Evidence map›Paper›PMID 42249912›Full record

ReviewExperimental brain research2026

Molecular neurobiological insights on integrative role of Trk neurotrophic receptors and their small-molecule agonists in neurodegenerative conditions.

Megha Sanjai, Jeyaram Bharathi Jeyabalan, Vignesh Pandi Alagesan, Shruthi Laya Saravanan, James Premdoss Clement, Antony Justin

Abstract readReview
In one paragraph

Review in Experimental brain research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Megha SanjaiCentre for Neuropharmacology and Experimental Neuroscience, Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Ooty, The Nilgiris, Tamil Nadu, 643 001, India.
Jeyaram Bharathi JeyabalanCentre for Neuropharmacology and Experimental Neuroscience, Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Ooty, The Nilgiris, Tamil Nadu, 643 001, India.
Vignesh Pandi AlagesanCentre for Neuropharmacology and Experimental Neuroscience, Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Ooty, The Nilgiris, Tamil Nadu, 643 001, India.
Shruthi Laya SaravananCentre for Neuropharmacology and Experimental Neuroscience, Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Ooty, The Nilgiris, Tamil Nadu, 643 001, India.
James Premdoss ClementFaculty of Life and Health Sciences, University of Exeter, Exeter, UK.
Antony JustinCentre for Neuropharmacology and Experimental Neuroscience, Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Ooty, The Nilgiris, Tamil Nadu, 643 001, India. justin@jssuni.edu.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurodegenerative conditions signify an irreversible, progressive loss of neurons eventually resulting in a wide array of symptoms including cognitive decline, gradual loss of memory, compromised motor functions. Conventional therapies available principally attempt to either restore neurotransmitter levels, or activate its subordinate receptors; while underlying disease pathology of neurodegeneration being overlooked. This narrowed therapeutic approach ultimately results in irreversible, augmented neurodegeneration, leading to hastened disease progression, resulting in long-term complications, and impaired quality of life. This poses an imperative need for newer treatments to curb the progression of the disease. Neurotrophins; NGF and BDNF are proteins that are classically acknowledged during the development of vertebrate nervous system. Proneurotrophins and Mature neurotrophins activate their specific p75NTR and Trk receptors, which initiate intracellular neuronal survival signaling cascades that play an imperative role in maintaining survival of neurons, apoptosis, and synaptic plasticity. Such neuroprotective effects, native neurotrophins could mainly be a potent strategy in the treatment of neurodegenerative disorders. Due to their deprived drugability, neurotrophins failed to pass on further. Hence, small molecule neurotrophin mimetics that corresponds to its receptor domains might show promising results by increasing receptor-induced neuronal survival, differentiation, and initiation of downstream signalling pathways. Prospects that these small molecule mimetics possesses influential neurotrophic effects might as well lead to the application of such compounds that might be crucial to treat the underlying pathology of neurodegeneration that extends beyond the standard symptomatic treatments of neurodegenerative disorders.

Indexed as

Nerve Growth FactorsNeurodegenerative DiseasesNeuroprotective AgentsReceptors, Nerve Growth FactorAnimalsHumansNerve Growth FactorsNeuroprotective AgentsReceptors, Nerve Growth FactorNeurodegenerationNeuronal survivalNeurotrophinsSmall-molecule agonistsTrk receptor

Identifiers

PMID42249912
PMCPMC13242386

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LicenceCC BY-NC-ND
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Registered trials

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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.