Preclinical evaluation of the abuse potential of Pitolisant, a histamine H3 receptor inverse agonist/antagonist compared with Modafinil
Background and Purpose Pitolisant, a histamine H3 receptor inverse agonist/antagonist is currently under Phase III clinical trials for treatment of excessive daytime sleepiness namely in narcoleptic patients. Its drug abuse potential was investigated using in vivo models in rodents and monkeys and c...
Gespeichert in:
Veröffentlicht in: | British journal of pharmacology 2013-06, Vol.169 (3), p.632-644 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 644 |
---|---|
container_issue | 3 |
container_start_page | 632 |
container_title | British journal of pharmacology |
container_volume | 169 |
creator | Uguen, M Perrin, D Belliard, S Ligneau, X Beardsley, PM Lecomte, JM Schwartz, JC |
description | Background and Purpose
Pitolisant, a histamine H3 receptor inverse agonist/antagonist is currently under Phase III clinical trials for treatment of excessive daytime sleepiness namely in narcoleptic patients. Its drug abuse potential was investigated using in vivo models in rodents and monkeys and compared with those of Modafinil, a psychostimulant currently used in the same indications.
Experimental Approach
Effects of Pitolisant on dopamine release in the nucleus accumbens, on spontaneous and cocaine‐induced locomotion, locomotor sensitization were monitored. It was also tested in three standard drug abuse tests i.e. conditioned place preference in rats, self‐administration in monkeys and cocaine discrimination in mice as well as in a physical dependence model.
Key Results
Pitolisant did not elicit any significant changes in dopaminergic indices in rat nucleus accumbens whereas Modafinil increased dopamine release. In rodents, Pitolisant was without any effect on locomotion and reduced the cocaine‐induced hyperlocomotion. In addition, no locomotor sensitization and no conditioned hyperlocomotion were evidenced with this compound in rats whereas significant effects were elicited by Modafinil. Finally, Pitolisant was devoid of any significant effects in the three standard drug abuse tests (including self‐administration in monkeys) and in the physical dependence model.
Conclusions and Implications
No potential drug abuse liability for Pitolisant was evidenced in various in vivo rodent and primate models, whereas the same does not seem so clear in the case of Modafinil. |
doi_str_mv | 10.1111/bph.12149 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3682710</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3316013031</sourcerecordid><originalsourceid>FETCH-LOGICAL-p3699-70f559b6b805577ae17e5d8e16de295ebbe4215d339a3653aeb8a8dfe11031233</originalsourceid><addsrcrecordid>eNpVkc1u1DAUhS0EotOBBS-ALLFtOv6JY2eDRKvCILXqLGBt3UxuGlcZOzjOVH0CXht3OlTgja_u-Xyu7UPIB87OeV6rZuzPueBl_YoseKmrQknDX5MFY0wXnBtzQk6n6Z6xLGr1lpwIWWqhS74gvzcRt4PzbgsDxT0MMyQXPA0dTT1SaOYJ6RgS-uQykdsbl8LgJvDpjALt3ZRg5zzStaTZCscUInV-jzEfhLvgM7DK8LGk27AbIWJLH1zq6U1oocvTh3fkTQfDhO-P-5L8_Hr143JdXN9--3755boYZVXXhWadUnVTNYYppTUg16hag7xqUdQKmwZLwVUrZQ2yUhKwMWDaDjlnkgspl-Tzs-84Nztst_ldEQY7RreD-GgDOPu_4l1v78LeysoInU2W5NPRIIZfM07J3oc5-nxny5UwlSjlgfr475gX_78fn4HVM_DgBnx80TmzT4nanKg9JGovNutDIf8A0S6WJA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1528624310</pqid></control><display><type>article</type><title>Preclinical evaluation of the abuse potential of Pitolisant, a histamine H3 receptor inverse agonist/antagonist compared with Modafinil</title><source>Wiley Free Content</source><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Uguen, M ; Perrin, D ; Belliard, S ; Ligneau, X ; Beardsley, PM ; Lecomte, JM ; Schwartz, JC</creator><creatorcontrib>Uguen, M ; Perrin, D ; Belliard, S ; Ligneau, X ; Beardsley, PM ; Lecomte, JM ; Schwartz, JC</creatorcontrib><description>Background and Purpose
Pitolisant, a histamine H3 receptor inverse agonist/antagonist is currently under Phase III clinical trials for treatment of excessive daytime sleepiness namely in narcoleptic patients. Its drug abuse potential was investigated using in vivo models in rodents and monkeys and compared with those of Modafinil, a psychostimulant currently used in the same indications.
