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...

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Veröffentlicht in:British journal of pharmacology 2013-06, Vol.169 (3), p.632-644
Hauptverfasser: Uguen, M, Perrin, D, Belliard, S, Ligneau, X, Beardsley, PM, Lecomte, JM, Schwartz, JC
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container_start_page 632
container_title British journal of pharmacology
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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
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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. 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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. 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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>
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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
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