Methoxphenidine (MXP) induced abnormalities: Addictive and schizophrenia‐related behaviours based on an imbalance of neurochemicals in the brain
Background and Purpose Methoxphenidine is a dissociative‐based novel psychoactive designer drug. Although fatal accidents from methoxphenidine abuse have been reported, recreational use of the drug continues. We aim to provide scientific supportfor legal regulation of recreational abuse of methoxphe...
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Veröffentlicht in: | British journal of pharmacology 2021-10, Vol.178 (19), p.3869-3887 |
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creator | Hur, Kwang‐Hyun Kim, Seong‐Eon Ma, Shi‐Xun Lee, Bo‐Ram Ko, Yong‐Hyun Seo, Jee‐Yeon Kim, Seon‐Kyung Kim, Young‐Jung Sung, Su‐Jeong Lee, Youyoung Jung, Young Hoon Lee, Yong‐Sup Lee, Seok‐Yong Jang, Choon‐Gon |
description | Background and Purpose
Methoxphenidine is a dissociative‐based novel psychoactive designer drug. Although fatal accidents from methoxphenidine abuse have been reported, recreational use of the drug continues. We aim to provide scientific supportfor legal regulation of recreational abuse of methoxphenidine by demonstrating its the pharmacological action.
Experimental Approach
Addictive potential of methoxphenidine was examined using intravenous self‐administration test with rats and conditioned place preference test with mice. Further, a series of behavioural tests (open field test, elevated plus maze test, novel object recognition test, social interaction test and tail suspension test) performed to assess whether methoxphenidine caused schizophrenia‐related symptoms in mice. Additionally, neurotransmitter enzyme‐linked immunosorbent assay and western blot were used to confirm methoxphenidine‐induced neurochemical changes in specific brain regions related to abnormal behaviours.
Key Results
Methoxphenidine caused addictive behaviours via reinforcing and rewarding effects. Consistently, methoxphenidine induced over‐activation of dopamine pathways in the nuclear accumbens, indicating activation of the brain reward circuit. Also, methoxphenidine caused all categories of schizophrenia‐related symptoms, including positive symptoms (hyperactivity, impulsivity), negative symptoms (anxiety, social withdrawal, depression) and cognitive impairment. Consistently, methoxphenidine led to the disruption of the hippocampal–prefrontal cortex pathway that is considered to be pathological involved in schizophrenia.
Conclusions and Implications
We demonastrate that methoxphenidine causes addictive and schizophrenia‐like behaviours and induces neurochemical changes in brain regions associated with these behaviours. We propose that methoxphenidine could be used in developing useful animal disease models and that it also requires legal restrictions on its recreational use. |
doi_str_mv | 10.1111/bph.15528 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2571619496</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2571619496</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3888-6a2557e986c7ddde30f3b0741781a9f013b1077b84000ce02bcf4a284b4a91173</originalsourceid><addsrcrecordid>eNp1kMtO3DAUhq2KqgyXRV-gssSmLDLYudnpDhAwSIyYBUjsIl9OFKPETu2EdrriERCPyJPUZabd9WyOdPyd_1gfQp8pmdNYJ3Jo57QoUv4BzWjOyqTION1BM0IISyjlfBfthfBISHxkxSe0m2UVZzxlM_S6hLF1P4cWrNHGAv66fFgdY2P1pEBjIa3zvejMaCB8w6daGzWaJ8DCahxUa365ofVxV7w9v3joxBiXJLTiybjJByxFiANnI49NL0UnrALsGmxh8k610BsluhDv4bEFLL0w9gB9bOIMDrd9H91fXtydL5Kb26vr89ObRGWc86QUaVEwqHipmNYaMtJkkrCcMk5F1RCaSUoYkzyPGhSQVKomFynPZS4qSlm2j442uYN33ycIY_0Y_2zjyTotGC1plVdlpI43lPIuBA9NPXjTC7-uKan_2K-j_frdfmS_bBMn2YP-R_7VHYGTDfDDdLD-f1J9tlpsIn8DroiQ2w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2571619496</pqid></control><display><type>article</type><title>Methoxphenidine (MXP) induced abnormalities: Addictive and schizophrenia‐related behaviours based on an imbalance of neurochemicals in the brain</title><source>Wiley Online Library Free Content</source><source>Access via Wiley Online Library</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Hur, Kwang‐Hyun ; Kim, Seong‐Eon ; Ma, Shi‐Xun ; Lee, Bo‐Ram ; Ko, Yong‐Hyun ; Seo, Jee‐Yeon ; Kim, Seon‐Kyung ; Kim, Young‐Jung ; Sung, Su‐Jeong ; Lee, Youyoung ; Jung, Young Hoon ; Lee, Yong‐Sup ; Lee, Seok‐Yong ; Jang, Choon‐Gon</creator><creatorcontrib>Hur, Kwang‐Hyun ; Kim, Seong‐Eon ; Ma, Shi‐Xun ; Lee, Bo‐Ram ; Ko, Yong‐Hyun ; Seo, Jee‐Yeon ; Kim, Seon‐Kyung ; Kim, Young‐Jung ; Sung, Su‐Jeong ; Lee, Youyoung ; Jung, Young Hoon ; Lee, Yong‐Sup ; Lee, Seok‐Yong ; Jang, Choon‐Gon</creatorcontrib><description>Background and Purpose
Methoxphenidine is a dissociative‐based novel psychoactive designer drug. Although fatal accidents from methoxphenidine abuse have been reported, recreational use of the drug continues. We aim to provide scientific supportfor legal regulation of recreational abuse of methoxphenidine by demonstrating its the pharmacological action.
Experimental Approach
Addictive potential of methoxphenidine was examined using intravenous self‐administration test with rats and conditioned place preference test with mice. Further, a series of behavioural tests (open field test, elevated plus maze test, novel object recognition test, social interaction test and tail suspension test) performed to assess whether methoxphenidine caused schizophrenia‐related symptoms in mice. Additionally, neurotransmitter enzyme‐linked immunosorbent assay and western blot were used to confirm methoxphenidine‐induced neurochemical changes in specific brain regions related to abnormal behaviours.
Key Results
Methoxphenidine caused addictive behaviours via reinforcing and rewarding effects. Consistently, methoxphenidine induced over‐activation of dopamine pathways in the nuclear accumbens, indicating activation of the brain reward circuit. Also, methoxphenidine caused all categories of schizophrenia‐related symptoms, including positive symptoms (hyperactivity, impulsivity), negative symptoms (anxiety, social withdrawal, depression) and cognitive impairment. Consistently, methoxphenidine led to the disruption of the hippocampal–prefrontal cortex pathway that is considered to be pathological involved in schizophrenia.
Conclusions and Implications
We demonastrate that methoxphenidine causes addictive and schizophrenia‐like behaviours and induces neurochemical changes in brain regions associated with these behaviours. We propose that methoxphenidine could be used in developing useful animal disease models and that it also requires legal restrictions on its recreational use.