# Plant essential oil supplementation promotes growth and attenuates lipopolysaccharide (LPS)-induced acute liver injury through SIRT1/PGC-1α signaling pathway in nursery pigs

**Authors:** Yu Niu, Xinru Song, Yiying Chen, Yiting Xu, Yiru Chen, Qingzhou Lin, Jintian He, Jinsong Liu, Ruiqiang Zhang, Caimei Yang

PMC · DOI: 10.5713/ab.25.0066 · 2025-06-04

## TL;DR

Adding plant essential oils to piglet diets improves growth and reduces liver damage caused by inflammation, with coated oils being more effective.

## Contribution

Shows that plant essential oils, especially coated ones, reduce liver inflammation in pigs via the SIRT1/PGC-1α pathway.

## Key findings

- PEO and CEO improved growth and feed efficiency in LPS-challenged piglets.
- CEO had stronger antioxidant effects than PEO, increasing IgA, IgM, and antioxidant enzymes.
- Both PEO and CEO activated the SIRT1/PGC-1α pathway to reduce liver oxidative damage.

## Abstract

This study aimed to evaluate whether dietary supplementation with plant essential oil (PEO) and coated plant essential oil (CEO) could promote growth and alleviate liver oxidative damage in nursery piglets challenged with lipopolysaccharide (LPS) by modulating mitochondrial function in the liver.

Twenty-four 21-day-old piglets were randomly assigned to four groups, with six replicates per group. The CON and LPS groups received a basal diet, while the LPS+PEO and LPS+CEO groups were received the basal diet supplemented with 500 mg/kg of PEO and 500 mg/kg of CEO, respectively. The experimental period lasted for 28 days. On day 49, piglets in the LPS, LPS+PEO, and LPS+CEO groups were injected intraperitoneally with LPS at a dose of 100 μg/kg body weight, while those in the CON group received an equal volume of saline. All piglets were weighed and euthanized four hours after the LPS or saline injection. Blood and liver samples were collected for further analysis.

Piglets in the LPS+PEO and LPS+CEO groups showed higher (p<0.05) average daily gain and better feed conversion ratio, and increased mRNA expressions of liver HO-1, NQO1 and Trx2 compared to the LPS and CON groups. Diet supplemented with PEO and CEO increased (p<0.05) the contents of immunoglobulin A (IgA), immunoglobulin G and immunoglobulin M (IgM), and the protein expressions of SIRT1 and PGC-1α in the liver of LPS-induced nursery piglets. Furthermore, piglets in the LPS+CEO group exhibited higher (p<0.05) levels of IgA, IgM, total antioxidant capacity, and the mRNA expressions of SOD2 and Trx2 in the liver than those of the LPS+PEO group.

Dietary supplementation with PEO or CEO improved growth performance in nursery piglets and alleviated LPS-induced liver oxidative damage in nursery piglets through activation of the SIRT1/PGC-1α signaling pathway. In addition, CEO supplementation demonstrated a more pronounced antioxidant effect than PEO.

## Linked entities

- **Genes:** SIRT1 (sirtuin 1) [NCBI Gene 23411], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891], HMOX1 (heme oxygenase 1) [NCBI Gene 3162], NQO1 (NAD(P)H quinone dehydrogenase 1) [NCBI Gene 1728], KMT2B (lysine methyltransferase 2B) [NCBI Gene 9757], SOD2 (superoxide dismutase 2) [NCBI Gene 6648]
- **Chemicals:** PEO (PubChem CID 784), CEO (PubChem CID 446820), IgA (PubChem CID 76900), IgM (PubChem CID 71581418)
- **Species:** Sus scrofa (taxon 9823)

## Full-text entities

- **Genes:** NQO1 (NAD(P)H quinone dehydrogenase 1) [NCBI Gene 100286873] {aka NADPH-d}, SIRT1 (sirtuin 1) [NCBI Gene 751859], SOD2 (superoxide dismutase 2) [NCBI Gene 100154319], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 397013] {aka PGC1, PGC1A, PPARGC-1, PPARGC1}, HMOX1 (heme oxygenase 1) [NCBI Gene 445512] {aka HSP32}
- **Diseases:** liver oxidative damage (MESH:D008107), acute liver injury (MESH:D017114)
- **Chemicals:** LPS (MESH:D008070), CEO (-)
- **Species:** Sus scrofa (pig, species) [taxon 9823]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12580957/full.md

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Source: https://tomesphere.com/paper/PMC12580957