# Postbiotic Metabolites of Proanthocyanidins Reduce Adipogenesis In Vitro by Suppressing De Novo Lipogenesis

**Authors:** Wasitha P. D. W. Thilakarathna, Madumani Amararathna, H. P. Vasantha Rupasinghe

PMC · DOI: 10.3390/molecules31040695 · Molecules · 2026-02-17

## TL;DR

This study shows that two metabolites from proanthocyanidins reduce fat cell formation in lab tests by blocking fat production pathways.

## Contribution

The study identifies 3-aminophenol and 4-hydroxyphenylacetamide as novel antiadipogenic metabolites from proanthocyanidins.

## Key findings

- 3-aminophenol and 4-hydroxyphenylacetamide significantly reduced lipid accumulation in preadipocytes.
- These metabolites suppressed de novo lipogenesis by targeting PPAR-γ, ACC, and FAS pathways.
- Molecular docking suggests 3-aminophenol may inhibit insulin receptors to downregulate PPAR-γ.

## Abstract

Proanthocyanidins (PACs) are a key group of bioactive phytochemicals known to provide health benefits. Most PACs are non-bioavailable polymeric molecules that need to be biotransformed by colonic microbes into simple metabolites to exert their pharmacological effects. In this study, six previously unexamined PAC metabolites from Saccharomyces cerevisiae, 3-aminophenol (3-AMP), 3-aminosalicylic acid, 2,4-dihydroxy-6-methylbenzaldehyde, 4-hydroxyphenylacetamide (4-HPA), 3-phenyllactic acid, and 2,4,6-trihydroxyacetophenone, were tested for their antiadipogenic activity using an insulin-dependent 3T3-L1 preadipocyte differentiation model. Lipid accumulation in differentiating preadipocytes was visualized and measured with the Oil Red O assay. Only 3-AMP and 4-HPA significantly reduced lipid accumulation at a concentration of 25 µM. To understand the cellular mechanisms, protein levels of key regulators of adipogenesis and lipid metabolism were analyzed using Western blotting. 3-AMP and 4-HPA may attenuate lipid accumulation by suppressing de novo lipogenesis, with 3-AMP downregulating the peroxisome proliferator-activated receptor (PPAR)-γ/acetyl-CoA carboxylase (ACC)/fatty acid synthase (FAS) axis and 4-HPA primarily inhibiting ACC/FAS signaling. Molecular docking studies indicated that 3-AMP may downregulate PPAR-γ expression through competitive inhibition of insulin receptors. These preliminary findings suggest that 3-AMP and 4-HPA exhibit potential antiadipogenic effects, highlighting PAC-derived postbiotics as promising nutraceuticals for mitigating obesity risk.

## Linked entities

- **Proteins:** PPARG (peroxisome proliferator activated receptor gamma), CAC2 (acetyl Co-enzyme a carboxylase biotin carboxylase subunit), FASN1 (Fatty acid synthase 1)
- **Chemicals:** 3-aminophenol (PubChem CID 11568), 4-hydroxyphenylacetamide (PubChem CID 86986), proanthocyanidins (PubChem CID 107876)
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** INSR (insulin receptor) [NCBI Gene 3643] {aka CD220, HHF5}, POTEF (POTE ankyrin domain family member F) [NCBI Gene 728378] {aka A26C1B, POTE2alpha, POTEACTIN}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, Pparg (peroxisome proliferator activated receptor gamma) [NCBI Gene 19016] {aka Nr1c3, PPAR-gamma, PPAR-gamma2, PPARgamma, PPARgamma2}, Acc (anterior capsular cataract) [NCBI Gene 104371], ACACA (acetyl-CoA carboxylase alpha) [NCBI Gene 31] {aka ACAC, ACACAD, ACACalpha, ACC, ACC1, ACCA}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, FAS (Fas cell surface death receptor) [NCBI Gene 355] {aka ALPS1A, APO-1, APT1, CD95, FAS1, FASTM}, FASN (fatty acid synthase) [NCBI Gene 2194] {aka FAS, OA-519, SDR27X1}, Insr (insulin receptor) [NCBI Gene 16337] {aka 4932439J01Rik, CD220, D630014A15Rik, IR, IR-A, IR-B}, PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}
- **Diseases:** Overweight (MESH:D050177), Obesity (MESH:D009765), microbial infections (MESH:D015163), diabetes (MESH:D003920), cancers (MESH:D009369), non-alcoholic fatty liver disease (MESH:D065626), cardiovascular, neurodegenerative, kidney, lung, and liver diseases (MESH:D019636), injury to (MESH:D014947), inflammatory (MESH:D007249), adipocyte hyperplasia (MESH:D006965), Toxicity (MESH:D064420), weight loss (MESH:D015431), cardiovascular diseases (MESH:D002318), premature death (MESH:D003643)
- **Chemicals:** isopropanol (MESH:D019840), alkaloids (MESH:D000470), NaF (MESH:D012969), Catechin (MESH:D002392), ORO (MESH:C011049), terpenoids (MESH:D013729), peptides (MESH:D010455), phenolic acids (MESH:C017616), 4-HPA (MESH:C074036), PC B2 (MESH:C034280), water (MESH:D014867), 3-AMP (MESH:C055528), streptomycin (MESH:D013307), 3-PLA (MESH:C017648), 3-HPA (MESH:C047158), triglycerides (MESH:D014280), Triton X-100 (MESH:D017830), stilbenes (MESH:D013267), EDTA (MESH:D004492), Pi (MESH:D010716), NaCl (MESH:D012965), sodium deoxycholate (MESH:D003840), flavan-3-ol (MESH:C404987), glucose (MESH:D005947), flavonoid (MESH:D005419), PVDF (MESH:C024865), (epi)gallocatechin (MESH:C057580), hydrogen (MESH:D006859), PBS (MESH:D007854), 2,4-DHMB (MESH:C430484), 2,4,6-trihydroxyacetophenone (MESH:C107067), palmitic acid (MESH:D019308), paraformaldehyde (MESH:C003043), Lipid (MESH:D008055), prebiotics (MESH:D056692), CO2 (MESH:D002245), L-glutamine (MESH:D005973), Polyphenols (MESH:D059808), fatty acid (MESH:D005227), carbohydrates (MESH:D002241), PACs (MESH:D044945), (epi)afzelechin (MESH:C120647), 5-tetradecyloxy-2-furoic acid (MESH:C014289), 3-isobutyl-1-methylxanthine (MESH:D015056), dexamethasone (MESH:D003907), lignans (MESH:D017705), penicillin (MESH:D010406), PAC (MESH:C013221), 2,4-dihydroxy-6-methylbenzaldehyde (MESH:C514789), PAC B2 (MESH:C479580), 2,4,6-THPA (-)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Glu706 to Ala, Arg252 to Cys
- **Cell lines:** Hep3B — Homo sapiens (Human), Childhood hepatocellular carcinoma, Cancer cell line (CVCL_0326), CL-173TM — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_3872), 3T3-L1 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0123), MRC-5 — Homo sapiens (Human), Finite cell line (CVCL_0440)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943237/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943237/full.md

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Source: https://tomesphere.com/paper/PMC12943237