Methylphenidate and desipramine combined treatment improves PTSD symptomatology in a rat model
Antidepressant medication constitutes the first line pharmacological treatment for posttraumatic stress disorder (PTSD), however, because many patients display no beneficial drug effects it has been suggested that combinations of antidepressants with additional drugs may be necessary. The defining s...
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creator | Aga-Mizrachi, S Cymerblit-Sabba, A Gurman, O Balan, A Shwam, G Deshe, R Miller, L Gorodetsky, N Heinrich, N Tzezana, O Zubedat, S Grinstein, D Avital, A |
description | Antidepressant medication constitutes the first line pharmacological treatment for posttraumatic stress disorder (PTSD), however, because many patients display no beneficial drug effects it has been suggested that combinations of antidepressants with additional drugs may be necessary. The defining symptoms of PTSD include re-experiencing, avoidance and hyperarousal. In addition, PTSD patients were shown to become easily distracted and often suffer from poor concentration together with indications of comorbidity with attention-deficit hyperactivity disorder (ADHD). Methylphenidate (MPH) is the most common and effective drug treatment for ADHD, thus we aimed to investigate the effects of MPH treatment, by itself or in combination with the antidepressants fluoxetine (FLU) or desipramine (DES). We modified an animal model of PTSD by exposing rats to chronic stress and evaluating the subsequent development of behavioral PTSD-like symptoms, as well as the effects on proinflammatory cytokines, which were implicated in PTSD. We report that while FLU or DES had a beneficial effect on avoidance and hyperarousal symptoms, MPH improved all three symptoms. Moreover, the combination of MPH with DES produced the most dramatic beneficial effects. Serum levels of interleukin-1β (IL-1β) and IL-6 were elevated in the PTSD-like group compared with the control group, and were decreased by MPH, FLU, DES or the combination drug treatments, with the combination of DES+MPH producing the most complete rescue of the inflammatory response. Considering the versatile symptoms of PTSD, our results suggest a new combined treatment for PTSD comprising the antidepressant DES and the psychostimulant MPH. |
doi_str_mv | 10.1038/tp.2014.82 |
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The defining symptoms of PTSD include re-experiencing, avoidance and hyperarousal. In addition, PTSD patients were shown to become easily distracted and often suffer from poor concentration together with indications of comorbidity with attention-deficit hyperactivity disorder (ADHD). Methylphenidate (MPH) is the most common and effective drug treatment for ADHD, thus we aimed to investigate the effects of MPH treatment, by itself or in combination with the antidepressants fluoxetine (FLU) or desipramine (DES). We modified an animal model of PTSD by exposing rats to chronic stress and evaluating the subsequent development of behavioral PTSD-like symptoms, as well as the effects on proinflammatory cytokines, which were implicated in PTSD. We report that while FLU or DES had a beneficial effect on avoidance and hyperarousal symptoms, MPH improved all three symptoms. Moreover, the combination of MPH with DES produced the most dramatic beneficial effects. Serum levels of interleukin-1β (IL-1β) and IL-6 were elevated in the PTSD-like group compared with the control group, and were decreased by MPH, FLU, DES or the combination drug treatments, with the combination of DES+MPH producing the most complete rescue of the inflammatory response. Considering the versatile symptoms of PTSD, our results suggest a new combined treatment for PTSD comprising the antidepressant DES and the psychostimulant MPH.