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Tannic acid modulates SARS-CoV-2 pathogenesis by curbing key host receptors and oxidative stress.

Authors :
Augustus AR
Radhakrishnan Y
Bhaskar JP
Ramamurthi S
Shunmugiah KP
Source :
Toxicology in vitro : an international journal published in association with BIBRA [Toxicol In Vitro] 2025 Mar; Vol. 103, pp. 105971. Date of Electronic Publication: 2024 Nov 16.
Publication Year :
2025

Abstract

The novel coronavirus SARS-CoV-2, which wrecked havoc around the world in the recent years through COVID-19, gains entry into the host cell through various receptors. Development of therapies targeting host-pathogen interaction will be a key to curb the infection as it potentially suppresses viral attachment and entry into the host. Boundless bioactives abundant in natural resources are the important source of new as well as safer alternatives. Tannic acid, a polyphenolic compound found abundantly in various plant sources, has gained much attention owing to its multifaceted pharmacological properties. This research paper presents a comprehensive investigation on antioxidant, anti-inflammatory and anti-viral abilities of tannic acid, substantiated through a triad of methodologies: in silico, in vitro and in vivo approaches. In vitro experiments, confirmed the antioxidant and anti-inflammatory efficacy as well as the host receptor modulating potential of tannic acid. In silico docking analyses elucidated the molecular interactions between tannic acid and key host receptors involved in inflammation and viral pathogenesis. Furthermore, the in vivo studies involving Danio rerio provided a holistic understanding of the systemic impact of tannic acid, including its antioxidant effects by mitigating the oxidative stress.<br />Competing Interests: Declaration of competing interest The authors declare no competing interests.<br /> (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1879-3177
Volume :
103
Database :
MEDLINE
Journal :
Toxicology in vitro : an international journal published in association with BIBRA
Publication Type :
Academic Journal
Accession number :
39551113
Full Text :
https://doi.org/10.1016/j.tiv.2024.105971