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Toll-like receptor 3 modulates the behavioral effects of cocaine in mice
The nucleus accumbens in the midbrain dopamine limbic system plays a key role in cocaine addiction. Toll-like receptors (TLRs) are important pattern-recognition receptors (PPRs) in the innate immune system that are also involved in drug dependence; however, the detailed mechanism is largely unknown....
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Published in: | Journal of neuroinflammation 2018-03, Vol.15 (1), p.93-93, Article 93 |
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container_title | Journal of neuroinflammation |
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creator | Zhu, Ruiming Bu, Qian Fu, Dengqi Shao, Xue Jiang, Linhong Guo, Wei Chen, Bo Liu, Bin Hu, Zhengtao Tian, Jingwei Zhao, Yinglan Cen, Xiaobo |
description | The nucleus accumbens in the midbrain dopamine limbic system plays a key role in cocaine addiction. Toll-like receptors (TLRs) are important pattern-recognition receptors (PPRs) in the innate immune system that are also involved in drug dependence; however, the detailed mechanism is largely unknown.
The present study was designed to investigate the potential role of TLR3 in cocaine addiction. Cocaine-induced conditioned place preference (CPP), locomotor activity, and self-administration were used to determine the effects of TLR3 in the rewarding properties of cocaine. Lentivirus-mediated re-expression of Tlr3 (LV-TLR3) was applied to determine if restoration of TLR3 expression in the NAc is sufficient to restore the cocaine effect in TLR3
mice. The protein levels of phospho-NF-κB p65, IKKβ, and p-IκBα both in the cytoplasm and nucleus of cocaine-induced CPP mice were detected by Western blot.
We showed that both TLR3 deficiency and intra-NAc injection of TLR3 inhibitors significantly attenuated cocaine-induced CPP, locomotor activity, and self-administration in mice. Importantly, the TLR3
mice that received intra-NAc injection of LV-TLR3 displayed significant increases in cocaine-induced CPP and locomotor activity. Finally, we found that TLR3 inhibitor reverted cocaine-induced upregulation of phospho-NF-κB p65, IKKβ, and p-IκBα.
Taken together, our results describe that TLR3 modulates cocaine-induced behaviors and provide further evidence supporting a role for central pro-inflammatory immune signaling in drug reward. We propose that TLR3 blockade could be a novel approach to treat cocaine addiction. |
doi_str_mv | 10.1186/s12974-018-1130-8 |
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The present study was designed to investigate the potential role of TLR3 in cocaine addiction. Cocaine-induced conditioned place preference (CPP), locomotor activity, and self-administration were used to determine the effects of TLR3 in the rewarding properties of cocaine. Lentivirus-mediated re-expression of Tlr3 (LV-TLR3) was applied to determine if restoration of TLR3 expression in the NAc is sufficient to restore the cocaine effect in TLR3
mice. The protein levels of phospho-NF-κB p65, IKKβ, and p-IκBα both in the cytoplasm and nucleus of cocaine-induced CPP mice were detected by Western blot.
We showed that both TLR3 deficiency and intra-NAc injection of TLR3 inhibitors significantly attenuated cocaine-induced CPP, locomotor activity, and self-administration in mice. Importantly, the TLR3
mice that received intra-NAc injection of LV-TLR3 displayed significant increases in cocaine-induced CPP and locomotor activity. Finally, we found that TLR3 inhibitor reverted cocaine-induced upregulation of phospho-NF-κB p65, IKKβ, and p-IκBα.
