Evidence map›Paper›PMID 40180689›Full record

ReviewMolecular neurobiology2025

Epigenetic and Mitochondrial Metabolic Dysfunction in Multiple Sclerosis: A Review of Herbal Drug Approaches and Current Clinical Trials.

Ashwani, Anjali Sharma, Mayank Kumar Choudhary, Dalapathi Gugulothu, Deepti Pandita, Surajpal Verma, Lalitkumar K Vora, Dharmendra Kumar Khatri, Debapriya Garabadu

Abstract readReview
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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

9 authors.

AshwaniDelhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, 110017, India.
Anjali SharmaCDSCO, FDA Bhawan, New Delhi, India.
Mayank Kumar ChoudharyDepartment of Pharmacology, School of Basic and Applied Sciences, Central University of Punjab, Bathinda, 151401, India.
Dalapathi GugulothuDelhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, 110017, India. dalugugulothu@gmail.com.
Deepti PanditaDelhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, 110017, India.
Surajpal VermaDelhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, 110017, India.
Lalitkumar K VoraSchool of Pharmacy, Medical Biology Centre, Queen'S University Belfast, 97 Lisburn Road, Belfast, Northern Ireland, BT9 7BL, UK. L.Vora@qub.ac.uk.ORCID http://orcid.org/0000-0001-8106-9066
Dharmendra Kumar KhatriDepartment of Pharmacology, NIMS Institute of Pharmacy, NIMS University Rajasthan, Jaipur, 303121, India. dkkhatri10@gmail.com.
Debapriya GarabaduDepartment of Pharmacology, School of Basic and Applied Sciences, Central University of Punjab, Bathinda, 151401, India. debapriya.garabadu@cup.edu.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is a complex autoimmune disease characterised by inflammation, demyelination, and neurodegeneration within the central nervous system (CNS). While the exact causes remain unclear, recent research highlights the significant role of epigenetic modifications and mitochondrial dysfunction in the disease's onset and progression. Epigenetic alterations, such as DNA methylation, histone modification, and microRNA regulation, influence gene expression without altering the DNA sequence, leading to immune dysregulation and inflammation. Similarly, mitochondrial dysfunction, marked by impaired oxidative phosphorylation, reduced adenosine triphosphate (ATP) production, and increased reactive oxygen species (ROS), contributes to neurodegeneration and impaired remyelination in MS. The growing interest in targeting these two interconnected mechanisms has opened new avenues for MS treatment. Herbal drugs, known for their multi-targeted effects, have shown potential in modulating epigenetic markers and enhancing mitochondrial function. Compounds such as resveratrol, curcumin, epigallocatechin-3-gallate (EGCG), quercetin, and omega-3 fatty acids demonstrate potential in regulating DNA methylation, histone deacetylation, and mitochondrial biogenesis. These natural agents offer dual-action therapies by reducing oxidative stress and inflammation while promoting neuronal survival and remyelination. This review explores the therapeutic potential of herbal drugs targeting epigenetic and mitochondrial pathways in MS, evaluating their mechanisms of action and highlighting their promise as novel therapeutic agents. While initial findings are encouraging, further research and clinical trials are required to validate the efficacy of these herbal treatments and fully understand their potential in slowing disease progression and improving patient outcomes in MS. Such exploration could pave the way for safer, multi-targeted therapies, offering new hope in the management of MS and other neurodegenerative diseases.

Indexed as

Clinical Trials as TopicEpigenesis, GeneticMitochondriaMultiple SclerosisAnimalsHumansClinical trialsEpigenetic dysregulationHerbal drugsMitochondria dysfunctionMultiple sclerosis

Identifiers

PMID40180689
PMCPMC12289784

What OpenQuestion holds

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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.