Effects of dietary l-carnitine were studied in juvenile black sea bream (Sparus macrocephalus). The semipurified basal diet [crude protein 450 g kg⁻¹ dry matter (DM); crude lipid 126 g kg⁻¹ DM] was formulated to choose white fishmeal as the protein source and fish oil plus corn oil (1 : 1) as the lipid source. Six diets (control + diets 1–5) containing 0.1, 0.12, 0.16, 0.24, 0.39 and 1.1 g of l-carnitine kg⁻¹ diet were fed to triplicate groups of black sea bream (initial weight 13.10 ± 0.05 g) for 8 weeks. At the end of the feeding trial, growth performance, body composition and antioxidant status were determined. The results showed that relative growth rate (RGR) was significantly improved by the elevation of dietary l-carnitine level from 0.1 to 0.24 g kg⁻¹, but decreased with further increment (P < 0.05). Lipid content decreased significantly (P < 0.05) in the dorsal muscle whereas increased (P < 0.05) in the liver with the addition of dietary l-carnitine. Dietary l-carnitine supplements elevated enzymatic antioxidants (superoxide dismutase, SOD; catalase, CAT; glutathione-S-transferase, GST) activities (P < 0.05) yet decreased the content of non-enzymatic factor, total sulphydryl groups (TSH) (P < 0.05). In summary, the optimum dietary l-carnitine level was 0.284 g kg⁻¹ diet by second-polynomial regression analysis based on RGR (y = −647.4x² +367.97x + 234.55; R² = 0.977, x = dietary l-carnitine levels, y = RGR), and dietary l-carnitine addition within the levels adopted in our study could depress lipid peroxidation in tissues of juvenile black sea bream.

An 8-week feeding trial was conducted to determine the effects of dietary methionine level on juvenile black sea bream Sparus macrocephalus. Fish (initial body weight: 14.21 ± 0.24 g) were reared in eighteen 350-L indoors flow-through circular fibreglass tanks (20 fish per tank). Isoenergetic and isonitrogenous diets contained six levels of L-methionine ranging from 7.5 to 23.5 g kg⁻¹ of dry diet in 3.0 g kg⁻¹ increments at a constant dietary cystine level of 3.1 g kg⁻¹. Growth performance and feed utilization were significantly influenced by dietary methionine levels (P < 0.05). Maximum weight gain (WG), specific growth rate (SGR), feed efficiency ratio, protein efficiency ratio and protein productive value (PPV) occurred at 17.2 g methionine kg⁻¹ diet, beyond which they showed declining tendency. Protein contents in whole fish body and dorsal muscle were positively correlated with dietary methionine level, while muscle lipid content was negatively correlated with it. Apparent digestibility coefficients (ADCs) of dietary nutrients were significantly affected by dietary treatments except for ADCs of crude lipid. Fish fed the grade level of methionine demonstrated a significant improvement in whole-body methionine content, total essential amino acids (∑EAA), total non-essential amino acids (∑NEAAs) and ∑EAA/∑NEAA ratio (P < 0.05). Regarding serum characteristics, significant differences were observed in total cholesterol, glucose and free methionine concentration (P > 0.05), while total protein level and triacylglycerol concentration kept relatively constant among treatments (P < 0.05). Analysis of dose response with second-order polynomial regression on the basis of either SGR or PPV, the optimum dietary methionine requirements of juvenile black sea bream were estimated to be 17.1 g kg⁻¹ of diet (45.0 g kg⁻¹ methionine of protein) and 17.2 g kg⁻¹ of diet (45.3 g kg⁻¹ methionine of protein) in the presence of 3.1 g kg⁻¹ cystine, respectively.

The present study investigated the influence of berberine (BBR) supplementation in normal and high-lipid (HL) diets on lipid metabolism and accumulation in black sea bream (Acanthopagrus schlegelii). BBR was supplemented at 50 mg/kg to control (Con, 11·1 % crude lipid) and high-lipid (HL, 20·2 % crude lipid) diets and named as ConB and HLB, respectively. After the 8-week feeding trial, fish body length and specific growth rate were significantly reduced by HL diets (P < 0·05). Muscle and whole-body crude lipid contents were significantly influenced by both BBR supplementation and dietary lipid level. Fish fed the HLB diet had significantly lower serum TAG, LDL-cholesterol contents and alanine aminotransferase activity compared with the HL group. The HL group presented vast lipid accumulation in the liver, and hypertrophied hepatocytes along with large lipid droplets, and translocation of nuclear to the cell periphery. These abnormalities in black sea bream were alleviated in the HLB group. BBR supplementation in the HL diet significantly down-regulated the hepatic expression levels of acetyl-CoA carboxylase α, sterol regulatory element-binding protein-1, 6-phosphogluconate dehydrogenase, glucose 6-phosphate dehydrogenase and pparγ, whereas the lipoprotein lipase, hormone-sensitive lipase and carnitine palmitoyltransferase 1a expression levels were significantly up-regulated. However, the expression levels of these genes showed opposite trends in muscle (except for pparγ). In conclusion, dietary BBR supplementation in the HL diet reduced hepatic lipid accumulation by down-regulating lipogenesis gene expression and up-regulating lipolysis gene expression, and it increased muscle lipid contents with opposite trends of the mechanism observed in the liver.

A feeding trial of eight weeks was conducted to examine the influence of food supplementation with lauric acid (LA) onAcanthopagrus schlegelii(juvenile black sea bream). A 24 percent fish meal baseline diet was created, while the other two diets were generated with dietary supplementation of graded points of LA at 0.1 percent and 0.8 percent, respectively. Each diet was given a triplicate tank with 20 fish weighing 6.22 ± 0.19 g. In comparison with the control group, the weight gain rate, growth rate, as well as feed efficiency of fish fed of 0.1 percent diet of LA were considerably (P < 0.05) greater. The total body and dorsal muscle proximate compositions did not change significantly between groups (P > 0.05). Triglyceride (TG) content was considerably (P < 0.05) greater in the LA-supplemented meals eating group in comparison with the control group. In the group eating LA-supplemented meals, the height of villus and the number of goblet cells/villus were considerably (P < 0.05) larger. The microbial makeup of the gut was also studied. The differences in phyla, class, and family level were not statistically significant (P > 0.05). Firmicutes in the phylum, Betaproteobacteri, Gammaproteobacteria, and Clostridia in the class, and Clostridiaceae in the family were all substantially increased with higher levels of LA supplementation (P < 0.05). According to the findings of this study, an LA-supplemented diet improves fish development, antioxidative capability, gut microbiota and intestinal health.