</description><identifier>ISSN: 2158-3188</identifier><identifier>EISSN: 2158-3188</identifier><identifier>DOI: 10.1038/tp.2014.82</identifier><identifier>PMID: 25247592</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/21 ; 631/443 ; 64/86 ; 692/699/476 ; Animals ; Antidepressive Agents, Tricyclic - pharmacology ; Behavioral Sciences ; Biological Psychology ; Central Nervous System Stimulants - pharmacology ; Desipramine - pharmacology ; Disease Models, Animal ; Drug Therapy, Combination ; Male ; Medicine ; Medicine & Public Health ; Methylphenidate - pharmacology ; Neurosciences ; Original ; original-article ; Pharmacotherapy ; Psychiatry ; Rats ; Rats, Wistar ; Stress Disorders, Post-Traumatic - drug therapy ; Treatment Outcome</subject><ispartof>Translational psychiatry, 2014-09, Vol.4 (9), p.e447-e447</ispartof><rights>The Author(s) 2014</rights><rights>Copyright Nature Publishing Group Sep 2014</rights><rights>Copyright © 2014 Macmillan Publishers Limited 2014 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-53b4f451a12520340e343dc2f7ae4a294e28194711bdca9524c725dfe07004ed3</citedby><cites>FETCH-LOGICAL-c475t-53b4f451a12520340e343dc2f7ae4a294e28194711bdca9524c725dfe07004ed3</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/PMC4203011/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203011/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25247592$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aga-Mizrachi, S</creatorcontrib><creatorcontrib>Cymerblit-Sabba, A</creatorcontrib><creatorcontrib>Gurman, O</creatorcontrib><creatorcontrib>Balan, A</creatorcontrib><creatorcontrib>Shwam, G</creatorcontrib><creatorcontrib>Deshe, R</creatorcontrib><creatorcontrib>Miller, L</creatorcontrib><creatorcontrib>Gorodetsky, N</creatorcontrib><creatorcontrib>Heinrich, N</creatorcontrib><creatorcontrib>Tzezana, O</creatorcontrib><creatorcontrib>Zubedat, S</creatorcontrib><creatorcontrib>Grinstein, D</creatorcontrib><creatorcontrib>Avital, A</creatorcontrib><title>Methylphenidate and desipramine combined treatment improves PTSD symptomatology in a rat model</title><title>Translational psychiatry</title><addtitle>Transl Psychiatry</addtitle><addtitle>Transl Psychiatry</addtitle><description>Antidepressant medication constitutes the first line pharmacological treatment for posttraumatic stress disorder (PTSD), however, because many patients display no beneficial drug effects it has been suggested that combinations of antidepressants with additional drugs may be necessary. The defining symptoms of PTSD include re-experiencing, avoidance and hyperarousal. In addition, PTSD patients were shown to become easily distracted and often suffer from poor concentration together with indications of comorbidity with attention-deficit hyperactivity disorder (ADHD). Methylphenidate (MPH) is the most common and effective drug treatment for ADHD, thus we aimed to investigate the effects of MPH treatment, by itself or in combination with the antidepressants fluoxetine (FLU) or desipramine (DES). We modified an animal model of PTSD by exposing rats to chronic stress and evaluating the subsequent development of behavioral PTSD-like symptoms, as well as the effects on proinflammatory cytokines, which were implicated in PTSD. We report that while FLU or DES had a beneficial effect on avoidance and hyperarousal symptoms, MPH improved all three symptoms. Moreover, the combination of MPH with DES produced the most dramatic beneficial effects. Serum levels of interleukin-1β (IL-1β) and IL-6 were elevated in the PTSD-like group compared with the control group, and were decreased by MPH, FLU, DES or the combination drug treatments, with the combination of DES+MPH producing the most complete rescue of the inflammatory response. Considering the versatile symptoms of PTSD, our results suggest a new combined treatment for PTSD comprising the antidepressant DES and the psychostimulant MPH.