Anti-inflammatory effect of Kaba Sura Kudineer (AYUSH approved COVID-19 drug)-A Siddha poly-herbal formulation against lipopolysaccharide induced inflammatory response in RAW-264.7 macrophages cells.
Animals
Anti-Inflammatory Agents
/ pharmacology
Dietary Supplements
Inflammation
/ drug therapy
Lipopolysaccharides
/ toxicity
Macrophages
/ drug effects
Medicine, Ayurvedic
Mice
Pharmaceutical Preparations
Phytotherapy
Plant Preparations
/ pharmacology
RAW 264.7 Cells
SARS-CoV-2
COVID-19 Drug Treatment
Cycloxygenase-2
Inflammation
Interleukins-6
Kaba sura kudineer
NF-ӄB
Nitric oxide
Journal
Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310
Informations de publication
Date de publication:
30 Jan 2022
30 Jan 2022
Historique:
received:
17
06
2021
revised:
02
10
2021
accepted:
09
10
2021
pubmed:
16
10
2021
medline:
20
11
2021
entrez:
15
10
2021
Statut:
ppublish
Résumé
Medicinal importance and potential activity of Siddha herbal formulations have proved over several centuries against a wide range of causative agents as Influenza, Dengue, Chikungunya, and Tuberculosis. The traditional medicine system of Siddha is a valuable therapeutic approach for treating viral respiratory infections like Coronavirus disease 2019 (COVID-19) and can be effectively employed to target the host response and preventive care to boost the immune system. Kaba Sura Kudineer (KSK), an official polyherbal formulation has been used in Siddha traditional medicine for centuries. However, the role of KSK in regulating inflammation and the underlying molecular mechanisms has remained elusive. The goal of this study was to evaluate the anti-inflammatory effect of KSK using lipopolysaccharide (LPS) stimulated RAW 264.7 murine macrophage cells. Raw 264.7 murine macrophage cells were used for this study. The Inflammatory mediators and cytokines were measured by enzyme-linked immunosorbent assay (ELISA). The NF-κB nulcear translocation and protein expression of iNOS, COX-2 was analyzed with westernblot. KSK supplementation decreased LPS mediated TLR-4 production and secretion of pro-inflammatory mediators and cytokines including IL-6, TNF-α, COX-2 and PGE-2. Moreover, it inhibited the production of nitric oxide (NO) and thereby inhibited the expression of iNOS in the cell. The Western blot analysis further confirmed that KSK strongly prevented the LPS-induced degradation of IκB which is normally required for the activation of NF-κB and hereby suppressed nuclear translocation of NF-κB. The protein expression of iNOS, COX-2 was significantly decreased with the presence of KSK treatment. Results suggested that KSK manipulates its anti-inflammatory effects mainly through blocking the TLR mediated NF-κB signal transduction pathways. Together, this study has proven that KSK could be a potential therapeutic drug for alleviating excessive inflammation in many inflammation-associated diseases like COVID-19.
Identifiants
pubmed: 34653521
pii: S0378-8741(21)00967-3
doi: 10.1016/j.jep.2021.114738
pmc: PMC8507575
pii:
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Lipopolysaccharides
0
Pharmaceutical Preparations
0
Plant Preparations
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
114738Informations de copyright
Copyright © 2021 Elsevier B.V. All rights reserved.
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