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Metabolite profiling, hypolipidemic, and anti-atherosclerosis activity of mixed vegetable fermentation extract

Although positive association between fermented vegetables intake with the risk of coronary heart disease (CHD) has increased attention nowadays, the metabolite profiling and the mechanism of action are still elusive. This study designed to investigate the secondary metabolites, hypolipidemic, and a...

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Autores principales: Rachmawati, Ermin, Suharti, Suharti, Sargowo, Djanggan, Sekar Kinasih, Larasati, Octaviano, Yudi Her, Mutiah, Roihatul, Ismail, Mahrus, Munjin Nasih, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172600/
https://www.ncbi.nlm.nih.gov/pubmed/37181140
http://dx.doi.org/10.1016/j.jsps.2023.03.004
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author Rachmawati, Ermin
Suharti, Suharti
Sargowo, Djanggan
Sekar Kinasih, Larasati
Octaviano, Yudi Her
Mutiah, Roihatul
Ismail, Mahrus
Munjin Nasih, Ahmad
author_facet Rachmawati, Ermin
Suharti, Suharti
Sargowo, Djanggan
Sekar Kinasih, Larasati
Octaviano, Yudi Her
Mutiah, Roihatul
Ismail, Mahrus
Munjin Nasih, Ahmad
author_sort Rachmawati, Ermin
collection PubMed
description Although positive association between fermented vegetables intake with the risk of coronary heart disease (CHD) has increased attention nowadays, the metabolite profiling and the mechanism of action are still elusive. This study designed to investigate the secondary metabolites, hypolipidemic, and anti-atherogenic effect of mixed vegetable fermentation extract (MVFE). The metabolite screening of the MVFE was assessed using the Liquid Chromatography Tandem Mass Spectrophotometer (LC-MS/MS) method. The result of LC-MS/MS was used as ligands to inhibit the binding of oxidized LDL (oxLDL) and Cluster Differentiation 36 (CD36), Scavenger Receptor A1 (SRA1), Lectin-type oxidized LDL receptor 1 (LOX1). This work was performed with molecular docking using Discovery Studio 2021, PyRx 0.9, and Autodock Vina 4.2 followed by analyzing Network Pharmacology, Protein Protein Interaction (PPI) using Cytoscape 3.9.1 and String 2.0.0. Finally, the clinical effect of MVFE was evaluated using in vivo study. Twenty rabbits were assigned to normal, negative control, and MVFE group that were fed with standard diet, high fat diet (HFD), HFD supplemented with MVFE 100, 200 mg/kg BW, respectively. The serum level of Total Cholesterol (TC) and Low-Density Lipoprotein (LDL-c) were detected at the end of week 4. The LC-MS/MS analysis identified 17 compounds categorized as peptides, fatty acids, polysaccharides, nucleoside, flavonoids, flavanols, and phenolic compounds. Based on the docking study, more negative binding affinity was observed in the interaction between metabolites with the scavenger receptors (SR) than simvastatin. The number of nodes and edges based on Network Pharmacology analysis were 268 and 482, respectively. The PPI network showed that MVFE metabolites exerts its athero-protective effect by modulating various cellular processes including inflammation, improvement of endothelial function, and modulation of lipid metabolism. Blood TC and LDL-c concentrations in the negative control (458.82 ± 82.03; 191.87 ± 92.16 mg/dL) were higher significantly compared to the normal group (87.03 ± 29.27; 43.33 ± 5.75 mg/dL). The MVFE administration decreased the TC (100, 200 mg/kg BW MVFE: 269.96 ± 85.34; 130.17 ± 45.02 mg/dL) and LDL-c level (100, 200 mg/kg BW MVFE = 87.24 ± 22.85; 41.82 ± 11.08 mg/dL) dose-dependently (p < 0,001). The secondary metabolites derived from fermented mixed vegetables extract might be developed as a potential strategy to prevent CHD by targeting the multiple pathways in atherosclerosis.
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spelling pubmed-101726002023-05-12 Metabolite profiling, hypolipidemic, and anti-atherosclerosis activity of mixed vegetable fermentation extract Rachmawati, Ermin Suharti, Suharti Sargowo, Djanggan Sekar Kinasih, Larasati Octaviano, Yudi Her Mutiah, Roihatul Ismail, Mahrus Munjin Nasih, Ahmad Saudi Pharm J Original Article Although positive association between fermented vegetables intake with the risk of coronary heart disease (CHD) has increased attention nowadays, the metabolite profiling and the mechanism of action are still elusive. This study designed to investigate the secondary metabolites, hypolipidemic, and anti-atherogenic effect of mixed vegetable fermentation extract (MVFE). The metabolite screening of the MVFE was assessed using the Liquid Chromatography Tandem Mass Spectrophotometer (LC-MS/MS) method. The result of LC-MS/MS was used as ligands to inhibit the binding of oxidized LDL (oxLDL) and Cluster Differentiation 36 (CD36), Scavenger Receptor A1 (SRA1), Lectin-type oxidized LDL receptor 1 (LOX1). This work was performed with molecular docking using Discovery Studio 2021, PyRx 0.9, and Autodock Vina 4.2 followed by analyzing Network Pharmacology, Protein Protein Interaction (PPI) using Cytoscape 3.9.1 and String 2.0.0. Finally, the clinical effect of MVFE was evaluated using in vivo study. Twenty rabbits were assigned to normal, negative control, and MVFE group that were fed with standard diet, high fat diet (HFD), HFD supplemented with MVFE 100, 200 mg/kg BW, respectively. The serum level of Total Cholesterol (TC) and Low-Density Lipoprotein (LDL-c) were detected at the end of week 4. The LC-MS/MS analysis identified 17 compounds categorized as peptides, fatty acids, polysaccharides, nucleoside, flavonoids, flavanols, and phenolic compounds. Based on the docking study, more negative binding affinity was observed in the interaction between metabolites with the scavenger receptors (SR) than simvastatin. The number of nodes and edges based on Network Pharmacology analysis were 268 and 482, respectively. The PPI network showed that MVFE metabolites exerts its athero-protective effect by modulating various cellular processes including inflammation, improvement of endothelial function, and modulation of lipid metabolism. Blood TC and LDL-c concentrations in the negative control (458.82 ± 82.03; 191.87 ± 92.16 mg/dL) were higher significantly compared to the normal group (87.03 ± 29.27; 43.33 ± 5.75 mg/dL). The MVFE administration decreased the TC (100, 200 mg/kg BW MVFE: 269.96 ± 85.34; 130.17 ± 45.02 mg/dL) and LDL-c level (100, 200 mg/kg BW MVFE = 87.24 ± 22.85; 41.82 ± 11.08 mg/dL) dose-dependently (p < 0,001). The secondary metabolites derived from fermented mixed vegetables extract might be developed as a potential strategy to prevent CHD by targeting the multiple pathways in atherosclerosis. Elsevier 2023-05 2023-03-10 /pmc/articles/PMC10172600/ /pubmed/37181140 http://dx.doi.org/10.1016/j.jsps.2023.03.004 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Rachmawati, Ermin
Suharti, Suharti
Sargowo, Djanggan
Sekar Kinasih, Larasati
Octaviano, Yudi Her
Mutiah, Roihatul
Ismail, Mahrus
Munjin Nasih, Ahmad
Metabolite profiling, hypolipidemic, and anti-atherosclerosis activity of mixed vegetable fermentation extract
title Metabolite profiling, hypolipidemic, and anti-atherosclerosis activity of mixed vegetable fermentation extract
title_full Metabolite profiling, hypolipidemic, and anti-atherosclerosis activity of mixed vegetable fermentation extract
title_fullStr Metabolite profiling, hypolipidemic, and anti-atherosclerosis activity of mixed vegetable fermentation extract
title_full_unstemmed Metabolite profiling, hypolipidemic, and anti-atherosclerosis activity of mixed vegetable fermentation extract
title_short Metabolite profiling, hypolipidemic, and anti-atherosclerosis activity of mixed vegetable fermentation extract
title_sort metabolite profiling, hypolipidemic, and anti-atherosclerosis activity of mixed vegetable fermentation extract
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172600/
https://www.ncbi.nlm.nih.gov/pubmed/37181140
http://dx.doi.org/10.1016/j.jsps.2023.03.004
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