Evidence map›Paper›PMID 39415580›Full record

ReviewCentral nervous system agents in medicinal chemistry2025

A Brief Review on Caenorhabditis elegans Role in Modelling Neurodegenerative Disease.

Himangi Vig, Priyanka Shukla, Anamika Mishra, Ayushi Pal, Ankita Wal

Abstract readReview
PubMed Publisher
In one paragraph

Review in Central nervous system agents in medicinal chemistry, 2025. 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

5 authors.

Himangi VigDepartment of Pharmacy, PSIT-Pranveer Singh Institute of Technology (Pharmacy) NH 19, Kanpur, India.
Priyanka ShuklaDepartment of Pharmacy, PSIT-Pranveer Singh Institute of Technology (Pharmacy) NH 19, Kanpur, India.
Anamika MishraDepartment of Pharmacy, PSIT-Pranveer Singh Institute of Technology (Pharmacy) NH 19, Kanpur, India.
Ayushi PalDepartment of Pharmacy, PSIT-Pranveer Singh Institute of Technology (Pharmacy) NH 19, Kanpur, India.
Ankita WalDepartment of Pharmacy, PSIT-Pranveer Singh Institute of Technology (Pharmacy) NH 19, Kanpur, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A small, translucent nematode known as Caenorhabditis elegans, or C. elegans, is frequently utilized as a model organism in biomedical studies. These worms, which are around 1 mm long and feed on bacteria, are usually found in soil. For accessible and effective research on genetics, developmental biology, neuroscience, cell biology, and aging, C. elegans provide an ideal model. Its simplicity, which includes a translucent body and a nervous system with only 302 neurons, makes it possible to see cellular and developmental processes in great detail. Because of its special benefits, the worm Caenorhabditis elegans allows for a thorough characterization of the cellular and molecular processes causing age-related neurodegenerative diseases. This is a general review of the life cycle, experimental methodologies, and the use of C. elegans to model brain diseases, including those related to molecular and genetic factors that cause neurodegenerative diseases. Additionally, we go over how C. elegans is a perfect model organism for studying neurons in instances of prevalent age-related neurodegenerative illnesses due to a combination of its biological traits and new analytical techniques. The literature review process was carried out step-by-step using online search databases such as Web of Science, PubMED, Embase, Google Scholar, Medline, and Google Patents. In the first searches, keywords like C.elegans, disease modelling, and neuroprotective activity were employed. Because of C. elegans's physiological transparency, it is possible to track the development of neurodegeneration in aging organisms by using co-expressed fluorescent proteins. Importantly, a fully characterized connectome provides a unique ability to precisely connect cellular death with behavioural instability or phenotypic diversity in vivo, thus permitting a deep knowledge of the detrimental effect of neurodegeneration on wellbeing. In addition, pharmacological therapies and both forward and reverse gene screening speed up the discovery of modifiers that change neurodegeneration. These chemical-genetic investigations work together to determine important threshold states that either increase or decrease cellular stress in order to unravel related pathways.

Indexed as

Caenorhabditis elegansDisease Models, AnimalNeurodegenerative DiseasesAgingAnimalsHumansAlzheimer’s diseaseCaenorhabditis elegansgenetic screeningmitochondrial dysfunctionneurodegenerationParkinson’s disease.

Identifiers

What Socratic 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 Socratic graph.