Literature DB >> 12685917

Dopaminergic deficit and the role of amisulpride in the treatment of mood disorders.

Stuart A Montgomery1.   

Abstract

Amisulpride has now been investigated extensively in placebo controlled and in comparator controlled studies in patients suffering from dysthymia, both pure dysthymia and dysthymia with major depression. The clinical trial programme, which has shown the significant efficacy of amisulpride compared with placebo in three placebo controlled studies, has provided useful evidence of the value of a dopaminergic compound in the treatment of mood disorders. Amisulpride was superior to sertraline, an established treatment for depression and for dysthymia, on some measures and had a faster onset of effect. Retrospective analysis of the individual scale items showed that amisulpride had a broad range of effect on depressive symptoms with possible superiority on certain symptoms thought to be related to dopaminergic mechanisms. The body of studies supports the view that amisulpride is an effective and well-tolerated treatment for dysthymia and dysthymia with major depression.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12685917

Source DB:  PubMed          Journal:  Int Clin Psychopharmacol        ISSN: 0268-1315            Impact factor:   1.659


  15 in total

1.  Effects of amisulpride on human resting cerebral perfusion.

Authors:  Roberto Viviani; Heiko Graf; Maike Wiegers; Birgit Abler
Journal:  Psychopharmacology (Berl)       Date:  2013-04-13       Impact factor: 4.530

2.  Pharmacological blockade of 5-HT7 receptors as a putative fast acting antidepressant strategy.

Authors:  Ouissame Mnie-Filali; Céline Faure; Laura Lambás-Señas; Mostafa El Mansari; Hassina Belblidia; Elise Gondard; Adeline Etiévant; Hélène Scarna; Anne Didier; Anne Berod; Pierre Blier; Nasser Haddjeri
Journal:  Neuropsychopharmacology       Date:  2011-02-16       Impact factor: 7.853

3.  The 5-HT(7) receptor as a mediator and modulator of antidepressant-like behavior.

Authors:  Gor Sarkisyan; Amanda J Roberts; Peter B Hedlund
Journal:  Behav Brain Res       Date:  2010-01-25       Impact factor: 3.332

4.  Antipsychotics possessing antidepressive efficacy increase Golf protein in rat striatum.

Authors:  Hideki Taoka; Takashi Hamamura; Shiro Endo; Shinji Miyata; Kishio Toma; Takeshi Ishihara; Shigetoshi Kuroda
Journal:  Psychopharmacology (Berl)       Date:  2008-09-06       Impact factor: 4.530

5.  Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings.

Authors:  Gabriel S Dichter; Cara A Damiano; John A Allen
Journal:  J Neurodev Disord       Date:  2012-07-06       Impact factor: 4.025

6.  Amisulpride is a potent 5-HT7 antagonist: relevance for antidepressant actions in vivo.

Authors:  Atheir I Abbas; Peter B Hedlund; Xi-Ping Huang; Thuy B Tran; Herbert Y Meltzer; Bryan L Roth
Journal:  Psychopharmacology (Berl)       Date:  2009-04-01       Impact factor: 4.530

7.  Efficacy of quetiapine in patients with bipolar I and II depression: a multicenter, prospective, open-label, observational study.

Authors:  Jong-Hyun Jeong; Won-Myong Bahk; Young Sup Woo; Ho-Jun Seo; Seung-Chul Hong; Duk-In Jon; Kyung Joon Min; Bo-Hyun Yoon
Journal:  Neuropsychiatr Dis Treat       Date:  2013-02-08       Impact factor: 2.570

8.  Erotic stimulus processing under amisulpride and reboxetine: a placebo-controlled fMRI study in healthy subjects.

Authors:  Heiko Graf; Maike Wiegers; Coraline D Metzger; Martin Walter; Georg Grön; Birgit Abler
Journal:  Int J Neuropsychopharmacol       Date:  2014-10-31       Impact factor: 5.176

9.  Update on the management of symptoms in schizophrenia: focus on amisulpride.

Authors:  Ann M Mortimer
Journal:  Neuropsychiatr Dis Treat       Date:  2009-05-20       Impact factor: 2.570

10.  Amisulpride plus valproate vs haloperidol plus valproate in the treatment of acute mania of bipolar I patients: a multicenter, open-label, randomized, comparative trial.

Authors:  Pierre Thomas; Eduard Vieta
Journal:  Neuropsychiatr Dis Treat       Date:  2008-06       Impact factor: 2.570

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.