饲料L-肉碱优化卵形鲳鲹幼鱼脂质稳态:促进肌肉脂肪沉积与肝脏脂肪分解的平衡策略

Dietary L-carnitine optimizes lipid homeostasis in juvenile Trachinotus ovatus: a balancing strategy for promoting muscle fat deposition and hepatic lipid catabolism

  • 摘要:
    目的 探究饲料中适宜L-肉碱水平添加对卵形鲳鲹幼鱼促进肌肉脂肪沉积与肝脏脂肪分解,实现跨组织的脂质稳态平衡,同时优化生长性能与抗氧化状态的调控作用。
    方法 本实验设置肉碱水平分别为0、200、400、600 和800 mg/kg的5组等氮等脂饲料(D1~D5),在网箱中进行8周养殖实验。
    结果 随饲料中L-肉碱水平升高,终体重(BW)、增重率(WG)和特定生长率(SGR)呈先上升后持平趋势,D2组达到最大值。在脂质代谢方面,随着L-肉碱添加量升高,肝脏粗脂肪含量下降脂质沉积减少,肌肉粗脂肪增加脂质沉积增多,肝脏各脂肪酸无显著影响,肝脏脂质代谢基因肉碱转移酶1(cpt1)、载脂蛋白b-100(apob-100)、肝型脂肪酸结合蛋白(l-fabp)和过氧化物酶体增殖物激活受体αppar-α)基因表达量随添加量升高而上调,在D2组有最大值,脂肪酸合成酶(fas)则逐渐下调,在D4组时最低。肌肉脂质代谢基因cpt1和ppar-α表达量D3-D5组显著低于D1和D2组。在D5组有最小值。在抗氧化指标方面,D1组血清总抗氧化能力最低,血清超氧化物歧化酶(SOD)随添加量升高而降低,丙二醛(MDA)随添加量升高而升高。肝脏硫氧还蛋白(trx1)和过氧化物还原酶(prx1)基因表达均在D3组时最低,热休克蛋白70(hsp70)在D4组有最大值。在血清生理生化指标方面,D2组高密度脂蛋白(HDL)显著高于D1和D5组,D4组总蛋白最低。
    结论 随着饲料L-肉碱水平添加,卵形鲳鲹幼鱼肌肉粗脂肪含量增加和肝脏粗脂含量减少,促进脂肪沉积和肝脏脂肪分解,在400 mg/kg添加水平有着最适生长性能,同时维持肝脏良好的脂质代谢能力和鱼体良好的抗氧化应激能力,研究结果补充L-肉碱对卵形鲳鲹幼鱼脂质调控方面的研究,为该物种制定均衡饮食和推进健康水产养殖实践提供重要见解。。

     

    Abstract: Given that functional additives have species-specific effects on lipid metabolism in fish muscles and livers, determining the appropriate addition amount is of great significance for a single species. This study aimed to investigate the regulatory effects of dietary L-carnitine supplementation on juvenile Trachinotus ovatus, focusing on promoting muscle fat deposition and hepatic lipid catabolism to achieve cross-tissue lipid homeostasis, while optimizing growth performance and antioxidant status.Five iso-nitrogenous and iso-lipidic diets (D1 to D5) were formulated with L-carnitine levels of 0, 200, 400, 600, and 800 mg/kg, respectively. An 8-week feeding trial was conducted in sea cages.As dietary L-carnitine levels increased, the final body weight (FBW), weight gain rate (WGR), and specific growth rate (SGR) showed an initial increase followed by stabilization, reaching their peak in the D2 group(P<0.05). In terms of lipid metabolism, increasing L-carnitine supplementation resulted in a decrease in hepatic crude fat content and lipid deposition, while muscle crude fat content and lipid deposition increased. No significant effect was observed on liver fatty acid composition (P>0.05). The expression levels of hepatic lipid metabolism-related genes-carnitine palmitoyltransferase 1 (cpt1), apolipoprotein B-100 (*apob-100*), liver-type fatty acid-binding protein (l-fabp), and peroxisome proliferator-activated receptor alpha (ppar-α)—increased with the supplementation level, peaking in group D2 before gradually declining in group D4(P<0.05). In muscle, the expression levels of cpt1 and ppar-α in groups D3 to D5 were significantly lower than those in groups D1 and D2(P<0.05), reaching the minimum in group D5. Regarding antioxidant indices, serum total antioxidant capacity was lowest in group D1(P<0.05). Serum superoxide dismutase (SOD) activity decreased with increasing L-carnitine levels(P<0.05), while malondialdehyde (MDA) levels increased(P<0.05) Hepatic gene expression of thioredoxin (trx1) and peroxiredoxin (prx1) was lowest in group D3(P<0.05), and heat shock protein 70 (hsp70) reached its highest level in group D4(P<0.05). For serum physiological and biochemical parameters, high-density lipoprotein (HDL) cholesterol was significantly higher in group D2 than in groups D1 and D5(P<0.05), and total protein was lowest in group D4(P<0.05).In summary, dietary L-carnitine supplementation increased muscle crude fat content and decreased hepatic crude fat content in juvenile T. ovatus, promoting muscle fat deposition and hepatic lipid catabolism. The optimal growth performance was achieved at the supplementation level of 400 mg/kg. This level also supported favorable hepatic lipid metabolism and systemic antioxidant capacity. These findings provide valuable scientific data on lipid regulation by L-carnitine in T. ovatus.

     

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