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砷通过 PANoptosis 途径诱导鸡肝毒性。

Arsenic induces hepatotoxicity in chickens via PANoptosis pathway.

机构信息

College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, China.

College of Life Science, Yantai University, Yantai City 264005, Shandong Province, China.

出版信息

Pestic Biochem Physiol. 2024 Sep;204:106064. doi: 10.1016/j.pestbp.2024.106064. Epub 2024 Jul 30.

Abstract

Environmental pollution caused by arsenic or its compounds is called arsenic pollution. Arsenic pollution mainly comes from people's mining and smelting of arsenic compounds. In addition, the widespread use of arsenic compounds, such as the use and production of arsenic-containing pesticides, is also a source of arsenic contamination. Arsenic contamination leads to an increased risk of arsenic exposure, and the multi-organ toxicity induced by arsenic exposure is a global health problem. As a non-mammalian vertebrate with high nutrient levels, chickens readily absorb and accumulate arsenic from their food. Relevant studies have shown that arsenic exposure induces hepatotoxicity in chickens, and there has been a steady stream of research into the specific mechanisms involved. PANoptosis, a newly discovered and unique mode of programmed cell death (PCD) characterized by both apoptosis, cellular pyroptosis, and necroptosis. There are no studies to indicate whether chicken liver toxicity due to arsenic is associated with PANoptosis. Therefore, we established chicken animal models and chicken primary hepatocyte models exposed to different arsenic concentrations to dissect the role and mechanism of PANoptosis in arsenic exposure-induced hepatotoxicity in chickens. Our histopathological results showed that arsenic treatment caused dose-dependent damage to chicken liver structure. Meanwhile, different doses of arsenic treatment groups caused significant up-regulation of the protein level of ZBP1, a key factor of PANoptosis. And then consequently triggered the abnormal gene and protein expression levels of apoptosis-associated factors (Caspase-8, Caspase-7, Caspase-3), cellular pyroptosis-associated factors (NLRP3, ASC, GSDMD) and necroptosis-associated factors (RIPK1, RIPK3, MLKL). In conclusion, our study revealed that PANoptosis is involved in arsenic-induced chicken hepatotoxicity. Our findings provide a new perspective on the pathogenesis of arsenic exposure-induced hepatotoxicity in chickens.

摘要

环境污染是由砷或其化合物引起的,被称为砷污染。砷污染主要来自人们对砷化合物的开采和冶炼。此外,砷化合物的广泛使用,如含砷农药的使用和生产,也是砷污染的来源。砷污染导致砷暴露的风险增加,砷暴露引起的多器官毒性是一个全球性的健康问题。鸡作为一种营养水平较高的非哺乳动物,很容易从食物中吸收和积累砷。相关研究表明,砷暴露会导致鸡的肝毒性,并且有源源不断的研究探讨其具体涉及的机制。PANoptosis 是一种新发现的、独特的程序性细胞死亡(PCD)方式,具有凋亡、细胞焦亡和坏死性凋亡的特征。目前尚无研究表明,砷引起的鸡肝毒性是否与 PANoptosis 有关。因此,我们建立了暴露于不同砷浓度的鸡动物模型和鸡原代肝细胞模型,以剖析 PANoptosis 在砷暴露诱导鸡肝毒性中的作用和机制。我们的组织病理学结果表明,砷处理导致鸡肝结构呈剂量依赖性损伤。同时,不同剂量的砷处理组导致 PANoptosis 的关键因子 ZBP1 的蛋白水平显著上调。进而导致凋亡相关因子(Caspase-8、Caspase-7、Caspase-3)、细胞焦亡相关因子(NLRP3、ASC、GSDMD)和坏死性凋亡相关因子(RIPK1、RIPK3、MLKL)的异常基因和蛋白表达水平。总之,我们的研究表明,PANoptosis 参与了砷诱导的鸡肝毒性。我们的研究结果为砷暴露诱导鸡肝毒性的发病机制提供了新的视角。

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