酶解鸡肝膏替代鱼粉对大口黑鲈生长性能、糖脂代谢及肌肉品质的影响

Effects of enzymatically hydrolyzed chicken liver paste replacing fish meal on growth performance, glycolipid metabolism and muscle quality of Micropterus salmoides

  • 摘要:
    目的 探究酶解鸡肝膏替代鱼粉对大口黑鲈生长性能、饲料利用、糖脂代谢及肌肉品质的调控效应,明确适宜替代比例。
    方法 以酶解鸡肝膏替代饲料中0%、5%、10%和15%的鱼粉,配制4种等氮(粗蛋白43%)等脂(粗脂肪15%)饲料,饲喂初始体重(14.03±0.96) g的大口黑鲈8周。
    结果 各实验组鱼末均重、增重率、特定生长率、蛋白质效率、肝体比、脏体比、全鱼营养成分及肌肉弹性、黏聚性和回复性均无显著差异。与鱼粉组相比,酶解鸡肝膏替代处理可提升鱼摄食、饲料利用与机体抗氧化水平,上调肌肉蛋白合成、肝脂分解及肝脏糖酵解相关基因表达,提高肌肉蛋白含量与肉质硬度、胶着性等质构指标;同时降低机体血糖、血脂、氧化损伤产物及肌肉脂肪沉积,抑制肝脏糖异生与脂肪合成关键基因转录。多数功能指标随替代比例升高呈先升后降规律,10% 替代组综合表现最优,肌肉粗蛋白、肉质咀嚼特性、抗氧化及脂解相关指标达到峰值;15% 替代仍可正向调控肌肉蛋白合成相关通路。
    结论 饲料中酶解鸡肝膏替代 15% 鱼粉不损伤大口黑鲈生长性能,且能够促进肌肉蛋白合成;10% 鱼粉替代为最优添加比例,可改善摄食效率、机体抗氧化能力、蛋白沉积与肌肉品质。

     

    Abstract: Micropterus salmoides is an economically important carnivorous freshwater fish in China relying heavily on fishmeal for balanced nutrition. Global fishmeal supply shortage and soaring prices greatly raise breeding costs and hinder sustainable largemouth bass culture. Enzymatically hydrolyzed chicken liver paste, a low-cost livestock by-product rich in peptides, amino acids and attractants, serves a promising fishmeal substitute, yet relevant aquatic research remains scarce. Carnivorous M. salmoides has weak hepatic carbohydrate and lipid regulation; inappropriate dietary protein sources easily cause hepatic steatosis and deteriorated fillet texture. Dietary protein sources regulate mTOR-mediated protein anabolism and hepatic lipid metabolism, jointly determining fish growth, antioxidant status and meat quality. Therefore, this trial partially replaced fishmeal with graded levels of enzymatically hydrolyzed chicken liver paste, and investigated its effects on growth performance, hepatic glucolipid metabolism and fillet quality to determine its optimal replacement ratio for largemouth bass feeds. The application effect of EMCLP replacing fish meal was evaluated based on growth performance, biochemical indices, nutrient metabolism and muscle quality. Four isonitrogenous (crude protein 43%) and isolipidic (crude fat 15%) experimental diets were formulated by replacing 0%, 5%, 10% and 15% of fish meal with EMCLP. Juvenile largemouth bass with an initial body weight of (14.03±0.96) g was fed for 8 weeks. No significant differences were observed in final body weight, weight gain rate, specific growth rate, protein efficiency ratio, hepatosomatic index, viscerosomatic index, whole-body proximate composition, or muscle texture parameters (springiness, cohesiveness, and resilience) among all dietary groups. Compared with the fish meal group, EMCLP substitution enhanced fish feed intake, feed utilization, and systemic antioxidant capacity, upregulated the expression of genes related to muscle protein synthesis (e.g., akt, mtor, s6k1, s6, and 4ebp1), hepatic lipolysis (e.g., pparα, cpt1, and aco1), and hepatic glycolysis (e.g., glut2, gk, pk, and hk), and increased muscle crude protein content and textural properties including hardness and gumminess. Concurrently, the substitution reduced plasma glucose, triglycerides, and oxidative damage products; decreased hepatic triglycerides, malondialdehyde, and cholesterol contents; lowered muscle fat deposition; and suppressed the transcription of key genes involved in hepatic gluconeogenesis (e.g., pepck and g6pase) and lipogenesis (e.g., acc1 and fas). Most functional parameters exhibited a quadratic response to increasing replacement levels, with the 10% replacement group achieving the optimal comprehensive performance, as evidenced by peak values in muscle crude protein, chewing-related texture attributes, antioxidant capacity, and lipolysis-related indicators. Notably, the 15% replacement group maintained positive regulatory effects on muscle protein synthesis-related pathways. Dietary replacement of fish meal with up to 15% EMCLP did not compromise the growth performance of largemouth bass and promoted muscle protein synthesis. The 10% replacement level represented the optimal inclusion rate, improving feed intake efficiency, systemic antioxidant capacity, protein deposition, and muscle quality.

     

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