Experimental Approach
Effects of Pitolisant on dopamine release in the nucleus accumbens, on spontaneous and cocaine‐induced locomotion, locomotor sensitization were monitored. It was also tested in three standard drug abuse tests i.e. conditioned place preference in rats, self‐administration in monkeys and cocaine discrimination in mice as well as in a physical dependence model.
Key Results
Pitolisant did not elicit any significant changes in dopaminergic indices in rat nucleus accumbens whereas Modafinil increased dopamine release. In rodents, Pitolisant was without any effect on locomotion and reduced the cocaine‐induced hyperlocomotion. In addition, no locomotor sensitization and no conditioned hyperlocomotion were evidenced with this compound in rats whereas significant effects were elicited by Modafinil. Finally, Pitolisant was devoid of any significant effects in the three standard drug abuse tests (including self‐administration in monkeys) and in the physical dependence model.
Conclusions and Implications
No potential drug abuse liability for Pitolisant was evidenced in various in vivo rodent and primate models, whereas the same does not seem so clear in the case of Modafinil.</description><identifier>ISSN: 0007-1188</identifier><identifier>EISSN: 1476-5381</identifier><identifier>DOI: 10.1111/bph.12149</identifier><identifier>PMID: 23472741</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject><![CDATA[Animals ; Behavior, Addictive - chemically induced ; Behavior, Addictive - prevention & control ; Behavior, Animal - drug effects ; Benzhydryl Compounds - adverse effects ; Central Nervous System Stimulants - adverse effects ; Cocaine ; conditioned place preference ; discrimination ; Dopamine ; Dopamine - chemistry ; Dopamine - metabolism ; Dopaminergic Neurons - drug effects ; Dopaminergic Neurons - metabolism ; Dose-Response Relationship, Drug ; Drug abuse ; Drug Antagonism ; Drug Evaluation, Preclinical ; Drug Inverse Agonism ; Drugs, Investigational - administration & dosage ; Drugs, Investigational - adverse effects ; Drugs, Investigational - therapeutic use ; H3 receptor ; histamine ; Histamine Agonists - administration & dosage ; Histamine Agonists - adverse effects ; Histamine Agonists - therapeutic use ; Histamine Antagonists - administration & dosage ; Histamine Antagonists - adverse effects ; Histamine Antagonists - therapeutic use ; Macaca mulatta ; Male ; Mice ; Modafinil ; monkeys ; Motor Activity - drug effects ; Nucleus Accumbens - drug effects ; Nucleus Accumbens - metabolism ; Piperidines - administration & dosage ; Piperidines - adverse effects ; Piperidines - therapeutic use ; Pitolisant ; Rats ; Receptors, Histamine H3 - chemistry ; Receptors, Histamine H3 - metabolism ; Research Papers ; Rodents ; self‐administration ; sensitization ; Wakefulness-Promoting Agents - administration & dosage ; Wakefulness-Promoting Agents - adverse effects ; Wakefulness-Promoting Agents - therapeutic use]]></subject><ispartof>British journal of pharmacology, 2013-06, Vol.169 (3), p.632-644</ispartof><rights>2013 The Authors. British Journal of Pharmacology © 2013 The British Pharmacological Society</rights><rights>2013 The Authors. British Journal of Pharmacology © 2013 The British Pharmacological Society.</rights><rights>British Journal of Pharmacology © 2013 The British Pharmacological Society</rights><rights>British Journal of Pharmacology © 2013 The British Pharmacological Society 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682710/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682710/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,1411,1427,27901,27902,45550,45551,46384,46808,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23472741$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uguen, M</creatorcontrib><creatorcontrib>Perrin, D</creatorcontrib><creatorcontrib>Belliard, S</creatorcontrib><creatorcontrib>Ligneau, X</creatorcontrib><creatorcontrib>Beardsley, PM</creatorcontrib><creatorcontrib>Lecomte, JM</creatorcontrib><creatorcontrib>Schwartz, JC</creatorcontrib><title>Preclinical evaluation of the abuse potential of Pitolisant, a histamine H3 receptor inverse agonist/antagonist compared with Modafinil</title><title>British journal of pharmacology</title><addtitle>Br J Pharmacol</addtitle><description>Background and Purpose
Pitolisant, a histamine H3 receptor inverse agonist/antagonist is currently under Phase III clinical trials for treatment of excessive daytime sleepiness namely in narcoleptic patients. Its drug abuse potential was investigated using in vivo models in rodents and monkeys and compared with those of Modafinil, a psychostimulant currently used in the same indications.
