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A Combined Water Extract of Frankincense and Myrrh Alleviates Neuropathic Pain in Mice via Modulation of TRPV1
Frankincense and myrrh are widely used in clinics as a pair of herbs to obtain a synergistic effect for relieving pain. To illuminate the analgesia mechanism of frankincense and myrrh, we assessed its effect in a neuropathic pain mouse model. Transient receptor potential vanilloid 1 (TRPV1) plays a...
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Published in: | Journal of neural transplantation & plasticity 2017-01, Vol.2017 (2017), p.1-11 |
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creator | Yu, Lei Gu, Leying Yuan, Xiaolin Wang, Zhongli Yu, Guang Tang, Zongxiang Shi, Hao Zhu, Chan Yang, Yan Yang, Niuniu Su, Shulan Li, Fengxian Wang, Changming Hu, Danyou Geng, Xiao |
description | Frankincense and myrrh are widely used in clinics as a pair of herbs to obtain a synergistic effect for relieving pain. To illuminate the analgesia mechanism of frankincense and myrrh, we assessed its effect in a neuropathic pain mouse model. Transient receptor potential vanilloid 1 (TRPV1) plays a crucial role in neuropathic pain and influences the plasticity of neuronal connectivity. We hypothesized that the water extraction of frankincense and myrrh (WFM) exerted its analgesia effect by modulating the neuronal function of TRPV1. In our study, WFM was verified by UHPLC-TQ/MS assay. In vivo study showed that nociceptive response in mouse by heat and capsaicin induced were relieved by WFM treatment. Furthermore, thermal hypersensitivity and mechanical allodynia were also alleviated by WFM treatment in a chronic constriction injury (CCI) mouse model. CCI resulted in increased TRPV1 expression at both the mRNA and protein levels in predominantly small-to-medium neurons. However, after WFM treatment, TRPV1 expression was reverted in real-time PCR, Western blot, and immunofluorescence experiments. Calcium response to capsaicin was also decreased in cultured DRG neurons from CCI model mouse after WFM treatment. In conclusion, WFM alleviated CCI-induced mechanical allodynia and thermal hypersensitivity via modulating TRPV1. |
doi_str_mv | 10.1155/2017/3710821 |
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To illuminate the analgesia mechanism of frankincense and myrrh, we assessed its effect in a neuropathic pain mouse model. Transient receptor potential vanilloid 1 (TRPV1) plays a crucial role in neuropathic pain and influences the plasticity of neuronal connectivity. We hypothesized that the water extraction of frankincense and myrrh (WFM) exerted its analgesia effect by modulating the neuronal function of TRPV1. In our study, WFM was verified by UHPLC-TQ/MS assay. In vivo study showed that nociceptive response in mouse by heat and capsaicin induced were relieved by WFM treatment. Furthermore, thermal hypersensitivity and mechanical allodynia were also alleviated by WFM treatment in a chronic constriction injury (CCI) mouse model. CCI resulted in increased TRPV1 expression at both the mRNA and protein levels in predominantly small-to-medium neurons. However, after WFM treatment, TRPV1 expression was reverted in real-time PCR, Western blot, and immunofluorescence experiments. Calcium response to capsaicin was also decreased in cultured DRG neurons from CCI model mouse after WFM treatment. In conclusion, WFM alleviated CCI-induced mechanical allodynia and thermal hypersensitivity via modulating TRPV1.</description><identifier>ISSN: 2090-5904</identifier><identifier>ISSN: 0792-8483</identifier><identifier>EISSN: 1687-5443</identifier><identifier>DOI: 10.1155/2017/3710821</identifier><identifier>PMID: 28740739</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Acids ; Analgesics - administration & dosage ; Animals ; Care and treatment ; Cells, Cultured ; Drug withdrawal ; Experiments ; Frankincense - administration & dosage ; Frankincense - chemistry ; Ganglia, Spinal - drug effects ; Gas flow ; Health aspects ; Male ; Medical research ; Mice, Inbred C57BL ; Myrrh ; Neuralgia - drug therapy ; Neuralgia - metabolism ; Neurons ; Neurons - drug effects ; Neurons - metabolism ; Pain ; Pain Threshold - drug effects ; Peripheral nerve diseases ; Resins, Plant - administration & dosage ; Resins, Plant - chemistry ; TRPV Cation Channels - metabolism ; Water - administration & dosage</subject><ispartof>Journal of neural transplantation & plasticity, 2017-01, Vol.2017 (2017), p.1-11</ispartof><rights>Copyright © 2017 Danyou Hu et al.</rights><rights>COPYRIGHT 2017 John Wiley & Sons, Inc.</rights><rights>Copyright © 2017 Danyou Hu et al. