Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Molecular pain 2020, Vol.16, p.1744806920909993-1744806920909993
Main Authors: Yu, Jiachuan, Luo, Yuanyuan, Jin, Huidan, Lv, Jiaxin, Zhou, Tingting, Yabasin, Iddrisu Baba, Wen, Qingping
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c462t-b048af8fadab9d1a23c6e740190904ce48ea2bca68b5a199cc6dda7a673b386b3
cites cdi_FETCH-LOGICAL-c462t-b048af8fadab9d1a23c6e740190904ce48ea2bca68b5a199cc6dda7a673b386b3
container_end_page 1744806920909993
container_issue
container_start_page 1744806920909993
container_title Molecular pain
container_volume 16
creator Yu, Jiachuan
Luo, Yuanyuan
Jin, Huidan
Lv, Jiaxin
Zhou, Tingting
Yabasin, Iddrisu Baba
Wen, Qingping
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
format article
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 &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Health &amp; 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>
fulltext fulltext
identifier ISSN: 1744-8069
ispartof Molecular pain, 2020, Vol.16, p.1744806920909993-1744806920909993
issn 1744-8069
1744-8069
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7054730
source Publicly Available Content Database; SAGE Open Access Journals; PubMed Central; Free Full-Text Journals in Chemistry
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T04%3A04%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Scorpion%20alleviates%20bone%20cancer%20pain%20through%20inhibition%20of%20bone%20destruction%20and%20glia%20activation&rft.jtitle=Molecular%20pain&rft.au=Yu,%20Jiachuan&rft.date=2020&rft.volume=16&rft.spage=1744806920909993&rft.epage=1744806920909993&rft.pages=1744806920909993-1744806920909993&rft.issn=1744-8069&rft.eissn=1744-8069&rft_id=info:doi/10.1177/1744806920909993&rft_dat=%3Cproquest_pubme%3E2691742951%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c462t-b048af8fadab9d1a23c6e740190904ce48ea2bca68b5a199cc6dda7a673b386b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2691742951&rft_id=info:pmid/32052691&rft_sage_id=10.1177_1744806920909993&rfr_iscdi=true