Experimental Approach
Effects of Pitolisant on dopamine release in the nucleus accumbens, on spontaneous and cocaine‐induced locomotion, locomotor sensitization were monitored. It was also tested in three standard drug abuse tests i.e. conditioned place preference in rats, self‐administration in monkeys and cocaine discrimination in mice as well as in a physical dependence model.
Key Results
Pitolisant did not elicit any significant changes in dopaminergic indices in rat nucleus accumbens whereas Modafinil increased dopamine release. In rodents, Pitolisant was without any effect on locomotion and reduced the cocaine‐induced hyperlocomotion. In addition, no locomotor sensitization and no conditioned hyperlocomotion were evidenced with this compound in rats whereas significant effects were elicited by Modafinil. Finally, Pitolisant was devoid of any significant effects in the three standard drug abuse tests (including self‐administration in monkeys) and in the physical dependence model.
Conclusions and Implications
No potential drug abuse liability for Pitolisant was evidenced in various in vivo rodent and primate models, whereas the same does not seem so clear in the case of Modafinil.</description><subject>Animals</subject><subject>Behavior, Addictive - chemically induced</subject><subject>Behavior, Addictive - prevention & control</subject><subject>Behavior, Animal - drug effects</subject><subject>Benzhydryl Compounds - adverse effects</subject><subject>Central Nervous System Stimulants - adverse effects</subject><subject>Cocaine</subject><subject>conditioned place preference</subject><subject>discrimination</subject><subject>Dopamine</subject><subject>Dopamine - chemistry</subject><subject>Dopamine - metabolism</subject><subject>Dopaminergic Neurons - drug effects</subject><subject>Dopaminergic Neurons - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug abuse</subject><subject>Drug Antagonism</subject><subject>Drug Evaluation, Preclinical</subject><subject>Drug Inverse Agonism</subject><subject>Drugs, Investigational - administration & dosage</subject><subject>Drugs, Investigational - adverse effects</subject><subject>Drugs, Investigational - therapeutic use</subject><subject>H3 receptor</subject><subject>histamine</subject><subject>Histamine Agonists - administration & dosage</subject><subject>Histamine Agonists - adverse effects</subject><subject>Histamine Agonists - therapeutic use</subject><subject>Histamine Antagonists - administration & dosage</subject><subject>Histamine Antagonists - adverse effects</subject><subject>Histamine Antagonists - therapeutic use</subject><subject>Macaca mulatta</subject><subject>Male</subject><subject>Mice</subject><subject>Modafinil</subject><subject>monkeys</subject><subject>Motor Activity - drug effects</subject><subject>Nucleus Accumbens - drug effects</subject><subject>Nucleus Accumbens - metabolism</subject><subject>Piperidines - administration & dosage</subject><subject>Piperidines - adverse effects</subject><subject>Piperidines - therapeutic use</subject><subject>Pitolisant</subject><subject>Rats</subject><subject>Receptors, Histamine H3 - chemistry</subject><subject>Receptors, Histamine H3 - metabolism</subject><subject>Research Papers</subject><subject>Rodents</subject><subject>self‐administration</subject><subject>sensitization</subject><subject>Wakefulness-Promoting Agents - administration & dosage</subject><subject>Wakefulness-Promoting Agents - adverse effects</subject><subject>Wakefulness-Promoting Agents - therapeutic use</subject><issn>0007-1188</issn><issn>1476-5381</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc1u1DAUhS0EotOBBS-ALLFtOv6JY2eDRKvCILXqLGBt3UxuGlcZOzjOVH0CXht3OlTgja_u-Xyu7UPIB87OeV6rZuzPueBl_YoseKmrQknDX5MFY0wXnBtzQk6n6Z6xLGr1lpwIWWqhS74gvzcRt4PzbgsDxT0MMyQXPA0dTT1SaOYJ6RgS-uQykdsbl8LgJvDpjALt3ZRg5zzStaTZCscUInV-jzEfhLvgM7DK8LGk27AbIWJLH1zq6U1oocvTh3fkTQfDhO-P-5L8_Hr143JdXN9--3755boYZVXXhWadUnVTNYYppTUg16hag7xqUdQKmwZLwVUrZQ2yUhKwMWDaDjlnkgspl-Tzs-84Nztst_ldEQY7RreD-GgDOPu_4l1v78LeysoInU2W5NPRIIZfM07J3oc5-nxny5UwlSjlgfr475gX_78fn4HVM_DgBnx80TmzT4nanKg9JGovNutDIf8A0S6WJA</recordid><startdate>201306</startdate><enddate>201306</enddate><creator>Uguen, M</creator><creator>Perrin, D</creator><creator>Belliard, S</creator><creator>Ligneau, X</creator><creator>Beardsley, PM</creator><creator>Lecomte, JM</creator><creator>Schwartz, JC</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>5PM</scope></search><sort><creationdate>201306</creationdate><title>Preclinical