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The present study was aimed at investigating the interactive effects of starvation and dietary lipid level in the previous feeding period on lipid-related composition of turbot. Turbot with an average initial body weight of 26 g were firstly fed diets with different lipid levels, namely, 8%, 12%, and 16%, for 9 weeks, and then subjected to starvation for 30 days. Each diet was fed to sextuplicate tanks of 35 fish in the feeding trial. Tissue samples were collected at the end of the feeding trial and at 10, 20, and 30 days after starvation. The results showed that 30-day starvation decreased the lipid content in the liver and the subcutaneous tissue around the fin (STF), but increased the lipid content in the muscle. A synergetic increase of muscle lipid by starvation and dietary lipid level was observed. Starvation mobilized different fatty acids among the three tissues, namely, MUFA (16:1n-7 and 18:1n-9) in the muscle, SFA (14:0 and 16:0), MUFA (16:1n-7, 18:1n-9 and 20:1n-9), and 18C-PUFA (18:2n-6 and 18:3n-3) in the liver, and unexpectedly n-3 PUFA (18:3n-3, EPA, and DHA) in the STF, respectively. The 30-day starvation decreased the muscle hardness and resilience, but affected other texture parameters in a starvation time-dependent manner. Up-regulation of expression of lipolytic genes by starvation occurred later in the STF than in the liver. Interactive effects of starvation and dietary lipid level were observed mainly on tissue fatty acid compositions. Results of this study suggested that combined manipulation of starvation time and dietary lipid level could be used as an effective means of fish quality regulation in terms of lipid/fatty acid-related composition., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Fatty acid-binding proteins (fabps) play important roles in lipid homeostasis. In the present study, 7 fabp isoforms, namely, fabp1, fabp2, fabp3, fabp4, fabp6, fabp7, and fabp10, in two marine teleosts, were characterized. In general, turbot and tiger puffer fabp genes showed high identity to their orthologs in other fish species and mammals, but tiger puffer Fabp6 shared the lowest identity to its known orthologs in zebrafish and human. The tissue distribution patterns of fabps were generally in accordance with their function features. However, tiger puffer fabps, in particular Fabp1, Fabp2, Fabp6 and Fabp7, may have functions distinct from other teleosts, as indicated by the phylogenetic tree and tissue distribution patterns. In both species, high dietary lipid levels downregulated the expression of fabp2, fabp3, fabp6, and fabp7a but tended to upregulate the fabp1 expression. Starvation downregulated the expression of most fabps in both fish species, but the downregulation of fabp expression in turbot was much more drastic and earlier compared to tiger puffer. Long-term (30-day) starvation increased the fabp7 expression in tiger puffer and tended to increase the fabp6 expression in turbot. Results of this study contribute to fish fabp physiology and its nutritional regulation. [ABSTRACT FROM AUTHOR]

A 56-day feeding trial was conducted in a flow-through seawater system to investigate the effects of lysophosphatidylcholine (LPC) on growth performance and lipid metabolism of turbot. Four experimental diets were prepared, differing only in the LPC supplementation, namely, 0 (LPC-0, control), 0.1 (LPC-0.1), 0.25 (LPC-0.25), and 0.5% (LPC-0.5) of dry matter. Each diet was randomly fed to triplicate tanks. LPC-0.1 and LPC-0.25 led to significantly higher weight gain than the control diet, and the highest weight gain was observed in LPC-0.1. Compared to the control group, the LPC-supplemented groups had higher survival and lower hepatosomatic index and viscerosomatic index. LPC-0.25 led to significantly lower contents of crude lipid and ash in whole fish. Dietary LPC supplementation led to a basic decrease in the lipid metabolism-related biochemical parameters in serum but had only very minor influence on the fatty acid composition in the liver and subcutaneous tissue around the fin (STF). High LPC levels upregulated the mRNA expression of BSAL and ApoEα in both the liver and STF. In conclusion, dietary LPC supplementation (0.1-0.25%) enhanced the growth, lowered the lipid accumulation in juvenile turbot, and significantly regulated the lipid metabolism. However, it seldom influenced the fatty acid composition. [ABSTRACT FROM AUTHOR]

A 12-week feeding trial was conducted to evaluate the effects of dietary fish oil (FO) replacement by beef tallow (BT) on the growth performance and body composition of juvenile turbot (average initial weight, 19.6 g). The control diet contained 6% added FO (of dry matter, Diet FO-C). Beef tallow was supplemented into Diet FO-C, replacing added FO at different levels, i.e., 25%, 50%, 75%, and 100%, formulating the other 4 experimental diets, designated as 25BT, 50BT, 75BT, and 100BT, respectively. The feeding trial was conducted in a flow-through seawater system. Each diet was randomly fed to triplicate tanks (30 fish in each tank). The results showed that a cubic regression relationship was observed between weight gain and dietary FO replacement level. Although total FO replacement by BT significantly reduced the growth of juvenile turbot, no significant difference was observed between FO-C and 75BT. Diet BT decreased the whole-body crude lipid content but increased the whole-body moisture and ash contents. Dietary BT regulated the proximate composition of fish tissues in a dose dependent manner. High dietary BT levels did not reduce the n-3 long-chain polyunsaturated fatty acid content (% total fatty acid) in the muscle. Partial FO replacement (25 and 50%) by BT even significantly increased the muscle DHA content. The fatty acid composition of the liver, subcutaneous adipose tissue around the fin, and intestine generally reflected those of the diets. No significant difference was observed in muscle and liver mitochondrial DNA copy number among groups, indicating the similar general energy supply status. Dietary BT significantly reduced the concentration of triacylglycerol, cholesterol and malondialdehyde in the serum. The volatile flavor compound in muscle was analyzed with gas chromatography-ion migration spectrometry (GC-IMS). Dietary BT resulted in lower number and abundance of flavor aldehydes and alcohols in the muscle. In conclusion, beef tallow can replace 75% added fish oil (appr. 45% of total fish oil including the residual fish oil in fishmeal) in the diets of turbot, without reducing fish growth. Dietary beef tallow significantly affected the body composition and volatile flavor compound composition in the muscle. • Beef tallow can replace 75% added fish oil in turbot diets. • Partial fish oil replacement by beef tallow increased the muscle DHA content. • Dietary beef tallow resulted in lower abundance of flavor aldehydes and alcohols. • Dietary beef tallow decreased the whole-body crude lipid content. [ABSTRACT FROM AUTHOR]