Selank: Safety Profile & Research Summary
Preclinical Research Summary
Animal Studies
| Model | Species | Key Findings | Ref |
|---|---|---|---|
| Anxiety (UCMS) | Wistar rats | Selank+Diazepam → OA time 8.9× higher than saline; prevented stress deterioration | [19] |
| Anxiety Phenotypes | BALB/c vs C57BL/6 mice | Selective anxiolytic in high-anxiety BALB/c; strain-dependent monoamine modulation | [13] |
| Primate Neurosis | Monkeys | Eliminated fear and aggression; increased exploratory activity, long-lasting effect | [2] |
| Alcohol Withdrawal | Outbred rats | ↑ EPM open arms (p<0.01); restored mechanical sensitivity; did NOT affect alcohol intake | [16] |
| Morphine Withdrawal | Outbred rats | ↓ withdrawal index 39.6%; ↑ tactile sensitivity 9×; attenuated convulsions (p<0.0001) | [17] |
| Memory Trace | Wistar rats | 30-day memory stability via serotonin metabolism activation | [13] |
| GABAergic Genes | Wistar rats | 45 genes altered at 1h; Gabre ↓20×, Hcrt ↑128× at 3h (explains no sedation) | [9] |
| BDNF Expression | Rats | ↑ Bdnf mRNA at 3h; ↑ BDNF protein at 24h | [12] |
| Gut Microbiota | Wistar rats | Prevented stress-induced microflora changes; ↓ corticosterone | [18] |
| Influenza (H3N2) | Mice | ↑ survival; IFN-α induction; Th1/Th2 normalization | [14] |
Clinical Studies / Human Data
| Study | Design | n= | Key Outcome | Ref |
|---|---|---|---|---|
| Zozulya 2008 (Phase II) | RCT vs medazepam | 62 | Comparable anxiolytic efficacy to medazepam; + anti-asthenic/psychostimulant effects; onset 1-3 days | [5] |
| Medvedev 2015 (Add-on) | Add-on to Phenazepam | 70 | Earlier onset of benzo effects; decreased attention/memory impairment from Phenazepam | [20] |
| Medvedev 2014 (Comparison) | vs Phenazepam | 60 | Pronounced anxiolytic + mild nootropic; effects persist 1 week post-dose | [21] |
| Elderly Vascular Study | Clinical | — | Reduced anxiety, improved concentration, increased reaction speed in elderly | [3] |
| Uchakina 2008 (Immune) | Immunological | — | Completely suppressed IL-6 gene expression in anxious subjects; normalized Th1/Th2 balance | [14] |
Pharmacokinetic Parameters
| Parameter | Value | Ref |
|---|---|---|
| Intranasal Bioavailability | 92.8% (exceptional for a peptide) | [7] |
| Plasma Half-life | ~2 minutes | [7] |
| Duration of Experimental Effects | 20–24 hours (trigger mechanism) | [7] |
| CNS Penetration | Detected in brain within 2 minutes (intranasal) | [7] |
| GABA-A Modulation | Positive allosteric modulator (non-BZD site) | [8] |
| Enkephalinase IC₅₀ | 15–20 μM (human serum) | [10] |
Comparison: Selank vs. Benzodiazepines
| Feature | Selank | Benzodiazepines |
|---|---|---|
| Anxiolytic Effect | Comparable (Phase II) | Established |
| Sedation | None | Common |
| Muscle Relaxation | None | Common |
| Cognitive Impairment | None (nootropic effect) | Amnesia risk |
| Dependence | None observed | High risk |
| Withdrawal | None observed | Significant risk |
| Mechanism | GABA-A PAM + enkephalinase | GABA-A BZD site |
| Additional Effects | Nootropic + immunomodulatory | None |
Comparison: Selank vs. Semax
| Feature | Selank | Semax |
|---|---|---|
| Parent Molecule | Tuftsin (IgG fragment) | ACTH(4-7) |
| Sequence | TKPRPGP (7 aa) | MEHFPGP (7 aa) |
| Primary Focus | Anxiolytic / immunomodulation | Nootropic / neuroprotection |
| Unique Mechanism | GABA-A PAM + enkephalinase | MC4/MC5 antagonist + BDNF/TrkB |
| PGP Stabilizer | Yes | Yes |
| Developer | IMG RAS + Zakusov Institute | IMG RAS |
The products offered on this website are furnished for in-vitro studies only. In-vitro studies (Latin: in glass) are performed outside of the body. These products are not medicines or drugs and have not been approved by the FDA to prevent, treat or cure any medical condition, ailment or disease. Bodily introduction of any kind into humans or animals is strictly forbidden by law.
For Laboratory Research Only. Not for human use, medical use, diagnostic use, or veterinary use.
ALL ARTICLES AND PRODUCT INFORMATION PROVIDED ON THIS WEBSITE ARE FOR INFORMATIONAL AND EDUCATIONAL PURPOSES ONLY.
References
- Kolomin TA, Shadrina M, Slominsky P, Limborska SA, Myasoedov NF. A New Generation of Drugs: Synthetic Peptides Based on Natural Regulatory Peptides. Neuroscience & Medicine. 2013;4(4):223–252.
- Vyunova TV, Andreeva LA, Shevchenko KV, Myasoedov NF. Peptide-based Anxiolytics: The Molecular Aspects of Heptapeptide Selank Biological Activity. Protein & Peptide Letters. 2018;25(10):914–923.