evaluation of the abuse potential of Pitolisant, a histamine H3 receptor inverse agonist/antagonist compared with Modafinil</title><author>Uguen, M ; Perrin, D ; Belliard, S ; Ligneau, X ; Beardsley, PM ; Lecomte, JM ; Schwartz, JC</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p3699-70f559b6b805577ae17e5d8e16de295ebbe4215d339a3653aeb8a8dfe11031233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Behavior, Addictive - chemically induced</topic><topic>Behavior, Addictive - prevention & control</topic><topic>Behavior, Animal - drug effects</topic><topic>Benzhydryl Compounds - adverse effects</topic><topic>Central Nervous System Stimulants - adverse effects</topic><topic>Cocaine</topic><topic>conditioned place preference</topic><topic>discrimination</topic><topic>Dopamine</topic><topic>Dopamine - chemistry</topic><topic>Dopamine - metabolism</topic><topic>Dopaminergic Neurons - drug effects</topic><topic>Dopaminergic Neurons - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug abuse</topic><topic>Drug Antagonism</topic><topic>Drug Evaluation, Preclinical</topic><topic>Drug Inverse Agonism</topic><topic>Drugs, Investigational - administration & dosage</topic><topic>Drugs, Investigational - adverse effects</topic><topic>Drugs, Investigational - therapeutic use</topic><topic>H3 receptor</topic><topic>histamine</topic><topic>Histamine Agonists - administration & dosage</topic><topic>Histamine Agonists - adverse effects</topic><topic>Histamine Agonists - therapeutic use</topic><topic>Histamine Antagonists - administration & dosage</topic><topic>Histamine Antagonists - adverse effects</topic><topic>Histamine Antagonists - therapeutic use</topic><topic>Macaca mulatta</topic><topic>Male</topic><topic>Mice</topic><topic>Modafinil</topic><topic>monkeys</topic><topic>Motor Activity - drug effects</topic><topic>Nucleus Accumbens - drug effects</topic><topic>Nucleus Accumbens - metabolism</topic><topic>Piperidines - administration & dosage</topic><topic>Piperidines - adverse effects</topic><topic>Piperidines - therapeutic use</topic><topic>Pitolisant</topic><topic>Rats</topic><topic>Receptors, Histamine H3 - chemistry</topic><topic>Receptors, Histamine H3 - metabolism</topic><topic>Research Papers</topic><topic>Rodents</topic><topic>self‐administration</topic><topic>sensitization</topic><topic>Wakefulness-Promoting Agents - administration & dosage</topic><topic>Wakefulness-Promoting Agents - adverse effects</topic><topic>Wakefulness-Promoting Agents - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uguen, M</creatorcontrib><creatorcontrib>Perrin, D</creatorcontrib><creatorcontrib>Belliard, S</creatorcontrib><creatorcontrib>Ligneau, X</creatorcontrib><creatorcontrib>Beardsley, PM</creatorcontrib><creatorcontrib>Lecomte, JM</creatorcontrib><creatorcontrib>Schwartz, JC</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uguen, M</au><au>Perrin, D</au><au>Belliard, S</au><au>Ligneau, X</au><au>Beardsley, PM</au><au>Lecomte, JM</au><au>Schwartz, JC</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preclinical evaluation of the abuse potential of Pitolisant, a histamine H3 receptor inverse agonist/antagonist compared with Modafinil</atitle><jtitle>British journal of pharmacology</jtitle><addtitle>Br J Pharmacol</addtitle><date>2013-06</date><risdate>2013</risdate><volume>169</volume><issue>3</issue><spage>632</spage><epage>644</epage><pages>632-644</pages><issn>0007-1188</issn><eissn>1476-5381</eissn><abstract>Background and Purpose
Pitolisant, a histamine H3 receptor inverse agonist/antagonist is currently under Phase III clinical trials for treatment of excessive daytime sleepiness namely in narcoleptic patients. Its drug abuse potential was investigated using in vivo models in rodents and monkeys and compared with those of Modafinil, a psychostimulant currently used in the same indications.
