Shi Lei, Feng Lin, Jiang Wei-Dan, Liu Yang, Jiang Jun, Wu Pei, Kuang Sheng-Yao, Tang Ling, Tang Wu-Neng, Zhang Yong-An, Zhou Xiao-Qiu
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; Key Laboratory for Animal Disease-Resistance Nutrition of China Ministry of Education, Sichuan Agricultural University, Chengdu 611130, China.
Fish Shellfish Immunol. 2016 Apr;51:405-419. doi: 10.1016/j.fsi.2016.02.029. Epub 2016 Mar 8.
This investigation used the same growth trial as the previous study, which showed that folic acid deficiency retarded growth in young grass carp (the percent weight gain of Groups 1-6 were 102.32 ± 3.41%, 137.25 ± 10.48%, 179.78 ± 3.95%, 164.33 ± 3.21%, 143.35 ± 8.12% and 115.28 ± 2.66%) [1]. In the present study, we investigated the effects of dietary folic acid on the immune response, antioxidant status and tight junctions in the intestine of young grass carp (Ctenopharyngodon idella). A total of 540 young grass carp were fed diets containing graded levels of folic acid at 0.10, 0.47, 1.03, 1.48, 1.88 and 3.12 mg kg(-1) diet for 8 weeks. The results indicated that acid phosphatase and lysozyme activities, and the complement component 3 content in the proximal intestine (PI), mid intestine (MI) and distal intestine (DI) were decreased with folic acid deficiency (0.1 mg kg(-1)) (P < 0.05). Folic acid deficiency (0.1 mg kg(-1)) up-regulated interleukin 1β, interleukin 8, tumor necrosis factor α, nuclear factor κB p65 (NF-κB p65), IκB kinase α (IKK-α), IKK-β and IKK-γ gene expression, meanwhile down-regulated interleukin 10, transforming growth factor β, IκB and target of rapamycin gene expression in the PI, MI and DI (P < 0.05). These data suggested that folic acid deficiency decreased fish intestinal innate immune function may be partly contributed to the regulation of NF-κB p65 pathway. Moreover, the activities and corresponding gene expression of glutathione content, Cu/Zn superoxide dismutase, catalase, glutathione peroxidase, glutathione s-transferases and glutathione reductase in fish intestine were depressed by deficient folic acid diet (0.1 mg kg(-1)) (P < 0.05). Furthermore, folic acid deficiency (0.1 mg kg(-1)) down-regulated NF-E2-related factor 2 (Nrf2) gene expression, up-regulated Kelch-like-ECH-associated protein 1a (Keap1a) and Keap1b gene expression in fish intestine (P < 0.05). These data indicated that deficient folic acid diet damaged fish intestinal antioxidant capacity partly by regulating Nrf2/Keap1 pathway. Additionally, folic acid deficiency (0.1 mg kg(-1)) down-regulated claudin-b, claudin-c, claudin-3, occludin and zonula occludens 1 gene expression; whereas folic acid deficiency (0.1 mg kg(-1)) up-regulated claudin-12, claudin-15, myosin light chain kinase (MLCK) and p38 mitogen activated protein kinase (p38 MAPK) gene expression in the PI, MI and DI (P < 0.05), suggesting that folic acid deficiency may damage fish intestinal tight junctions associated with the mediation of MLCK and p38 MAPK gene expression. In conclusion, folic acid deficiency (0.1 mg kg(-1)) impaired fish intestinal immunity, antioxidant capacity and tight junctions.
本研究采用了与之前研究相同的生长试验,之前的研究表明叶酸缺乏会阻碍草鱼幼鱼的生长(第1 - 6组的体重增加百分比分别为102.32 ± 3.41%、137.25 ± 10.48%、179.78 ± 3.95%、164.33 ± 3.21%、143.35 ± 8.12%和115.28 ± 2.66%)[1]。在本研究中,我们调查了饲料中叶酸对草鱼幼鱼(草鱼)肠道免疫反应、抗氧化状态和紧密连接的影响。总共540尾草鱼幼鱼被投喂含有0.10、0.47、1.03、1.48、1.88和3.12 mg kg(-1)不同叶酸水平的饲料,持续8周。结果表明,叶酸缺乏(0.1 mg kg(-1))会导致草鱼前肠(PI)、中肠(MI)和后肠(DI)中的酸性磷酸酶和溶菌酶活性以及补体成分3含量降低(P < 0.05)。叶酸缺乏(0.1 mg kg(-1))上调了白细胞介素1β、白细胞介素8、肿瘤坏死因子α、核因子κB p65(NF-κB p65)、IκB激酶α(IKK-α)、IKK-β和IKK-γ基因的表达,同时下调了PI、MI和DI中白细胞介素10、转化生长因子β、IκB和雷帕霉素靶基因的表达(P < 0.05)。这些数据表明,叶酸缺乏导致鱼类肠道先天免疫功能下降可能部分归因于NF-κB p65途径的调节。此外,叶酸缺乏饲料(含量为0.1 mg kg(-1))会降低鱼类肠道中谷胱甘肽含量、铜/锌超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶、谷胱甘肽S-转移酶和谷胱甘肽还原酶的活性以及相应基因的表达(P < 0.05)。此外,叶酸缺乏(0.1 mg kg(-1))下调了鱼类肠道中NF-E2相关因子2(Nrf2)基因的表达,上调了Kelch样-ECH相关蛋白1a(Keap1a)和Keap1b基因的表达(P < 0.05)。这些数据表明,叶酸缺乏饲料通过调节Nrf2/Keap1途径部分损害了鱼类肠道的抗氧化能力。另外,叶酸缺乏(0.1 mg kg(-1))下调了claudin-b、claudin-c、claudin-3、闭合蛋白和紧密连接蛋白1基因的表达;而叶酸缺乏(0.1 mg kg(-1))上调了PI、MI和DI中claudin-12、claudin-15、肌球蛋白轻链激酶(MLCK)和p38丝裂原活化蛋白激酶(p38 MAPK)基因的表达(P < 0.05),这表明叶酸缺乏可能通过MLCK和p38 MAPK基因表达的介导损害鱼类肠道的紧密连接。总之,叶酸缺乏(0.1 mg kg(-1))会损害鱼类肠道的免疫力、抗氧化能力和紧密连接。