Blocking brown adipocyte β 3 -adrenoceptor attenuates blood-spinal cord barrier impairment and chronic postsurgical pain in a rat model of preoperative stress
Preoperative stress has been recognized as an independent risk factor for chronic postsurgical pain (CPSP). However, the underlying mechanisms of CPSP influenced by preoperative stress remain elusive. Previous studies indicated that excessive stress could induce disruption of the blood-spinal cord b...
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Veröffentlicht in: | International immunopharmacology 2024-02, Vol.128, p.111530 |
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description | Preoperative stress has been recognized as an independent risk factor for chronic postsurgical pain (CPSP). However, the underlying mechanisms of CPSP influenced by preoperative stress remain elusive. Previous studies indicated that excessive stress could induce disruption of the blood-spinal cord barrier (BSCB). We wondered whether and how BSCB involves in CPSP by using a single prolonged stress (SPS) combining plantar incision model in male rats to mimic preoperative stress-related postsurgical pain. Here, we observed that preoperative SPS-exposed rats exhibited relentless incisional pain, which was accompanied by impairment of BSCB and persistent elevation of serum IL-6. Intraperitoneal injections of Tocilizumab (an IL-6 receptor monoclonal antibody) not only mitigated BSCB breakdown but also alleviated pain behaviors. In addition, intervening β
-adrenoceptor (ADRB3) signaling in brown adipocytes by SR59230a (a specific ADRB3 antagonist) treatment or removal of brown adipose tissues could effectively decrease serum IL-6 levels, ameliorate BSCB disruption, and alleviate incisional pain. Further results displayed that SI-exposed rats also showed markedly spinal microglia activation. And exogenous His-tagged IL-6 could pass through the disrupted BSCB, which might contribute to microglia activation. Injection of SR59230a or ablation of brown adipose tissues could effectively reduce the activation of spinal microglia. Thus, our findings suggest that serum IL-6 induced by brown adipocyte ADRB3 signaling contributed to BSCB disruption and spinal microglia activation, which might be involved in preoperative stress mediated CPSP. This work indicates a promising treatment strategy for preoperative stress induced CPSP by blocking ADRB3. |
doi_str_mv | 10.1016/j.intimp.2024.111530 |
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-adrenoceptor (ADRB3) signaling in brown adipocytes by SR59230a (a specific ADRB3 antagonist) treatment or removal of brown adipose tissues could effectively decrease serum IL-6 levels, ameliorate BSCB disruption, and alleviate incisional pain. Further results displayed that SI-exposed rats also showed markedly spinal microglia activation. And exogenous His-tagged IL-6 could pass through the disrupted BSCB, which might contribute to microglia activation. Injection of SR59230a or ablation of brown adipose tissues could effectively reduce the activation of spinal microglia. Thus, our findings suggest that serum IL-6 induced by brown adipocyte ADRB3 signaling contributed to BSCB disruption and spinal microglia activation, which might be involved in preoperative stress mediated CPSP. This work indicates a promising treatment strategy for preoperative stress induced CPSP by blocking ADRB3.</description><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2024.111530</identifier><identifier>PMID: 38278068</identifier><language>eng</language><publisher>Netherlands</publisher><subject>Adipocytes, Brown - metabolism ; Animals ; Interleukin-6 - metabolism ; Male ; Pain, Postoperative ; Propanolamines ; Rats ; Rats, Sprague-Dawley ; Receptors, Adrenergic - metabolism ; Receptors, Adrenergic, beta-3 - metabolism ; Spinal Cord ; Spinal Cord Injuries - metabolism</subject><ispartof>International immunopharmacology, 