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

被引:51
作者
Feng, Lin [1 ,2 ,3 ]
Li, Wen [1 ]
Liu, Yang [1 ,2 ,3 ]
Jiang, Wei-Dan [1 ,2 ,3 ]
Kuang, Sheng-Yao [4 ]
Wu, Pei [1 ,2 ,3 ]
Jiang, Jun [1 ,2 ,3 ]
Tang, Ling [4 ]
Tang, Wu-Neng [4 ]
Zhang, Yong-An [5 ]
Zhou, Xiao-Qiu [1 ,2 ,3 ]
机构
[1] Sichuan Agr Univ, Inst Anim Nutr, Chengdu 611130, Sichuan, Peoples R China
[2] Sichuan Agr Univ, Fish Nutr & Safety Prod Univ, Key Lab Sichuan Prov, Chengdu 611130, Sichuan, Peoples R China
[3] Sichuan Agr Univ, Key Lab Anim Dis Resistance Nutr, China Minist Educ, Chengdu 611130, Sichuan, Peoples R China
[4] Sichuan Acad Anim Sci, Inst Anim Nutr, Chengdu 610066, Peoples R China
[5] Chinese Acad Sci, Inst Hydrobiol, Wuhan 430072, Peoples R China
关键词
Phenylalanine; Gill; Tight junction; Signalling molecule; Immune; CARP CTENOPHARYNGODON-IDELLA; MESSENGER-RNA; MAMMALIAN TARGET; ANTIOXIDANT DEFENSES; GENE-TRANSCRIPTION; PROTEIN TRANSCRIPT; BARRIER HEALTH; JUVENILE JIAN; TNF-ALPHA; COPPER;
D O I
10.1016/j.fsi.2016.11.048
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
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(-1)) 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 down regulation 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 (Keap1 a) 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 down regulation of interleukin 10 (IL-10), transforming growth factor beta (TGF-beta) and inhibitor factor kappa B alpha (i kappa B alpha) and the upregulation of relative mRNA expression of interleukin 1 beta (IL-1 beta), interleukin 8 (IL-8), tumour necrosis factor-alpha (TNF-alpha) and nuclear transcription factor-kappa B p65 (NF-kappa B 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-kappa B p65, i kappa B alpha, TOR, Nrf2, Keap1 and apoptosis-related genes in the fish gills. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:185 / 196
页数:12
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