</description><identifier>ISSN: 0007-1188</identifier><identifier>EISSN: 1476-5381</identifier><identifier>DOI: 10.1111/bph.15528</identifier><identifier>PMID: 33987827</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>addiction ; Addictive behaviors ; Animal diseases ; Animal models ; Brain ; Cognitive ability ; dissociative drug ; Emotional behavior ; Hippocampus ; Hyperactivity ; Impulsive behavior ; Intravenous administration ; Mental disorders ; methoxphenidine ; MXP ; NMDA receptor antagonist ; Nucleus accumbens ; Open-field behavior ; Pattern recognition ; Place preference conditioning ; Prefrontal cortex ; Reinforcement ; Schizophrenia ; Social interactions ; Withdrawal</subject><ispartof>British journal of pharmacology, 2021-10, Vol.178 (19), p.3869-3887</ispartof><rights>2021 The British Pharmacological Society</rights><rights>This article is protected by copyright. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3888-6a2557e986c7ddde30f3b0741781a9f013b1077b84000ce02bcf4a284b4a91173</citedby><cites>FETCH-LOGICAL-c3888-6a2557e986c7ddde30f3b0741781a9f013b1077b84000ce02bcf4a284b4a91173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fbph.15528$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbph.15528$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33987827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hur, Kwang‐Hyun</creatorcontrib><creatorcontrib>Kim, Seong‐Eon</creatorcontrib><creatorcontrib>Ma, Shi‐Xun</creatorcontrib><creatorcontrib>Lee, Bo‐Ram</creatorcontrib><creatorcontrib>Ko, Yong‐Hyun</creatorcontrib><creatorcontrib>Seo, Jee‐Yeon</creatorcontrib><creatorcontrib>Kim, Seon‐Kyung</creatorcontrib><creatorcontrib>Kim, Young‐Jung</creatorcontrib><creatorcontrib>Sung, Su‐Jeong</creatorcontrib><creatorcontrib>Lee, Youyoung</creatorcontrib><creatorcontrib>Jung, Young Hoon</creatorcontrib><creatorcontrib>Lee, Yong‐Sup</creatorcontrib><creatorcontrib>Lee, Seok‐Yong</creatorcontrib><creatorcontrib>Jang, Choon‐Gon</creatorcontrib><title>Methoxphenidine (MXP) induced abnormalities: Addictive and schizophrenia‐related behaviours based on an imbalance of neurochemicals in the brain</title><title>British journal of pharmacology</title><addtitle>Br J Pharmacol</addtitle><description>Background and Purpose
Methoxphenidine is a dissociative‐based novel psychoactive designer drug. Although fatal accidents from methoxphenidine abuse have been reported, recreational use of the drug continues. We aim to provide scientific supportfor legal regulation of recreational abuse of methoxphenidine by demonstrating its the pharmacological action.
Experimental Approach
Addictive potential of methoxphenidine was examined using intravenous self‐administration test with rats and conditioned place preference test with mice. Further, a series of behavioural tests (open field test, elevated plus maze test, novel object recognition test, social interaction test and tail suspension test) performed to assess whether methoxphenidine caused schizophrenia‐related symptoms in mice. Additionally, neurotransmitter enzyme‐linked immunosorbent assay and western blot were used to confirm methoxphenidine‐induced neurochemical changes in specific brain regions related to abnormal behaviours.
Key Results
Methoxphenidine caused addictive behaviours via reinforcing and rewarding effects. Consistently, methoxphenidine induced over‐activation of dopamine pathways in the nuclear accumbens, indicating activation of the brain reward circuit. Also, methoxphenidine caused all categories of schizophrenia‐related symptoms, including positive symptoms (hyperactivity, impulsivity), negative symptoms (anxiety, social withdrawal, depression) and cognitive impairment. Consistently, methoxphenidine led to the disruption of the hippocampal–prefrontal cortex pathway that is considered to be pathological involved in schizophrenia.
