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Argon blocks the expression of locomotor sensitization to amphetamine through antagonism at the vesicular monoamine transporter-2 and mu-opioid receptor in the nucleus accumbens.
David, H N; Dhilly, M; Degoulet, M; Poisnel, G; Meckler, C; Vallée, N; Blatteau, J-É; Risso, J-J; Lemaire, M; Debruyne, D; Abraini, J H.
Afiliación
  • David HN; 1] Centre de Recherche Hôtel-Dieu de Lévis, CSSS Alphonse-Desjardins, Lévis, QC, Canada [2] Département d'Anesthésiologie, Université Laval, Québec, QC, Canada.
  • Dhilly M; 1] ISTCT UMR 6301, CEA DSV/I2BM, LDM-TEP Group, Caen, France [2] ISTCT UMR 6301, CNRS, Caen, France [3] ISTCT UMR 6301, Université de Caen Basse-Normandie, Normandie-Université, Caen, France.
  • Degoulet M; Faculté de Médecine, Université de Caen Basse-Normandie, Normandie-Université, Caen, France.
  • Poisnel G; 1] ISTCT UMR 6301, CEA DSV/I2BM, LDM-TEP Group, Caen, France [2] ISTCT UMR 6301, CNRS, Caen, France [3] ISTCT UMR 6301, Université de Caen Basse-Normandie, Normandie-Université, Caen, France.
  • Meckler C; Institut de Recherche Biomédicale des Armées, Toulon, France.
  • Vallée N; Institut de Recherche Biomédicale des Armées, Toulon, France.
  • Blatteau JÉ; Institut de Recherche Biomédicale des Armées, Toulon, France.
  • Risso JJ; Institut de Recherche Biomédicale des Armées, Toulon, France.
  • Lemaire M; Air Liquide, Centre de Recherche Claude-Delorme, Paris-Saclay, France.
  • Debruyne D; 1] ISTCT UMR 6301, CEA DSV/I2BM, LDM-TEP Group, Caen, France [2] ISTCT UMR 6301, CNRS, Caen, France [3] ISTCT UMR 6301, Université de Caen Basse-Normandie, Normandie-Université, Caen, France.
  • Abraini JH; 1] Département d'Anesthésiologie, Université Laval, Québec, QC, Canada [2] Faculté de Médecine, Université de Caen Basse-Normandie, Normandie-Université, Caen, France [3] Institut de Recherche Biomédicale des Armées, Toulon, France.
Transl Psychiatry ; 5: e594, 2015 Jul 07.
Article en En | MEDLINE | ID: mdl-26151922
We investigated the effects of the noble gas argon on the expression of locomotor sensitization to amphetamine and amphetamine-induced changes in dopamine release and mu-opioid neurotransmission in the nucleus accumbens. We found (1) argon blocked the increase in carrier-mediated dopamine release induced by amphetamine in brain slices, but, in contrast, potentiated the decrease in KCl-evoked dopamine release induced by amphetamine, thereby suggesting that argon inhibited the vesicular monoamine transporter-2; (2) argon blocked the expression of locomotor and mu-opioid neurotransmission sensitization induced by repeated amphetamine administration in a short-term model of sensitization in rats; (3) argon decreased the maximal number of binding sites and increased the dissociation constant of mu-receptors in membrane preparations, thereby indicating that argon is a mu-receptor antagonist; (4) argon blocked the expression of locomotor sensitization and context-dependent locomotor activity induced by repeated administration of amphetamine in a long-term model of sensitization. Taken together, these data indicate that argon could be of potential interest for treating drug addiction and dependence.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Argón / Receptores Opioides mu / Proteínas de Transporte Vesicular de Monoaminas / Anfetamina / Locomoción / Núcleo Accumbens Límite: Animals Idioma: En Revista: Transl Psychiatry Año: 2015 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Argón / Receptores Opioides mu / Proteínas de Transporte Vesicular de Monoaminas / Anfetamina / Locomoción / Núcleo Accumbens Límite: Animals Idioma: En Revista: Transl Psychiatry Año: 2015 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos