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Scorpion alleviates bone cancer pain through inhibition of bone destruction and glia activation
Background Bone cancer pain is common in patients with advanced cancers as tumor metastasizes to bone. The inefficient clinical treatment severely reduces quality of life of bone cancer pain patients. During the pain status, activated spinal astrocytes and microglia release various inflammatory cyto...
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Published in: | Molecular pain 2020, Vol.16, p.1744806920909993-1744806920909993 |
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description | Background
Bone cancer pain is common in patients with advanced cancers as tumor metastasizes to bone. The inefficient clinical treatment severely reduces quality of life of bone cancer pain patients. During the pain status, activated spinal astrocytes and microglia release various inflammatory cytokines, resulting in spinal inflammation and the development of neuron sensitization. Scorpion is the dry body of Buthus martensii Karsch and is often used for various pain management in clinical practice. However, its function on bone cancer pain is unclear.
Methods
We investigated the effects of intragastric administration of scorpion on bone cancer pain induced by left tibial cavity injection of Walker 256 cells. Nociceptive behavior was measured using the von Frey filaments test and the spontaneous ambulatory pain score. The bone destruction was assessed by tibial radiographs. Expression of spinal cord astrocyte marker glial fibrillary acidic protein and microglial marker Iba1 was monitored by Western blot assay and immunofluorescence. Tumor necrosis factor-alpha (TNF-α), interleukin (IL)-6, and IL-1β was detected by real-time polymerase chain reaction. The proliferation of Walker 256 cells was evaluated by CCK8 assay.
Results
Intragastric administration of scorpion reduced bone cancer pain behavior and relieved bone destruction, accompanied by decreased expression of spinal glial fibrillary acidic protein and Iba1 protein level and TNF-α, IL-6, and IL-1β mRNA level. Besides, scorpion inhibited proliferation of Walker 256 cells in a dose- and time-dependent manner.
Conclusion
Our results demonstrate that scorpion produces an analgesic effect in a rat model of bone cancer pain via inhibiting bone destruction and activation of spinal cord astrocytes and microglia. |
doi_str_mv | 10.1177/1744806920909993 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7054730</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_1744806920909993</sage_id><sourcerecordid>2691742951</sourcerecordid><originalsourceid>FETCH-LOGICAL-c462t-b048af8fadab9d1a23c6e740190904ce48ea2bca68b5a199cc6dda7a673b386b3</originalsourceid><addsrcrecordid>eNp1kUtPxCAUhYnR-N67Mk3cuKnyGigbE2N8JSYu1DW5UDqD6cAI7ST-e1vHd-IKOHz3XA4XoQOCTwiR8pRIzissFMUKK6XYGtoepXLU1n_st9BOzs8YM4kF2URbjOIJFYpsI_1gY1r4GApoW7f00LlcmBhcYSFYl4oF-FB0sxT76azwYeaN70Y8NiusdrlLvX3XINTFtPVQwHBewqjtoY0G2uz2P9Zd9HR1-XhxU97dX99enN-VlgvalQbzCpqqgRqMqglQZoWTHJMhF-bW8coBNRZEZSZAlLJW1DVIEJIZVgnDdtHZynfRm7mrrQtdglYvkp9DetURvP59E_xMT-NSSzzhkuHB4PjDIMWXfgil5z5b17YQXOyzpmzkBGVkQI_-oM-xT2GIp8dPlZyqyUjhFWVTzDm55usxBOtxevrv9IaSw58hvgo-xzUA5QrIMHXfXf81fAMxl6Qu</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2691742951</pqid></control><display><type>article</type><title>Scorpion alleviates bone cancer pain through inhibition of bone destruction and glia activation</title><source>Publicly Available Content Database</source><source>SAGE Open Access Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Yu, Jiachuan ; Luo, Yuanyuan ; Jin, Huidan ; Lv, Jiaxin ; Zhou, Tingting ; Yabasin, Iddrisu Baba ; Wen, Qingping</creator><creatorcontrib>Yu, Jiachuan ; Luo, Yuanyuan ; Jin, Huidan ; Lv, Jiaxin ; Zhou, Tingting ; Yabasin, Iddrisu Baba ; Wen, Qingping</creatorcontrib><description>Background
Bone cancer pain is common in patients with advanced cancers as tumor metastasizes to bone. The inefficient clinical treatment severely reduces quality of life of bone cancer pain patients. During the pain status, activated spinal astrocytes and microglia release various inflammatory cytokines, resulting in spinal inflammation and the development of neuron sensitization. Scorpion is the dry body of Buthus martensii Karsch and is often used for various pain management in clinical practice. However, its function on bone cancer pain is unclear.
