Resveratrol alleviates inorganic arsenic-induced ferroptosis in chicken brain via activation of the Nrf2 signaling pathway

被引:0
|
作者
Pang, Shan [1 ]
Han, Biqi [1 ]
Wu, Pengfei [1 ]
Yang, Xu [1 ]
Liu, Yunfeng [1 ]
Li, Jiayi [1 ]
Lv, Zhanjun [1 ]
Zhang, Zhigang [1 ]
机构
[1] Northeast Agr Univ, Coll Vet Med, 600 Changjiang Rd, Harbin 150030, Peoples R China
基金
中国国家自然科学基金;
关键词
Resveratrol; Arsenic; Brain; Ferroptosis; Nrf2; INDUCED LUNG INJURY; DIETARY LUTEOLIN; INFLAMMATION; GROUNDWATER; APOPTOSIS; PROTECTS; EXPOSURE; ACID; MICE;
D O I
10.1016/j.pestbp.2024.105885
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inorganic arsenic (iAs) is a well-recognized environmental pollutant that induces severe brain injury in humans and animals. The antioxidant, anti-inflammatory, and anti-ferroptotic effects of resveratrol (Res) were demonstrated in multiple animal experiments. In order to investigate the protective effect of Res on iAs-induced chicken brain injury, the 40 chickens (19-d-old, female) brain injury model was established by oral administration of iAs (30 mg/L NaAsO2) for 6 weeks. All chickens had free access to both food and water during the experiment. The biochemical indices, hematoxylin-eosin staining, and related protein levels of oxidative stress, inflammation and ferroptosis were then determined. Our results indicated that Res (1000 mg/kg) alleviated the iAs-induced brain injury after 6 weeks of oral administration, primarily by reducing the interleukin-1 beta mRNA expression and nuclear factor kappa B and malondialdehyde level, and increasing the antioxidant enzyme activity and the mRNA expression of nuclear factor erythroid 2-related factor 2 (Nrf2). Taken together, our study demonstrates that Res effectively inhibits iAs-induced oxidative stress and ferroptosis by mediating the Nrf2 signaling pathway, thereby alleviating iAs-induced brain injury in chickens. This is the first time that the amelioration effects of Res on the iAs-induced brain have been investigated from multiple perspectives.
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页数:10
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