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Effect of various antagonists on the Channa striatus fillet extract antinociception in mice
The effects of an aqueous supernatant of haruan (ASH) (Channa striatus) fillet extract on various antinociception receptor system activities were examined using a mouse abdominal-constriction model. Mice that were pretreated with distilled water, s.c., followed 10 min later by administration of 25%,...
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Published in: | Canadian journal of physiology and pharmacology 2005-07, Vol.83 (7), p.635-642 |
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container_title | Canadian journal of physiology and pharmacology |
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creator | Zakaria, Z A Sulaiman, M R Jais, A M. Mat Somchit, M N |
description | The effects of an aqueous supernatant of haruan (ASH) (Channa striatus) fillet extract on various antinociception receptor system activities were examined using a mouse abdominal-constriction model. Mice that were pretreated with distilled water, s.c., followed 10 min later by administration of 25%, 50%, and 100% concentration ASH, s.c., produced a significant concentration-dependent antinociceptive activity (p < 0.001). Pretreatment with naloxone (0.3, 1.0, and 3.0 mg/kg body mass), 10 min before ASH administration, failed to block the extract antinociception. Pretreatment of the 100% concentration ASH with mecamylamine (5 mg/kg), pindolol (10 mg/kg), and haloperidol (1 mg/kg) also did not cause any significant change in its antinociception. However, pretreatment with atropine (5 mg/kg), bicuculline (10 mg/kg), phenoxybenzamine (10mg/kg), and methysergide (5 mg/kg) were found to reverse ASH antinociception. Based on the above findings, the ASH is suggested to contain different types of bioactive compounds that act synergistically on muscarinic, GABA
A
, α-adrenergic, and serotonergic receptor systems to produce the observed antinocicep tion.
Key words: Haruan (Channa striatus), antinociceptive, writhing test, receptor systems |
doi_str_mv | 10.1139/y05-050 |
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A
, α-adrenergic, and serotonergic receptor systems to produce the observed antinocicep tion.
Key words: Haruan (Channa striatus), antinociceptive, writhing test, receptor systems</description><identifier>ISSN: 0008-4212</identifier><identifier>EISSN: 1205-7541</identifier><identifier>DOI: 10.1139/y05-050</identifier><identifier>PMID: 16091789</identifier><identifier>CODEN: CJPPA3</identifier><language>eng</language><publisher>Ottawa, Canada: NRC Research Press</publisher><subject>Amino acids ; Analgesics ; Animals ; Anti-Inflammatory Agents, Non-Steroidal - pharmacology ; Aspirin - pharmacology ; Biological and medical sciences ; Diet ; Dose-Response Relationship, Drug ; Fatty acids ; Fish ; Fundamental and applied biological sciences. Psychology ; Male ; Medical applications ; Mice ; Mice, Inbred BALB C ; Muscle Contraction - drug effects ; Muscle, Skeletal - physiology ; Naloxone - pharmacology ; Narcotic Antagonists - pharmacology ; Pain Measurement - drug effects ; Perciformes - physiology ; Reaction Time - drug effects ; Receptors, Cell Surface - antagonists & inhibitors ; Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors ; Tissue Extracts - antagonists & inhibitors ; Tissue Extracts - physiology ; Vertebrates: nervous system and sense organs ; Wound healing</subject><ispartof>Canadian journal of physiology and pharmacology, 2005-07, Vol.83 (7), p.635-642</ispartof><rights>2006 INIST-CNRS</rights><rights>Copyright National Research Council of Canada Jul 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-a2656f758ba47faada78746d104041047359ad9063d124b8bb195a9ee5d98fc03</citedby><cites>FETCH-LOGICAL-c402t-a2656f758ba47faada78746d104041047359ad9063d124b8bb195a9ee5d98fc03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17213482$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16091789$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zakaria, Z A</creatorcontrib><creatorcontrib>Sulaiman, M R</creatorcontrib><creatorcontrib>Jais, A M. Mat</creatorcontrib><creatorcontrib>Somchit, M N</creatorcontrib><title>Effect of various antagonists on the Channa striatus fillet extract antinociception in mice</title><title>Canadian journal of physiology and pharmacology</title><addtitle>Revue canadienne de physiologie et pharmacologie</addtitle><description>The effects of an aqueous supernatant of haruan (ASH) (Channa striatus) fillet extract on various antinociception receptor system activities were examined using a mouse abdominal-constriction model. Mice that were pretreated with distilled water, s.c., followed 10 min later by administration of 25%, 50%, and 100% concentration ASH, s.c., produced a significant concentration-dependent antinociceptive activity (p < 0.001). Pretreatment with naloxone (0.3, 1.0, and 3.0 mg/kg body mass), 10 min before ASH administration, failed to block the extract antinociception. Pretreatment of the 100% concentration ASH with mecamylamine (5 mg/kg), pindolol (10 mg/kg), and haloperidol (1 mg/kg) also did not cause any significant change in its antinociception. However, pretreatment with atropine (5 mg/kg), bicuculline (10 mg/kg), phenoxybenzamine (10mg/kg), and methysergide (5 mg/kg) were found to reverse ASH antinociception. Based on the above findings, the ASH is suggested to contain different types of bioactive compounds that act synergistically on muscarinic, GABA
A
, α-adrenergic, and serotonergic receptor systems to produce the observed antinocicep tion.
