Literature DB >> 3045107

Clinical effects of serotonin reuptake inhibitors in the treatment of depressive illness.

G D Burrows1, I M McIntyre, F K Judd, T R Norman.   

Abstract

The serotonergic hypothesis of depression has stimulated the development of a range of chemically diverse compounds that have an exclusive effect on this neurotransmitter for potential use as antidepressant drugs. The group of serotonin reuptake inhibitors are at various stages of clinical development. The authors review the efficacy, side effect profiles, and toxicity of zimelidine, fluvoxamine, and citalopram in detail and ifoxetine, fluoxetine, indalpine, paroxetine, and sertraline in brief. Evidence suggests that, compared with tricyclic antidepressants, these drugs may cause fewer anticholinergic effects and lower cardiotoxicity in the treatment of major depressive disorders. These advantages need to be weighed against an emerging pattern of gastrointestinal complaints, insomnia, and akathisia. The place of serotonin reuptake inhibitors in therapy can be fully evaluated only after further studies, particularly those involving long-term use. The adverse experience associated with zimelidine suggests that caution and vigilance should be exercised in future studies of agents in this class. These drugs will undoubtedly provide important insights into depressive illness and some anxiety disorders and may fulfill their initial promise.

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Year:  1988        PMID: 3045107

Source DB:  PubMed          Journal:  J Clin Psychiatry        ISSN: 0160-6689            Impact factor:   4.384


  5 in total

Review 1.  Sertraline. A pharmacoeconomic evaluation of its use in depression.

Authors:  R Davis; M I Wilde
Journal:  Pharmacoeconomics       Date:  1996-10       Impact factor: 4.981

2.  Terbinafine increases the plasma concentration of paroxetine after a single oral administration of paroxetine in healthy subjects.

Authors:  Norio Yasui-Furukori; Manabu Saito; Yoshimasa Inoue; Takenori Niioka; Yasushi Sato; Shoko Tsuchimine; Sunao Kaneko
Journal:  Eur J Clin Pharmacol       Date:  2006-11-24       Impact factor: 2.953

3.  Effect of sertraline treatment on benzodiazepine receptors in the rat brain.

Authors:  L Giardino; M Zanni; A Velardo; G Amato; L Calzà
Journal:  J Neural Transm Gen Sect       Date:  1993

4.  The influence of 5-HTTLPR genotype on the association between the plasma concentration and therapeutic effect of paroxetine in patients with major depressive disorder.

Authors:  Tetsu Tomita; Norio Yasui-Furukori; Taku Nakagami; Shoko Tsuchimine; Masamichi Ishioka; Ayako Kaneda; Norio Sugawara; Sunao Kaneko
Journal:  PLoS One       Date:  2014-05-23       Impact factor: 3.240

5.  Sex differences in the prediction of the effectiveness of paroxetine for patients with major depressive disorder identified using a receiver operating characteristic curve analysis for early response.

Authors:  Tetsu Tomita; Norio Yasui-Furukori; Yasui-Furukori Norio; Yasushi Sato; Taku Nakagami; Shoko Tsuchimine; Ayako Kaneda; Sunao Kaneko
Journal:  Neuropsychiatr Dis Treat       Date:  2014-04-08       Impact factor: 2.570

  5 in total

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