- Medvedev VE, Tereshchenko ON, Kost NV, et al. Optimization of the treatment of anxiety disorders with selank. Zhurnal Nevrologii i Psikhiatrii. 2015;115(6):33–40.
- U.S. Food and Drug Administration. Bulk Drug Substances Used in Compounding Under Section 503B. FDA Compounding Database. 2023.
- Zozulya AA, Neznamov GG, Syunyakov TS, et al. Efficacy and possible mechanisms of action of a new peptide anxiolytic selank in the therapy of generalized anxiety disorders and neurasthenia. Zhurnal Nevropatologii i Psikhiatrii. 2008;108(4):38–48.
- Kozlovskii II, Danchev ND. The optimizing action of the synthetic peptide Selank on a conditioned active avoidance reflex in rats. Neuroscience and Behavioral Physiology. 2003;33(7):639–643.
- Kolomin TA, Agapova T, Agniullin YV, et al. Changes in the Transcription Profile of the Hippocampus in Response to Administration of the Tuftsin Analog Selank. Neuroscience and Behavioral Physiology. 2014;44(8):849–855.
- V'yunova TV, Andreeva LA, Shevchenko KV, et al. Peptide regulation of specific ligand-receptor interactions of GABA with the plasma membranes of nerve cells. Neurochemical Journal. 2014;8(4):259–264.
- Volkova A, Shadrina M, Kolomin T, et al. Selank Administration Affects the Expression of Some Genes Involved in GABAergic Neurotransmission. Frontiers in Pharmacology. 2016;7:31.
- Kost NV, Sokolov OY, Gabaeva MV, et al. Semax and Selank Inhibit the Enkephalin-Degrading Enzymes of Human Serum. Russian Journal of Bioorganic Chemistry. 2001;27(3):180–183.
- Zozulya AA, Kost NV, Sokolov OY, et al. The Inhibitory Effect of Selank on Enkephalin-Degrading Enzymes as a Possible Mechanism of Its Anxiolytic Activity. Bull Exp Biol Med. 2001;131(4):315–317.
- Inozemtseva LS, Karpenko EA, Dolotov OV, et al. Intranasal administration of the peptide Selank regulates BDNF expression in the rat hippocampus in vivo. Doklady Biological Sciences. 2008;421:241–243.
- Narkevich VB, Kudrin VS, Klodt PM, et al. Effects of Selank on monoamine neurotransmitters in the brain of BALB/c and C57BL/6 mice. Bull Exp Biol Med. 2008;145(1):68–71.
- Uchakina ON, Uchakin PN, Miasoedov NF, et al. Immunomodulatory effects of selank in patients with anxiety-asthenic disorders. Zhurnal Nevrologii i Psikhiatrii. 2008;108(5):71–75.
- Kozlovskii II, Andreeva LA, Kozlovskaya MM. The role of the endogenous opioid system in the anxiolytic action of Selank. Bull Exp Biol Med. 2012;153(5):728–730.
- Kolik LG, Nadorova AV, Kozlovskaya MM. Efficacy of Peptide Anxiolytic Selank during Modeling of Withdrawal Syndrome in Rats with Stable Alcoholic Motivation. Bull Exp Biol Med. 2014;157(1):61–65.
- Konstantinopolsky MA, Kolik LG, Chernyakova IV. Selank, a Peptide Analog of Tuftsin, Attenuates Aversive Signs of Morphine Withdrawal in Rats. Bull Exp Biol Med. 2022;173(6):730–733.
- Mukhina AY, et al. Effects of Selank on intestinal microbiota and stress-induced changes. Russian Journal of Physiology. 2019/2020.
- Kasian A, Kolomin T, Andreeva L, et al. Peptide Selank Enhances the Effect of Diazepam in Reducing Anxiety in Unpredictable Chronic Mild Stress Conditions in Rats. Behavioural Neurology. 2017;2017:5091027.
- Kolik LG, Nadorova AV, Antipova TA, Durnev AD. Selank, Peptide Analogue of Tuftsin, Protects Against Ethanol-Induced Memory Impairment by Regulating of BDNF Content. Bull Exp Biol Med. 2019;167(5):641–644.
- Medvedev VE, Tereshchenko ON, Israelian AI, et al. A comparison of the anxiolytic effect and tolerability of selank and phenazepam. Zhurnal Nevrologii i Psikhiatrii. 2014;114(7):17–22.
- Semenova TP, Kozlovskii II, Zakharova NM, Kozlovskaya MM. Experimental optimization of learning and memory processes by selank. Eksperimental'naia i Klinicheskaia Farmakologiia. 2010;73(8):2–5.
- Filatova E, Kasian A, Kolomin T, et al. GABA, Selank, and Olanzapine Affect the Expression of Genes Involved in GABAergic Neurotransmission in IMR-32 Cells. Frontiers in Pharmacology. 2017;8:89.
- Kolomin TA, Shadrina M, Andreeva LA, et al. Expression of inflammation-related genes in mouse spleen under tuftsin analog Selank. Regulatory Peptides. 2011;170(1-3):18–23.
- Andreeva LA, Nagaev IY, Mezentseva MV, et al. Antiviral properties of structural fragments of the peptide Selank. Doklady Biological Sciences. 2010;431:79–82.
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