Key words: Haruan (Channa striatus), antinociceptive, writhing test, receptor systems</description><subject>Amino acids</subject><subject>Analgesics</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - pharmacology</subject><subject>Aspirin - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Diet</subject><subject>Dose-Response Relationship, Drug</subject><subject>Fatty acids</subject><subject>Fish</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Male</subject><subject>Medical applications</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle, Skeletal - physiology</subject><subject>Naloxone - pharmacology</subject><subject>Narcotic Antagonists - pharmacology</subject><subject>Pain Measurement - drug effects</subject><subject>Perciformes - physiology</subject><subject>Reaction Time - drug effects</subject><subject>Receptors, Cell Surface - antagonists & inhibitors</subject><subject>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors</subject><subject>Tissue Extracts - antagonists & inhibitors</subject><subject>Tissue Extracts - physiology</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Wound healing</subject><issn>0008-4212</issn><issn>1205-7541</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp90F1rFDEUBuAgil2r-A8kCFYQRvM1k-SyLG0VCt7olRfhTCZxU2Yza5IV--89sgMFQW-SHHjOSfIS8pKz95xL--Ge9R3r2SOy4QKPulf8MdkwxkynBBdn5Fmtd1gORpqn5IwPzHJt7IZ8u4ox-EaXSH9CScuxUsgNvi851VbpkmnbBbrdQc5AaysJGpKY5jk0Gn61AtiMHSkvPvlwaAlbUqZ7LJ6TJxHmGl6s-zn5en31Zfuxu_1882l7edt5xUTrQAz9EHVvRlA6AkygjVbDxJliChctewuTZYOcuFCjGUdue7Ah9JM10TN5Ti5Ocw9l-XEMtbl9qj7MM-SAH3KDUYOyUiJ8_Re8W44l49ucEFwLIa1G9PaEfFlqLSG6Q0l7KPeOM_cnbIdhOwwb5at13HHch-nBrekieLMCqB7mWCD7VB-cFlwqI9C9O7lcfAk1QPG7_9x68W-8IneYovwNHD-hjQ</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Zakaria, Z A</creator><creator>Sulaiman, M R</creator><creator>Jais, A M. 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Mat ; Somchit, M N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-a2656f758ba47faada78746d104041047359ad9063d124b8bb195a9ee5d98fc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Amino acids</topic><topic>Analgesics</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - pharmacology</topic><topic>Aspirin - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Diet</topic><topic>Dose-Response Relationship, Drug</topic><topic>Fatty acids</topic><topic>Fish</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Male</topic><topic>Medical applications</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle, Skeletal - physiology</topic><topic>Naloxone - pharmacology</topic><topic>Narcotic Antagonists - pharmacology</topic><topic>Pain Measurement - drug effects</topic><topic>Perciformes - physiology</topic><topic>Reaction Time - drug effects</topic><topic>Receptors, Cell Surface - antagonists & inhibitors</topic><topic>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. 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Mat</au><au>Somchit, M N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of various antagonists on the Channa striatus fillet extract antinociception in mice</atitle><jtitle>Canadian journal of physiology and pharmacology</jtitle><addtitle>Revue canadienne de physiologie et pharmacologie</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>83</volume><issue>7</issue><spage>635</spage><epage>642</epage><pages>635-642</pages><issn>0008-4212</issn><eissn>1205-7541</eissn><coden>CJPPA3</coden><abstract>The effects of an aqueous supernatant of haruan (ASH) (Channa striatus) fillet extract on various antinociception receptor system activities were examined using a mouse abdominal-constriction model. Mice that were pretreated with distilled water, s.c., followed 10 min later by administration of 25%, 50%, and 100% concentration ASH, s.c., produced a significant concentration-dependent antinociceptive activity (p < 0.001). Pretreatment with naloxone (0.3, 1.0, and 3.0 mg/kg body mass), 10 min before ASH administration, failed to block the extract antinociception. Pretreatment of the 100% concentration ASH with mecamylamine (5 mg/kg), pindolol (10 mg/kg), and haloperidol (1 mg/kg) also did not cause any significant change in its antinociception. However, pretreatment with atropine (5 mg/kg), bicuculline (10 mg/kg), phenoxybenzamine (10mg/kg), and methysergide (5 mg/kg) were found to reverse ASH antinociception. Based on the above findings, the ASH is suggested to contain different types of bioactive compounds that act synergistically on muscarinic, GABA
A
, α-adrenergic, and serotonergic receptor systems to produce the observed antinocicep tion.
Key words: Haruan (Channa striatus), antinociceptive, writhing test, receptor systems</abstract><cop>Ottawa, Canada</cop><pub>NRC Research Press</pub><pmid>16091789</pmid><doi>10.1139/y05-050</doi><tpages>8</tpages></addata></record> |
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subjects | Amino acids Analgesics Animals Anti-Inflammatory Agents, Non-Steroidal - pharmacology Aspirin - pharmacology Biological and medical sciences Diet Dose-Response Relationship, Drug Fatty acids Fish Fundamental and applied biological sciences. Psychology Male Medical applications Mice Mice, Inbred BALB C Muscle Contraction - drug effects Muscle, Skeletal - physiology Naloxone - pharmacology Narcotic Antagonists - pharmacology Pain Measurement - drug effects Perciformes - physiology Reaction Time - drug effects Receptors, Cell Surface - antagonists & inhibitors Somesthesis and somesthetic pathways (proprioception, exteroception, nociception) interoception electrolocation. Sensory receptors Tissue Extracts - antagonists & inhibitors Tissue Extracts - physiology Vertebrates: nervous system and sense organs Wound healing |
title | Effect of various antagonists on the Channa striatus fillet extract antinociception in mice |
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