Modulation of neuropathological pathways by bioactive peptides and proteins/polypeptides: Targeting oxidative stress in neurodegenerative diseases.
Giri. Sushil S; Chandra. Phool P
Key Findings
- Semax can modulate oxidative stress and neuroinflammation, supporting neuroprotection
- It helps preserve mitochondrial function and enhances synaptic plasticity in preclinical models
- Delivery to the brain is a major challenge, but new technologies (nanoparticles, AI‑guided design) are being explored
Practical Outcomes
- For now, semax looks promising as a neuroprotective agent, but there’s no clear, safe dosage or administration guide for self‑experimenters. Until delivery methods improve and clinical data expand, it’s best to focus on proven lifestyle strategies for brain health while monitoring future research on semax.
Summary
This review says that the peptide semax (along with other brain‑derived factors) can help protect brain cells by lowering oxidative stress, calming inflammation, keeping mitochondria healthy, and boosting synaptic plasticity, which are all important in diseases like Alzheimer’s and Parkinson’s. However, the paper is a broad overview and doesn’t give specific dosing or real‑world protocols, and it notes big hurdles like getting the peptide across the blood‑brain barrier and preventing it from breaking down.
Abstract
Neurodegenerative disorders (NDDs) pose a growing global health burden, primarily due to their progressive nature and the limited efficacy of existing treatments. Bioactive peptides and proteins/polypeptides, particularly those derived from dietary and natural sources, show promise in modulating neurobiological pathways central to neurodegeneration. This review aims to critically examine the neuroprotective roles of Bioactive peptides and proteins/polypeptides in NDDs, elucidating their mechanisms of action, potential therapeutic applications in conditions like Alzheimer's, Parkinso's disease, Huntington's disease, and others, as well as the trends in peptide-based therapeutics. Bioactive peptides and proteins/polyspeptides, such as NGF, BDNF, GDNF, Semax, and Exendin-4, have been found to modulate several critical mechanisms, including the reduction of oxidative stress (OS), inhibition of neuroinflammation, preservation of mitochondria, and enhancement of synaptic plasticity. These peptides have demonstrated efficacy in preclinical and early-phase clinical trials across a spectrum of NDDs. Delivery challenges, such as blood-brain barrier (BBB) permeability and enzymatic degradation, have been acknowledged. Ongoing innovations in peptide engineering, nanoparticle-based delivery systems, CRISPR-assisted design, and AI-driven screening are addressing these limitations. By targeting multiple pathogenic mechanisms simultaneously, peptide-based therapeutics present a rational and innovative approach to NDD management. Their multifunctional action profiles and ability to target specific molecular pathways highlight their potential as next-generation neuroprotective agents. However, future clinical validation and advanced strategies are essential for translating these promising molecules into effective treatments.
Study Information
pubmed
2025
2025-09-21T00:00:00.000Z
10.1016/j.npep.2025.102563
1
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