Miscellaneous. Osteoarticular involvement in other diseases</topic><topic>Neostigmine - administration & dosage</topic><topic>Neuropharmacology</topic><topic>Ondansetron</topic><topic>Pain - etiology</topic><topic>Pain Management</topic><topic>Pain Measurement - methods</topic><topic>Pain Threshold - physiology</topic><topic>Pharmacology. Drug treatments</topic><topic>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reaction Time - physiology</topic><topic>Serotonin Antagonists - administration & dosage</topic><topic>Spiro Compounds - administration & dosage</topic><topic>Spiroxatrine</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baek, Yong Hyeon</creatorcontrib><creatorcontrib>Choi, Do Young</creatorcontrib><creatorcontrib>Yang, Hyung In</creatorcontrib><creatorcontrib>Park, Dong Suk</creatorcontrib><collection>Pascal-Francis</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><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baek, Yong Hyeon</au><au>Choi, Do Young</au><au>Yang, Hyung In</au><au>Park, Dong Suk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analgesic effect of electroacupuncture on inflammatory pain in the rat model of collagen-induced arthritis: Mediation by cholinergic and serotonergic receptors</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2005-09-28</date><risdate>2005</risdate><volume>1057</volume><issue>1</issue><spage>181</spage><epage>185</epage><pages>181-185</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>The analgesic effect and its mechanism of electroacupuncture (EA) on inflammatory pain, especially in the rat model of collagen-induced arthritis (CIA), have not yet been studied. This study was designed to investigate the analgesic effect and its cholinergic and serotonergic mechanism of EA in the CIA rat model. To induce CIA, male Sprague–Dawley rats were immunized with bovine type II collagen emulsified in Freund's incomplete adjuvant, followed by a booster injection 14 days later. The analgesic effect was evaluated by tail flick latency (TFL). After induction of arthritis, the inflammatory pain threshold decreased as time passed and there was no big change of the pain threshold after 3 weeks. Three weeks after the first immunization, low frequency EA stimulation (2 Hz, 0.07 mA, 0.3 ms) delivered to Zusanli (ST
36) for 30 min showed the analgesic effect. Also, the analgesic effect of EA was blocked by pretreatment with atropine (muscarinic cholinergic receptor antagonist, 1 mg/kg i.p.), spiroxatrine (5-HT1a receptor antagonist, 1 mg/kg i.p.), and ondansetron (5-HT3 receptor antagonist, 0.5 mg/kg i.p.), but not by pretreatment with ketanserin (5-HT2 receptor antagonist, 1 mg/kg i.p.). These results suggest that low frequency EA can relieve inflammatory pain in CIA and the analgesic effect of EA can be mediated by muscarinic cholinergic receptor, 5-HT1a and 5-HT3 receptors, but not by 5-HT2 receptor.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>16139820</pmid><doi>10.1016/j.brainres.2005.07.014</doi><tpages>5</tpages></addata></record> |
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subjects | Acupuncture Points Analgesics Analysis of Variance Animals Arthritis, Experimental - therapy Atropine Biological and medical sciences Cholinesterase Inhibitors - administration & dosage Collagen-induced arthritis Dioxanes - administration & dosage Disease Models, Animal Diseases of the osteoarticular system Drug Interactions Electroacupuncture Inflammation - complications Inflammation - therapy Ketanserin Male Medical sciences Miscellaneous Miscellaneous. Osteoarticular involvement in other diseases Neostigmine - administration & dosage Neuropharmacology Ondansetron Pain - etiology Pain Management Pain Measurement - methods Pain Threshold - physiology Pharmacology. Drug treatments Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) Rats Rats, Sprague-Dawley Reaction Time - physiology Serotonin Antagonists - administration & dosage Spiro Compounds - administration & dosage Spiroxatrine Time Factors |
title | Analgesic effect of electroacupuncture on inflammatory pain in the rat model of collagen-induced arthritis: Mediation by cholinergic and serotonergic receptors |
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