Drug intelligence / Profile preview

escitalopram + pindolol

Development stage
Preclinical
Lead developer
Lundbeck
Modality
Small Molecules
Administration
Oral
01

Overview

Escitalopram + pindolol is a combination of two pharmaceutical agents used experimentally to enhance and accelerate antidepressant response in major depressive disorder. Escitalopram is a selective serotonin re-uptake inhibitor (SSRI) that increases serotonergic neurotransmission by inhibiting the serotonin transporter (SERT), both at the orthosteric and allosteric sites, leading to increased synaptic serotonin levels[1]. Pindolol is a non-selective beta-adrenoceptor antagonist (beta blocker) with partial agonist activity at beta-1 and beta-2 adrenergic receptors as well as antagonistic activity at 5-hydroxytryptamine receptor 1A (5-HT1A)[2][6]. When combined with SSRIs like escitalopram, pindolol may block presynaptic 5-HT1A autoreceptors in the raphe nuclei. This action prevents SSRI-induced inhibition of serotonergic neuron firing early in treatment and can accelerate or potentiate antidepressant effects[6][8]. The combination has been studied for its potential to produce faster onset of antidepressant action compared to SSRI monotherapy.

Brand names
CipralexViskazide
02

Targets

SERT allosteric site (Serotonin transporter allosteric site)ADRB2 (β2)ADRB1 (β1)HTR1A (Serotonin receptor 1A (5-hydroxytryptamine receptor 1A))

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