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    饲料维生素D3对不同密度拥挤应激下“中科五号”异育银鲫幼鱼抗氧化能力及铁死亡的影响

    VITAMIN D3 SUPPLEMENTATION ON ANTIOXIDANT CAPACITY AND FERROPTOSIS IN JUVENILE GIBEL CARP (CARASSIUS AURATUS GIBELIO VAR. CAS V) AT DIFFERENT STOCKING DENSITIES

    • 摘要: 在鱼类早期发育阶段, 高密度养殖引起的拥挤胁迫严重威胁鱼类健康。本研究旨在探究维生素D3(VD3)对缓解高密度养殖诱导的铁死亡的作用及其潜在分子机制, 以初始体重为(0.47±0.03)g/尾的“中科五号”异育银鲫(Carassius auratus gibelio var. CAS Ⅴ)幼鱼为研究对象, 采用双因素实验设计, 在两种养殖密度(低密度组L: 70尾/缸; 高密度组H: 210尾/缸)下, 分别投喂3种不同VD3添加水平(0组: 不添加; 1000 IU/kg组: 低剂量; 5000 IU/kg组: 高剂量)的实验饲料, 进行为期71 d的养殖实验。结果显示, 各组间生长指标未出现显著差异, 但高密度组肝脏谷丙转氨酶(GPT)活性显著降低, 而谷胱甘肽过氧化物酶4(GPx4)活性和还原型谷胱甘肽(GSH)含量出现代偿性的异常升高。此外, H0组肝脏中大量蓄积了脂质过氧化物(LPO)和游离铁(Fe2+)。而饲料中添加VD3显著降低了肝脏LPO和Fe2+含量, 有效缓解了上述铁死亡相关标志物的蓄积。透射电镜(TEM)观察显示, 高密度组肝细胞线粒体明显固缩且嵴消失, 呈现典型的铁死亡超微结构特征, 而VD3的干预显著改善了损伤程度。转录组学分析进一步表明, VD3处理组的差异表达基因显著富集于铁死亡、半胱氨酸与蛋氨酸代谢以及脂肪酸生物合成等通路。实时荧光定量PCR结果证实, VD3干预显著上调了关键抗氧化基因(nrf2gpx4aprdx6)的表达, 并下调了促铁死亡基因(acsl4a)的表达, 与转录组学表达趋势一致。综上表明, 高密度养殖诱发了异育银鲫幼鱼显著的肝脏铁死亡及代谢失调, 而在饲料中适量添加VD3(1000 IU/kg)能够有效缓解由拥挤胁迫产生的负面影响。

       

      Abstract: High-density crowding stress during the initial feeding stage poses severe challenges to fish health, promoting lipid peroxidation. This study aimed to assess the protective effects of vitamin D3 (VD3) against crowding stress and investigate its underlying mechanisms. A two-factor design was employed using juvenile gibel carp (Carassius auratus gibelio var. CAS Ⅴ)(0.47±0.03) g/fish for a 71-days feeding trial, three experimental diets with different VD3 concentrations VD0 IU/kg (no VD3), VD1000 IU/kg (low concentration), and VD5000 IU/kg (high concentration) were applied under two different rearing densities (L: 70 fish/tank, H: 210 fish/tank). Although macroscopic growth parameters showed no significant differences, hepatic biochemical and molecular profiles indicated a severe underlying metabolic burden. Specifically, at the metabolic level, hepatic GPT activity was significantly decreased under high density, while GPx4 activity and GSH content were abnormally elevated in a compensatory manner. Furthermore, the unsupplemented high-density group exhibited substantial accumulation of lipid hydroperoxide (LPO) and labile iron (Fe2+). Notably, dietary VD3 supplementation significantly reduced both hepatic LPO and Fe2+ contents, effectively attenuating these ferroptosis-related markers. Transmission electron microscopy (TEM) examination revealed significantly shrunken mitochondria and vanished cristae, indicating typical ferroptosis, which were remarkably mitigated by VD3 supplementation. Transcriptomic analysis further demonstrated that differentially expressed genes in the VD3-treated group were enriched in ferroptosis, cysteine and methionine metabolism, and fatty acid biosynthesis pathways. qPCR validation confirmed the significant upregulation of key antioxidant genes (nrf2, gpx4a, and prdx6) and the downregulation of the pro-ferroptosis gene (acsl4a) by VD3, aligning with transcriptomic trends. In conclusion, high-density rearing triggered pronounced hepatic ferroptosis and metabolic dysregulation in juvenile C. auratus gibelio, whereas dietary VD3 supplementation effectively ameliorated lipid peroxidation and restored mitochondrial ultrastructure. These findings offer mechanistic insights into nutritional interventions for alleviating crowding stress and inform early-life nutritional programming strategies in this species.

       

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