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2017 Danyou Hu et al. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c635t-fd024acb44bf3e096ca0f2f0f2a63b5b6e29700cf63379b822831baf7b8901fa3</citedby><cites>FETCH-LOGICAL-c635t-fd024acb44bf3e096ca0f2f0f2a63b5b6e29700cf63379b822831baf7b8901fa3</cites><orcidid>0000-0001-7918-0160 ; 0000-0003-2803-0984</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2407660658/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2407660658?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28740739$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Pan, Fang</contributor><contributor>Fang Pan</contributor><creatorcontrib>Yu, Lei</creatorcontrib><creatorcontrib>Gu, Leying</creatorcontrib><creatorcontrib>Yuan, Xiaolin</creatorcontrib><creatorcontrib>Wang, Zhongli</creatorcontrib><creatorcontrib>Yu, Guang</creatorcontrib><creatorcontrib>Tang, Zongxiang</creatorcontrib><creatorcontrib>Shi, Hao</creatorcontrib><creatorcontrib>Zhu, Chan</creatorcontrib><creatorcontrib>Yang, Yan</creatorcontrib><creatorcontrib>Yang, Niuniu</creatorcontrib><creatorcontrib>Su, Shulan</creatorcontrib><creatorcontrib>Li, Fengxian</creatorcontrib><creatorcontrib>Wang, Changming</creatorcontrib><creatorcontrib>Hu, Danyou</creatorcontrib><creatorcontrib>Geng, Xiao</creatorcontrib><title>A Combined Water Extract of Frankincense and Myrrh Alleviates Neuropathic Pain in Mice via Modulation of TRPV1</title><title>Journal of neural transplantation & plasticity</title><addtitle>Neural Plast</addtitle><description>Frankincense and myrrh are widely used in clinics as a pair of herbs to obtain a synergistic effect for relieving pain. To illuminate the analgesia mechanism of frankincense and myrrh, we assessed its effect in a neuropathic pain mouse model. Transient receptor potential vanilloid 1 (TRPV1) plays a crucial role in neuropathic pain and influences the plasticity of neuronal connectivity. We hypothesized that the water extraction of frankincense and myrrh (WFM) exerted its analgesia effect by modulating the neuronal function of TRPV1. In our study, WFM was verified by UHPLC-TQ/MS assay. In vivo study showed that nociceptive response in mouse by heat and capsaicin induced were relieved by WFM treatment. Furthermore, thermal hypersensitivity and mechanical allodynia were also alleviated by WFM treatment in a chronic constriction injury (CCI) mouse model. CCI resulted in increased TRPV1 expression at both the mRNA and protein levels in predominantly small-to-medium neurons. However, after WFM treatment, TRPV1 expression was reverted in real-time PCR, Western blot, and immunofluorescence experiments. Calcium response to capsaicin was also decreased in cultured DRG neurons from CCI model mouse after WFM treatment. In conclusion, WFM alleviated CCI-induced mechanical allodynia and thermal hypersensitivity via modulating TRPV1.</description><subject>Acids</subject><subject>Analgesics - administration & dosage</subject><subject>Animals</subject><subject>Care and treatment</subject><subject>Cells, Cultured</subject><subject>Drug withdrawal</subject><subject>Experiments</subject><subject>Frankincense - administration & dosage</subject><subject>Frankincense - chemistry</subject><subject>Ganglia, Spinal - drug effects</subject><subject>Gas flow</subject><subject>Health aspects</subject><subject>Male</subject><subject>Medical research</subject><subject>Mice, Inbred C57BL</subject><subject>Myrrh</subject><subject>Neuralgia - drug therapy</subject><subject>Neuralgia - metabolism</subject><subject>Neurons</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Pain</subject><subject>Pain Threshold - drug effects</subject><subject>Peripheral nerve diseases</subject><subject>Resins, Plant - administration & dosage</subject><subject>Resins, Plant - chemistry</subject><subject>TRPV Cation Channels - metabolism</subject><subject>Water - administration & dosage</subject><issn>2090-5904</issn><issn>0792-8483</issn><issn>1687-5443</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl1rFDEUhgdR7Fq981oCggi6bTL5mOSmsCytFrpapOplyGSSnayzyZrMVPvvzbhr2xUvJBMCyXMemPeconiO4BFClB6XEFXHuEKQl-hBMUGMV1NKCH5YTEoo4JQKSA6KJymtICSMUvq4OCh5RWCFxaTwMzAP69p504CvqjcRnP7so9I9CBacReW_Oa-NTwYo34DFTYwtmHWduXYZTuCDGWLYqL51Glwq50H-Fk4bkN_BIjRDp3oX_Ci7-nT5BT0tHlnVJfNsdx4Wn89Or-bvpxcf353PZxdTzTDtp7aBJVG6JqS22EDBtIK2tHkrhmtaM1OKCkJtGcaVqHlZcoxqZauaC4iswofF-dbbBLWSm-jWKt7IoJz8fRHiUqrYO90ZyWFNOc_1FWIE6YZjrBnkFHKElbEmu062rs1Qr02T08gBdXvS_RfvWrkM15JSSASlWfB6J4jh-2BSL9cuadN1ypswJIlEiRHCkMCMvvwLXYUh-hyVLHPHGIOM8jtqqfIPOG_D2LJRKmeUMI4FEiJTR_-g8mrM2ungjXX5fq_g1b2C1qiub1PohrGDaR98uwV1DClFY2_DQFCOQynHoZS7ocz4i_sB3sJ_pjADb7ZA63yjfrj_1JnMGKvu6BykqCr8C7fE73M</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Yu, Lei</creator><creator>Gu, Leying</creator><creator>Yuan, Xiaolin</creator><creator>Wang, Zhongli</creator><creator>Yu, Guang</creator><creator>Tang, Zongxiang</creator><creator>Shi, Hao</creator><creator>Zhu, Chan</creator><creator>Yang, Yan</creator><creator>Yang, Niuniu</creator><creator>Su, Shulan</creator><creator>Li, Fengxian</creator><creator>Wang, Changming</creator><creator>Hu, Danyou</creator><creator>Geng, Xiao</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>K9.