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黄芩苷抑制对氧磷酶毒性的坏死性凋亡和炎症;涉及鲤鱼鳃中的内质网应激和氧化应激。

Baicalin suppressed necroptosis and inflammation against chlorpyrifos toxicity; involving in ER stress and oxidative stress in carp gills.

机构信息

College of Animal Science and Technology, Northeast Agricultural University, Harbin, 150030, PR China.

College of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China.

出版信息

Fish Shellfish Immunol. 2023 Aug;139:108883. doi: 10.1016/j.fsi.2023.108883. Epub 2023 Jun 5.

Abstract

Chlorpyrifos (CPF) has caused large-scale pollution worldwide and posed a threat to non-target organisms. Baicalein (BAI) is a flavonoid extract with anti-oxidant and anti-inflammatory activities. The gills are the mucosal immune organ and the first physical barrier of fish. However, it is not clear whether BAI counteracts organophosphorus pesticide CPF exposure-caused gill damage. Therefore, we established the CPF exposure and BAI intervention models by adding 23.2 μg/L CPF in water and/or 0.15 g/kg BAI in feed for 30 days. The results showed that CPF exposure could cause gill histopathology lesions. Moreover, CPF exposure led to endoplasmic reticulum (ER) stress, caused oxidative stress and Nrf2 pathway activation, and triggered NF-κB-mediated inflammation reaction and necroptosis in carp gills. BAI adding effectively relieved the pathological changes, and lighten inflammation and necroptosis involving in the elF2α/ATF4 and ATF6 pathways through binding to GRP78 protein. Moreover, BAI could ease oxidative stress, but did not affect Nrf2 pathway in carp gills under CPF exposure. These results suggested that BAI feeding could alleviate necroptosis and inflammation against chlorpyrifos toxicity through elF2α/ATF4 and ATF6 axis. The results partially explained the poisoning effect of CPF, and showed BAI could be act as an antidote for organophosphorus pesticides.

摘要

毒死蜱(CPF)在全球范围内造成了大规模污染,对非目标生物构成了威胁。黄芩素(BAI)是一种具有抗氧化和抗炎活性的类黄酮提取物。鳃是鱼类的黏膜免疫器官和第一道物理屏障。然而,目前尚不清楚 BAI 是否能对抗有机磷农药 CPF 暴露引起的鳃损伤。因此,我们通过在水中添加 23.2μg/L CPF 和/或在饲料中添加 0.15g/kg BAI 建立了 CPF 暴露和 BAI 干预模型,持续 30 天。结果表明,CPF 暴露会导致鳃组织病理学损伤。此外,CPF 暴露导致内质网(ER)应激,引起氧化应激和 Nrf2 通路激活,并触发 NF-κB 介导的炎症反应和鲤鱼鳃细胞的坏死性凋亡。BAI 添加有效地缓解了病理变化,并通过与 GRP78 蛋白结合,减轻了涉及 elF2α/ATF4 和 ATF6 途径的炎症和坏死性凋亡。此外,BAI 可以缓解氧化应激,但在 CPF 暴露下对鲤鱼鳃中的 Nrf2 通路没有影响。这些结果表明,BAI 喂养可以通过 elF2α/ATF4 和 ATF6 轴缓解坏死性凋亡和炎症对毒死蜱毒性的影响。结果部分解释了 CPF 的中毒作用,并表明 BAI 可以作为有机磷农药的解毒剂。

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