Conclusions and Implications
We demonastrate that methoxphenidine causes addictive and schizophrenia‐like behaviours and induces neurochemical changes in brain regions associated with these behaviours. We propose that methoxphenidine could be used in developing useful animal disease models and that it also requires legal restrictions on its recreational use.</description><subject>addiction</subject><subject>Addictive behaviors</subject><subject>Animal diseases</subject><subject>Animal models</subject><subject>Brain</subject><subject>Cognitive ability</subject><subject>dissociative drug</subject><subject>Emotional behavior</subject><subject>Hippocampus</subject><subject>Hyperactivity</subject><subject>Impulsive behavior</subject><subject>Intravenous administration</subject><subject>Mental disorders</subject><subject>methoxphenidine</subject><subject>MXP</subject><subject>NMDA receptor antagonist</subject><subject>Nucleus accumbens</subject><subject>Open-field behavior</subject><subject>Pattern recognition</subject><subject>Place preference conditioning</subject><subject>Prefrontal cortex</subject><subject>Reinforcement</subject><subject>Schizophrenia</subject><subject>Social interactions</subject><subject>Withdrawal</subject><issn>0007-1188</issn><issn>1476-5381</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kMtO3DAUhq2KqgyXRV-gssSmLDLYudnpDhAwSIyYBUjsIl9OFKPETu2EdrriERCPyJPUZabd9WyOdPyd_1gfQp8pmdNYJ3Jo57QoUv4BzWjOyqTION1BM0IISyjlfBfthfBISHxkxSe0m2UVZzxlM_S6hLF1P4cWrNHGAv66fFgdY2P1pEBjIa3zvejMaCB8w6daGzWaJ8DCahxUa365ofVxV7w9v3joxBiXJLTiybjJByxFiANnI49NL0UnrALsGmxh8k610BsluhDv4bEFLL0w9gB9bOIMDrd9H91fXtydL5Kb26vr89ObRGWc86QUaVEwqHipmNYaMtJkkrCcMk5F1RCaSUoYkzyPGhSQVKomFynPZS4qSlm2j442uYN33ycIY_0Y_2zjyTotGC1plVdlpI43lPIuBA9NPXjTC7-uKan_2K-j_frdfmS_bBMn2YP-R_7VHYGTDfDDdLD-f1J9tlpsIn8DroiQ2w</recordid><startdate>202110</startdate><enddate>202110</enddate><creator>Hur, Kwang‐Hyun</creator><creator>Kim, Seong‐Eon</creator><creator>Ma, Shi‐Xun</creator><creator>Lee, Bo‐Ram</creator><creator>Ko, Yong‐Hyun</creator><creator>Seo, Jee‐Yeon</creator><creator>Kim, Seon‐Kyung</creator><creator>Kim, Young‐Jung</creator><creator>Sung, Su‐Jeong</creator><creator>Lee, Youyoung</creator><creator>Jung, Young Hoon</creator><creator>Lee, Yong‐Sup</creator><creator>Lee, Seok‐Yong</creator><creator>Jang, Choon‐Gon</creator><general>Blackwell Publishing Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>202110</creationdate><title>Methoxphenidine (MXP) induced abnormalities: Addictive and schizophrenia‐related behaviours based on an imbalance of neurochemicals in the brain</title><author>Hur, Kwang‐Hyun ; Kim, Seong‐Eon ; Ma, Shi‐Xun ; Lee, Bo‐Ram ; Ko, Yong‐Hyun ; Seo, Jee‐Yeon ; Kim, Seon‐Kyung ; Kim, Young‐Jung ; Sung, Su‐Jeong ; Lee, Youyoung ; Jung, Young Hoon ; Lee, Yong‐Sup ; Lee, Seok‐Yong ; Jang, Choon‐Gon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3888-6a2557e986c7ddde30f3b0741781a9f013b1077b84000ce02bcf4a284b4a91173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>addiction</topic><topic>Addictive behaviors</topic><topic>Animal diseases</topic><topic>Animal models</topic><topic>Brain</topic><topic>Cognitive ability</topic><topic>dissociative drug</topic><topic>Emotional behavior</topic><topic>Hippocampus</topic><topic>Hyperactivity</topic><topic>Impulsive behavior</topic><topic>Intravenous administration</topic><topic>Mental disorders</topic><topic>methoxphenidine</topic><topic>MXP</topic><topic>NMDA receptor antagonist</topic><topic>Nucleus accumbens</topic><topic>Open-field behavior</topic><topic>Pattern recognition</topic><topic>Place preference conditioning</topic><topic>Prefrontal cortex</topic><topic>Reinforcement</topic><topic>Schizophrenia</topic><topic>Social interactions</topic><topic>Withdrawal</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hur, Kwang‐Hyun</creatorcontrib><creatorcontrib>Kim, Seong‐Eon</creatorcontrib><creatorcontrib>Ma, Shi‐Xun</creatorcontrib><creatorcontrib>Lee, Bo‐Ram</creatorcontrib><creatorcontrib>Ko, Yong‐Hyun</creatorcontrib><creatorcontrib>Seo, Jee‐Yeon</creatorcontrib><creatorcontrib>Kim, Seon‐Kyung</creatorcontrib><creatorcontrib>Kim, Young‐Jung</creatorcontrib><creatorcontrib>Sung, Su‐Jeong</creatorcontrib><creatorcontrib>Lee, Youyoung</creatorcontrib><creatorcontrib>Jung, Young