FAS and SREBP-1c Inhibition via AMPK Activation in HepG2 Cells by Biovip, Tox-off, and Traphanoside GO1 from Glinus oppositifolius.


Journal

Biological & pharmaceutical bulletin
ISSN: 1347-5215
Titre abrégé: Biol Pharm Bull
Pays: Japan
ID NLM: 9311984

Informations de publication

Date de publication:
2023
Historique:
medline: 4 8 2023
pubmed: 3 8 2023
entrez: 2 8 2023
Statut: ppublish

Résumé

Glinus oppositifolius is an endemic herbaceous plant found in tropical Asian countries and is native in Vietnam. It is used in traditional folk medicine because of its flavor and antiseptic and laxative effects. In the current research, the effects of Tox-off, Biovip, and the purified compounds isolated from G. oppositifolius in the previous study were evaluated on the activation of adenosine 5'-monophosphate-activated protein kinase (AMPK)-activated protein kinase (AMPK) and acetyl-coenzyme A carboxylase (ACC) in C2C12 myoblasts. In addition, the most potent active compounds, traphanoside-GO1 (TRA-GO1) and TRA-GO5 have validated the reduction of fatty acid synthase (FAS) and sterol regulatory element binding protein (SREBP)-1c in HepG2 cells. We found that Tox-off and Biovip significantly increased the phosphorylation of AMPK and ACC in C2C12 myoblasts. Furthermore, TRA-GO1 and TRA-GO5 significantly increased the AMPK activation and phosphorylation of its downstream substrate ACC in a concentration-dependent way compared to the dimethyl sulfoxide (DMSO) control. Besides, the protein level of FAS and SREBP-1c decreased by TRA-GO1 and TRA-GO5 in a concentration-dependent manner. Taken together, our results showed that the increased AMPK and ACC phosphorylation by active components of G. oppositifolius may activate the AMPK signaling pathways, which are useful for the anti-obesity and its related metabolic disorders.

Identifiants

pubmed: 37532557
doi: 10.1248/bpb.b22-00892
doi:

Substances chimiques

Sterol Regulatory Element Binding Protein 1 0
AMP-Activated Protein Kinases EC 2.7.11.31
Fatty Acid Synthases EC 2.3.1.85
Acetyl-CoA Carboxylase EC 6.4.1.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1057-1064

Auteurs

Vinh Hue Thi Nguyen (VHT)

Traphaco Joint Stock Company.
Faculty of Medicine and Pharmacy, Dainam University.

Ha Thi Do (HT)

National Institute of Medical Materials.

Hien Thi Tran (HT)

Thai Binh University Medicine and Pharmacy.

Huong Thuy Vu (HT)

Traphaco Joint Stock Company.

Thu Thi Nguyen (TT)

National Institute of Medical Materials.

Diep Thi Vu (DT)

National Institute of Medical Materials.

Ha Ly Thi Nguyen (HLT)

National Institute of Medical Materials.

Huy Van Nguyen (HV)

Traphaco Joint Stock Company.

Quang Luc Tran (QL)

Traphaco Joint Stock Company.

Van Anh Thi Nguyen (VAT)

Traphaco Joint Stock Company.

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Classifications MeSH