猪胆囊粉替代鱼粉对黄鳝幼鱼生长、肝脏抗氧化能力及肝脏脂代谢的影响

REPLACING FISH MEAL WITH PORCINE GALLBLADDER MEAL ON GROWTH, HEPATIC ANTIOXIDANT CAPACITY, AND LIPID METABOLISM IN JUVENILE RICE FIELD EEL (MONOPTERUS ALBUS)

  • 摘要: 为探究猪胆囊粉猪胆囊粉替代鱼粉对黄鳝Monopterus albus, 初体重(30.00±0.01) g幼鱼生长性能及健康状况的影响, 设计5种等蛋白(粗蛋白水平41%, 粗脂肪水平6.3%)、等脂肪的实验饲料, 分别以0 (对照, P0)、15% (P15)、30% (P30)、45% (P45)和60% (P60)比例替代鱼粉中的蛋白源。实验周期为8周。与对照组相比, P15组黄鳝末重与增重率显著升高, 饵料系数显著降低; P45与P60组则表现出生长抑制和饵料利用率下降, P60组还出现肝体比显著升高。同时, 各替代组黄鳝肠道脂肪酶活性均显著上升, 而P45与P60组胰蛋白酶活性显著下降。与P0组相比, P15组饲料改善了黄鳝肠道组织结构, 而高比例组(P45和P60)黄鳝肠道组织出现损伤迹象。各实验组黄鳝血清TG、LDL-C、GLU及C4含量均显著升高, P45和P60组TC含量显著升高, HDL-C、TBA含量显著下降。实验组脂肪合成相关基因表达水平显著上调, P15组脂肪分解与氧化相关基因上调, 而P45与P60组则下调。P15组肝脏炎症因子基因表达水平下调, 抗氧化酶活力及相关基因表达上调, 表明炎症反应受到抑制, 抗氧化能力增强; 而P45与P60组则呈现出相反趋势。肝组织切片显示, 高比例替代组(P45和P60)肝细胞出现明显空泡样变性及炎性细胞聚集, 血清GPT、GOT活性显著升高, 组织结构破坏加剧。综上所述, 猪胆囊粉替代鱼粉比例在15%时鱼体生长性能提升, 同时健康状况得到改善; 超过≥45%替代水平对肝、肠健康及脂代谢造成负面影响。研究建议猪胆粉在黄鳝饲料中的替代比例不超过30%。

     

    Abstract: To evaluate the effects of replacing fish meal with porcine gallbladder meal on the growth performance and health status in juvenile rice field eel Monopterus albus, initial body weight: (30.00 ± 0.01) g, five isonitrogenous and isolipidic experimental diets were formulated with 0 (control, P0), 15% (P15), 30% (P30), 45% (P45), and 60% (P60) of fish meal protein replaced by porcine gallbladder meal. The feeding trial lasted for 8 weeks. Compared to the control, the P15 group showed significantly higher final body weight and weight gain rate, along with a lower feed conversion ratio. In contrast, the P45 and P60 groups exhibited growth suppression and reduced feed efficiency, with the P60 group also showing a significantly increased hepatosomatic index. Intestinal lipase activity was significantly elevated in all replacement groups, while trypsin activity decreased significantly in P45 and P60. Histological examination revealed improved intestinal structure in the P15, whereas structural damage was observed in the P45 and P60. Serum biochemical analysis showed significantly increased levels of TG, LDL-C, GLU, and C4 in all experimental groups. TC levels increased significantly in P45 and P60, while HDL-C and TBA levels significantly decreased. Genes related to lipid synthesis were upregulated across all experimental groups; lipid decomposition and oxidation-related genes were upregulated in P15 but downregulated in P45 and P60. In P15, hepatic inflammatory cytokine expression was downregulated, and antioxidant enzyme activities and related gene expression were upregulated, indicating suppressed inflammation and enhanced antioxidant capacity. Conversely, P45 and P60 exhibited increased expression of inflammatory genes and impaired antioxidant responses. Liver histology revealed pronounced vacuolar degeneration and inflammatory cell infiltration in the high-replacement groups (P45 and P60), along with significantly elevated serum GPT and GOT levels and aggravated structural damage. In conclusion, at a replacement level of 15%, porcine gallbladder powder effectively improved growth performance and overall health status in juvenile M. albus, while high replacement levels (≥45%) impair hepatic and intestinal health and disturb lipid metabolism. It is recommended that porcine gallbladder powder substitution not exceed 30% in M. albus diets.

     

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