# Metabolomics-Based Elucidation of the Lipid-Lowering Mechanisms of Monascus Vinegar Polysaccharides

**Authors:** Yanhua Liu, Yueyue Wu, Shuo Wang, Senzhen Lin, Bingning Gao, Chenyu Yang, Jia Song, Min Wang

PMC · DOI: 10.3390/foods15040654 · Foods · 2026-02-11

## TL;DR

This study explores how Monascus vinegar polysaccharides lower lipids in mice by affecting specific metabolic pathways.

## Contribution

The study identifies specific metabolic pathways modulated by Monascus vinegar polysaccharides in lipid and antioxidant regulation.

## Key findings

- MVP significantly reduced serum and liver lipid levels in hyperlipidemia mice.
- MVP improved liver histopathology and increased antioxidant enzyme activity.
- Key metabolic pathways affected include arachidonic acid and glutathione metabolism.

## Abstract

Monascus vinegar (MV) is a functional food containing various bioactive components, which has attracted significant research attention due to the unique health benefits conferred by these active functional ingredients. This study aimed to investigate the mechanism by which Monascus vinegar polysaccharides (MVPs) prevent hyperlipidemia. We established a hyperlipidemia mouse model using a high-fat diet (HFD) and conducted an 8-week intervention experiment. Results showed that MVP significantly reduced serum and liver lipid levels in mice, increased the activity of liver antioxidant enzymes, and downregulated the expression of serum proinflammatory cytokines. Hematoxylin and eosin (H&E) staining revealed that MVP significantly improved liver histopathological abnormalities. Enrichment analysis of key differential metabolites identified four potential metabolic pathways and mapped them to the MVP and model groups. The analysis revealed the involvement of pathways related to arachidonic acid metabolism, glutathione metabolism, alanine–aspartate–glutamate metabolism, and pyrimidine metabolism. After MVP intervention, key metabolites within these pathways were significantly improved. MVP may influence lipid metabolism through modulation of these pathways. This study provides theoretical support for the application and development of MVP in the functional food sector.

## Linked entities

- **Diseases:** hyperlipidemia (MONDO:0021187)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Cldn1 (claudin 1) [NCBI Gene 12737], Vip (vasoactive intestinal polypeptide) [NCBI Gene 22353], Cox4i1 (cytochrome c oxidase subunit 4I1) [NCBI Gene 12857] {aka COX, COX IV-1, COXIV, Cox4, Cox4a, IV-1}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Lpl (lipoprotein lipase) [NCBI Gene 16956], Cpt1a (carnitine palmitoyltransferase 1a, liver) [NCBI Gene 12894] {aka C730027G07, CPTI, Cpt1}, Il2 (interleukin 2) [NCBI Gene 16183] {aka Il-2}, Cxcl15 (C-X-C motif chemokine ligand 15) [NCBI Gene 20309] {aka Il8, Scyb15, lungkine, weche}, Lox (lysyl oxidase) [NCBI Gene 16948] {aka TSC-160, rrg}, Acc (anterior capsular cataract) [NCBI Gene 104371], Ocln (occludin) [NCBI Gene 18260] {aka Ocl}, Mvp (major vault protein) [NCBI Gene 78388] {aka 2310009M24Rik, LRP, VAULT1}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Lipc (lipase C, hepatic type) [NCBI Gene 15450] {aka HL, Hpl}, Acaa2 (acetyl-CoA acyltransferase 2) [NCBI Gene 52538] {aka 0610011L04Rik, D18Ertd240e}, Crp (C-reactive protein, pentraxin-related) [NCBI Gene 12944], Dgat1 (diacylglycerol O-acyltransferase 1) [NCBI Gene 13350] {aka ARAT, D15Ertd23e, Dgat}, Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}
- **Diseases:** Lipid metabolism disorder (MESH:D052439), diabetic complications (MESH:D048909), atherosclerosis (MESH:D050197), cardiovascular diseases (MESH:D002318), cytotoxic (MESH:D064420), mucosal damage (MESH:D052016), cardiac hypertrophy (MESH:D006332), liver injury (MESH:D017093), necrosis (MESH:D009336), blood lipid disorders (MESH:D011017), tissue injury (MESH:D017695), liver histopathological abnormalities (MESH:D008107), chronic inflammation (MESH:D007249), fatty (MESH:D008067), injury to (MESH:D014947), metabolic disturbances (MESH:D024821), fibrosis (MESH:D005355), hyperlipidemia (MESH:D006949), dyslipidemia (MESH:D050171), mitochondrial (MESH:D028361), non-alcoholic fatty liver disease (MESH:D065626), swelling (MESH:D004487), HL (OMIM:614025), glutathione (MESH:C536835), hepatic fatty degeneration (MESH:D005234), obese (MESH:D009765), metabolic disease (MESH:D008659), metabolic dysregulation (MESH:D021081)
- **Chemicals:** 13(S)-HPOT (-), H&amp;E (MESH:D006371), bile acid (MESH:D001647), alpha-ketoglutarate (MESH:D007656), polyunsaturated fatty acid (MESH:D005231), n-butanol (MESH:D020001), haematoxylin (MESH:D006416), aspartate (MESH:D001224), leukotrienes (MESH:D015289), amino acid (MESH:D000596), phenylalanine (MESH:D010649), arginine (MESH:D001120), fatty acid (MESH:D005227), MDA (MESH:D008315), carbohydrate (MESH:D002241), polyphenols (MESH:D059808), oxylipins (MESH:D054883), Butyric acid (MESH:D020148), protriptyline (MESH:D011530), GSH (MESH:D005978), p-fluorophenylalanine (MESH:D010135), Lipid (MESH:D008055), chloroform (MESH:D002725), dimethyl trisulfide (MESH:C054170), 4-hydroxycinnamic acid (MESH:C495469), PBS (MESH:D007854), sphingolipid (MESH:D013107), calcitriol (MESH:D002117), Cytidine (MESH:D003562), eosin (MESH:D004801), organoheterocyclic compounds (MESH:D006571), myo-inositol (MESH:D007294), ethyl icosapentate (MESH:C035276), formalin (MESH:D005557), 8,9-EET (MESH:C050715), calcium (MESH:D002118), SCFA (MESH:D005232), paraffin (MESH:D010232), Fat (MESH:D005223), saline (MESH:D012965), linoleic acid (MESH:D019787), methanol (MESH:D000432), phosphorus (MESH:D010758), phosphoinositide (MESH:D010716), formic acid (MESH:C030544), DEPC (MESH:D004047), sugar (MESH:D000073893), Uridine (MESH:D014529), Polysaccharides (MESH:D011134), xylene (MESH:D014992), quercetin (MESH:D011794), nitrogen (MESH:D009584), prostaglandins (MESH:D011453), TG (MESH:D014280), acetonitrile (MESH:C032159), alanine (MESH:D000409), pentose phosphate (MESH:D010428), water (MESH:D014867), phospholipids (MESH:D010743), alpha-linolenic acid (MESH:D017962)
- **Species:** Sargassum fusiforme (species) [taxon 590727], Homo sapiens (human, species) [taxon 9606], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Caulerpa lentillifera (species) [taxon 148947], gut metagenome (species) [taxon 749906], Mus musculus (house mouse, species) [taxon 10090], Monascus purpureus (species) [taxon 5098]
- **Mutations:** C at 5, C at 40, Q2, R2, R2Y

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12939243/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939243/full.md

## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939243/full.md

---
Source: https://tomesphere.com/paper/PMC12939243