# Eucalyptus globulus oil supplementation improves growth performance by regulating serum biochemistry, antioxidant, intestinal health, and lung health of broilers from 1 to 21 days of age

**Authors:** Zhenzhen Ji, Zhiqiang Miao, Yuanyang Dong, Miaomiao Han, Chenxuan Huang, Jianhui Li

PMC · DOI: 10.3389/fvets.2026.1798261 · Frontiers in Veterinary Science · 2026-03-17

## TL;DR

Eucalyptus globulus oil improves broiler growth and health by enhancing antioxidant activity, intestinal function, and lung immunity in young chickens.

## Contribution

This study demonstrates the novel use of Eucalyptus globulus oil as a feed supplement that positively affects multiple physiological systems in broiler chickens.

## Key findings

- EGO supplementation increased average daily gain and decreased feed-to-gain ratio in broilers.
- EGO enhanced antioxidant capacity and reduced oxidative stress markers in serum.
- EGO modulated intestinal and lung immune responses by regulating cytokines and tight junction proteins.

## Abstract

Eucalyptus globulus oil (EGO) is distinguished by its elevated 1,8-cineole content and is gaining attention as a natural feed additive due to its multifunctional bioactivities. However, the specific impacts of EGO on broiler physiology, including serum biochemical parameters and organ barrier functions, are not yet fully understood. The objective of this research was to ascertain the impact of EGO on the growth of broiler chickens. This investigation encompassed various parameters, including serum biochemistry, antioxidant capacity, intestinal and lung immunological function, and barrier function aspects.

A total of 288 one-day-old male Cobb broilers with similar weight (45.18 ± 1.01 g) were randomly divided into four groups of six replicates of 12 birds each. The control group (CON) was fed a basal diet, while the other three groups received a basal diet supplemented with 100, 200, or 300 mg/kg of EGO. The trial lasted 21 days. Performance indices, including average daily gain (ADG), average daily feed intake (ADFI), and feed-to-gain ratio (F/G), were evaluated at 7, 14, and 21 days of age. One bird per replicate was euthanized to collect blood, immune organ, lung, and jejunal tissue samples for further analysis at 21 days of age.

This supplementation increased ADG by 3.90% and decreased F/G by 3.97% (p < 0.05). It was evident that both ADG and F/G demonstrated a quadratic response to elevated EGO levels (p < 0.05). Serum analysis revealed linear and quadratic increases in alkaline phosphatase (ALP) and creatinine (Cr) levels with higher EGO doses (p < 0.05), while lysozyme (LZM) activity increased linearly (p < 0.05). The antioxidant capacity was enhanced, showing linear and quadratic improvements in superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities, and a reduction in malondialdehyde (MDA) (p < 0.05). In the jejunum, EGO was observed to down-regulate pro-inflammatory cytokines interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), and interferon-γ (IFN-γ), and up-regulate the anti-inflammatory cytokine interleukin-10 (IL-10) (p < 0.05). Concurrently, EGO increased the expression of tight junction proteins occludin (OCLN), claudin-1 (CLDN1), tight junction protein 1 (TJP1), and mucin 2 (MUC2) (p < 0.05). In contrast, EGO has been demonstrated to up-regulate avian beta-defensin 5 (AvBD5), IFN-γ, and IL-10 in lung tissue (p < 0.05). Furthermore, EGO has been shown to enhance CLDN1 and TJP1 expression (p < 0.05), while significantly reducing OCLN levels (p < 0.05).

These findings suggest that, given growth performance, safety, and efficacy, an additive dosage of 200 mg/kg is recommended.

## Linked entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553], TNF (tumor necrosis factor) [NCBI Gene 7124], IFNG (interferon gamma) [NCBI Gene 3458], IL10 (interleukin 10) [NCBI Gene 3586], OCLN (occludin) [NCBI Gene 100506658], CLDN1 (claudin 1) [NCBI Gene 9076], TJP1 (tight junction protein 1) [NCBI Gene 7082], MUC2 (mucin 2, oligomeric mucus/gel-forming) [NCBI Gene 4583], AvBD5 (avian beta-defensin 5) [NCBI Gene 414340]
- **Proteins:** GPX2 (glutathione peroxidase 2), si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3), CLDN7 (claudin 7), MUC2 (mucin 2, oligomeric mucus/gel-forming)
- **Chemicals:** 1,8-cineole (PubChem CID 2758)

## Full-text entities

- **Genes:** INFG (interferon gamma) [NCBI Gene 396054] {aka IFNG}, CLDN1 (claudin 1) [NCBI Gene 424910], TJP1 (tight junction protein 1) [NCBI Gene 415388], IL10 (interleukin 10) [NCBI Gene 428264] {aka IL-10, interleukin-10}, OCLN (occludin) [NCBI Gene 396026], LITAF (lipopolysaccharide induced TNF factor) [NCBI Gene 374125] {aka TNF-alpha}, IL1B (interleukin 1, beta) [NCBI Gene 395196] {aka IL-1BETA, IL1beta}, MUC2 (mucin 2, oligomeric mucus/gel-forming) [NCBI Gene 423101] {aka MUC5AC, mucin, mucin2}
- **Diseases:** inflammatory (MESH:D007249)
- **Chemicals:** EGO (MESH:D000078122), 1,8-cineole (MESH:D000077591), Cr (MESH:D003404), MDA (MESH:D008315)
- **Species:** Gallus gallus (bantam, species) [taxon 9031]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13035509/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC13035509/full.md

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Source: https://tomesphere.com/paper/PMC13035509