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Science6 min read

Semax: a review of the research literature on this ACTH-derived neurotrophic peptide

A heptapeptide devoid of corticotropic activity, studied for its influence on BDNF and NGF: an overview of the research literature on Semax.

Contents

Semax is a synthetic heptapeptide derived from the ACTH(4-10) fragment, initially developed in Russia and extensively studied since in the fundamental neuropharmacology literature.

An ACTH derivative without corticotropic activity

Unlike full-length ACTH, Semax lacks significant corticotropic activity: it does not stimulate the hypothalamic-pituitary-adrenal axis and does not notably raise cortisol in the studied models. This dissociation between the ACTH-derived sequence and the absence of an adrenal hormonal effect is one of the most well-documented points in the literature devoted to this peptide.

Reported effects on neurotrophic factors

The literature (published preclinical studies, notably PMID 16996037 and 16635254) reports a rapid increase in the expression of BDNF (Brain-Derived Neurotrophic Factor) and NGF (Nerve Growth Factor) in the hippocampus and frontal cortex of murine models, with an associated modulation of TrkA/TrkB receptors. These two neurotrophic factors are central subjects of study in fundamental neuroscience, involved in synaptic plasticity.

Modulation of neurotransmission systems

Beyond neurotrophic factors, published work describes a modulation of the dopaminergic, serotonergic and cholinergic systems, an increase in endogenous enkephalin, as well as a reduction in neuronal oxidative stress in the studied models.

Preclinical ischemia models

A significant portion of the Semax literature comes from preclinical models of cerebral ischemia and stroke, where neuroprotective effects via inhibition of BAX-mediated neuronal apoptosis have been reported, alongside improved mnemonic and attentional performance in these same animal models.

A peptide studied alongside other cognitive compounds

In our catalog, Selank — another Russian peptide, derived from tuftsin — is frequently cited in the same literature for its anxiolytic properties and its modulation of BDNF, offering an interesting comparative research axis with Semax.

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