Kulkarni · Psychopharmacology 2008 · Controlled animal laboratory experiment · n=?

Antidepressant activity of curcumin: involvement of serotonin and dopamine system.

Cited 344 times in the scientific literature.

Level 5 - mechanism / opinion, no new human data

Preclinical animal and laboratory study in mice

PubMed 18766332 · doi:10.1007/s00213-008-1300-y · record verified 2026-08-28

What was done

Researchers evaluated the antidepressant-like mechanisms of curcumin (10–80 mg/kg, i.p.) in mice, tested alone, combined with subthreshold doses of standard antidepressants (fluoxetine, venlafaxine, bupropion, imipramine, and desipramine), and coadministered with the bioavailability enhancer piperine (2.5 mg/kg, i.p.). Assessments included behavioral testing via the forced swim test, monoamine oxidase (MAO-A and MAO-B) enzyme inhibition, and measurement of brain neurotransmitter levels (serotonin, dopamine, and norepinephrine).

What was found

The abstract reports directional findings without exact numerical values. Curcumin dose-dependently decreased immobility time in the forced swim test, increased serotonin levels, elevated dopamine levels at higher doses, and inhibited both MAO-A and MAO-B at higher doses. Curcumin (20 mg/kg) enhanced the anti-immobility effects and synergistically increased serotonin levels when combined with subthreshold fluoxetine, venlafaxine, or bupropion, but produced no significant change with imipramine or desipramine. Norepinephrine levels did not change. Piperine (2.5 mg/kg) potentiated the pharmacological, biochemical, and neurochemical effects of curcumin (20 and 40 mg/kg).

Why it matters

This study outlines specific monoaminergic and enzymatic mechanisms underlying curcumin's antidepressant-like properties in rodents, demonstrating potential synergy with certain conventional antidepressants and piperine.

Limits

The study is restricted to an acute rodent behavioral model (forced swim test), which does not fully model human clinical depression or chronic treatment responses. Dosing was administered via intraperitoneal injection rather than oral intake, and the abstract omits sample sizes (n), numerical metrics, and statistical confidence intervals.

Cited by