Taken together, our results describe that TLR3 modulates cocaine-induced behaviors and provide further evidence supporting a role for central pro-inflammatory immune signaling in drug reward. We propose that TLR3 blockade could be a novel approach to treat cocaine addiction.</description><identifier>ISSN: 1742-2094</identifier><identifier>EISSN: 1742-2094</identifier><identifier>DOI: 10.1186/s12974-018-1130-8</identifier><identifier>PMID: 29571298</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Cocaine ; Drug addiction ; NF-κB ; TLR3</subject><ispartof>Journal of neuroinflammation, 2018-03, Vol.15 (1), p.93-93, Article 93</ispartof><rights>The Author(s). 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-24c289410d7db975ecfcf1ce641f35670f7ce0a94604cf53483c76a994c8b3933</citedby><cites>FETCH-LOGICAL-c465t-24c289410d7db975ecfcf1ce641f35670f7ce0a94604cf53483c76a994c8b3933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865345/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865345/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29571298$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Ruiming</creatorcontrib><creatorcontrib>Bu, Qian</creatorcontrib><creatorcontrib>Fu, Dengqi</creatorcontrib><creatorcontrib>Shao, Xue</creatorcontrib><creatorcontrib>Jiang, Linhong</creatorcontrib><creatorcontrib>Guo, Wei</creatorcontrib><creatorcontrib>Chen, Bo</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><creatorcontrib>Hu, Zhengtao</creatorcontrib><creatorcontrib>Tian, Jingwei</creatorcontrib><creatorcontrib>Zhao, Yinglan</creatorcontrib><creatorcontrib>Cen, Xiaobo</creatorcontrib><title>Toll-like receptor 3 modulates the behavioral effects of cocaine in mice</title><title>Journal of neuroinflammation</title><addtitle>J Neuroinflammation</addtitle><description>The nucleus accumbens in the midbrain dopamine limbic system plays a key role in cocaine addiction. Toll-like receptors (TLRs) are important pattern-recognition receptors (PPRs) in the innate immune system that are also involved in drug dependence; however, the detailed mechanism is largely unknown.
The present study was designed to investigate the potential role of TLR3 in cocaine addiction. Cocaine-induced conditioned place preference (CPP), locomotor activity, and self-administration were used to determine the effects of TLR3 in the rewarding properties of cocaine. Lentivirus-mediated re-expression of Tlr3 (LV-TLR3) was applied to determine if restoration of TLR3 expression in the NAc is sufficient to restore the cocaine effect in TLR3
mice. The protein levels of phospho-NF-κB p65, IKKβ, and p-IκBα both in the cytoplasm and nucleus of cocaine-induced CPP mice were detected by Western blot.
We showed that both TLR3 deficiency and intra-NAc injection of TLR3 inhibitors significantly attenuated cocaine-induced CPP, locomotor activity, and self-administration in mice. Importantly, the TLR3
mice that received intra-NAc injection of LV-TLR3 displayed significant increases in cocaine-induced CPP and locomotor activity. Finally, we found that TLR3 inhibitor reverted cocaine-induced upregulation of phospho-NF-κB p65, IKKβ, and p-IκBα.
Taken together, our results describe that TLR3 modulates cocaine-induced behaviors and provide further evidence supporting a role for central pro-inflammatory immune signaling in drug reward. We propose that TLR3 blockade could be a novel approach to treat cocaine addiction.</description><subject>Cocaine</subject><subject>Drug addiction</subject><subject>NF-κB</subject><subject>TLR3</subject><issn>1742-2094</issn><issn>1742-2094</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkU1PFTEUhidGIwj8ADemSzej_f7YmBiiQkLiBtZN58wptzgzvbZzSfj39nKRwKpNz3mfc5qn6z4y-oUxq79Wxp2RPWW2Z0zQ3r7pjpmRvOfUybcv7kfdh1rvKBVcaf6-O-JOmZa1x93FdZ6mfkp_kBQE3K65EEHmPO6msGIl6wbJgJtwn3IJE8EYEdZKciSQIaQFSVrInABPu3cxTBXPns6T7ubnj-vzi_7q96_L8-9XPUit1p5L4NZJRkczDs4ohAiRAWrJolDa0GgAaXBSUwlRCWkFGB2ck2AH4YQ46S4P3DGHO78taQ7lweeQ_ONDLrc-lDXBhN6qYeTg0IFi0ig1SNkwkY6jCWG0qrG-HVjb3TDjCLis7ZOvoK8rS9r423zvldVttT3g8xOg5L87rKufUwWcprBg3lXPmxrKpXamtbJDK5Rca8H4PIZRv7fpDzZ9i_i9TW9b5tPL_Z4T__WJfxVOmsM</recordid><startdate>20180323</startdate><enddate>20180323</enddate><creator>Zhu, Ruiming</creator><creator>Bu, Qian</creator><creator>Fu, Dengqi</creator><creator>Shao, Xue</creator><creator>Jiang, Linhong</creator><creator>Guo, Wei</creator><creator>Chen, Bo</creator><creator>Liu, Bin</creator><creator>Hu, Zhengtao</creator><creator>Tian, Jingwei</creator><creator>Zhao, Yinglan</creator><creator>Cen, Xiaobo</creator><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20180323</creationdate><title>Toll-like