Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Laetitia, Cistarelli"'
Autor:
Ines S Amorim, Sylvie Challal, Laetitia Cistarelli, Thierry Dorval, Laurene Abjean, Manuelle Touzard, Nicolas Arbez, Arnaud François, Fany Panayi, Ross Jeggo, Erika Cecon, Atsuro Oishi, Julie Dam, Ralf Jockers, Patricia Machado
Publikováno v:
PLoS ONE, Vol 18, Iss 4, p e0283941 (2023)
Intracellular accumulation of tau protein is a hallmark of Alzheimer's Disease and Progressive Supranuclear Palsy, as well as other neurodegenerative disorders collectively known as tauopathies. Despite our increasing understanding of the mechanisms
Externí odkaz:
https://doaj.org/article/8015c54627e64350a7b3b92db676e019
Autor:
Nathalie Dumas, Esther Schenker, Arnaud François, Ross Jeggo, Sylvie Girardon, Laetitia Cistarelli, Catherine Liard, Alain P. Gobert, Gaelle Rollin-Jego, Rodolphe Billiras
Publikováno v:
Alzheimer's & Dementia. 14
Autor:
Jean A. Boutin, P. Monika Verdouw, Marianne Rodriguez, Roberto Maggio, Philippe Vayer, Takashi Yoshitake, Gabriella Aloisi, Catherine de Montrion, Brian P. Lockhart, Mauricette Brocco, Jean-Michel Rivet, Per Svenningsson, Jean-Pierre Galizzi, Lotte De Groote, Benjamin Di Cara, Francis Cogé, Laetitia Cistarelli, Sylvie Veiga, Lucianne Groenink, Ebba Gregorsson Lundius, Millan Mark, Alain Gobert
Publikováno v:
The Journal of Neuroscience. 31:16928-16940
“Ecstasy” [3,4-methylenedioxymetamphetamine (MDMA)] is of considerable interest in light of its prosocial properties and risks associated with widespread recreational use. Recently, it was found to bind trace amine-1 receptors (TA1Rs), which modu
Autor:
Anne Dekeyne, Sylvie Veiga, Loretta Iob, Elisabeth Mocaer, Mauricette Brocco, Martin Egeland, Alan R. Crossman, Carmen Muńoz, Per Svenningsson, Françoise Lejeune, Sylvie Girardon, Michael A. Hill, Benjamin Di Cara, Nitza Thomasson, Millan Mark, Laetitia Cistarelli, Alain Gobert, Charles R. Ashby
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 324:600-611
The novel benzopyranopyrrolidine, S33138 [N-[4-[2-[(3aS,9bR)-8-cyano-1,3a,4,9b-tetrahydro[1]benzopyrano[3,4-c]pyrrol-2(3H)-yl)-ethyl]phenylacetamide], is a preferential antagonist of cloned human D(3) versus D(2L) and D(2S) receptors. In mice, S33138
Publikováno v:
Journal of Neuroscience Methods. 140:141-152
Information concerning striatal levels of noradrenaline (NA) remains inconsistent. Here we have addressed this issue using a sensitive method of HPLC coupled to amperometric detection. The NA reuptake-inhibitor, reboxetine, selectively elevated level
Publikováno v:
Journal of Neurochemistry. 66:2209-2212
In freely moving rats, the novel, selective dopamine (DA) D 3 receptor agonist PD 128,907 dose-dependently [effective dose (ED 25 ) = 0.07 mg/kg, s.c.] reduced dialysate levels of DA in the frontal cortex, a structure innervated by the ventral tegmen
Publikováno v:
Journal of Neurochemistry. 69:2616-2619
Evidence exists that a reinforcement in monoaminergic transmission in the frontal cortex (FCX) is associated with antidepressant (AD) properties. Herein, we examined whether blockade of alpha2-adrenergic receptors modified the influence of monoamine
Autor:
Christophe Melon, Millan Mark, Loretta Iob, Alain P. Gobert, Laetitia Cistarelli, Anne Dekeyne
Publikováno v:
Psychopharmacology. 158:213-218
Rationale: Although drug discrimination procedures have proven difficult to apply to antidepressant agents, we recently characterized discriminative stimulus properties of the selective serotonin (5-HT) reuptake inhibitor, citalopram, in rats. Howeve
Autor:
Adrian Newman-Tancredi, Jean-Michel Rivet, Laetitia Cistarelli, Agnes Adhumeau‐Auclair, Françoise Lejeune, Millan Mark, Alain P. Gobert, Christophe Melon, Jean-Paul Nicolas
Publikováno v:
Synapse. 36:205-221
The present study evaluated, via a combined electrophysiological and dialysis approach, the potential influence of serotonin (5-HT)2C as compared to 5-HT2A and 5-HT2B receptors on dopaminergic, adrenergic, and serotonergic transmission in frontal cor
Publikováno v:
Neuroscience. 93:1251-1262
The serotonin1A receptor partial agonist, buspirone, also displays antagonist properties at D2 receptors and is metabolized to the alpha2-adrenergic receptor antagonist, 1-(2-pyrimidinyl-piperazine). Herein, we examined mechanisms underlying the infl