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Inhibition on acid‐sensing ion channels and analgesic activities of flavonoids isolated from dragon's blood resin
Acid‐sensing ion channel (ASIC) serves important roles in the transmission of nociceptive information. To confirm the analgesic mechanism of dragon's blood resin, patch–clamp technique, in vivo animal experiments, and immunohistochemical staining were used to observe the effects of the three fl...
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Published in: | Phytotherapy research 2019-03, Vol.33 (3), p.718-727 |
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description | Acid‐sensing ion channel (ASIC) serves important roles in the transmission of nociceptive information. To confirm the analgesic mechanism of dragon's blood resin, patch–clamp technique, in vivo animal experiments, and immunohistochemical staining were used to observe the effects of the three flavonoids (loureirin B, cochinchinemin A, and cochinchinemin B) isolated from dragon's blood resin on ASIC. Results showed that the three flavonoids exerted various inhibitory effects on ASIC currents in rat dorsal root ganglion (DRG) neurons. The combination of the three flavonoids with total concentration of 6.5 μM could decrease (53.8 ± 4.3%) of the peak amplitude and (45.8 ± 4.5%) of the sustained portion of ASIC currents. The combination of the three flavonoids was fully efficacious on complete Freud's adjuvant (CFA)–induced inflammatory thermal hyperalgesia at a dose of 6.5 mM similar with amiloride at 10 mM. The analgesic effects of the combination could be weakened by an ASIC activator 2‐guanidine‐4‐methylquinazoline. CFA‐induced hyperalgesia was accompanied by c‐Fos up‐regulation in DRG neurons, and the combination rescued thermal hyperalgesia through down‐regulation of c‐Fos and ASIC3 expression in CFA‐induced inflammation. These collective results suggested that the flavonoids isolated from dragon's blood resin could be considered as the chemical compounds that exert analgesic effects on inflammatory thermal pain due to action on ASIC. |
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To confirm the analgesic mechanism of dragon's blood resin, patch–clamp technique, in vivo animal experiments, and immunohistochemical staining were used to observe the effects of the three flavonoids (loureirin B, cochinchinemin A, and cochinchinemin B) isolated from dragon's blood resin on ASIC. Results showed that the three flavonoids exerted various inhibitory effects on ASIC currents in rat dorsal root ganglion (DRG) neurons. The combination of the three flavonoids with total concentration of 6.5 μM could decrease (53.8 ± 4.3%) of the peak amplitude and (45.8 ± 4.5%) of the sustained portion of ASIC currents. The combination of the three flavonoids was fully efficacious on complete Freud's adjuvant (CFA)–induced inflammatory thermal hyperalgesia at a dose of 6.5 mM similar with amiloride at 10 mM. The analgesic effects of the combination could be weakened by an ASIC activator 2‐guanidine‐4‐methylquinazoline. CFA‐induced hyperalgesia was accompanied by c‐Fos up‐regulation in DRG neurons, and the combination rescued thermal hyperalgesia through down‐regulation of c‐Fos and ASIC3 expression in CFA‐induced inflammation. These collective results suggested that the flavonoids isolated from dragon's blood resin could be considered as the chemical compounds that exert analgesic effects on inflammatory thermal pain due to action on ASIC.</description><identifier>ISSN: 0951-418X</identifier><identifier>EISSN: 1099-1573</identifier><identifier>DOI: 10.1002/ptr.6262</identifier><identifier>PMID: 30618119</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Acidity ; Acids ; acid‐sensing ion channel ; Amiloride ; Analgesics ; Animal research ; Blood ; Chemical compounds ; Dorsal root ganglia ; dorsal root ganglion neuron ; dragon's blood resin ; flavonoid ; Flavonoids ; Guanidine ; Hyperalgesia ; In vivo methods and tests ; Inflammation ; inflammatory thermal hyperalgesia model ; Ion channels ; Neurons ; Organic chemistry ; Pain ; Pain perception ; Resins ; Sodium channels</subject><ispartof>Phytotherapy research, 2019-03, Vol.33 (3), p.718-727</ispartof><rights>2019 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3492-bce810de5aae1d008823fe4bf222932eaff2ac25b3fcddb53cb06adb0e9223373</citedby><cites>FETCH-LOGICAL-c3492-bce810de5aae1d008823fe4bf222932eaff2ac25b3fcddb53cb06adb0e9223373</cites><orcidid>0000-0001-5922-6344</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30618119$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wan, Ying</creatorcontrib><creatorcontrib>Yu, Yi</creatorcontrib><creatorcontrib>Pan, Xinxin</creatorcontrib><creatorcontrib>Mo, Xiaoqiang</creatorcontrib><creatorcontrib>Gong, Weifan</creatorcontrib><creatorcontrib>Liu, Xiangming</creatorcontrib><creatorcontrib>Chen, Su</creatorcontrib><title>Inhibition on acid‐sensing ion channels and analgesic activities of flavonoids isolated from dragon's blood resin</title><title>Phytotherapy research</title><addtitle>Phytother Res</addtitle><description>Acid‐sensing ion channel (ASIC) serves important roles in the transmission of nociceptive information. To confirm the analgesic mechanism of dragon's blood resin, patch–clamp technique, in vivo animal experiments, and immunohistochemical staining were used to observe the effects of the three flavonoids (loureirin B, cochinchinemin A, and cochinchinemin B) isolated from dragon's blood resin on ASIC. Results showed that the three flavonoids exerted various inhibitory effects on ASIC currents in rat dorsal root ganglion (DRG) neurons. The combination of the three flavonoids with total concentration of 6.5 μM could decrease (53.8 ± 4.3%) of the peak amplitude and (45.8 ± 4.5%) of the sustained portion of ASIC currents. The combination of the three flavonoids was fully efficacious on complete Freud's adjuvant (CFA)–induced inflammatory thermal hyperalgesia at a dose of 6.5 mM similar with amiloride at 10 mM. The analgesic effects of the combination could be weakened by an ASIC activator 2‐guanidine‐4‐methylquinazoline. CFA‐induced hyperalgesia was accompanied by c‐Fos up‐regulation in DRG neurons, and the combination rescued thermal hyperalgesia through down‐regulation of c‐Fos and ASIC3 expression in CFA‐induced inflammation. These collective results suggested that the flavonoids isolated from dragon's blood resin could be considered as the chemical compounds that exert analgesic effects on inflammatory thermal pain due to action on ASIC.</description><subject>Acidity</subject><subject>Acids</subject><subject>acid‐sensing ion channel</subject><subject>Amiloride</subject><subject>Analgesics</subject><subject>Animal research</subject><subject>Blood</subject><subject>Chemical compounds</subject><subject>Dorsal root ganglia</subject><subject>dorsal root ganglion neuron</subject><subject>dragon's blood resin</subject><subject>flavonoid</subject><subject>Flavonoids</subject><subject>Guanidine</subject><subject>Hyperalgesia</subject><subject>In vivo methods and tests</subject><subject>Inflammation</subject><subject>inflammatory thermal hyperalgesia model</subject><subject>Ion channels</subject><subject>Neurons</subject><subject>Organic chemistry</subject><subject>Pain</subject><subject>Pain perception</subject><subject>Resins</subject><subject>Sodium channels</subject><issn>0951-418X</issn><issn>1099-1573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kdtKXDEUhkOp1FELfYIS6EW92XYlmX3IZZFaBcFSLHi3yWFljGSSabJH8c5H6DP6JGY8FQqFhED4_g_W-gn5wOCAAfAvqykfdLzjb8iMgZQNa3vxlsxAtqyZs-Fim-yUcgUAksP8HdkW0LGBMTkj5SReeu0nnyKtRxlv7-_-FIzFxwXd_JpLFSOGQlW09aqwwOJNJSd_XXNYaHLUBXWdYvK2UF9SUBNa6nJaUpvVIsXPheqQkqW5ZuMe2XIqFHz__O6SX0ffzg-Pm9Oz7yeHX08bI-aSN9rgwMBiqxQyCzAMXDica8c5l4Kjco4rw1stnLFWt8Jo6JTVgJJzIXqxS_afvKucfq-xTOPSF4MhqIhpXUbOuhbkIPu2op_-Qa_SOtdhN5SEnres53-FJqdSMrpxlf1S5duRwbgpYqxFjJsiKvrxWbjWS7Sv4MvmK9A8ATc-4O1_ReOP85-PwgeCypSn</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Wan, Ying</creator><creator>Yu, Yi</creator><creator>Pan, Xinxin</creator><creator>Mo, Xiaoqiang</creator><creator>Gong, Weifan</creator><creator>Liu, Xiangming</creator><creator>Chen, Su</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5922-6344</orcidid></search><sort><creationdate>201903</creationdate><title>Inhibition on acid‐sensing ion channels and analgesic activities of flavonoids isolated from dragon's blood resin</title><author>Wan, Ying ; Yu, Yi ; Pan, Xinxin ; Mo, Xiaoqiang ; Gong, Weifan ; Liu, Xiangming ; Chen, Su</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3492-bce810de5aae1d008823fe4bf222932eaff2ac25b3fcddb53cb06adb0e9223373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acidity</topic><topic>Acids</topic><topic>acid‐sensing ion channel</topic><topic>Amiloride</topic><topic>Analgesics</topic><topic>Animal research</topic><topic>Blood</topic><topic>Chemical compounds</topic><topic>Dorsal root ganglia</topic><topic>dorsal root ganglion neuron</topic><topic>dragon's blood resin</topic><topic>flavonoid</topic><topic>Flavonoids</topic><topic>Guanidine</topic><topic>Hyperalgesia</topic><topic>In vivo methods and tests</topic><topic>Inflammation</topic><topic>inflammatory thermal hyperalgesia model</topic><topic>Ion channels</topic><topic>Neurons</topic><topic>Organic chemistry</topic><topic>Pain</topic><topic>Pain perception</topic><topic>Resins</topic><topic>Sodium channels</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wan, Ying</creatorcontrib><creatorcontrib>Yu, Yi</creatorcontrib><creatorcontrib>Pan, Xinxin</creatorcontrib><creatorcontrib>Mo, Xiaoqiang</creatorcontrib><creatorcontrib>Gong, Weifan</creatorcontrib><creatorcontrib>Liu, Xiangming</creatorcontrib><creatorcontrib>Chen, Su</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Phytotherapy research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wan, Ying</au><au>Yu, Yi</au><au>Pan, Xinxin</au><au>Mo, Xiaoqiang</au><au>Gong, Weifan</au><au>Liu, Xiangming</au><au>Chen, Su</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition on acid‐sensing ion channels and analgesic activities of flavonoids isolated from dragon's blood resin</atitle><jtitle>Phytotherapy research</jtitle><addtitle>Phytother Res</addtitle><date>2019-03</date><risdate>2019</risdate><volume>33</volume><issue>3</issue><spage>718</spage><epage>727</epage><pages>718-727</pages><issn>0951-418X</issn><eissn>1099-1573</eissn><abstract>Acid‐sensing ion channel (ASIC) serves important roles in the transmission of nociceptive information. To confirm the analgesic mechanism of dragon's blood resin, patch–clamp technique, in vivo animal experiments, and immunohistochemical staining were used to observe the effects of the three flavonoids (loureirin B, cochinchinemin A, and cochinchinemin B) isolated from dragon's blood resin on ASIC. Results showed that the three flavonoids exerted various inhibitory effects on ASIC currents in rat dorsal root ganglion (DRG) neurons. The combination of the three flavonoids with total concentration of 6.5 μM could decrease (53.8 ± 4.3%) of the peak amplitude and (45.8 ± 4.5%) of the sustained portion of ASIC currents. The combination of the three flavonoids was fully efficacious on complete Freud's adjuvant (CFA)–induced inflammatory thermal hyperalgesia at a dose of 6.5 mM similar with amiloride at 10 mM. The analgesic effects of the combination could be weakened by an ASIC activator 2‐guanidine‐4‐methylquinazoline. CFA‐induced hyperalgesia was accompanied by c‐Fos up‐regulation in DRG neurons, and the combination rescued thermal hyperalgesia through down‐regulation of c‐Fos and ASIC3 expression in CFA‐induced inflammation. These collective results suggested that the flavonoids isolated from dragon's blood resin could be considered as the chemical compounds that exert analgesic effects on inflammatory thermal pain due to action on ASIC.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30618119</pmid><doi>10.1002/ptr.6262</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-5922-6344</orcidid></addata></record> |
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subjects | Acidity Acids acid‐sensing ion channel Amiloride Analgesics Animal research Blood Chemical compounds Dorsal root ganglia dorsal root ganglion neuron dragon's blood resin flavonoid Flavonoids Guanidine Hyperalgesia In vivo methods and tests Inflammation inflammatory thermal hyperalgesia model Ion channels Neurons Organic chemistry Pain Pain perception Resins Sodium channels |
title | Inhibition on acid‐sensing ion channels and analgesic activities of flavonoids isolated from dragon's blood resin |
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