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苯丙氨酸通过Nrf2、TOR和NF-κB信号分子对ROS诱导的鱼类鳃氧化损伤、细胞凋亡和紧密连接损伤的保护作用。

Protective role of phenylalanine on the ROS-induced oxidative damage, apoptosis and tight junction damage via Nrf2, TOR and NF-κB signalling molecules in the gill of fish.

作者信息

Feng Lin, Li Wen, Liu Yang, Jiang Wei-Dan, Kuang Sheng-Yao, Wu Pei, Jiang Jun, Tang Ling, Tang Wu-Neng, Zhang Yong-An, Zhou Xiao-Qiu

机构信息

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

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

出版信息

Fish Shellfish Immunol. 2017 Jan;60:185-196. doi: 10.1016/j.fsi.2016.11.048. Epub 2016 Nov 23.

Abstract

This study explored the possible preventive effects of dietary phenylalanine (Phe) on antioxidant responses, apoptosis and tight junction protein transcription in the gills of young grass carp (Ctenopharyngodon idella). Fish were fed six different experimental diets containing graded levels of Phe (3.4-16.8 g kg) for 8 weeks. The results showed that Phe deficiency induced protein oxidation and lipid peroxidation by decreasing the glutathione content and the activities and mRNA levels of Cu/Zn superoxide dismutase (SOD1), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR) and glutathione-S-transferase (GST) in fish gill (P < 0.05). These results may be ascribed to the downregulation of NF-E2-related factor 2 (Nrf2), target of rapamycin (TOR) and ribosomal protein S6 kinase 1 (S6K1), and the upregulation of Kelch-like-ECH-associated protein 1 a (Keap1a) expression in grass carp gills (P < 0.05). Additionally, Phe deficiency induced DNA fragmentation via the up-regulation of Caspase 3, Caspase 8 and Caspase 9 mRNA expression (P < 0.05). These results may be ascribed to the improvement in reactive oxygen species (ROS) levels in the fish gills (P < 0.05). Furthermore, the results indicated that Phe deficiency decreased Claudin b, Claudin 3, Occludin and ZO-1 transcription and increased Claudin 15 expression in the fish gills (P < 0.05). These effects were partly due to the downregulation of interleukin 10 (IL-10), transforming growth factor β (TGF-β) and inhibitor factor κBα (iκBα) and the upregulation of relative mRNA expression of interleukin 1β (IL-1β), interleukin 8 (IL-8), tumour necrosis factor-α (TNF-α) and nuclear transcription factor-κB p65 (NF-κB p65) (P < 0.05). Taken together, the results showed that Phe deficiency impaired the structural integrity of fish gills by regulating the expression of tight junction proteins, cytokines, antioxidant enzymes, NF-κB p65, iκBα, TOR, Nrf2, Keap1 and apoptosis-related genes in the fish gills.

摘要

本研究探讨了日粮苯丙氨酸(Phe)对草鱼幼鱼鳃抗氧化反应、细胞凋亡和紧密连接蛋白转录的潜在预防作用。给鱼投喂六种不同的实验日粮,其Phe含量呈梯度变化(3.4 - 16.8 g/kg),持续8周。结果表明,Phe缺乏通过降低草鱼鳃中谷胱甘肽含量、铜/锌超氧化物歧化酶(SOD1)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPx)、谷胱甘肽还原酶(GR)和谷胱甘肽 - S - 转移酶(GST)的活性及mRNA水平,诱导了蛋白质氧化和脂质过氧化(P < 0.05)。这些结果可能归因于草鱼鳃中核因子E2相关因子2(Nrf2)、雷帕霉素靶蛋白(TOR)和核糖体蛋白S6激酶1(S6K1)的下调,以及kelch样ECH相关蛋白1a(Keap1a)表达的上调(P < 0.05)。此外,Phe缺乏通过上调半胱天冬酶3、半胱天冬酶8和半胱天冬酶9的mRNA表达诱导DNA片段化(P < 0.05)。这些结果可能归因于草鱼鳃中活性氧(ROS)水平的升高(P < 0.05)。此外,结果表明,Phe缺乏降低了鱼鳃中Claudin b、Claudin 3、闭合蛋白和紧密连接蛋白1(ZO - 1)的转录,并增加了Claudin 15的表达(P < 0.05)。这些影响部分归因于白细胞介素10(IL - 10)、转化生长因子β(TGF - β)和抑制因子κBα(iκBα)的下调,以及白细胞介素1β(IL - 1β)、白细胞介素8(IL - 8)、肿瘤坏死因子 - α(TNF - α)和核转录因子κB p65(NF - κB p65)相对mRNA表达的上调(P < 0.05)。综上所述,结果表明,Phe缺乏通过调节鱼鳃中紧密连接蛋白、细胞因子、抗氧化酶、NF - κB p65、iκBα、TOR、Nrf2、Keap1和凋亡相关基因的表达,损害了鱼鳃的结构完整性。

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