Amisulpride is approved for clinical use in treating schizophrenia in a number of European countries and also for treating dysthymia, a mild form of depression, in Italy. Amisulpride has also been demonstrated to be an antidepressant for patients with major depression in many clinical trials. In part because of the selective D2/D3 receptor antagonist properties of amisulpride, it has long been widely assumed that dopaminergic modulation is the proximal event responsible for mediating its antidepressant and antipsychotic properties
Amisulpride is a substituted benzamide antipsychotic with nanomolar affinity and high selectivity fo...
Atypical antipsychotic drugs are classically associated with lower propensity to extrapyramidal symp...
Background: Reduced mismatch negativity and P3a amplitude have been suggested to be among the core d...
Amisulpride is approved for clinical use in treating schizophrenia in a number of European countries...
The benzamide derivative amisulpride shows a unique thera-peutic profile being antipsychotic, at hig...
A wide body of evidence suggests that 5-HT7 receptors are implicated in a variety of central nervous...
The class of substituted benzamides includes compounds able to modulate dopaminergic neurons selecti...
Amisulpride (AMS) in low dosage has been used effectively for treatment of dysthymia. Yet there is a...
One of the most stimulating problems posed by second generation antipsychotics is the question of wh...
F17464 (N-(3-{4-[4-(8-Oxo-8H-[1,3]-dioxolo-[4,5-g]-chromen-7-yl)-butyl]-piperazin-1-yl}-phenyl)-meth...
Abstract Antinociceptive effects of various neuroleptics in animal acute pain-models have been descr...
Dopamine is implicated in the pathogenesis of both the positive and the negative symptoms of schizop...
Objective: Amisulpride is a novel atypical antipsychotic withpreferential affinity for presynaptic d...
See Caravaggio and Graff-Guerrero (doi:10.1093/awx023) for a scientific commentary on this article.A...
All FDA-approved antipsychotic drugs (APDs) target primarily dopamine D2 or serotonin (5-HT2A) recep...
Amisulpride is a substituted benzamide antipsychotic with nanomolar affinity and high selectivity fo...
Atypical antipsychotic drugs are classically associated with lower propensity to extrapyramidal symp...
Background: Reduced mismatch negativity and P3a amplitude have been suggested to be among the core d...
Amisulpride is approved for clinical use in treating schizophrenia in a number of European countries...
The benzamide derivative amisulpride shows a unique thera-peutic profile being antipsychotic, at hig...
A wide body of evidence suggests that 5-HT7 receptors are implicated in a variety of central nervous...
The class of substituted benzamides includes compounds able to modulate dopaminergic neurons selecti...
Amisulpride (AMS) in low dosage has been used effectively for treatment of dysthymia. Yet there is a...
One of the most stimulating problems posed by second generation antipsychotics is the question of wh...
F17464 (N-(3-{4-[4-(8-Oxo-8H-[1,3]-dioxolo-[4,5-g]-chromen-7-yl)-butyl]-piperazin-1-yl}-phenyl)-meth...
Abstract Antinociceptive effects of various neuroleptics in animal acute pain-models have been descr...
Dopamine is implicated in the pathogenesis of both the positive and the negative symptoms of schizop...
Objective: Amisulpride is a novel atypical antipsychotic withpreferential affinity for presynaptic d...
See Caravaggio and Graff-Guerrero (doi:10.1093/awx023) for a scientific commentary on this article.A...
All FDA-approved antipsychotic drugs (APDs) target primarily dopamine D2 or serotonin (5-HT2A) recep...
Amisulpride is a substituted benzamide antipsychotic with nanomolar affinity and high selectivity fo...
Atypical antipsychotic drugs are classically associated with lower propensity to extrapyramidal symp...
Background: Reduced mismatch negativity and P3a amplitude have been suggested to be among the core d...