Hoon</creatorcontrib><creatorcontrib>Lee, Yong‐Sup</creatorcontrib><creatorcontrib>Lee, Seok‐Yong</creatorcontrib><creatorcontrib>Jang, Choon‐Gon</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>British journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hur, Kwang‐Hyun</au><au>Kim, Seong‐Eon</au><au>Ma, Shi‐Xun</au><au>Lee, Bo‐Ram</au><au>Ko, Yong‐Hyun</au><au>Seo, Jee‐Yeon</au><au>Kim, Seon‐Kyung</au><au>Kim, Young‐Jung</au><au>Sung, Su‐Jeong</au><au>Lee, Youyoung</au><au>Jung, Young Hoon</au><au>Lee, Yong‐Sup</au><au>Lee, Seok‐Yong</au><au>Jang, Choon‐Gon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methoxphenidine (MXP) induced abnormalities: Addictive and schizophrenia‐related behaviours based on an imbalance of neurochemicals in the brain</atitle><jtitle>British journal of pharmacology</jtitle><addtitle>Br J Pharmacol</addtitle><date>2021-10</date><risdate>2021</risdate><volume>178</volume><issue>19</issue><spage>3869</spage><epage>3887</epage><pages>3869-3887</pages><issn>0007-1188</issn><eissn>1476-5381</eissn><abstract>Background and Purpose
Methoxphenidine is a dissociative‐based novel psychoactive designer drug. Although fatal accidents from methoxphenidine abuse have been reported, recreational use of the drug continues. We aim to provide scientific supportfor legal regulation of recreational abuse of methoxphenidine by demonstrating its the pharmacological action.
Experimental Approach
Addictive potential of methoxphenidine was examined using intravenous self‐administration test with rats and conditioned place preference test with mice. Further, a series of behavioural tests (open field test, elevated plus maze test, novel object recognition test, social interaction test and tail suspension test) performed to assess whether methoxphenidine caused schizophrenia‐related symptoms in mice. Additionally, neurotransmitter enzyme‐linked immunosorbent assay and western blot were used to confirm methoxphenidine‐induced neurochemical changes in specific brain regions related to abnormal behaviours.
Key Results
Methoxphenidine caused addictive behaviours via reinforcing and rewarding effects. Consistently, methoxphenidine induced over‐activation of dopamine pathways in the nuclear accumbens, indicating activation of the brain reward circuit. Also, methoxphenidine caused all categories of schizophrenia‐related symptoms, including positive symptoms (hyperactivity, impulsivity), negative symptoms (anxiety, social withdrawal, depression) and cognitive impairment. Consistently, methoxphenidine led to the disruption of the hippocampal–prefrontal cortex pathway that is considered to be pathological involved in schizophrenia.
Conclusions and Implications
We demonastrate that methoxphenidine causes addictive and schizophrenia‐like behaviours and induces neurochemical changes in brain regions associated with these behaviours. We propose that methoxphenidine could be used in developing useful animal disease models and that it also requires legal restrictions on its recreational use.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>33987827</pmid><doi>10.1111/bph.15528</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record> |
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subjects | addiction Addictive behaviors Animal diseases Animal models Brain Cognitive ability dissociative drug Emotional behavior Hippocampus Hyperactivity Impulsive behavior Intravenous administration Mental disorders methoxphenidine MXP NMDA receptor antagonist Nucleus accumbens Open-field behavior Pattern recognition Place preference conditioning Prefrontal cortex Reinforcement Schizophrenia Social interactions Withdrawal |
title | Methoxphenidine (MXP) induced abnormalities: Addictive and schizophrenia‐related behaviours based on an imbalance of neurochemicals in the brain |
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