</scope><scope>M0S</scope><scope>M2M</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-7918-0160</orcidid><orcidid>https://orcid.org/0000-0003-2803-0984</orcidid></search><sort><creationdate>20170101</creationdate><title>A Combined Water Extract of Frankincense and Myrrh Alleviates Neuropathic Pain in Mice via Modulation of TRPV1</title><author>Yu, Lei ; Gu, Leying ; Yuan, Xiaolin ; Wang, Zhongli ; Yu, Guang ; Tang, Zongxiang ; Shi, Hao ; Zhu, Chan ; Yang, Yan ; Yang, Niuniu ; Su, Shulan ; Li, Fengxian ; Wang, Changming ; Hu, Danyou ; Geng, Xiao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c635t-fd024acb44bf3e096ca0f2f0f2a63b5b6e29700cf63379b822831baf7b8901fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acids</topic><topic>Analgesics - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of neural transplantation & plasticity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Lei</au><au>Gu, Leying</au><au>Yuan, Xiaolin</au><au>Wang, Zhongli</au><au>Yu, Guang</au><au>Tang, Zongxiang</au><au>Shi, Hao</au><au>Zhu, Chan</au><au>Yang, Yan</au><au>Yang, Niuniu</au><au>Su, Shulan</au><au>Li, Fengxian</au><au>Wang, Changming</au><au>Hu, Danyou</au><au>Geng, Xiao</au><au>Pan, Fang</au><au>Fang Pan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Combined Water Extract of Frankincense and Myrrh Alleviates Neuropathic Pain in Mice via Modulation of TRPV1</atitle><jtitle>Journal of neural transplantation & plasticity</jtitle><addtitle>Neural Plast</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>2017</volume><issue>2017</issue><spage>1</spage><epage>11</epage><pages>1-11</pages><issn>2090-5904</issn><issn>0792-8483</issn><eissn>1687-5443</eissn><abstract>Frankincense and myrrh are widely used in clinics as a pair of herbs to obtain a synergistic effect for relieving pain. To illuminate the analgesia mechanism of frankincense and myrrh, we assessed its effect in a neuropathic pain mouse model. Transient receptor potential vanilloid 1 (TRPV1) plays a crucial role in neuropathic pain and influences the plasticity of neuronal connectivity. We hypothesized that the water extraction of frankincense and myrrh (WFM) exerted its analgesia effect by modulating the neuronal function of TRPV1. In our study, WFM was verified by UHPLC-TQ/MS assay. In vivo study showed that nociceptive response in mouse by heat and capsaicin induced were relieved by WFM treatment. Furthermore, thermal hypersensitivity and mechanical allodynia were also alleviated by WFM treatment in a chronic constriction injury (CCI) mouse model. CCI resulted in increased TRPV1 expression at both the mRNA and protein levels in predominantly small-to-medium neurons. However, after WFM treatment, TRPV1 expression was reverted in real-time PCR, Western blot, and immunofluorescence experiments. Calcium response to capsaicin was also decreased in cultured DRG neurons from CCI model mouse after WFM treatment. In conclusion, WFM alleviated CCI-induced mechanical allodynia and thermal hypersensitivity via modulating TRPV1.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>28740739</pmid><doi>10.1155/2017/3710821</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-7918-0160</orcidid><orcidid>https://orcid.org/0000-0003-2803-0984</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acids Analgesics - administration & dosage Animals Care and treatment Cells, Cultured Drug withdrawal Experiments Frankincense - administration & dosage Frankincense - chemistry Ganglia, Spinal - drug effects Gas flow Health aspects Male Medical research Mice, Inbred C57BL Myrrh Neuralgia - drug therapy Neuralgia - metabolism Neurons Neurons - drug effects Neurons - metabolism Pain Pain Threshold - drug effects Peripheral nerve diseases Resins, Plant - administration & dosage Resins, Plant - chemistry TRPV Cation Channels - metabolism Water - administration & dosage |
title | A Combined Water Extract of Frankincense and Myrrh Alleviates Neuropathic Pain in Mice via Modulation of TRPV1 |
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