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ARA 290

Cibinetide, PHBSP, PH-BSP, Helix B surface peptide

Quick Stats
Studies 51
Trials 5
Score 2
2015 pubmed 10 citations

Testing the antidepressant properties of the peptide ARA290 in a human neuropsychological model of drug action.

Cerit. Hilâl H; Veer. Ilya M IM; Dahan. Albert A; Niesters. Marieke M; Harmer. Catherine J CJ; Miskowiak. Kamilla W KW; Rombouts. Serge A R B SA; Van der Does. Willem W

Key Findings

  • ARA290 reduced brain activity to happy faces in the fusiform gyrus.
  • Participants were slightly less accurate at recognizing happy and disgusted faces and were faster at categorizing positive versus negative words.
  • No changes were seen in overall mood or affective symptoms after the dose.

Practical Outcomes

  • For biohackers looking for a mood‑enhancing or antidepressant effect, ARA290 does not appear promising based on this small study. The single 2 mg dose showed only minor shifts in emotional processing and no real mood benefit, so it’s not recommended for routine use in this context.

Summary

A single 2 mg dose of the peptide ARA290 was tested in healthy volunteers to see if it acts like an antidepressant. A week later, participants showed subtle changes in how they processed happy and negative emotions, but there were no mood improvements. Overall, the results don’t strongly support ARA290 as a mood‑boosting supplement.

Abstract

Studies on the neural effects of Erythropoietin (EPO) indicate that EPO may have antidepressant effects. Due to its hematopoietic effects, EPO may cause serious side-effects with repeated administration if patients are not monitored extensively. ARA290 is an EPO-analog peptide without such hematopoietic side-effects but may have neurotrophic and antidepressant effects. The aim of this study was to investigate the possible antidepressant effects of ARA290 in a neuropsychological model of drug action. Healthy participants (N=36) received ARA290 (2mg) or placebo in a double-blind, randomized, parallel-group design. Neural and cognitive effects were assessed one week after administration. Primary outcome measures were the neural processing of fearful vs happy faces and the behavioral recognition of emotional facial expressions. ARA290-treated individuals displayed lower neural responses to happy faces in the fusiform gyrus. ARA290 tended to lower the recognition of happy and disgust facial expressions. Although ARA290 was not associated with a better memory for positive words, it was associated with faster categorization of positive vs negative words. Finally, ARA290 increased attention towards positive emotional pictures. No effects were observed on mood and affective symptoms. ARA290 may modulate some aspects of emotional processing, however, the direction and the strength of its effects do not unequivocally support an antidepressant-like profile for ARA290. Future studies may investigate the effects of different timing and dose.

Study Information

Provider

pubmed

Year

2015

Date

2015-09-18T00:00:00.000Z

DOI

10.1016/j.euroneuro.2015.09.005

Citations

10

References

55