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Effects of dietary melatonin on growth performance, nutrient composition, and lipid metabolism of Pacific white shrimp (Penaeus vannamei)

肝胰腺 生物 小虾 对虾 斑节对虾 六烯酸 脂质代谢 立陶宛 花生四烯酸 脂肪酸 生物化学 体重增加 动物科学 食品科学 内分泌学 内科学 多不饱和脂肪酸 生态学 体重 医学
作者
Yucong Ye,Siwen Li,Bihong Zhu,Ying Yang,Xinglin Du,Yiming Li,Yunlong Zhao
出处
期刊:Aquaculture [Elsevier BV]
卷期号:578: 740095-740095 被引量:1
标识
DOI:10.1016/j.aquaculture.2023.740095
摘要

The goal of this study was to investigate the effects of dietary melatonin (MT) on the growth physiology and lipid metabolism of Penaeus vannamei (P. vannamei). We prepared six experimental diets with varying MT levels (0 (control), 22.5, 41.2, 82.7, 165.1, 329.2 mg/kg) and fed six groups of shrimp with these diets for 2 months. The highest survival, body length growth rate, weight gain, and specific growth rates occurred in shrimp that were fed the diet containing 82.7 mg/kg MT, and the highest levels of docosahexaenoic acid (DHA) and arachidonic acid (ARA) were also found in this treatment group. Compared with the control group, there were no significant differences in moisture, crude protein, and ash contents in shrimp fed with MT, but the crude lipid content was significantly decreased in the high concentration MT supplemented group. Compared to the control group, shrimp fed 82.7 mg/kg MT had better morphology and structure of the hepatopancreas, whereas the hepatopancreas tissues were damaged in shrimp from the high dose MT groups. Analysis of lipid metabolism-related enzymes and genes in the hepatopancreas showed that dietary MT greatly decreased fatty acid synthase and acetyl-CoA carboxylase activities but increased carnitine palmitoyltransferase 1 activity. At the transcriptional level, dietary MT reduced hepatopancreas fat accumulation by upregulating lipid oxidation genes and downregulating lipid synthesis genes. A broken-line model revealed that the ideal MT concentration was in the range of 59.59–71.97 mg/kg. We found that MT supplementation improved P. vannamei growth performance, enhanced fatty acid β oxidation, and prevented fat deposition in the hepatopancreas.

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