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黄曲霉毒素 B1 通过 Keap1a/Nrf2/MLCK 信号通路和 NF-κB/TOR 信号通路破坏草鱼(Ctenopharyngodon idella)鳃的结构屏障和免疫屏障。

Aflatoxin B1 damaged structural barrier through Keap1a/Nrf2/ MLCK signaling pathways and immune barrier through NF-κB/ TOR signaling pathways in gill of grass carp (Ctenopharyngodon idella).

机构信息

Animal Nutrition Institute, Sichuan Agricultural University, Chengdu 611130, China.

Animal Nutrition Institute, Sichuan Agricultural University, Chengdu 611130, China; Fish Nutrition and Safety Production University Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu 611130, China; Laboratory of Animal Disease-Resistance Nutrition, Ministry of Education, Ministry of Agriculture and Rural Affairs, Key Laboratory of Sichuan Province, Sichuan 611130, China.

出版信息

Aquat Toxicol. 2023 Apr;257:106424. doi: 10.1016/j.aquatox.2023.106424. Epub 2023 Feb 10.

Abstract

Aquafeeds are susceptible to contamination caused by aflatoxin B1 (AFB1). The gill of fish is an important respiratory organ. However, few studies have investigated the effects of dietary AFB1 exposure on gill. This study aimed to discuss the effects of AFB1 on the structural and immune barrier of grass carp gill. Dietary AFB1 increased reactive oxygen species (ROS) levels, protein carbonyl (PC) and malondialdehyde (MDA) contents, which consequently caused oxidative damage. In contrast, dietary AFB1 decreased antioxidant enzymes activities, relative genes expression (except MnSOD) and the contents of glutathione (GSH) (P < 0.05), which are partly regulated by NF-E2-related factor 2 (Nrf2/Keap1a). Moreover, dietary AFB1 caused DNA fragmentation. The relative genes of apoptosis (except Bcl-2, McL-1 and IAP) were significantly upregulated (P < 0.05), and apoptosis was likely upregulated through p38 mitogen-activated protein kinase (p38MAPK). The relative expressions of genes associated with tight junction complexes (TJs) (except ZO-1 and claudin-12) were significantly decreased (P < 0.05), and TJs were likely regulated by myosin light chain kinase (MLCK). Overall, dietary AFB1 disrupted the structural barrier of gill. Furthermore, AFB1 increased gill sensitivity to F. columnare, increased Columnaris disease and decreased the production of antimicrobial substances (P < 0.05) in grass carp gill, and upregulated the expression of genes involved with pro-inflammatory factors (except TNF-α and IL-8) and the pro-inflammatory response partly attributed to the regulation by nuclear factor κB (NF-κB). Meanwhile, the anti-inflammatory factors were downregulated (P < 0.05) in grass carp gill after challenge with F. columnare, which was partly attributed to the target of rapamycin (TOR). These results suggested that AFB1 aggravated the disruption of the immune barrier of grass carp gill after being challenge with F. columnare. Finally, the upper limit of safety of AFB1 for grass carp, based on Columnaris disease, was 31.10 μg/kg diet.

摘要

水产饲料容易受到黄曲霉毒素 B1(AFB1)的污染。鱼类的鳃是重要的呼吸器官。然而,很少有研究探讨膳食 AFB1 暴露对鳃的影响。本研究旨在讨论 AFB1 对草鱼鳃结构和免疫屏障的影响。膳食 AFB1 增加了活性氧(ROS)水平、蛋白质羰基(PC)和丙二醛(MDA)含量,导致氧化损伤。相反,膳食 AFB1 降低了抗氧化酶活性、相对基因表达(MnSOD 除外)和谷胱甘肽(GSH)含量(P < 0.05),这部分受到核因子 E2 相关因子 2(Nrf2/Keap1a)的调节。此外,膳食 AFB1 导致 DNA 片段化。凋亡相关基因(除 Bcl-2、McL-1 和 IAP 外)显著上调(P < 0.05),凋亡可能通过丝裂原活化蛋白激酶 p38(p38MAPK)上调。与紧密连接复合物(TJs)相关的基因(除 ZO-1 和 claudin-12 外)的相对表达显著降低(P < 0.05),TJs 可能受肌球蛋白轻链激酶(MLCK)调节。总的来说,膳食 AFB1 破坏了鳃的结构屏障。此外,AFB1 增加了草鱼对柱状屈挠杆菌的易感性,增加了柱状屈挠杆菌病,降低了草鱼鳃中抗菌物质的产生(P < 0.05),并上调了参与促炎因子(除 TNF-α和 IL-8 外)和促炎反应的基因表达,部分归因于核因子 κB(NF-κB)的调节。同时,草鱼鳃中抗炎因子下调(P < 0.05),这部分归因于雷帕霉素靶蛋白(TOR)。这些结果表明,AFB1 加剧了草鱼在受到柱状屈挠杆菌挑战后对免疫屏障的破坏。最后,基于柱状屈挠杆菌病,草鱼 AFB1 的安全上限为 31.10μg/kg 饲料。

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