ORIGINAL PAPER
Naringenin and caffeic acid supplementation alleviates heat stress-induced liver damage by maintaining endoplasmic reticulum homeostasis in broilers
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1
An Kang University, School of Medicine, Department of Nursing, 725000 AnKang, China
2
Universiti Malaysia Sabah, Faculty of Medicine and Health Sciences, Department of Biomedical Sciences, 88400 Kota Kinabalu, Malaysia
3
Shaanxi Provincial University, Engineering Research Center for Development & Utilization of Qinba Traditional Chinese Medicine Resources, 725000 AnKang, China
4
Universiti Malaysia Sabah, Faculty of Medicine and Health Sciences, Department of Public Health Medicine, 88400 Kota Kinabalu, Malaysia
5
Universiti Malaysia Sabah, Faculty of Medicine and Health Sciences, Department of Surgery, 88400 Kota Kinabalu, Malaysia
6
Universiti Malaysia Sabah, Faculty of Medicine and Health Sciences, Borneo Medical and Health Research Centre, 88400 Kota Kinabalu, Malaysia
Publication date: 2025-06-10
Corresponding author
J. Chen
An Kang University, School of Medicine, Department of Nursing, 725000 AnKang, China
KEYWORDS
TOPICS
ABSTRACT
Heat stress (HS) is a major challenge to poultry production, with
significant implications for animal health and performance. This study explored
the protective role of naringenin (NAR) and caffeic acid (CA) on liver health in
HS-exposed broilers. First, an in vitro screening experiment was performed in
chicken embryo fibroblast (DF-1) cells. Our results demonstrated that NAR and
CA significantly reduced the expression of heat shock protein 70 (HSP70) and
heat shock transcription factor 1 (HSF1), while restoring superoxide dismutase
(SOD) activity and total antioxidant capacity (T-AOC) compared to the HS group
(P < 0.05). For the in vivo trial, broilers subjected to chronic HS (37 ± 2 °C for
6 weeks) were supplemented with 0.1% NAR, 0.1% CA, or their combination.
Dietary NAR and CA significantly improved broiler growth performance under
HS. Both compounds markedly reduced serum and liver levels of HSP70 and
HSF-1, while enhancing antioxidant capacity (SOD and T-AOC; P < 0.05).
Additionally, NAR and CA protected against HS-induced liver damage, as
evidenced by reduced serum aspartate transaminase and alanine transaminase
activity (P < 0.05). Mechanistically, NAR and CA preserved liver homeostasis
by modulating the endoplasmic reticulum stress response signalling involving
PKR-like ER kinase, activating transcription factor 4, activating transcription
factor 6, eukaryotic translation initiation factor 2 alpha, C/EBP homologous
protein, X-box-binding protein 1, and glucose-regulated protein 78.
CONFLICT OF INTEREST
The Authors declare that there is no conflict of
interest.
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