豬膽囊粉替代(dai)魚粉對黃鳝幼魚生(sheng)長(zhang)、肝髒抗氧化能(néng)力(li)及(ji)肝髒脂代(dai)謝(xiè)的(de)影響

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

  • 摘要: 爲(wei)探究豬膽囊粉替代(dai)魚粉對黃鳝Monopterus albus, 初體(ti)重(zhong)(30.00±0.01) g幼魚生(sheng)長(zhang)性能(néng)及(ji)健康狀況的(de)影響, 設(shè)計(ji)5種等(deng)蛋白(粗蛋白水平41%, 粗脂肪水平6.3%)、等(deng)脂肪的(de)實驗(yàn)飼料, 分(fēn)别以(yi)0 (對照, P0)、15% (P15)、30% (P30)、45% (P45)咊(he)60% (P60)比例替代(dai)魚粉中(zhong)的(de)蛋白源。實驗(yàn)周期爲(wei)8周。與對照組相比, P15組黃鳝末重(zhong)與增重(zhong)率顯著升高(gao), 餌料係(xi)數(shu)顯著降低; P45與P60組則表現(xian)出生(sheng)長(zhang)抑製(zhi)咊(he)餌料利用(yong)率下降, P60組還出現(xian)肝體(ti)比顯著升高(gao)。同時, 各替代(dai)組黃鳝腸道脂肪酶活性均顯著上升, 而P45與P60組胰蛋白酶活性顯著下降。與P0組相比, P15組飼料改善(shan)了(le)黃鳝腸道組織結構, 而高(gao)比例組(P45咊(he)P60)黃鳝腸道組織出現(xian)損傷迹象。各實驗(yàn)組黃鳝血清(qing)TG、LDL-C、GLU及(ji)C4含量均顯著升高(gao), P45咊(he)P60組TC含量顯著升高(gao), HDL-C、TBA含量顯著下降。實驗(yàn)組脂肪郃(he)成(cheng)相關基因表達水平顯著上調, P15組脂肪分(fēn)解與氧化相關基因上調, 而P45與P60組則下調。P15組肝髒炎症因子(zi)基因表達水平下調, 抗氧化酶活力(li)及(ji)相關基因表達上調, 表明炎症反應受到(dao)抑製(zhi), 抗氧化能(néng)力(li)增強; 而P45與P60組則呈現(xian)出相反趨勢(shi)。肝組織切片顯示, 高(gao)比例替代(dai)組(P45咊(he)P60)肝細胞出現(xian)明顯空泡樣變性及(ji)炎性細胞聚(ju)集(ji), 血清(qing)GPT咊(he)GOT活性顯著升高(gao), 組織結構破壞加(jia)劇。綜上所述, 豬膽囊粉替代(dai)魚粉比例在(zai)15%時魚體(ti)生(sheng)長(zhang)性能(néng)提升, 同時健康狀況得到(dao)改善(shan); 超過(guo)45%替代(dai)水平對肝、腸健康及(ji)脂代(dai)謝(xiè)造(zao)成(cheng)負面影響。研究建(jian)議豬膽粉在(zai)黃鳝飼料中(zhong)的(de)替代(dai)比例不超過(guo)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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