Research Topics
Genomes and GenesSpecies | L BardinSummaryAffiliation: Centre de Recherche Pierre Fabre Country: France Publications
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Publications
The complex role of serotonin and 5-HT receptors in chronic painLaurent Bardin
Division of Neurobiology 2, Centre de Recherche Pierre Fabre, Castres, France
Behav Pharmacol 22:390-404. 2011....
Chronic restraint stress induces mechanical and cold allodynia, and enhances inflammatory pain in rat: Relevance to human stress-associated painful pathologiesL Bardin
Division of Neurobiology 2, Centre de Recherche Pierre Fabre, 17, avenue Jean Moulin, 81106 Castres, France
Behav Brain Res 205:360-6. 2009....
Pharmacological profiles in rats of novel antipsychotics with combined dopamine D2/serotonin 5-HT1A activity: comparison with typical and atypical conventional antipsychoticsLaurent Bardin
Division of Neurobiology, Pierre Fabre Research Centre, Castres, France
Behav Pharmacol 18:103-18. 2007....
Antipsychotic-like vs cataleptogenic actions in mice of novel antipsychotics having D2 antagonist and 5-HT1A agonist propertiesLaurent Bardin
Division of Neurobiology 2, Centre de Recherche Pierre Fabre, Castres, France
Neuropsychopharmacology 31:1869-79. 2006..Further, they indicate that the balance of affinity and/or efficacy between D2 and 5-HT1A receptors profoundly influences their pharmacological activities, and will likely impact their therapeutic profiles...
Comparison of milnacipran, duloxetine and pregabalin in the formalin pain test and in a model of stress-induced ultrasonic vocalizations in ratsL Bardin
Division of Neurobiology 2, Centre de Recherche Pierre Fabre, 17, avenue Jean Moulin, 81106 Castres, France
Neurosci Res 66:135-40. 2010..To summarize, reduction of formalin-induced paw licking/late phase might constitute a useful indicator of potential activity against inflammatory/centrally sensitized pain, as might be expressed in fibromyalgia...
Dual, hyperalgesic, and analgesic effects of the high-efficacy 5-hydroxytryptamine 1A (5-HT1A) agonist F 13640 [(3-chloro-4-fluoro-phenyl)-[4-fluoro-4-{[(5-methyl-pyridin-2-ylmethyl)-amino]-methyl}piperidin-1-yl]methanone, fumaric acid salt]: relationshipLaurent Bardin
Department of General Pharmacology, Centre de Recherche Pierre Fabre, 17 avenue Jean Moulin, 81106 Castres Cedex, France
J Pharmacol Exp Ther 312:1034-42. 2005..These results demonstrate that F 13640 induces hyperalgesia and/or analgesia with a time course that parallels the occupancy of 5-HT(1A) receptors and the presence of the compound in blood and brain...
Role of spinal 5-HT(1A) receptors in morphine analgesia and tolerance in ratsLaurent Bardin
Centre de Recherche Pierre Fabre, 17 avenue Jean Moulin, Castres Cédex F 81106, France
Eur J Pain 8:253-61. 2004..These findings demonstrate that 5-HT(1A) receptor agonists can act in the spinal cord to produce both hyper- and hypo-algesic effects and play a major role in the opioid analgesia and tolerance...
Profound, non-opioid analgesia produced by the high-efficacy 5-HT(1A) agonist F 13640 in the formalin model of tonic nociceptive painL Bardin
Centre de Recherche Pierre Fabre, 17 avenue Jean Moulin, F 81106 Castres Cedex, France
Pharmacology 67:182-94. 2003....
F15063, a compound with D2/D3 antagonist, 5-HT 1A agonist and D4 partial agonist properties. II. Activity in models of positive symptoms of schizophreniaR Depoortere
Division of Neurobiology 2, Centre de Recherche Pierre Fabre, Castres, France
Br J Pharmacol 151:253-65. 2007..Here, the profile of F15063 was evaluated in models of positive symptoms of schizophrenia and motor side-effects...
Large-amplitude 5-HT1A receptor activation: a new mechanism of profound, central analgesiaF C Colpaert
Centre de Recherche Pierre Fabre, 17, avenue Jean Moulin, 81106 Castres Cedex, France
Neuropharmacology 43:945-58. 2002....
In the formalin model of tonic nociceptive pain, 8-OH-DPAT produces 5-HT1A receptor-mediated, behaviorally specific analgesiaL Bardin
Centre de Recherche Pierre Fabre, 17 avenue Jean Moulin, F 81106 Cedex, Castres, France
Eur J Pharmacol 421:109-14. 2001..e., forepaw treading) of the 5-HT syndrome which 8-OH-DPAT also induces...