Methods
We investigated the effects of intragastric administration of scorpion on bone cancer pain induced by left tibial cavity injection of Walker 256 cells. Nociceptive behavior was measured using the von Frey filaments test and the spontaneous ambulatory pain score. The bone destruction was assessed by tibial radiographs. Expression of spinal cord astrocyte marker glial fibrillary acidic protein and microglial marker Iba1 was monitored by Western blot assay and immunofluorescence. Tumor necrosis factor-alpha (TNF-α), interleukin (IL)-6, and IL-1β was detected by real-time polymerase chain reaction. The proliferation of Walker 256 cells was evaluated by CCK8 assay.
Results
Intragastric administration of scorpion reduced bone cancer pain behavior and relieved bone destruction, accompanied by decreased expression of spinal glial fibrillary acidic protein and Iba1 protein level and TNF-α, IL-6, and IL-1β mRNA level. Besides, scorpion inhibited proliferation of Walker 256 cells in a dose- and time-dependent manner.
Conclusion
Our results demonstrate that scorpion produces an analgesic effect in a rat model of bone cancer pain via inhibiting bone destruction and activation of spinal cord astrocytes and microglia.</description><identifier>ISSN: 1744-8069</identifier><identifier>EISSN: 1744-8069</identifier><identifier>DOI: 10.1177/1744806920909993</identifier><identifier>PMID: 32052691</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Analgesics ; Animals ; Astrocytes ; Astrocytes - metabolism ; Behavior, Animal ; Biological Products - therapeutic use ; Bone and Bones - pathology ; Bone cancer ; Bone Neoplasms - drug therapy ; Bone Neoplasms - physiopathology ; Bone tumors ; Cancer Pain - drug therapy ; Cancer Pain - physiopathology ; Cell Line, Tumor ; Cell proliferation ; Female ; Filaments ; Glial fibrillary acidic protein ; Hyperalgesia ; IL-1β ; Immunofluorescence ; Inflammation ; Interleukin 6 ; Interleukin-1beta - metabolism ; Interleukin-6 - metabolism ; Mammary Neoplasms, Animal - pathology ; Microglia ; mRNA ; Neoplasm Transplantation ; Neuroglia - drug effects ; Neuroglia - metabolism ; Pain ; Pain perception ; Patients ; Proteins ; Quality of life ; Rats ; Rats, Sprague-Dawley ; Scorpions - chemistry ; Spinal cord ; Spinal Cord - metabolism ; Spinal Cord - pathology ; Stomach ; Tumor Necrosis Factor-alpha - metabolism ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α</subject><ispartof>Molecular pain, 2020, Vol.16, p.1744806920909993-1744806920909993</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/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>The Author(s) 2020 2020 SAGE Publications Inc., unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-b048af8fadab9d1a23c6e740190904ce48ea2bca68b5a199cc6dda7a673b386b3</citedby><cites>FETCH-LOGICAL-c462t-b048af8fadab9d1a23c6e740190904ce48ea2bca68b5a199cc6dda7a673b386b3</cites><orcidid>0000-0002-3311-9230</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/PMC7054730/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2691742951?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,4010,21945,25731,27830,27900,27901,27902,36989,36990,44566,44921,45309,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32052691$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Jiachuan</creatorcontrib><creatorcontrib>Luo, Yuanyuan</creatorcontrib><creatorcontrib>Jin, Huidan</creatorcontrib><creatorcontrib>Lv, Jiaxin</creatorcontrib><creatorcontrib>Zhou, Tingting</creatorcontrib><creatorcontrib>Yabasin, Iddrisu Baba</creatorcontrib><creatorcontrib>Wen, Qingping</creatorcontrib><title>Scorpion alleviates bone cancer pain through inhibition of bone destruction and glia activation</title><title>Molecular pain</title><addtitle>Mol Pain</addtitle><description>Background
Bone cancer pain is common in patients with advanced cancers as tumor metastasizes to bone. The inefficient clinical treatment severely reduces quality of life of bone cancer pain patients. During the pain status, activated spinal astrocytes and microglia release various inflammatory cytokines, resulting in spinal inflammation and the development of neuron sensitization. Scorpion is the dry body of Buthus martensii Karsch and is often used for various pain management in clinical practice. However, its function on bone cancer pain is unclear.
Methods
We investigated the effects of intragastric administration of scorpion on bone cancer pain induced by left tibial cavity injection of Walker 256 cells. Nociceptive behavior was measured using the von Frey filaments test and the spontaneous ambulatory pain score. The bone destruction was assessed by tibial radiographs. Expression of spinal cord astrocyte marker glial fibrillary acidic protein and microglial marker Iba1 was monitored by Western blot assay and immunofluorescence. Tumor necrosis factor-alpha (TNF-α), interleukin (IL)-6, and IL-1β was detected by real-time polymerase chain reaction. The proliferation of Walker 256 cells was evaluated by CCK8 assay.
