Evidence map›Paper›PMID 41747606›Full record

ArticleJournal of Ayurveda and integrative medicine

A preliminary study on Tapyadi Loha for the treatment of hepatic encephalopathy based on Insilico and Invitro analysis.

Shruti Chindam, Urmila Aswar, Chinmay Phondekar

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Article in Journal of Ayurveda and integrative medicine. 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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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Shruti ChindamDepartment of Pharmacology, Poona College of Pharmacy, Bharati Vidyapeeth Deemed to be University, Pune, Maharashtra, India.
Urmila AswarDepartment of Pharmacology, Poona College of Pharmacy, Bharati Vidyapeeth Deemed to be University, Pune, Maharashtra, India. Electronic address: urmila.aswar@bharatividyapeeth.edu.
Chinmay PhondekarConsultant Ayurvedic Physician, Bhargava Ayurved Chikitsalaya, Dombivali, Maharashtra, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatic encephalopathy (HE) is a neuropsychiatric disorder linked to liver dysfunction, commonly occurring in cirrhosis or acute liver failure. Existing treatments like lactulose and rifaximin provide only symptomatic relief and cause gastrointestinal side effects, emphasizing the need for alternative therapies. Tapyadi Loha (TL), a classical Ayurvedic herbomineral formulation, is traditionally used in clinical practice for HE lacks scientific evidence.

objectivesTo perform preliminary evaluation of TL in the management of HE through in silico and in vitro analysis. MATERIAL AND

methodsActivity markers of TL were screened using IMPPAT, SwissADME, and MolSoft based on ≥30 % oral bioavailability and drug-likeness scores of 0-1. Potential HE-related targets were identified through SwissTarget Prediction, SuperPred, BindingDB, and GeneCards, with overlapping targets analyzed via PPI networks using STRING and Cytoscape. Molecular docking in Schrodinger's Maestro revealed good binding affinity phytoconstituents, which were quantified by LC-MS/MS as per CCRAS guidelines. Their hepatoprotective activity was validated in HepG2 cells, while antioxidant effects were confirmed using the DPPH assay.

resultsGene ontology and KEGG analyses revealed enrichment in cancer and hepatitis B pathways, notably NF-κB, TNF, and TLR signalling. Docking studies identified strong binding of gallic acid, quercetin, ascorbic acid, and luteolin, validated by LC-MS/MS. In vitro, TL treatment significantly improved HepG2 cell viability in thioacetamide-induced toxicity in a dose dependent manner, confirming its hepatoprotective potential. Additionally, TL demonstrated antioxidant activity in the DPPH assay.

conclusionThe study examined the potential molecular targets, important genes, and signalling pathways of TL and its connection to HE using a network pharmacology approach. HepG2 cell line research showed that TL increased cell viability in a dose-dependent way. The study supports TL's possible neuroprotective and hepatoprotective benefits.

Indexed as

Hepatic encephalopathyHerbomineral formulationMolecular dockingNetwork pharmacologyTapyadi Loha

Identifiers

PMID41747606
PMCPMC12955553

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