The novel analgesic, F 13640, produces intra- and postoperative analgesia in a rat model of surgical painIvan Kiss
, Intensivmedizin und Schmerztherapie, Alfried Krupp Krankenhaus, 45117 Essen, Germany
Eur J Pharmacol 523:29-39. 2005..Unlike the opioid, remifentanil, F 13640 caused no hyperalgesia with ongoing postoperative pain, and should remain effective with protracted postoperative use...
F15063, a compound with D2/D3 antagonist, 5-HT 1A agonist and D4 partial agonist properties. III. Activity in models of cognition and negative symptomsR Depoortere
Division of Neurobiology 2, Centre de Recherche Pierre Fabre, Castres, France
Br J Pharmacol 151:266-77. 2007..However F15063 induced neither catalepsy nor the 'serotonin syndrome'. Here, we evaluated its profile in rat models predictive of efficacy against negative symptoms/cognitive deficits of schizophrenia...
5-HT1A receptors are involved in the effects of xaliproden on G-protein activation, neurotransmitter release and nociceptionJ C Martel
Division of Neurobiology 2, Centre de Recherche Pierre Fabre, Castres, France
Br J Pharmacol 158:232-42. 2009..The present study investigated its profile on in vitro transduction, neurochemical responses and acute nociceptive pain tests in rats...
Effects of antipsychotics and reference monoaminergic ligands on marble burying behavior in miceLiesbeth A Bruins Slot
Department of Cellular and Molecular Biology bDivision of Neurobiology 2, Pierre Fabre Research Centre, Castres Cedex, France
Behav Pharmacol 19:145-52. 2008..Inhibition of marble burying behavior may result from the interplay of several receptor systems, including 5-HT2 receptor blockade, dopamine D2 partial agonism and serotonin 5-HT1A agonism...
The antipsychotics clozapine and olanzapine increase plasma glucose and corticosterone levels in rats: comparison with aripiprazole, ziprasidone, bifeprunox and F15063Marie Bernadette Assié
Neurobiology II Division, Centre de Recherche Pierre Fabre, 17 avenue Jean Moulin, 81106 Castres Cedex, France
Eur J Pharmacol 592:160-6. 2008....
Apomorphine-induced emesis in dogs: differential sensitivity to established and novel dopamine D2/5-HT(1A) antipsychotic compoundsRonan Depoortere
Division of Neurobiology 2, Centre de Recherche Pierre Fabre, 17, avenue Jean Moulin, 81106 Castres, France
Eur J Pharmacol 597:34-8. 2008..This model can thus be advantageously used to investigate the pharmacological activity of novel D2 receptor antagonists/partial agonists in dogs...
Penile erection and yawning induced by dopamine D2-like receptor agonists in rats: influence of strain and contribution of dopamine D2, but not D3 and D4 receptorsRonan Depoortere
Division of Neurobiology 2, Centre de Recherche Pierre Fabre, Castres, France
Behav Pharmacol 20:303-11. 2009..5 mg/kg). The present data do not support a major implication of either DA D3 or D4 receptors in the control of PE and YA in rats, but indicate a preponderant role of DA D2 receptors...
F15599, a preferential post-synaptic 5-HT1A receptor agonist: activity in models of cognition in comparison with reference 5-HT1A receptor agonistsRonan Depoortere
Neurobiology 2 Division, Centre de Recherche Pierre Fabre, 17, avenue Jean Moulin, 81106 Castres, France
Eur Neuropsychopharmacol 20:641-54. 2010..This suggests that preferential activation of post-synaptic 5-HT(1A) receptors could prove useful in pathologies characterized by cognitive/memory deficiencies, such as schizophrenia and depression...
F15063, a potential antipsychotic with dopamine D(2)/D(3) antagonist, 5-HT(1A) agonist and D(4) partial agonist properties: (IV) duration of brain D2-like receptor occupancy and antipsychotic-like activity versus plasma concentration in miceMarie Bernadette Assié
Centre de Recherche Pierre Fabre, 17 avenue Jean Moulin, 81106 Castres Cedex, France
Naunyn Schmiedebergs Arch Pharmacol 375:241-50. 2007..In addition, the durations of action of F15063 and haloperidol in a behavioural model of antipsychotic-like activity were closely correlated to their occupancy of central D2-like receptors, and much longer than their presence in plasma...
