Search Results - "Carfagna, Nicola"

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  1. 1

    Reboxetine: a pharmacologically potent, selective, and specific norepinephrine reuptake inhibitor by Wong, Erik H.F., Sonders, Mark S., Amara, Susan G., Tinholt, Paula M., Piercey, Montford F.P., Hoffmann, William P., Hyslop, Deborah K., Franklin, Stanley, Porsolt, Roger D., Bonsignori, Alberto, Carfagna, Nicola, McArthur, Robert A.

    Published in Biological psychiatry (1969) (01-05-2000)
    “…Background: Reboxetine is a potent antidepressant, with efficacy comparable to that of imipramine, desipramine, and fluoxetine, and has improved side-effect…”
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  2. 2

    Neuroprotective effects of nicergoline in immortalized neurons by Sortino, Maria Angela, Battaglia, Angelo, Pamparana, Franco, Carfagna, Nicola, Post, Claes, Canonico, Pier Luigi

    Published in European journal of pharmacology (05-03-1999)
    “…We studied the potential neuroprotective action of nicergoline in immortalized hypothalamic GT1-7 cells exposed to agents which deplete levels of reduced…”
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  3. 3

    Modulation of hippocampal ACh release by chronic nicergoline treatment in freely moving young and aged rats by Carfagna, Nicola, Di Clemente, Angelo, Cavanus, Stefano, Damiani, Domenico, Gerna, Marco, Salmoiraghi, Patrizia, Cattaneo, Barbara, Post, Claes

    Published in Neuroscience letters (15-09-1995)
    “…The effects of nicergoline on basal and K +-stimulated release of ACh in the hippocampus of 3- and 19-month old rats has been studied by microdialysis. A…”
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  4. 4

    Antioxidant properties of MDL and MMDL, two nicergoline metabolites, during chronic administration of haloperidol by Vairetti, Mariapia, Battaglia, Angelo, Carfagna, Nicola, Luigi Canonico, Pier, Bertè, Francantonio, Richelmi, Plinio

    Published in European journal of pharmacology (18-10-2002)
    “…We evaluated the effects of 10-alpha-methoxy-9,10-dihydrolysergol (MDL) and 1-methyl-10-alpha-methoxy-9,10-dihydrolysergol (MMDL), two nicergoline metabolites,…”
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  5. 5

    Nicergoline in dementia: A review of its pharmacological properties and therapeutic potential by WINBLAD, Bengt, CARFAGNA, Nicola, BONURA, Luisa, ROSSINI, Bianca M, WONG, Eric H. F, BATTAGLIA, Angelo

    Published in CNS drugs (01-10-2000)
    “…Nicergoline is a semisynthetic ergoline derivative indicated for the treatment of cognitive impairment in various forms of dementia. It is currently available…”
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  6. 6

    Modulation of phosphoinositide turnover by chronic nicergoline in rat brain by Carfagna, Nicola, Cavanus, Stefano, Damiani, Domenico, Salmoiraghi, Patrizia, Fariello, Ruggero, Post, Claes

    Published in Neuroscience letters (17-05-1996)
    “…Basal and agonist-stimulated phosphoinositide (PI) turnover and inositol 1,4,5 -trisphospate (InsP 3) content in rat brain were investigated after chronic…”
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  7. 7

    Effects of Nicergoline on Age-Related Decrements in Radial Maze Performance and Acetylcholine Levels by McArthur, Robert A., Carfagna, Nicola, Banfi, Laura, Cavanus, Stefano, Cervini, Maria Antonietta, Fariello, Ruggero, Post, Claes

    Published in Brain research bulletin (1997)
    “…The effects of chronic oral administration of nicergoline (5.0 mg/kg; bid) on locomotor activity, eight-arm radial maze performance plus striatal, cortical,…”
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  8. 8

    (E) and (Z)-3-Styrylpiperidines as sigma ligands by Mantegani, Sergio, Brambilla, Enzo, Cremonesi, Paolo, Caccia, Carla, Fornaretto, Maria Gioia, Carfagna, Nicola, Colombo, Monica, McArthur, Robert A., Varasi, Mario

    Published in Bioorganic & medicinal chemistry letters (17-06-1997)
    “…A class of (E) and (Z)-3-styrylpiperidine derivatives was prepared as racemates and evaluated for affinity at σ binding sites labeled with […”
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  9. 9

    Preparation of 7-oxaaporphine derivatives and evaluation of their dopaminergic activity by Banzatti, Carlo, Carfagna, Nicola, Commisso, Roberto, Heidempergher, Franco, Pegrassi, Lorenzo, Melloni, Piero

    Published in Journal of medicinal chemistry (01-07-1988)
    “…A series of 7-oxaaporphine derivatives was prepared. The compounds were evaluated as dopaminergic agents. None of them showed either affinity for dopamine…”
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