# Simulated Gastrointestinal Digestion Modulates Anticholinesterase, Antioxidant, and Anti-Inflammatory Activities of Vegan Soups Rich in Natural Cholinesterase Inhibitors

**Authors:** Dorota Gajowniczek-Ałasa, Roman Paduch, Ewa Baranowska-Wójcik, Oskar M. Szczepaniak, Dominik Szwajgier

PMC · DOI: 10.3390/nu18040698 · Nutrients · 2026-02-21

## TL;DR

This study shows how digestion changes the health benefits of vegan soups, especially their effects on brain and inflammation-related functions.

## Contribution

The novel contribution is evaluating how simulated digestion alters the bioactivity of vegan soups rich in natural cholinesterase inhibitors.

## Key findings

- Total polyphenol levels decreased during digestion but partially recovered in the colonic phase.
- Anticholinesterase and antioxidant activities varied by digestion stage and soup type.
- Colonic digestion is critical for assessing the functional food potential of plant-based soups.

## Abstract

Background/Objectives: Dietary strategies targeting oxidative stress, neuroinflammation and cholinergic dysfunction are increasingly investigated as supportive approaches for maintaining cognitive health. Soups constitute a practical functional food matrix due to their compositional complexity and suitability for regular consumption. However, their bioactivity may be substantially altered during digestion. Methods: Previously, we created optimized mushroom, asparagus, leek, and sea buckthorn vegan lunch soups rich in cholinesterase inhibitors. This study evaluated digestion-induced changes in anticholinesterase, antioxidant, and anti-inflammatory activities using a standardized static in vitro digestion model (INFOGEST). Results: Fresh soups contained 90.43–247.36 µg GAE/cm3 of total polyphenols, which significantly decreased during oral–intestinal digestion, followed by stabilization or partial recovery during the colonic phase. Acetylcholinesterase and butyrylcholinesterase inhibitory activities showed soup-specific and digestion stage-dependent patterns, with an overall decline after bacterial incubation. Antioxidant capacity assessed by DPPH•, ABTS•+, and cyclic voltammetry revealed dynamic redox shifts across digestion stages, while endogenous antioxidant enzymes (SOD, CAT, GR, GPx) and COX-2 activity were differentially modulated. Cell-based assays demonstrated low cytotoxicity and moderate, concentration-dependent cytokine modulation. Conclusions: Overall, gastrointestinal digestion and microbial activity markedly reshape the bioactivity of plant-based soups, indicating that the colonic phase is critical for realistic evaluation of functional food potential and supporting digestion-aware assessment of dietary strategies relevant to cognitive and inflammatory health.

## Linked entities

- **Proteins:** COX2 (cytochrome c oxidase subunit II), SOD1 (superoxide dismutase 1), CAT (catalase), NR3C1 (nuclear receptor subfamily 3 group C member 1), GPX (probable phospholipid hydroperoxide glutathione peroxidase)
- **Chemicals:** GAE (PubChem CID 3037582), ABTS•+ (PubChem CID 35688)

## Full-text entities

- **Diseases:** injury to (MESH:D014947), neurodegeneration (MESH:D019636), Inflammatory (MESH:D007249), colon cancer (MESH:D015179), AD (MESH:D000544), cytotoxicity (MESH:D064420), neuroinflammation (MESH:D000090862), cholinergic (MESH:C535672), colon adenocarcinoma (MESH:D003110)
- **Chemicals:** H2O2 (MESH:D006861), Pt (MESH:D010984), superoxide (MESH:D013481), PBS (-), acetylthiocholine (MESH:D000122), Trolox (MESH:C010643), molecular oxygen (MESH:D010100), penicillin (MESH:D010406), gallic acid (MESH:D005707), amphotericin B (MESH:D000666), EDTA (MESH:D004492), quercetin (MESH:D011794), 3,4-dihydroxyphenylacetic acid (MESH:D015102), 2,2'-diphenyl-1-picrylhydrazyl (MESH:C004931), ester (MESH:D004952), streptomycin (MESH:D013307), carbon (MESH:D002244), acetylsalicylic acid (MESH:D001241), protocatechuic acid (MESH:C009091), Polyphenol (MESH:D059808), water (MESH:D014867), CO2 (MESH:D002245), butyrylthiocholine (MESH:D002092), ABTS (MESH:C002502), phenolic acids (MESH:C017616), acetylcholine (MESH:D000109), KCl (MESH:D011189), DTNB (MESH:D004228), ascorbic acid (MESH:D001205), AgCl (MESH:C037548), hydrogen (MESH:D006859), anthocyanins (MESH:D000872), flavonoids (MESH:D005419), short-chain fatty acids (MESH:D005232), reactive oxygen species (MESH:D017382), glycoside (MESH:D006027), H2SO4 (MESH:C033158)
- **Species:** Agaricus bisporus (common mushroom, species) [taxon 5341], Asparagus (genus) [taxon 4685], Hippophae rhamnoides (sallowthorn, species) [taxon 193516], Allium ampeloprasum (leek, species) [taxon 4681], Homo sapiens (human, species) [taxon 9606], Astragalus membranaceus (species) [taxon 649199], Bythinella sp. GE (species) [taxon 989193]
- **Cell lines:** CRL-1807 — Homo sapiens (Human), 5' 10' methylenetetrahydrofolate reductase deficiency, Finite cell line (CVCL_RA67), CCD 841 CoTr — Homo sapiens (Human), Transformed cell line (CVCL_2872), HTB-38 — Mus musculus (Mouse), Hybridoma (CVCL_A8FQ), HT-29 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0320), CCD 841 — Homo sapiens (Human), Finite cell line (CVCL_2871)

## Full text

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## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943184/full.md

## References

65 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943184/full.md

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Source: https://tomesphere.com/paper/PMC12943184