Results
Intragastric administration of scorpion reduced bone cancer pain behavior and relieved bone destruction, accompanied by decreased expression of spinal glial fibrillary acidic protein and Iba1 protein level and TNF-α, IL-6, and IL-1β mRNA level. Besides, scorpion inhibited proliferation of Walker 256 cells in a dose- and time-dependent manner.
Conclusion
Our results demonstrate that scorpion produces an analgesic effect in a rat model of bone cancer pain via inhibiting bone destruction and activation of spinal cord astrocytes and microglia.</description><subject>Analgesics</subject><subject>Animals</subject><subject>Astrocytes</subject><subject>Astrocytes - metabolism</subject><subject>Behavior, Animal</subject><subject>Biological Products - therapeutic use</subject><subject>Bone and Bones - pathology</subject><subject>Bone cancer</subject><subject>Bone Neoplasms - drug therapy</subject><subject>Bone Neoplasms - physiopathology</subject><subject>Bone tumors</subject><subject>Cancer Pain - drug therapy</subject><subject>Cancer Pain - physiopathology</subject><subject>Cell Line, Tumor</subject><subject>Cell proliferation</subject><subject>Female</subject><subject>Filaments</subject><subject>Glial fibrillary acidic protein</subject><subject>Hyperalgesia</subject><subject>IL-1β</subject><subject>Immunofluorescence</subject><subject>Inflammation</subject><subject>Interleukin 6</subject><subject>Interleukin-1beta - metabolism</subject><subject>Interleukin-6 - metabolism</subject><subject>Mammary Neoplasms, Animal - pathology</subject><subject>Microglia</subject><subject>mRNA</subject><subject>Neoplasm Transplantation</subject><subject>Neuroglia - drug effects</subject><subject>Neuroglia - metabolism</subject><subject>Pain</subject><subject>Pain perception</subject><subject>Patients</subject><subject>Proteins</subject><subject>Quality of life</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Scorpions - chemistry</subject><subject>Spinal cord</subject><subject>Spinal Cord - metabolism</subject><subject>Spinal Cord - pathology</subject><subject>Stomach</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><issn>1744-8069</issn><issn>1744-8069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><recordid>eNp1kUtPxCAUhYnR-N67Mk3cuKnyGigbE2N8JSYu1DW5UDqD6cAI7ST-e1vHd-IKOHz3XA4XoQOCTwiR8pRIzissFMUKK6XYGtoepXLU1n_st9BOzs8YM4kF2URbjOIJFYpsI_1gY1r4GApoW7f00LlcmBhcYSFYl4oF-FB0sxT76azwYeaN70Y8NiusdrlLvX3XINTFtPVQwHBewqjtoY0G2uz2P9Zd9HR1-XhxU97dX99enN-VlgvalQbzCpqqgRqMqglQZoWTHJMhF-bW8coBNRZEZSZAlLJW1DVIEJIZVgnDdtHZynfRm7mrrQtdglYvkp9DetURvP59E_xMT-NSSzzhkuHB4PjDIMWXfgil5z5b17YQXOyzpmzkBGVkQI_-oM-xT2GIp8dPlZyqyUjhFWVTzDm55usxBOtxevrv9IaSw58hvgo-xzUA5QrIMHXfXf81fAMxl6Qu</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Yu, Jiachuan</creator><creator>Luo, Yuanyuan</creator><creator>Jin, Huidan</creator><creator>Lv, Jiaxin</creator><creator>Zhou, Tingting</creator><creator>Yabasin, Iddrisu Baba</creator><creator>Wen, Qingping</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>AFRWT</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>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</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>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3311-9230</orcidid></search><sort><creationdate>2020</creationdate><title>Scorpion alleviates bone cancer pain through inhibition of bone destruction and glia activation</title><author>Yu, Jiachuan ; Luo, Yuanyuan ; Jin, Huidan ; Lv, Jiaxin ; Zhou, Tingting ; Yabasin, Iddrisu Baba ; Wen, Qingping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-b048af8fadab9d1a23c6e740190904ce48ea2bca68b5a199cc6dda7a673b386b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Analgesics</topic><topic>Animals</topic><topic>Astrocytes</topic><topic>Astrocytes - metabolism</topic><topic>Behavior, Animal</topic><topic>Biological Products - therapeutic use</topic><topic>Bone and Bones - pathology</topic><topic>Bone cancer</topic><topic>Bone Neoplasms - drug therapy</topic><topic>Bone Neoplasms - physiopathology</topic><topic>Bone tumors</topic><topic>Cancer Pain - drug therapy</topic><topic>Cancer Pain - physiopathology</topic><topic>Cell Line, Tumor</topic><topic>Cell proliferation</topic><topic>Female</topic><topic>Filaments</topic><topic>Glial fibrillary acidic protein</topic><topic>Hyperalgesia</topic><topic>IL-1β</topic><topic>Immunofluorescence</topic><topic>Inflammation</topic><topic>Interleukin 6</topic><topic>Interleukin-1beta - metabolism</topic><topic>Interleukin-6 - metabolism</topic><topic>Mammary Neoplasms, Animal - pathology</topic><topic>Microglia</topic><topic>mRNA</topic><topic>Neoplasm