Serotonin selective reuptake inhibitors (SSRIs) have generally proven to be as effective as tricyclicantidepressants (TCAs) in the treatment of major depression and have an improved side effect profile.However, data suggest that the SSRIs are not as effective as the TCAs in certain subsets of depressedpatients, indicating the importance of norepinephrine reuptake inhibition for such patients. Evidencefor the role of norepinephrine in depression comes from early studies on excretion of catecholaminesand more recent studies on receptor function, second messenger systems, and gene modification.These data are reviewed in this article. Data from a multicenter, randomized, controlled clinical trialcomparing desipramine, a relatively norepinephrine-selective TCA, and the SSRI fluoxetine in moderateto marked major depression suggest a differential response depending on the antidepressant. The2 drugs were overall similar in efficacy; however, in severely ill patients, there was a suggestion thatdesipramine was more likely to induce remission than fluoxetine. Urinary metabolite 3-methoxy-4-hydroxyphenylglycol levels were a better predictor of likelihood of remission than severity of episodeor drug treatment. Desipramine and fluoxetine produced different longitudinal effects in catecholamineexcretion, indicating that the 2 agents act through different mechanisms. Given the good therapeuticprofile but relative risks associated with TCA therapy, selective norepinephrine reuptake inhibitors,such as reboxetine, which has a good safety profile, could be a major step forward in thetreatment of depression.
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