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Preclinical evaluation of the abuse potential of Pitolisant, a histamine H3 receptor inverse agonist/antagonist compared with Modafinil.
Uguen, M; Perrin, D; Belliard, S; Ligneau, X; Beardsley, P M; Lecomte, J M; Schwartz, J C.
Afiliación
  • Uguen M; Bioprojet-Biotech, Saint Grégoire Cedex, France.
Br J Pharmacol ; 169(3): 632-44, 2013 Jun.
Article en En | MEDLINE | ID: mdl-23472741
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.
Asunto(s)
Conducta Adictiva/inducido químicamente; Drogas en Investigación/efectos adversos; Agonistas de los Receptores Histamínicos/efectos adversos; Antagonistas de los Receptores Histamínicos/efectos adversos; Piperidinas/efectos adversos; Receptores Histamínicos H3/metabolismo; Promotores de la Vigilia/efectos adversos; Animales; Conducta Adictiva/prevención & control; Conducta Animal/efectos de los fármacos; Compuestos de Bencidrilo/efectos adversos; Estimulantes del Sistema Nervioso Central/efectos adversos; Dopamina/química; Dopamina/metabolismo; Neuronas Dopaminérgicas/efectos de los fármacos; Neuronas Dopaminérgicas/metabolismo; Relación Dosis-Respuesta a Droga; Antagonismo de Drogas; Evaluación Preclínica de Medicamentos; Agonismo Inverso de Drogas; Drogas en Investigación/administración & dosificación; Drogas en Investigación/uso terapéutico; Agonistas de los Receptores Histamínicos/administración & dosificación; Agonistas de los Receptores Histamínicos/uso terapéutico; Antagonistas de los Receptores Histamínicos/administración & dosificación; Antagonistas de los Receptores Histamínicos/uso terapéutico; Macaca mulatta; Masculino; Ratones; Modafinilo; Actividad Motora/efectos de los fármacos; Núcleo Accumbens/efectos de los fármacos; Núcleo Accumbens/metabolismo; Piperidinas/administración & dosificación; Piperidinas/uso terapéutico; Ratas; Receptores Histamínicos H3/química; Promotores de la Vigilia/administración & dosificación; Promotores de la Vigilia/uso terapéutico

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Piperidinas / Drogas en Investigación / Conducta Adictiva / Agonistas de los Receptores Histamínicos / Receptores Histamínicos H3 / Promotores de la Vigilia / Antagonistas de los Receptores Histamínicos Idioma: En Revista: Br J Pharmacol Año: 2013 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Piperidinas / Drogas en Investigación / Conducta Adictiva / Agonistas de los Receptores Histamínicos / Receptores Histamínicos H3 / Promotores de la Vigilia / Antagonistas de los Receptores Histamínicos Idioma: En Revista: Br J Pharmacol Año: 2013 Tipo del documento: Article