</description><subject>13/21</subject><subject>631/443</subject><subject>64/86</subject><subject>692/699/476</subject><subject>Animals</subject><subject>Antidepressive Agents, Tricyclic - pharmacology</subject><subject>Behavioral Sciences</subject><subject>Biological Psychology</subject><subject>Central Nervous System Stimulants - pharmacology</subject><subject>Desipramine - pharmacology</subject><subject>Disease Models, Animal</subject><subject>Drug Therapy, Combination</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Methylphenidate - pharmacology</subject><subject>Neurosciences</subject><subject>Original</subject><subject>original-article</subject><subject>Pharmacotherapy</subject><subject>Psychiatry</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Stress Disorders, Post-Traumatic - drug therapy</subject><subject>Treatment Outcome</subject><issn>2158-3188</issn><issn>2158-3188</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNplkVFLHDEQx0NRqqgv_QAl0BdR7prJJu7uiyBnbQWlhdrXhtxm9i6ySdYkJ9y3b-SsnJqXCcyP__yGIeQTsCmwqvmaxylnIKYN_0D2OchmUkHT7Gz998hRSvesPCkaqOEj2eOSi1q2fJ_8vcW8XA_jEr01OiPV3lCDyY5RO-uRdsHNSzU0R9TZoc_UujGGR0z0193vS5rWbszB6RyGsFhT66mmUWfqgsHhkOz2ekh49FwPyJ-rb3ezH5Obn9-vZxc3k6545Ims5qIXEjQUM1YJhpWoTMf7WqPQvBXIG2hFDTA3nW6LfVdzaXpkNWMCTXVAzje542ru0HRFM-pBjdE6HdcqaKted7xdqkV4VKKMYwAl4Pg5IIaHFaasnE0dDoP2GFZJgTw7AxDAREG_vEHvwyr6sp6Cui1ZjNeyUCcbqoshpYj9iwww9XQ5lUf1dDnV8AJ_3tZ_Qf_fqQCnGyCVll9g3Jr5Pu4fVH-iow</recordid><startdate>20140923</startdate><enddate>20140923</enddate><creator>Aga-Mizrachi, S</creator><creator>Cymerblit-Sabba, A</creator><creator>Gurman, O</creator><creator>Balan, A</creator><creator>Shwam, G</creator><creator>Deshe, R</creator><creator>Miller, L</creator><creator>Gorodetsky, N</creator><creator>Heinrich, N</creator><creator>Tzezana, O</creator><creator>Zubedat, S</creator><creator>Grinstein, D</creator><creator>Avital, A</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</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>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></search><sort><creationdate>20140923</creationdate><title>Methylphenidate and desipramine combined treatment improves PTSD symptomatology in a rat model</title><author>Aga-Mizrachi, S ; 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The defining symptoms of PTSD include re-experiencing, avoidance and hyperarousal. In addition, PTSD patients were shown to become easily distracted and often suffer from poor concentration together with indications of comorbidity with attention-deficit hyperactivity disorder (ADHD). Methylphenidate (MPH) is the most common and effective drug treatment for ADHD, thus we aimed to investigate the effects of MPH treatment, by itself or in combination with the antidepressants fluoxetine (FLU) or desipramine (DES). We modified an animal model of PTSD by exposing rats to chronic stress and evaluating the subsequent development of behavioral PTSD-like symptoms, as well as the effects on proinflammatory cytokines, which were implicated in PTSD. We report that while FLU or DES had a beneficial effect on avoidance and hyperarousal symptoms, MPH improved all three symptoms. Moreover, the combination of MPH with DES produced the most dramatic beneficial effects. Serum levels of interleukin-1β (IL-1β) and IL-6 were elevated in the PTSD-like group compared with the control group, and were decreased by MPH, FLU, DES or the combination drug treatments, with the combination of DES+MPH producing the most complete rescue of the inflammatory response. Considering the versatile symptoms of PTSD, our results suggest a new combined treatment for PTSD comprising the antidepressant DES and the psychostimulant MPH.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>25247592</pmid><doi>10.1038/tp.2014.82</doi><oa>free_for_read</oa></addata></record> |
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subjects | 13/21 631/443 64/86 692/699/476 Animals Antidepressive Agents, Tricyclic - pharmacology Behavioral Sciences Biological Psychology Central Nervous System Stimulants - pharmacology Desipramine - pharmacology Disease Models, Animal Drug Therapy, Combination Male Medicine Medicine & Public Health Methylphenidate - pharmacology Neurosciences Original original-article Pharmacotherapy Psychiatry Rats Rats, Wistar Stress Disorders, Post-Traumatic - drug therapy Treatment Outcome |
title | Methylphenidate and desipramine combined treatment improves PTSD symptomatology in a rat model |
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