Zobrazeno 1 - 10
of 243
pro vyhledávání: '"E Mocaër"'
Autor:
Lawrence P. Reagan, A.L. Bumgardner, C. Gabriel, M. Risher, E. Mocaër, Jim R. Fadel, A. Hang, Victoria A. Macht, Claudia A. Grillo, Gerardo G. Piroli
Publikováno v:
Neuroscience. 284:430-443
Major depressive illness is among the most prevalent neuropsychiatric disorders and is associated with neuroplasticity deficits in limbic structures such as the amygdala. Since exposure to stressful life events is proposed to contribute to depressive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06a8581b259c23ff9c5225898a9a15ac
https://doi.org/10.1016/j.neuroscience.2014.09.047
https://doi.org/10.1016/j.neuroscience.2014.09.047
Publikováno v:
Journal of Pineal Research. 37:176-184
The ability of daily melatonin and the melatonin receptor antagonist, S22153, to entrain circadian system function was investigated in mice with atypical melatonin rhythm. B6D2F(1) mice were first synchronized to a LD 12:12 for approximately 2 wk, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::034858dff746fa3a4e18eebeb2e5dc8e
https://doi.org/10.1111/j.1600-079x.2004.00152.x
https://doi.org/10.1111/j.1600-079x.2004.00152.x
Publikováno v:
Neuropharmacology. 39:1037-1043
8-OH-DPAT [8-hydroxy-2-(di-N-propylamino)tetralin], a 5-HT(1A) receptor agonist, and S 15535 (4-benzodioxan-5-yl)1-(indan-2-yl)piperazine, a partial agonist at 5-HT(1A) receptors, were administered into the dorsal raphe nucleus and dorsal hippocampus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab67f95da7141d7393f05159caea65e8
https://doi.org/10.1016/s0028-3908(99)00189-6
https://doi.org/10.1016/s0028-3908(99)00189-6
Publikováno v:
European Neuropsychopharmacology. 25:S432-S433
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5b44cc889b4d21738971605aedf0ffa
https://doi.org/10.1016/s0924-977x(15)30578-2
https://doi.org/10.1016/s0924-977x(15)30578-2
Publikováno v:
British journal of pharmacology. 171(15)
Agomelatine behaves both as a potent agonist at melatonin MT1 and MT2 receptors and as a neutral antagonist at 5-HT2C receptors. Accumulating evidence in a broad range of experimental procedures supports the notion that the psychotropic effects of ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3af74d998f9688072825b1fb61371c94
https://pubmed.ncbi.nlm.nih.gov/24724693
https://pubmed.ncbi.nlm.nih.gov/24724693
Publikováno v:
Magnetic Resonance in Chemistry. 30:1212-1219
The conformational behaviour of 7-[(3-chloro-6,11-dihydro-6-methyldibenzo[c, f][1,2]thiazepin-11-yl)amino] heptanoic acid 5,5 dioxide (tianeptine), a new antidepressant drug, was studied by means of 1H and 13C NMR. The ring skeleton exhibits two dist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76d9b3327d39878b9aa1692eb2388cdd
https://doi.org/10.1002/mrc.1260301210
https://doi.org/10.1002/mrc.1260301210
Publikováno v:
British Journal of Psychiatry. 160:56-60
Tianeptine is a tricyclic antidepressant with an unusual chemical structure (a long lateral chain grafted on to a substituted dibenzothiazepin nucleus), and with biochemical and animal-behavioural properties which are strikingly different from those
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::433dd73a243fddb790efedd2ef2c08d4
https://doi.org/10.1192/s0007125000296694
https://doi.org/10.1192/s0007125000296694
Publikováno v:
Psychopharmacology. 104:328-336
Unlike other antidepressant drugs, tianeptine, when administered to cats at doses ranging from 1.2 to 5 mg/kg, produces an increase in arousal associated with longer sequences of immobile attentiveness. The present study analyses tianeptine-induced e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e2d801351e57b1cfc857dc218c5d9ca
https://doi.org/10.1007/bf02246032
https://doi.org/10.1007/bf02246032
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 116
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a81695a0ed7bceadcc441d2948a50ae
https://doi.org/10.1055/s-0028-1096337
https://doi.org/10.1055/s-0028-1096337
Autor:
J. Matias, Antonio Portolés, N. Prieto, G. Paniagua, E. Mocaër, C. Gabriel, DG Parra, S. Naval, Ana Terleira, S. Alonso, Angel L. Montejo
Publikováno v:
Journal of psychopharmacology (Oxford, England). 24(1)
Sexual dysfunction (SD) is a common and underestimated effect of antidepressants. Healthy volunteers are the most adequate group to study this adverse event avoiding influence of depression itself. Sexual acceptability of agomelatine (a melatonergic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2b8d143d9b50f82a190dc6c544d6afb
https://pubmed.ncbi.nlm.nih.gov/18801825
https://pubmed.ncbi.nlm.nih.gov/18801825