# Transcriptional insights into aflatoxin B1 induced hepatotoxicity and comparative effects of medicinal herbs in pigs

**Authors:** Avon Augustin Nalpadan, Henry Reyer, Michael Oster, Nares Trakooljul, Siriluck Ponsuksili, Wojciech Kozera, Krzysztof Karpiesiuk, Katarzyna Kępka-Borkowska, Katarzyna Chałaśkiewicz, Mariusz Pierzchała, Hiroaki Taniguchi, Adam Lepczyński, Brygida Ślaska, Varunkumar Asediya, Chandra Shekhar Pareek, Klaus Wimmers

PMC · DOI: 10.1186/s12917-025-05270-1 · BMC Veterinary Research · 2026-01-15

## TL;DR

This study explores how aflatoxin B1 harms pig livers and how certain herbs may help protect against this damage.

## Contribution

The study provides new insights into how medicinal herbs can counteract aflatoxin B1-induced gene expression changes in pigs.

## Key findings

- AFB1 suppressed genes related to biotransformation, detoxification, and redox balance in pig livers.
- Kalmegh and milk thistle upregulated key hepatic pathways, suggesting hepatoprotective effects.
- Turmeric supplementation did not consistently affect target genes under the tested conditions.

## Abstract

Aflatoxin B1 (AFB1) contamination in animal feed poses a serious risk to livestock health due to its hepatotoxic effects. Many medicinal herbs which may be used as feed additives exhibit antioxidant and anti-inflammatory properties with potential hepatoprotective outcomes. We investigated effects of AFB1 in three concentrations (30 µg/kg BW, 60 µg/kg BW, 120 µg/kg BW) as well as three medicinal herbs, i.e., kalmegh (Andrographis paniculata), milk thistle (Silybum marianum), and turmeric (Curcuma longa) in pigs. Hepatic expression of genes involved in biotransformation, detoxification, antioxidation, energy homeostasis, and immunity were evaluated by high-throughput real-time PCR.

We found that AFB1 significantly suppressed genes involved in biotransformation (CYP2U1, CYP4V2, CYP7B1, CYP26A1, CYP51A1), detoxification (GSS, ABCC2, SULT1E1), redox balance (GPX1, PRDX4), lipid homeostasis (ACOX1), and immune regulation (CP, CRP). Kalmegh and, to a lesser extent, milk thistle supplementation provided a comprehensive upregulation of genes involved in key hepatic pathways maintaining liver integrity. Under the specific experimental conditions, the applied dietary turmeric supplement did not induce consistent effects on the analyzed target genes.

The results indicate that certain medicinal herbs could counteract AFB1-induced gene expression responses in liver. Their application as dietary supplements to reduce potentially harmful effects caused by AFB1 toxicity in farm animals might be an effective tool in improving animal health, productivity and food safety.

The online version contains supplementary material available at 10.1186/s12917-025-05270-1.

## Linked entities

- **Genes:** CYP2U1 (cytochrome P450 family 2 subfamily U member 1) [NCBI Gene 113612], CYP4V2 (cytochrome P450 family 4 subfamily V member 2) [NCBI Gene 285440], CYP7B1 (cytochrome P450 family 7 subfamily B member 1) [NCBI Gene 9420], CYP26A1 (cytochrome P450 family 26 subfamily A member 1) [NCBI Gene 1592], CYP51A1 (cytochrome P450 family 51 subfamily A member 1) [NCBI Gene 1595], GSS (glutathione synthetase) [NCBI Gene 2937], ABCC2 (ATP binding cassette subfamily C member 2) [NCBI Gene 1244], SULT1E1 (sulfotransferase family 1E member 1) [NCBI Gene 6783], GPX1 (glutathione peroxidase 1) [NCBI Gene 2876], PRDX4 (peroxiredoxin 4) [NCBI Gene 10549], ACOX1 (acyl-CoA oxidase 1) [NCBI Gene 51], CP (ceruloplasmin) [NCBI Gene 1356], CRP (C-reactive protein) [NCBI Gene 1401]
- **Chemicals:** aflatoxin B1 (PubChem CID 186907)

## Full-text entities

- **Genes:** NFE2L2 (nuclear factor, erythroid 2 like 2) [NCBI Gene 396014] {aka ECH, NRF2}, DNASE1 (deoxyribonuclease 1) [NCBI Gene 397051], GPX1 (glutathione peroxidase 1) [NCBI Gene 100857115] {aka GPx-1}, PRDX4 (peroxiredoxin 4) [NCBI Gene 418601], CRP (C-reactive protein) [NCBI Gene 100620468], ACOX1 (acyl-CoA oxidase 1) [NCBI Gene 100113422] {aka ACO}, TOP2B (DNA topoisomerase II beta) [NCBI Gene 100156319], RPL32 (ribosomal protein L32) [NCBI Gene 414419], CRP (C-reactive protein, pentraxin-related) [NCBI Gene 396842] {aka PTX1}, HMBS (hydroxymethylbilane synthase) [NCBI Gene 396581]
- **Diseases:** acute inflammation (MESH:D007249), acute illness (MESH:D000208), damage in (MESH:D020263), liver damage (MESH:D056486), death (MESH:D003643), toxicity (MESH:D064420), mitochondrial (MESH:D028361), Liver (MESH:D017093)
- **Chemicals:** AFP1 (MESH:C042410), silybin (MESH:D000077385), cholesterol (MESH:D002784), phenol (MESH:D019800), curcumin (MESH:D003474), sodium pentobarbital (MESH:D010424), triglyceride (MESH:D014280), SYBR Green I (MESH:C098022), Aflatoxin (MESH:D000348), hydroxycholesterol (MESH:D006888), H2O2 (MESH:D006861), aflatoxicol (MESH:C012170), NADPH (MESH:D009249), chloroform (MESH:D002725), 14-deoxy-12(R)-sulfo andrographolide (MESH:C487001), ROS (MESH:D017382), AFQ1 (MESH:C033759), AFB1 epoxide (-), epoxide (MESH:D004852), retinoid (MESH:D012176), beta-naphthoflavone (MESH:D019324), iron (MESH:D007501), AFM1 (MESH:D016607), monounsaturated fatty acids (MESH:D005229), vegetable oil (MESH:D010938), glutathione (MESH:D005978), lipid (MESH:D008055), fatty acid (MESH:D005227), oxysterol (MESH:D000072376), azaperone (MESH:D001376), Silymarin (MESH:D012838), nitrogen (MESH:D009584), arachidonic acid (MESH:D016718), guanine (MESH:D006147), AFB1 (MESH:D016604), Andrographolide (MESH:C030419), diterpenoid (MESH:D004224), benzanthracene (MESH:C030935)
- **Species:** Homo sapiens (human, species) [taxon 9606], Aspergillus (genus) [taxon 5052], Andrographis paniculata (species) [taxon 175694], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Rattus norvegicus (brown rat, species) [taxon 10116], Silybum marianum (blessed milkthistle, species) [taxon 92921], Bos taurus (bovine, species) [taxon 9913], Mus musculus (house mouse, species) [taxon 10090], Sus scrofa (pig, species) [taxon 9823], Anas platyrhynchos (duck, species) [taxon 8839], Gallus gallus (bantam, species) [taxon 9031], Curcuma longa (turmeric, species) [taxon 136217]
- **Mutations:** C - 24  C

## Full text

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## Figures

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## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12849138/full.md

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Source: https://tomesphere.com/paper/PMC12849138