饲料添加虾青素对青海湖裸鲤响应碱度胁迫的影响

Effects of astaxanthin addition in feeds on the response to alkalinity stress of Gymnocypris przewalskii

  • 摘要: 目的 探究饲料添加虾青素调节青海湖裸鲤响应碱度胁迫的作用机制,为虾青素在青海湖裸鲤饲料中的应用提供理论依据。方法 选择900尾1日龄青海湖裸鲤幼鱼,随机分成5组,对照组(AS0)饲喂基础饲料,试验组饲料中分别添加25 mg/kg(AS25)、50 mg/kg(AS50)、100 mg/kg(AS100)和200 mg/kg(AS200)虾青素。试验结束后,探究饲料添加虾青素对青海湖裸鲤生长性能、抗氧化能力和免疫功能的影响。选择饲喂最适添加量虾青素组的青海湖裸鲤进行碱度胁迫试验,分析饲料添加虾青素对青海湖裸鲤响应碱度胁迫的影响。结果 饲料中添加50 mg/kg虾青素显著提高了青海湖裸鲤的特定生长率、增重率和肝体比(P<0.05,下同)。AS50组青海湖裸鲤血清总蛋白含量显著高于AS0、AS25和AS200组,白蛋白含量显著高于AS0组,谷胱甘肽过氧化物酶活性和谷胱甘肽还原酶活性高于AS0、AS25、AS100和AS200组,总超氧化物歧化酶活性和过氧化氢酶活性在AS100组最高。青海湖裸鲤肝脏中总蛋白和丙二醛含量及总超氧化物歧化酶、谷胱甘肽过氧化物酶和过氧化氢酶活性均在AS50组最高,谷胱甘肽还原酶活性在AS100组最高。与AS0组相比,AS50组白介素-1β、白介素-6、白介素-8水平和肿瘤坏死因子α水平显著降低,白介素-10和转化生长因子β水平显著升高。AS0L96 vs AS0C组中铁死亡信号通路关键基因acsl4bacsl1btfr1bgpx4a在AS0L96组显著下调表达。AS50L96 vs AS0L96组中类固醇生物合成信号通路关键基因hsd17b7在AS50L96组显著上调表达。结论 青海湖裸鲤饲料中适宜的虾青素添加量为50~100 mg/kg,尤其以50 mg/kg的添加量抗碱度胁迫效果最佳。虾青素能通过调控青海湖裸鲤肝脏代谢和免疫响应等信号通路应对碱度胁迫,其中acsl4bacsl1btfr1bgpx4ahsd17b7基因可能在青海湖裸鲤响应碱度胁迫中发挥重要作用。

     

    Abstract: Objective This study aimed to investigate the mechanism of astaxanthin addition in feeds on the response to alkalinity stress of naked carp (Gymnocypris przewalskii), and to provide a theoretical basis for application of astaxanthin in feed of the naked carp.Method Nine hundred one-day-old juveniles were randomly divided into five groups: the control group (AS0) was fed a basal diet; while the experimental groups received feeds added with astaxanthin at 25 mg/kg (AS25), 50 mg/kg (AS50), 100 mg/kg (AS100), and 200 mg/kg (AS200), respectively. Following the experiment, the effects of astaxanthin addition in feeds on growth performance, antioxidant capacity, and immune functions were investigated. The alkalinity stress test was conducted on a group of naked carp fed diets with the optimal astaxanthin addition to analyze the effects of astaxanthin addition in feeds on the response of naked carp to alkalinity stress.Result Adding 50 mg/kg astaxanthin in feeds significantly increased the specific growth rate, weight gain rate, and liver-to-body ratio of naked carp (P<0.05, the same below). The serum total protein content in the AS50 group was significantly higher than those in the AS0, AS25, and AS200 groups; the albumin content in the AS50 group was significantly higher than that in the AS0 group; the glutathione peroxidase and glutathione reductase activities in the AS50 group were higher than those in the AS0, AS25, AS100, and AS200 groups; the highest total superoxide dismutase and catalase activities were observed in the AS100 group. In livers of the naked carp, the highest total protein content, malondialdehyde content, total superoxide dismutase activity, glutathione peroxidase activity, and catalase activity were observed in the AS50 group, while the highest glutathione reductase activity was observed in the AS100 group. Compared with the AS0 group, the AS50 group showed significantly decreases in interleukin-1β, interleukin-6, interleukin-8, and tumor necrosis factor-α, whereas significantly increases in of interleukin-10 and transforming growth factor-β. In the group of AS0L96 vs AS0C, key genes in the ferroptosis signaling pathway (acsl4bacsl1btfr1b, and gpx4a) were significantly down-regulated in the AS0L96 group. In the group of AS50L96 vs AS0L96, the key gene hsd17b7 in the steroid biosynthesis signaling pathway was significantly up-regulated in the AS50L96 group.Conclusion The optimal astaxanthin addition in feeds of naked carp was 50-100 mg/kg, and addition at 50 mg/kg is the most effective for resisting alkalinity stress. Astaxanthin can regulate signaling pathways such as liver metabolism and immune response in naked carp to respond to alkalinity stress, and among them, acsl4bacsl1btfr1bgpx4a and hsd17b7 genes may play important roles in the response of naked carp to alkalinity stress.

     

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