Transplantation</topic><topic>Neuroglia - drug effects</topic><topic>Neuroglia - metabolism</topic><topic>Pain</topic><topic>Pain perception</topic><topic>Patients</topic><topic>Proteins</topic><topic>Quality of life</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Scorpions - chemistry</topic><topic>Spinal cord</topic><topic>Spinal Cord - metabolism</topic><topic>Spinal Cord - pathology</topic><topic>Stomach</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumor necrosis factor-α</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Jiachuan</creatorcontrib><creatorcontrib>Luo, Yuanyuan</creatorcontrib><creatorcontrib>Jin, Huidan</creatorcontrib><creatorcontrib>Lv, Jiaxin</creatorcontrib><creatorcontrib>Zhou, Tingting</creatorcontrib><creatorcontrib>Yabasin, Iddrisu Baba</creatorcontrib><creatorcontrib>Wen, Qingping</creatorcontrib><collection>SAGE Open Access Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular pain</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Jiachuan</au><au>Luo, Yuanyuan</au><au>Jin, Huidan</au><au>Lv, Jiaxin</au><au>Zhou, Tingting</au><au>Yabasin, Iddrisu Baba</au><au>Wen, Qingping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Scorpion alleviates bone cancer pain through inhibition of bone destruction and glia activation</atitle><jtitle>Molecular pain</jtitle><addtitle>Mol Pain</addtitle><date>2020</date><risdate>2020</risdate><volume>16</volume><spage>1744806920909993</spage><epage>1744806920909993</epage><pages>1744806920909993-1744806920909993</pages><issn>1744-8069</issn><eissn>1744-8069</eissn><abstract>Background
Bone cancer pain is common in patients with advanced cancers as tumor metastasizes to bone. The inefficient clinical treatment severely reduces quality of life of bone cancer pain patients. During the pain status, activated spinal astrocytes and microglia release various inflammatory cytokines, resulting in spinal inflammation and the development of neuron sensitization. Scorpion is the dry body of Buthus martensii Karsch and is often used for various pain management in clinical practice. However, its function on bone cancer pain is unclear.
Methods
We investigated the effects of intragastric administration of scorpion on bone cancer pain induced by left tibial cavity injection of Walker 256 cells. Nociceptive behavior was measured using the von Frey filaments test and the spontaneous ambulatory pain score. The bone destruction was assessed by tibial radiographs. Expression of spinal cord astrocyte marker glial fibrillary acidic protein and microglial marker Iba1 was monitored by Western blot assay and immunofluorescence. Tumor necrosis factor-alpha (TNF-α), interleukin (IL)-6, and IL-1β was detected by real-time polymerase chain reaction. The proliferation of Walker 256 cells was evaluated by CCK8 assay.
Results
Intragastric administration of scorpion reduced bone cancer pain behavior and relieved bone destruction, accompanied by decreased expression of spinal glial fibrillary acidic protein and Iba1 protein level and TNF-α, IL-6, and IL-1β mRNA level. Besides, scorpion inhibited proliferation of Walker 256 cells in a dose- and time-dependent manner.
Conclusion
Our results demonstrate that scorpion produces an analgesic effect in a rat model of bone cancer pain via inhibiting bone destruction and activation of spinal cord astrocytes and microglia.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>32052691</pmid><doi>10.1177/1744806920909993</doi><orcidid>https://orcid.org/0000-0002-3311-9230</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analgesics Animals Astrocytes Astrocytes - metabolism Behavior, Animal Biological Products - therapeutic use Bone and Bones - pathology Bone cancer Bone Neoplasms - drug therapy Bone Neoplasms - physiopathology Bone tumors Cancer Pain - drug therapy Cancer Pain - physiopathology Cell Line, Tumor Cell proliferation Female Filaments Glial fibrillary acidic protein Hyperalgesia IL-1β Immunofluorescence Inflammation Interleukin 6 Interleukin-1beta - metabolism Interleukin-6 - metabolism Mammary Neoplasms, Animal - pathology Microglia mRNA Neoplasm Transplantation Neuroglia - drug effects Neuroglia - metabolism Pain Pain perception Patients Proteins Quality of life Rats Rats, Sprague-Dawley Scorpions - chemistry Spinal cord Spinal Cord - metabolism Spinal Cord - pathology Stomach Tumor Necrosis Factor-alpha - metabolism Tumor necrosis factor-TNF Tumor necrosis factor-α |
title | Scorpion alleviates bone cancer pain through inhibition of bone destruction and glia activation |
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