receptor 3 modulates the behavioral effects of cocaine in mice</title><author>Zhu, Ruiming ; Bu, Qian ; Fu, Dengqi ; Shao, Xue ; Jiang, Linhong ; Guo, Wei ; Chen, Bo ; Liu, Bin ; Hu, Zhengtao ; Tian, Jingwei ; Zhao, Yinglan ; Cen, Xiaobo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-24c289410d7db975ecfcf1ce641f35670f7ce0a94604cf53483c76a994c8b3933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Cocaine</topic><topic>Drug addiction</topic><topic>NF-κB</topic><topic>TLR3</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Ruiming</creatorcontrib><creatorcontrib>Bu, Qian</creatorcontrib><creatorcontrib>Fu, Dengqi</creatorcontrib><creatorcontrib>Shao, Xue</creatorcontrib><creatorcontrib>Jiang, Linhong</creatorcontrib><creatorcontrib>Guo, Wei</creatorcontrib><creatorcontrib>Chen, Bo</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><creatorcontrib>Hu, Zhengtao</creatorcontrib><creatorcontrib>Tian, Jingwei</creatorcontrib><creatorcontrib>Zhao, Yinglan</creatorcontrib><creatorcontrib>Cen, Xiaobo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Journal of neuroinflammation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Ruiming</au><au>Bu, Qian</au><au>Fu, Dengqi</au><au>Shao, Xue</au><au>Jiang, Linhong</au><au>Guo, Wei</au><au>Chen, Bo</au><au>Liu, Bin</au><au>Hu, Zhengtao</au><au>Tian, Jingwei</au><au>Zhao, Yinglan</au><au>Cen, Xiaobo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toll-like receptor 3 modulates the behavioral effects of cocaine in mice</atitle><jtitle>Journal of neuroinflammation</jtitle><addtitle>J Neuroinflammation</addtitle><date>2018-03-23</date><risdate>2018</risdate><volume>15</volume><issue>1</issue><spage>93</spage><epage>93</epage><pages>93-93</pages><artnum>93</artnum><issn>1742-2094</issn><eissn>1742-2094</eissn><abstract>The nucleus accumbens in the midbrain dopamine limbic system plays a key role in cocaine addiction. Toll-like receptors (TLRs) are important pattern-recognition receptors (PPRs) in the innate immune system that are also involved in drug dependence; however, the detailed mechanism is largely unknown.
The present study was designed to investigate the potential role of TLR3 in cocaine addiction. Cocaine-induced conditioned place preference (CPP), locomotor activity, and self-administration were used to determine the effects of TLR3 in the rewarding properties of cocaine. Lentivirus-mediated re-expression of Tlr3 (LV-TLR3) was applied to determine if restoration of TLR3 expression in the NAc is sufficient to restore the cocaine effect in TLR3
mice. The protein levels of phospho-NF-κB p65, IKKβ, and p-IκBα both in the cytoplasm and nucleus of cocaine-induced CPP mice were detected by Western blot.
We showed that both TLR3 deficiency and intra-NAc injection of TLR3 inhibitors significantly attenuated cocaine-induced CPP, locomotor activity, and self-administration in mice. Importantly, the TLR3
mice that received intra-NAc injection of LV-TLR3 displayed significant increases in cocaine-induced CPP and locomotor activity. Finally, we found that TLR3 inhibitor reverted cocaine-induced upregulation of phospho-NF-κB p65, IKKβ, and p-IκBα.
Taken together, our results describe that TLR3 modulates cocaine-induced behaviors and provide further evidence supporting a role for central pro-inflammatory immune signaling in drug reward. We propose that TLR3 blockade could be a novel approach to treat cocaine addiction.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>29571298</pmid><doi>10.1186/s12974-018-1130-8</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cocaine Drug addiction NF-κB TLR3 |
title | Toll-like receptor 3 modulates the behavioral effects of cocaine in mice |
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