Evidence map›Paper›PMID 40038194›Full record

ReviewMolecular neurobiology2025

Deciphering the Neuroprotective Action of Bee Venom Peptide Melittin: Insights into Mechanistic Interplay.

Pankaj Kadyan, Lovedeep Singh

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Pankaj KadyanUniversity Institute of Pharma Sciences, Chandigarh University, Mohali, Punjab, India.
Lovedeep SinghUniversity Institute of Pharma Sciences, Chandigarh University, Mohali, Punjab, India. lovedeep992s@gmail.com.ORCID http://orcid.org/0000-0002-2903-4293

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and multiple sclerosis, are characterized by progressive loss of neuronal structure and function. These conditions often lead to cognitive decline, motor dysfunction, and ultimately severe impairment of daily activities. A key feature of neurodegenerative diseases is chronic inflammation, which contributes to neuronal damage and exacerbates disease progression. Traditional treatments mainly focus on symptomatic relief rather than addressing the underlying causes, highlighting the need for novel therapeutic approaches. Melittin, a bioactive peptide derived from bee venom, has garnered attention for its multifaceted neuroprotective properties, particularly in the context of neuroinflammatory and neurodegenerative disorders. This review delves into the molecular mechanisms through which melittin exerts neuroprotective effects, with a focus on its ability to modulate neuroinflammation, apoptosis, and neurogenesis. Research indicates that melittin can downregulate pro-apoptotic pathways by inhibiting calpain-mediated activation of apoptosis-inducing factor and Bax, thereby reducing neuronal cell death. Additionally, melittin exerts its neuroprotective effects through the inhibition of neuroinflammatory processes, specifically by downregulating key inflammatory pathways such as NF-κB and MAPK. This modulation leads to decreased production of proinflammatory cytokines and prostaglandins, which are implicated in the pathogenesis of neurodegenerative disorders. Beyond its anti-inflammatory actions, melittin promotes neurogenesis, potentially through the modulation of the BDNF/Trk-B/CREB signaling pathway, which plays a crucial role in neuronal survival and plasticity. These properties suggest that melittin not only provides symptomatic relief but could also address the root causes of neuronal degeneration, presenting a promising avenue for the development of new treatments for neurodegenerative diseases. Further research is required to validate its efficacy and safety in clinical settings.

Indexed as

Bee VenomsMelittenNeuroprotective AgentsAnimalsApoptosisHumansNeurodegenerative DiseasesSignal TransductionBee VenomsMelittenNeuroprotective AgentsApoptosisBDNFMelittinNeuroprotectionNF-κBp38-MAPK

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.