Evidence map›Paper›PMID 41543687›Full record

ArticleApplied biochemistry and biotechnology2026

Investigation of the In Vitro Neuroprotective Potential of Aegiceras corniculatum against MPTP-induced Toxicity.

Nitu Kumari, Vaddi Damodara Reddy, Santosh Anand

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Article in Applied biochemistry and biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Nitu KumariDepartment of Biotechnology, School of Applied Sciences, REVA University, Bangalore, KA, India.
Vaddi Damodara ReddyDepartment of Biotechnology, School of Applied Sciences, REVA University, Bangalore, KA, India.
Santosh AnandDepartment of Biotechnology, School of Applied Sciences, REVA University, Bangalore, KA, India. santosh.anand@reva.edu.in.ORCID http://orcid.org/0000-0002-2445-8118

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aegiceras corniculatum (AC), a mangrove species widely recognized for its diverse pharmacological properties, has attracted significant attention recently due to its antioxidant, anti-inflammatory, and antimicrobial activities. Despite this, the neuroprotective potential of AC, particularly in the context of neurodegenerative disorders such as Parkinson's disease (PD), remains largely unexplored. Due to the growing interest in plant-derived compounds for the management of PD, investigating the therapeutic relevance of AC could provide new insights into alternative strategies for neuroprotection. The present study aimed to evaluate the neuroprotective ability of the leaf extract of AC against PD. Preliminary phytochemical analyses were conducted to identify the presence of bioactive compounds in the AC extract (ACE). The antioxidant capacity of ACE was evaluated using three standard assays: 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay, ferric reducing antioxidant power (FRAP) assay, and hydrogen peroxide (H₂O₂) scavenging assay. We used the MPTP-induced PD model established in an SH-SY5Y human neuroblastoma cell line as well as in the U87-MG glioblastoma cell line. MTT assay was conducted to measure the cell viability, and further, 2',7'-dichlorofluorescin diacetate (DCFDA) assay was used to measure the reactive oxygen species (ROS). Glutathione peroxidase (GPx) enzyme activity was determined by a chromogenic reaction-based assay. Western blot analysis was used to assess the expression levels of SNCA protein. The ACE was found to contain a diverse range of phytochemicals, including polyphenols, flavonoids, and terpenoids. Among the ethanolic, hydroethanolic, and aqueous extracts evaluated, ethanolic ACE (eACE) exhibited the highest antioxidant activity. The SH-SY5Y cell line demonstrated significantly higher neuroprotective potential to eACE treatment compared to the U87-MG cell line. Moreover, eACE markedly attenuated intracellular ROS levels and enhanced glutathione peroxidase (GP

Indexed as

1-Methyl-4-phenylpyridiniumNeuroprotective AgentsPlant ExtractsPrimulaceaeAntioxidantsCell Line, TumorCell SurvivalHumansOxidative StressParkinson Disease1-Methyl-4-phenylpyridiniumAntioxidantsNeuroprotective AgentsPlant ExtractsAegiceras corniculatumCytotoxicNeuroprotectionParkinson’s diseaseSH-SY5Y cell line

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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 Socratic graph.