Evidence map›Paper›PMID 41444312›Full record

ArticleScientific reports2025

Evaluation of anti-inflammatory and neuroprotective effect of walnut shell pectin.

O Sindhu, M N Chandraprabha, G Divyashri, T P Krishna Murthy

Abstract read
In one paragraph

Article in Scientific reports, 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
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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

4 authors.

O SindhuDepartment of Biotechnology, M S Ramaiah Institute of Technology, Bengaluru, 560054, India.
M N ChandraprabhaDepartment of Biotechnology, M S Ramaiah Institute of Technology, Bengaluru, 560054, India. chandra@msrit.edu.
G DivyashriHead, Bioproducts Research, Iom Bioworks Pvt., Ltd, Bengaluru, 560065, India. divyashri@iombio.com.
T P Krishna MurthyDepartment of Biotechnology, M S Ramaiah Institute of Technology, Bengaluru, 560054, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation and oxidative stress are key pathological drivers of many chronic and neurodegenerative disorders, prompting increasing interest in natural compounds that can safely modulate inflammatory responses and protect neural cells from oxidative damage. In this study, walnut shell pectin (WSP), extracted from Chilean walnut shells, was evaluated for its anti-inflammatory and neuroprotective potential using in vitro models. The anti-inflammatory effects were assessed in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages, while the neuroprotective effects were investigated in rotenone-treated SH-SY5Y neuroblastoma cells. WSP significantly reduced LPS-induced inflammation by downregulating the expression of pro-inflammatory cytokine TNF-α and enhancing the anti-inflammatory cytokine IL-10. In rotenone-exposed SH-SY5Y cells, WSP increased the activities of antioxidant enzymes, catalase and superoxide dismutase, thereby reducing oxidative stress and improving neuronal viability. The maximum protective concentration for both cell lines was determined to be 50 µg/ml. Overall, WSP exhibited strong anti-inflammatory and neuroprotective activities in vitro, highlighting its potential as a natural therapeutic compound for preventing and managing inflammation-associated and neurodegenerative disorders.

Indexed as

Anti-Inflammatory AgentsJuglansNeuroprotective AgentsPectinsAnimalsAntioxidantsCell Line, TumorCell SurvivalHumansInflammationLipopolysaccharidesMiceOxidative StressRAW 264.7 CellsAnti-Inflammatory AgentsAntioxidantsLipopolysaccharidesNeuroprotective AgentsPectinsAnti-inflammatory effectNeuroprotective effectRAW 264.7 cellsSH-SY5Y cellsWalnut shell pectin

Identifiers

PMID41444312
PMCPMC12738577

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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.