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semax nootropic preclinical animal n preclinical 2026-04-03 PubMed

Semax Effectively Reduces Stress-Induced Anxiety and Depression in Rats

[Influence of Semax on the emotional state of white rats in the norm and against the background of cholecystokinin-tetrapeptide action].

Background

Anxiety and depression are widespread mental health disorders with significant impact on quality of life. Current treatments often have side effects or limited efficacy, highlighting the need for novel therapeutic approaches. This study investigated whether Semax, an analog of adrenocorticotropic hormone (ACTH(4-10)), could modulate emotional states, particularly in response to chemically induced stress, to explore its potential as an anxiolytic and antidepressant.

Results

In normal, unstressed rats, Semax administration alone did not significantly influence the animals' emotional state. However, the CCK-4 injection successfully led to a clear increase in both anxiety and depression in the control rat group. Semax administration at both 0.05 mg/kg and 0.5 mg/kg intranasally effectively normalized the animal behavior disturbed by CCK-4, demonstrating significant anxiolytic and antidepressant effects. Specifically, treated rats showed a reversal of the CCK-4-induced anxious and depressive behaviors, performing similarly to normal, unstressed animals in the elevated plus-maze and forced swimming tests. This indicates a robust counteraction of the stress-induced emotional disturbances by Semax across the tested doses.

Why It Matters

This study provides strong preclinical evidence for Semax's potential as a therapeutic agent for stress-induced anxiety and depression. Given that Semax is a well-studied peptide already used clinically in some countries for cognitive enhancement, its established safety profile could significantly accelerate its development for these new psychiatric indications. These findings suggest Semax could be a valuable and rapidly translatable new treatment option for patients suffering from elevated anxiety and depression. Future research should focus on elucidating the precise neurobiological mechanisms underlying these effects and conducting further preclinical and eventually human clinical trials (e.g., Phase I/II) to confirm efficacy and safety in human populations.


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Source: pubmed:20387390 · Ingested 2026-04-03 · Digest: gemini-2.5-flash