Novel Functional Food Properties of Forest Onion ( Eleutherine bulbosa Merr.) Phytochemicals for Treating Metabolic Syndrome: New Insights from a Combined Computational and In Vitro Approach.
Happy Kurnia PermatasariNuril Farid AbshoriRony Abdi SyahputraUrip HarahapNurlinah AmaliaDian Aruni KumalawatiNelly MayuluNurpudji Astuti TaslimTrina Ekawati TalleiRaymond Rubianto TjandrawinataElvan WiyartaAdriyan PramonoBonlgee KimApollinaire TsopmoJ LLuís Serra-MajemFahrul NurkolisPublished in: Nutrients (2024)
Metabolic syndrome is a global health problem. The use of functional foods as dietary components has been increasing. One food of interest is forest onion extract (FOE). This study aimed to investigate the effect of FOE on lipid and glucose metabolism in silico and in vitro using the 3T3-L1 mouse cell line. This was a comprehensive study that used a multi-modal computational network pharmacology analysis and molecular docking in silico and 3T3-L1 mouse cells in vitro. The phytochemical components of FOE were analyzed using untargeted ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS). Next, an in silico analysis was performed to determine FOE's bioactive compounds, and a toxicity analysis, protein target identification, network pharmacology, and molecular docking were carried out. FOE's effect on pancreatic lipase, α-glucosidase, and α-amylase inhibition was determined. Finally, we determined its effect on lipid accumulation and MAPK8, PPARG, HMGCR, CPT-1, and GLP1 expression in the preadipocyte 3T3-L1 mouse cell line. We showed that the potential metabolites targeted glucose and lipid metabolism in silico and that FOE inhibited pancreatic lipase levels, α-glucosidase, and α-amylase in vitro. Furthermore, FOE significantly ( p < 0.05) inhibits targeted protein expressions of MAPK8, PPARG, HMGCR, CPT-1, and GLP-1 in vitro in 3T3-L1 mouse cells in a dose-dependent manner. FOE contains several metabolites that reduce pancreatic lipase levels, α-glucosidase, α-amylase, and targeted proteins associated with lipid and glucose metabolism in vitro.
Keyphrases
- molecular docking
- molecular dynamics simulations
- metabolic syndrome
- liquid chromatography tandem mass spectrometry
- ms ms
- oxidative stress
- induced apoptosis
- signaling pathway
- climate change
- simultaneous determination
- cell cycle arrest
- multiple sclerosis
- poor prognosis
- fatty acid
- public health
- binding protein
- drug delivery
- small molecule
- adipose tissue
- cardiovascular disease
- type diabetes
- high resolution
- blood pressure
- skeletal muscle
- solid phase extraction
- gas chromatography mass spectrometry