Clinical evidence for serotonin and norepinephrine reuptake inhibition of duloxetine

Madhukar H. Trivedi, Durisala Desaiah, Melissa J. Ossanna, Yili L. Pritchett, Stephen K. Brannan, Michael J. Detke

Research output: Contribution to journalReview article

43 Scopus citations

Abstract

Most antidepressants in clinical use are believed to function by enhancing neurotransmission of serotonin [5-hydroxytryptamine (5-HT)] and/or norepinephrine (NE) via inhibition of neurotransmitter reuptake. Agents that affect reuptake of both 5-HT and NE (serotonin-norepinephrine reuptake inhibitors) have been postulated to offer greater efficacy for the treatment of major depressive disorder (MDD). These dual-acting agents also display a broader spectrum of action, including efficacy for MDD and associated painful physical symptoms, diabetic peripheral neuropathic pain, generalized anxiety disorder, and fibromyalgia syndrome. Substantial preclinical evidence shows that duloxetine, an approved drug for the treatment of MDD, generalized anxiety disorder, and the management of diabetic peripheral neuropathic pain, inhibits reuptake of both 5-HT and NE. This paper reviews clinical and neurochemical evidence of duloxetine's effects on 5-HT and NE reuptake inhibition. The clinical evidence supporting duloxetine's effects on NE reuptake inhibition includes indirect measures such as altered excretion of NE metabolites, cardiovascular effects, and treatment-emergent adverse event profiles similar to those for other drugs believed to act through the inhibition of NE reuptake. In summary, the data presented in this report provide clinical evidence of a mechanism for duloxetine involving both 5-HT and NE reuptake inhibition in humans and are consistent with preclinical evidence for 5-HT/NE reuptake inhibition.

Original languageEnglish (US)
Pages (from-to)161-169
Number of pages9
JournalInternational Clinical Psychopharmacology
Volume23
Issue number3
DOIs
StatePublished - May 1 2008

Keywords

  • Dual reuptake inhibition
  • Duloxetine
  • Major depressive disorder
  • Norepinephrine
  • Pain
  • Serotonin

ASJC Scopus subject areas

  • Psychiatry and Mental health
  • Pharmacology (medical)

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