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Review
. 2022 Sep;239(9):2735-2752.
doi: 10.1007/s00213-022-06203-8. Epub 2022 Aug 10.

Psychopharmacological properties and therapeutic profile of the antidepressant venlafaxine

Affiliations
Review

Psychopharmacological properties and therapeutic profile of the antidepressant venlafaxine

Basile Coutens et al. Psychopharmacology (Berl). 2022 Sep.

Abstract

Major depression (MD) is one of the most common psychiatric disorders worldwide. Currently, the first-line treatment for MD targets the serotonin system but these drugs, notably the selective serotonin reuptake inhibitors, usually need 4 to 6 weeks before the benefit is felt and a significant proportion of patients shows an unsatisfactory response. Numerous treatments have been developed to circumvent these issues as venlafaxine, a mixed serotonin-norepinephrine reuptake inhibitor that binds and blocks both the SERT and NET transporters. Despite this pharmacological profile, it is difficult to have a valuable insight into its ability to produce more robust efficacy than single-acting agents. In this review, we provide an in-depth characterization of the pharmacological properties of venlafaxine from in vitro data to preclinical and clinical efficacy in depressed patients and animal models of depression to propose an indirect comparison with the most common antidepressants. Preclinical studies show that the antidepressant effect of venlafaxine is often associated with an enhancement of serotonergic neurotransmission at low doses. High doses of venlafaxine, which elicit a concomitant increase in 5-HT and NE tone, is associated with changes in different forms of plasticity in discrete brain areas. In particular, the hippocampus appears to play a crucial role in venlafaxine-mediated antidepressant effects notably by regulating processes such as adult hippocampal neurogenesis or the excitatory/inhibitory balance. Overall, depending on the dose used, venlafaxine shows a high efficacy on depressive-like symptoms in relevant animal models but to the same extent as common antidepressants. However, these data are counterbalanced by a lower tolerance. In conclusion, venlafaxine appears to be one of the most effective treatments for treatment of major depression. Still, direct comparative studies are warranted to provide definitive conclusions about its superiority.

Keywords: 5-HT; Antidepressants; Major depression disorder; NE; Venlafaxine.

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References

    1. Abdel-Wahab BA, Salama RH (2011) Venlafaxine protects against stress-induced oxidative DNA damage in hippocampus during antidepressant testing in mice. Pharmacol Biochem Behav 100:59–65 - PubMed - DOI
    1. Adrien J (2002) Neurobiological bases for the relation between sleep and depression. Sleep Med Rev 6:341–351 - PubMed - DOI
    1. Alaiyed S, Bozzelli PL, Caccavano A, Wu JY, Conant K (2019) Venlafaxine stimulates PNN proteolysis and MMP-9-dependent enhancement of gamma power; relevance to antidepressant efficacy. J Neurochem 148:810–821 - PubMed - PMC - DOI
    1. Alaiyed S, McCann M, Mahajan G, Rajkowska G, Stockmeier CA, Kellar KJ et al (2020) Venlafaxine stimulates an MMP-9-dependent increase in excitatory/inhibitory balance in a stress model of depression. J Neurosci 40:4418–4431 - PubMed - PMC - DOI
    1. Albiñana Pérez MS, Cea Pereira L, Bilbao Salcedo J, Rodríguez PI (2012) Possible serotonin syndrome associated with administration of venlafaxine and tramadol. Farm Hosp 36:548 - PubMed

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