2024-02, Vol.128, p.111530</ispartof><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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/38278068$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Jixiang</creatorcontrib><creatorcontrib>Hou, Bailing</creatorcontrib><creatorcontrib>Rong, Hui</creatorcontrib><creatorcontrib>Xu, Ke</creatorcontrib><creatorcontrib>Jiang, Li</creatorcontrib><creatorcontrib>Yang, Shuai</creatorcontrib><creatorcontrib>Zhu, Huijie</creatorcontrib><creatorcontrib>Yang, Haikou</creatorcontrib><creatorcontrib>Jiao, Yang</creatorcontrib><creatorcontrib>Liu, Yue</creatorcontrib><creatorcontrib>Ni, Kun</creatorcontrib><creatorcontrib>Ma, Zhengliang</creatorcontrib><title>Blocking brown adipocyte β 3 -adrenoceptor attenuates blood-spinal cord barrier impairment and chronic postsurgical pain in a rat model of preoperative stress</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>Preoperative stress has been recognized as an independent risk factor for chronic postsurgical pain (CPSP). However, the underlying mechanisms of CPSP influenced by preoperative stress remain elusive. Previous studies indicated that excessive stress could induce disruption of the blood-spinal cord barrier (BSCB). We wondered whether and how BSCB involves in CPSP by using a single prolonged stress (SPS) combining plantar incision model in male rats to mimic preoperative stress-related postsurgical pain. Here, we observed that preoperative SPS-exposed rats exhibited relentless incisional pain, which was accompanied by impairment of BSCB and persistent elevation of serum IL-6. Intraperitoneal injections of Tocilizumab (an IL-6 receptor monoclonal antibody) not only mitigated BSCB breakdown but also alleviated pain behaviors. In addition, intervening β
-adrenoceptor (ADRB3) signaling in brown adipocytes by SR59230a (a specific ADRB3 antagonist) treatment or removal of brown adipose tissues could effectively decrease serum IL-6 levels, ameliorate BSCB disruption, and alleviate incisional pain. Further results displayed that SI-exposed rats also showed markedly spinal microglia activation. And exogenous His-tagged IL-6 could pass through the disrupted BSCB, which might contribute to microglia activation. Injection of SR59230a or ablation of brown adipose tissues could effectively reduce the activation of spinal microglia. Thus, our findings suggest that serum IL-6 induced by brown adipocyte ADRB3 signaling contributed to BSCB disruption and spinal microglia activation, which might be involved in preoperative stress mediated CPSP. This work indicates a promising treatment strategy for preoperative stress induced CPSP by blocking ADRB3.</description><subject>Adipocytes, Brown - metabolism</subject><subject>Animals</subject><subject>Interleukin-6 - metabolism</subject><subject>Male</subject><subject>Pain, Postoperative</subject><subject>Propanolamines</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Adrenergic - metabolism</subject><subject>Receptors, Adrenergic, beta-3 - metabolism</subject><subject>Spinal Cord</subject><subject>Spinal Cord Injuries - metabolism</subject><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFT1tOwzAQtJAQLY8bILQXSGonbZNvEIgD8F9t7G1xSbzW2gH1NNyBg3Am_AHfSCPNaDQjzSh1a3RttNmujrUP2U-xbnSzro0xm1afqaXpu74ynd4s1GVKR62LXpsLtWj7puv1tl-qz_uR7ZsPBxiEPwKg85HtKRN8f0ELFTqhwJZiZgHMmcKMmRIMI7OrUvQBR7AsDgYU8SRQZqCXiUIGDA7sq3DwFiKnnGY5eFsKJRGgAEEww8SORuA9RCGOVCz_TpCyUErX6nyPY6KbX75Sd0-PLw_PVZyHidwuip9QTru_R-2_gR9N4GJp</recordid><startdate>20240215</startdate><enddate>20240215</enddate><creator>Zhu, Jixiang</creator><creator>Hou, Bailing</creator><creator>Rong, Hui</creator><creator>Xu, Ke</creator><creator>Jiang, Li</creator><creator>Yang, Shuai</creator><creator>Zhu, Huijie</creator><creator>Yang, Haikou</creator><creator>Jiao, Yang</creator><creator>Liu, Yue</creator><creator>Ni, Kun</creator><creator>Ma, Zhengliang</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20240215</creationdate><title>Blocking brown adipocyte β 3 -adrenoceptor attenuates blood-spinal cord barrier impairment and chronic postsurgical pain in a rat model of preoperative stress</title><author>Zhu, Jixiang ; Hou, Bailing ; Rong, Hui ; Xu, Ke ; Jiang, Li ; Yang, Shuai ; Zhu, Huijie ; Yang, Haikou ; Jiao, Yang ; Liu, Yue ; Ni, Kun ; Ma, Zhengliang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_382780683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adipocytes, Brown - metabolism</topic><topic>Animals</topic><topic>Interleukin-6 - metabolism</topic><topic>Male</topic><topic>Pain, Postoperative</topic><topic>Propanolamines</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Adrenergic - metabolism</topic><topic>Receptors, Adrenergic, beta-3 - metabolism</topic><topic>Spinal Cord</topic><topic>Spinal Cord Injuries - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Jixiang</creatorcontrib><creatorcontrib>Hou, Bailing</creatorcontrib><creatorcontrib>Rong, Hui</creatorcontrib><creatorcontrib>Xu, Ke</creatorcontrib><creatorcontrib>Jiang, Li</creatorcontrib><creatorcontrib>Yang, Shuai</creatorcontrib><creatorcontrib>Zhu, Huijie</creatorcontrib><creatorcontrib>Yang, Haikou</creatorcontrib><creatorcontrib>Jiao, Yang</creatorcontrib><creatorcontrib>Liu, Yue</creatorcontrib><creatorcontrib>Ni, Kun</creatorcontrib><creatorcontrib>Ma, Zhengliang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Jixiang</au><au>Hou, Bailing</au><au>Rong, Hui</au><au>Xu, Ke</au><au>Jiang, Li</au><au>Yang, Shuai</au><au>Zhu, Huijie</au><au>Yang, Haikou</au><au>Jiao, Yang</au><au>Liu, Yue</au><au>Ni, Kun</au><au>Ma, Zhengliang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blocking brown adipocyte β 3 -adrenoceptor attenuates blood-spinal cord barrier impairment and chronic postsurgical pain in a rat model of preoperative stress</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2024-02-15</date><risdate>2024</risdate><volume>128</volume><spage>111530</spage><pages>111530-</pages><eissn>1878-1705</eissn><abstract>Preoperative stress has been recognized as an independent risk factor for chronic postsurgical pain (CPSP). However, the underlying mechanisms of CPSP influenced by preoperative stress remain elusive. Previous studies indicated that excessive stress could induce disruption of the blood-spinal cord barrier (BSCB). We wondered whether and how BSCB involves in CPSP by using a single prolonged stress (SPS) combining plantar incision model in male rats to mimic preoperative stress-related postsurgical pain. Here, we observed that preoperative SPS-exposed rats exhibited relentless incisional pain, which was accompanied by impairment of BSCB and persistent elevation of serum IL-6. Intraperitoneal injections of Tocilizumab (an IL-6 receptor monoclonal antibody) not only mitigated BSCB breakdown but also alleviated pain behaviors. In addition, intervening β
-adrenoceptor (ADRB3) signaling in brown adipocytes by SR59230a (a specific ADRB3 antagonist) treatment or removal of brown adipose tissues could effectively decrease serum IL-6 levels, ameliorate BSCB disruption, and alleviate incisional pain. Further results displayed that SI-exposed rats also showed markedly spinal microglia activation. And exogenous His-tagged IL-6 could pass through the disrupted BSCB, which might contribute to microglia activation. Injection of SR59230a or ablation of brown adipose tissues could effectively reduce the activation of spinal microglia. Thus, our findings suggest that serum IL-6 induced by brown adipocyte ADRB3 signaling contributed to BSCB disruption and spinal microglia activation, which might be involved in preoperative stress mediated CPSP. This work indicates a promising treatment strategy for preoperative stress induced CPSP by blocking ADRB3.</abstract><cop>Netherlands</cop><pmid>38278068</pmid><doi>10.1016/j.intimp.2024.111530</doi></addata></record> |
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subjects | Adipocytes, Brown - metabolism Animals Interleukin-6 - metabolism Male Pain, Postoperative Propanolamines Rats Rats, Sprague-Dawley Receptors, Adrenergic - metabolism Receptors, Adrenergic, beta-3 - metabolism Spinal Cord Spinal Cord Injuries - metabolism |
title | Blocking brown adipocyte β 3 -adrenoceptor attenuates blood-spinal cord barrier impairment and chronic postsurgical pain in a rat model of preoperative stress |
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