Standardized ethanol extract of Tinospora crispa upregulates pro-inflammatory mediators release in LPS-primed U937 human macrophages through stimulation of MAPK, NF-κB and PI3K-Akt signaling networks.


Journal

BMC complementary medicine and therapies
ISSN: 2662-7671
Titre abrégé: BMC Complement Med Ther
Pays: England
ID NLM: 101761232

Informations de publication

Date de publication:
06 Aug 2020
Historique:
received: 06 03 2020
accepted: 27 07 2020
entrez: 9 8 2020
pubmed: 9 8 2020
medline: 2 2 2021
Statut: epublish

Résumé

Immunomodulatory effects of Tinospora crispa have been investigated due to its traditional use to treat several inflammatory disorders associated to the immune system. The present study reports the underlying mechanisms involved in the stimulation of 80% ethanol extract of T. crispa stems on pro-inflammatory mediators release in lipopolysaccharide (LPS)-primed U937 human macrophages via MyD88-dependent pathways. Release of interleukin (IL)-1β and tumor necrosis factor (TNF)-α, and production of prostaglandin E Qualitative and quantitative analyses of chromatographic data indicated that syringin and magnoflorine were found as the major components of the extract. T. crispa-treatment prompted activation of NF-κB by enhancing IKKα/β and NF-κB (p65) phosphorylation, and degradation of IκBα. The extract upregulated COX-2 protein expression, release of pro-inflammatory mediators and MAPKs (ERK, p38 and JNK) phosphorylation as well as Akt dose-dependently. T. crispa extract also upregulated the upstream signaling adaptor molecules, toll-like receptor 4 (TLR4) and MyD88. T. crispa-treatment also upregulated the pro-inflammatory markers mRNA expression. The results suggested that T. crispa extract stimulated the MyD88-dependent signaling pathways by upregulating the various immune inflammatory related parameters.

Sections du résumé

BACKGROUND BACKGROUND
Immunomodulatory effects of Tinospora crispa have been investigated due to its traditional use to treat several inflammatory disorders associated to the immune system. The present study reports the underlying mechanisms involved in the stimulation of 80% ethanol extract of T. crispa stems on pro-inflammatory mediators release in lipopolysaccharide (LPS)-primed U937 human macrophages via MyD88-dependent pathways.
METHODS METHODS
Release of interleukin (IL)-1β and tumor necrosis factor (TNF)-α, and production of prostaglandin E
RESULTS RESULTS
Qualitative and quantitative analyses of chromatographic data indicated that syringin and magnoflorine were found as the major components of the extract. T. crispa-treatment prompted activation of NF-κB by enhancing IKKα/β and NF-κB (p65) phosphorylation, and degradation of IκBα. The extract upregulated COX-2 protein expression, release of pro-inflammatory mediators and MAPKs (ERK, p38 and JNK) phosphorylation as well as Akt dose-dependently. T. crispa extract also upregulated the upstream signaling adaptor molecules, toll-like receptor 4 (TLR4) and MyD88. T. crispa-treatment also upregulated the pro-inflammatory markers mRNA expression.
CONCLUSION CONCLUSIONS
The results suggested that T. crispa extract stimulated the MyD88-dependent signaling pathways by upregulating the various immune inflammatory related parameters.

Identifiants

pubmed: 32762741
doi: 10.1186/s12906-020-03039-7
pii: 10.1186/s12906-020-03039-7
pmc: PMC7409646
doi:

Substances chimiques

Inflammation Mediators 0
Lipopolysaccharides 0
NF-kappa B 0
Plant Extracts 0
Proto-Oncogene Proteins c-akt EC 2.7.11.1
Mitogen-Activated Protein Kinases EC 2.7.11.24

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

245

Subventions

Organisme : Kementerian Pertanian dan Industri Asas Tani Malaysia
ID : NH1015D075

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Auteurs

Md Areeful Haque (MA)

Department of Pharmacy, International Islamic University Chittagong, Chittagong, 4318, Bangladesh.

Ibrahim Jantan (I)

Institute of Systems Biology (INBIOSIS), Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor, Malaysia. profibj@gmail.com.

Hemavathy Harikrishnan (H)

Department of Pharmacology, School of Medicine, Case Western Reserve University, Cleveland, OH, USA.

Waqas Ahmad (W)

School of Pharmaceutical Sciences, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia.

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Classifications MeSH