Drug intelligence / Profile preview

desipramine + lithium

Development stage
Unknown
Modality
Small Molecules
Administration
Oral
01

Overview

Desipramine + lithium is a combination of two pharmaceutical agents used primarily in the management of major depressive disorder, particularly in cases resistant to standard antidepressant therapy. Desipramine is a tricyclic antidepressant (TCA) that acts mainly as a potent inhibitor of norepinephrine reuptake and, to a lesser extent, serotonin reuptake. Lithium is an elemental mood stabilizer commonly used in bipolar disorder and as an augmenting agent for treatment-resistant depression. The combination has been shown to induce greater antidepressant effects than either drug alone, both in preclinical models and clinical studies. Mechanistically, chronic co-administration may enhance hippocampal cell proliferation and neuroplasticity beyond what is observed with monotherapy[1][2][6]. This regimen is typically considered when patients do not respond adequately to tricyclic antidepressants alone.

02

Targets

ADRB1 (β1)HRH1 (Histamine H1 Receptor)NMDAR (Glutamate receptor ionotropic, NMDA)mAChR (Muscarinic acetylcholine receptors)NCX1 (Sodium/calcium exchanger 1)GSK3 (Glycogen synthase kinase 3 beta)IMPA1 (Inositol Monophosphatase)ADRA1A (α1A)SERT (Sodium-dependent serotonin transporter)HTR2A (Serotonin receptor 5-HT2A)NET (Norepinephrine Transporter)

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