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    高脂饲料中添加L-肉碱对牛蛙生长性能、消化酶活性、抗氧化能力及脂代谢的影响

    L-carnitine supplementation in high-fat diets on growth performance, digestive enzyme activities, antioxidant capacity, and lipid metabolism in bullfrogs (Lithobates catesbeianus)

    • 摘要: 本研究旨在探讨高脂饲料中添加不同水平 L-肉碱对牛蛙(Lithobates catesbeianus)生长性能、消化酶活性、抗氧化能力及肝脏脂代谢相关基因表达的影响。选取初始均重约26.83 g的健康牛蛙234只, 随机分为6组, 分别投喂正常脂肪饲料(NFD组, 粗脂肪7.01%)、高脂饲料(HFD组, 粗脂肪10.56%)及高脂基础上添加0.075%、0.150%、0.225%、0.300% L-肉碱的饲料(HR1-HR4组), 养殖周期56d。结果显示, 与HFD组相比, HR1—HR3组牛蛙增重率、特定生长率和饲料效率显著提高(P<0.05), 其中HR1组上述指标显著高于NFD组(P<0.05), 其余添加组与NFD组无显著差异(P>0.05)。HR1—HR4组全体粗脂肪与NFD组无显著性差异, HR1—HR3组肌肉粗脂肪与NFD组无显著性差异(P>0.05)。HR1—HR4组血清总胆固醇含量相比于HFD组显著降低(P<0.05), 各添加组上述指标与NFD组无显著差异(P>0.05)。仅HR1组肠道胰蛋白酶活性、全体粗蛋白较HFD组显著提升(P<0.05); 各添加组肠道脂肪酶活性较HFD组显著降低(P<0.05), 上述消化酶指标与NFD组均无显著差异(P>0.05)。相比于HFD组, HR1—HR3组肝脏过氧化氢酶、超氧化物歧化酶活性显著提高, 丙二醛含量显著降低(P<0.05), 各添加组上述指标与NFD组无显著差异(P>0.05); 油红O染色显示HR1和HR2组肝脏脂肪沉积缓解效果较优。与HFD组相比, HR1—HR4组肝脏脂分解基因cpt1α表达显著上调, 脂合成基因fasacc1pparγ表达显著下调(P<0.05); HR3组与HR4组atgl表达量显著高于HFD组(P<0.05)。各添加组脂合成基因、HR1—HR3组cpt1α基因表达与NFD组无显著差异(P>0.05)。各组hsl基因无显著性差异(P>0.05)。综上, 高脂饲料中添加0.075% L-肉碱可通过调控肝脏脂代谢基因表达、改善肠道消化机能、提升抗氧化能力, 有效缓解高脂摄入导致的牛蛙生长受抑与脂肪过度沉积。

       

      Abstract: This study aimed to investigate the effects of dietary L-carnitine supplementation at different levels in high-fat diets on growth performance, digestive enzyme activities, serum biochemical indices, antioxidant capacity, and expression of hepatic lipid metabolism-related genes in bullfrogs (Lithobates catesbeianus). A total of 234healthy bullfrogs with an initial average body weight of approximately 26.83 g were randomly divided into 6 groups, which were fed a normal-fat diet (NFD group, crude lipid 7.01%), a high-fat diet (HFD group, crude lipid 10.56%), and high-fat diets supplemented with 0.075%, 0.150%, 0.225%, and 0.300% L-carnitine (HR1 to HR4 groups), respectively, with a feeding trial period of 56 days. The results showed that compared with the HFD group, weight gain rate, specific growth rate, and feed efficiency of bullfrogs in HR1-HR3 groups were significantly increased (P<0.05). Among them, the above indicators in the HR1 group were significantly higher than those in the NFD group (P<0.05), and there was no significant difference between the other supplemented groups and the NFD group (P>0.05). No significant difference in whole-body crude lipid of bullfrogs in HR1-HR4 groups compared with the NFD group. Furthermore, no significant difference in muscle crude lipid content of bullfrogs in HR1-HR3 groups compared with the NFD group (P>0.05). Bullfrogs in HR1-HR4 groups showed significantly decreased serum total cholesterol content compared with the HFD group (P<0.05); however, no significant differences in these parameters were observed between any of the L-carnitine-supplemented groups and the NFD group (P>0.05). Only the intestinal trypsin activity and whole-body crude protein content in the HR1 group were significantly higher than those in the HFD group (P<0.05); the intestinal lipase activity of all supplemented groups was significantly lower than that of the HFD group (P<0.05), and there was no significant difference in the above digestive enzyme indicators between all supplemented groups and the NFD group (P>0.05). Bullfrogs in HR1-HR3 groups showed significantly increased the activities of hepatic catalase and superoxide dismutase, and significantly decreased the malondialdehyde content (P<0.05), with no significant difference in the above indicators between all supplemented groups and the NFD group (P>0.05). Oil Red O staining showed that the HR1 and HR2 groups had the optimal alleviation effect on hepatic lipid deposition. Compared with the HFD group, bullfrogs in HR1-HR4 groups showed significantly up-regulated the expression of the hepatic lipolysis-related gene cpt1α, and significantly down-regulated the expression of the lipogenesis-related genes fas, acc1, and pparγ (P<0.05); the expression level of atgl in HR3 and HR4 groups was significantly higher than that in the HFD group (P<0.05). No significant differences were observed in the expression of lipogenic genes in all supplementation groups, as well as the cpt1α gene in HR1-HR3 groups, compared with the NFD group (P>0.05). Additionally, there were no significant differences in the expression of the hsl gene among all groups (P>0.05). In conclusion, 0.075% L-carnitine supplementation in high-fat diets can effectively alleviate the growth inhibition and excessive lipid deposition in bullfrogs caused by high-fat intake by regulating the expression of hepatic lipid metabolism-related genes, improving intestinal digestive function, and enhancing antioxidant capacity.

       

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