Experimental Approach
Effects of Pitolisant on dopamine release in the nucleus accumbens, on spontaneous and cocaine‐induced locomotion, locomotor sensitization were monitored. It was also tested in three standard drug abuse tests i.e. conditioned place preference in rats, self‐administration in monkeys and cocaine discrimination in mice as well as in a physical dependence model.
Key Results
Pitolisant did not elicit any significant changes in dopaminergic indices in rat nucleus accumbens whereas Modafinil increased dopamine release. In rodents, Pitolisant was without any effect on locomotion and reduced the cocaine‐induced hyperlocomotion. In addition, no locomotor sensitization and no conditioned hyperlocomotion were evidenced with this compound in rats whereas significant effects were elicited by Modafinil. Finally, Pitolisant was devoid of any significant effects in the three standard drug abuse tests (including self‐administration in monkeys) and in the physical dependence model.
Conclusions and Implications
No potential drug abuse liability for Pitolisant was evidenced in various in vivo rodent and primate models, whereas the same does not seem so clear in the case of Modafinil.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>23472741</pmid><doi>10.1111/bph.12149</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0007-1188 |
ispartof | British journal of pharmacology, 2013-06, Vol.169 (3), p.632-644 |
issn | 0007-1188 1476-5381 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3682710 |
source | Wiley Free Content; MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
subjects | Animals Behavior, Addictive - chemically induced Behavior, Addictive - prevention & control Behavior, Animal - drug effects Benzhydryl Compounds - adverse effects Central Nervous System Stimulants - adverse effects Cocaine conditioned place preference discrimination Dopamine Dopamine - chemistry Dopamine - metabolism Dopaminergic Neurons - drug effects Dopaminergic Neurons - metabolism Dose-Response Relationship, Drug Drug abuse Drug Antagonism Drug Evaluation, Preclinical Drug Inverse Agonism Drugs, Investigational - administration & dosage Drugs, Investigational - adverse effects Drugs, Investigational - therapeutic use H3 receptor histamine Histamine Agonists - administration & dosage Histamine Agonists - adverse effects Histamine Agonists - therapeutic use Histamine Antagonists - administration & dosage Histamine Antagonists - adverse effects Histamine Antagonists - therapeutic use Macaca mulatta Male Mice Modafinil monkeys Motor Activity - drug effects Nucleus Accumbens - drug effects Nucleus Accumbens - metabolism Piperidines - administration & dosage Piperidines - adverse effects Piperidines - therapeutic use Pitolisant Rats Receptors, Histamine H3 - chemistry Receptors, Histamine H3 - metabolism Research Papers Rodents self‐administration sensitization Wakefulness-Promoting Agents - administration & dosage Wakefulness-Promoting Agents - adverse effects Wakefulness-Promoting Agents - therapeutic use |
title | Preclinical evaluation of the abuse potential of Pitolisant, a histamine H3 receptor inverse agonist/antagonist compared with Modafinil |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T09%3A39%3A35IST&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=Preclinical%20evaluation%20of%20the%20abuse%20potential%20of%20Pitolisant,%20a%20histamine%20H3%20receptor%20inverse%20agonist/antagonist%20compared%20with%20Modafinil&rft.jtitle=British%20journal%20of%20pharmacology&rft.au=Uguen,%20M&rft.date=2013-06&rft.volume=169&rft.issue=3&rft.spage=632&rft.epage=644&rft.pages=632-644&rft.issn=0007-1188&rft.eissn=1476-5381&rft_id=info:doi/10.1111/bph.12149&rft_dat=%3Cproquest_pubme%3E3316013031%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1528624310&rft_id=info:pmid/23472741&rfr_iscdi=true |