Itaconic acid regulates endoplasmic reticulum stress and apoptosis via SERCA2 to alleviate ovarian dysfunction in laying hens with fatty liver hemorrhage syndrome

  • J Nutr Biochem. 2026 May 21:157:110418. doi: 10.1016/j.jnutbio.2026.110418.
Jiayi Ding  1 ,  Chun Zeng  2 ,  Yang Hu  3 ,  Zhongtao Li  2 ,  Wenjing Pu  2 ,  Panpan Cao  2 ,  Xiaoquan Guo  2 ,  Huabin Cao  2 ,  Chenghong Xing  2 ,  Guoliang Hu  2 ,  Yu Zhuang  4
Affiliations
  • 1. Jiangxi Provincial Key Laboratory for Animal Health, Institute of Animal Population Health, College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, PR China; Dantu District Animal Epidemic Prevention and Control Center, Dantu District Agriculture and Rural Bureau, Zhenjiang, Jiangsu, PR China.
  • 2. Jiangxi Provincial Key Laboratory for Animal Health, Institute of Animal Population Health, College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, PR China.
  • 3. College of Computer and Information Engineering, Jiangxi Agricultural University, Nanchang, Jiangxi, PR China.
  • 4. Jiangxi Provincial Key Laboratory for Animal Health, Institute of Animal Population Health, College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, PR China. Electronic address: [email protected].
PMID: 42173262 DOI: 10.1016/j.jnutbio.2026.110418
Abstract

Fatty liver hemorrhage syndrome (FLHS), a common nutritional metabolic disorder, exerts a significant impact on poultry egg production due to its detrimental effect on reproductive performance, while the underlying mechanism involving the ovaries remains unclear. Itaconic acid (IA), a metabolite discovered in the fungus, has garnered significant attention in therapeutic applications. This study aims to elucidate the pathological changes in the ovaries of hens with FLHS and to identify IA as a potential therapeutic agent for improving ovarian dysfunction in poultry. In vivo, a validated model of FLHS in laying hens, induced by a high-energy low-protein diet, was established. IA supplementation improved egg production, egg quality, follicle number, and histological integrity of ovaries, while reducing serum and tissue markers of lipid peroxidation, CA2+ disorder, endoplasmic reticulum stress, and Apoptosis. In vitro, given the poor cell membrane permeability of IA, 4-octyl itaconate (4-OI), a cell-permeable derivative that undergoes rapid intracellular hydrolysis to yield IA, was applied to ovarian granulosa cells challenged with free fatty acids. IA played a role in the restoration of sarcoplasmic reticulum/endoplasmic reticulum CA2+-ATPase 2 (SERCA2) expression, mitigating endoplasmic reticulum stress and Apoptosis. Importantly, inhibition of SERCA2 with thapsigargin reversed the protective effects of IA, establishing SERCA2 as an essential mediator. These findings elucidated the mechanism by which IA alleviates FLHS-induced ovarian dysfunction in laying hens, particularly highlighting its ameliorative effect on follicular atresia caused by ovarian granulosa cell Apoptosis, suggesting that dietary supplementation with IA may offer a nutritional strategy to alleviate FLHS-induced follicular atresia, maintain egg production performance, and ensure a high-quality egg supply in laying hens.

Keywords
Apoptosis; Endoplasmic reticulum stress; Fatty liver hemorrhage syndrome; Itaconic acid; Ovarian; SERCA2.
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