Dietary amino acid l-tryptophan requirement of fingerling Indian catfish, Heteropneustes fossilis (Bloch), estimated by growth and haemato-biochemical parameters

An 8-week feeding trial was conducted to determine the dietary tryptophan requirement of fingerling Indian catfish, Heteropneustes fossilis (6.10 ± 1.15 cm, 4.44 ± 0.50 g). Six isonitrogenous (40 g 100 g^?1) and isoenergetic (17.90 kJ g^?1) amino acid test diets were formulated with gradation of 0.1 g 100 g^?1 containing graded levels of l-tryptophan (0.04–0.54 g 100 g^?1, dry diet). Fish were stocked in triplicate groups, in 75-L circular trough with flow-through system and fed experimental diets at 4% BW/day twice daily. Maximum live weight gain (258%), best feed conversion ratio (FCR) (1.54) and protein efficiency ratio (PER) (1.62) were obtained in fish fed diet containing 0.34 g 100 g^?1 tryptophan. However, quadratic regression analysis of weight gain, FCR, PER and body protein deposition (BPD) data indicated requirements for dietary tryptophan at 0.37, 0.33, 0.32 and 0.33 g 100 g^?1 of dry diet, respectively. Significantly (P < 0.05) higher body protein, minimum moisture and intermediate fat contents were recorded at 0.34 g 100 g^?1 dietary tryptophan diet. Ash content was not significantly different (P > 0.05) among treatments except for diets 0.04 and 0.14 g 100 g^?1. Excellent somatic and haematological indices values were obtained at the requirement level. Based on above results, it is recommended that the diet for H. fossilis should contain tryptophan at 0.32 g 100 g^?1, dry diet, corresponding to 0.80 g 100 g^?1 dietary protein for optimum growth and efficient feed utilization.     

Effects of dietary arginine levels on growth, feed conversion, protein productive value and carcass composition of stinging catfish fingerling Heteropneustes fossilis (Bloch)

A 12-week feeding trial was conducted to evaluate the effects of varying levels of dietary arginine on growth, feed conversion, protein productive value and carcass composition of fingerling Heteropneustes fossilis (10.11?±?0.14?cm; 5.87?±?0.07?g). Casein and gelatin-based isonitrogenous (38% crude protein) and isocaloric (14.72 kJ?g^?1 digestible energy) amino acid test diets with varying levels of l-arginine (1.00, 1.25, 1.50, 1.75, 2.00 and 2.25?g 100?g^?1 of dry diet) were fed to randomly assigned triplicate groups of fish to apparent satiation twice daily at two feeding schedules (08.00 and 17.30?h). Thermal growth coefficient (TGC; 0.86), feed conversion ratio (FCR; 1.97) and protein productive value (PPV; 0.25) were best attained by the group fed diet containing 1.75?g arginine 100?g^?1 of dry diet (D4). Carcass protein content also peaked at the above level of dietary arginine whereas carcass lipid showed consistent drop with the increase in dietary arginine level up to 1.75?g 100?g^?1 of dry diet. Second-degree polynomial regression analysis at 95% maximum and minimum response of thermal growth coefficient, feed conversion, protein productive value, carcass protein and lipid productive value against varying levels of dietary arginine yielded that dietary arginine in the range of 1.51–1.66?g 100?g^?1 of dry diet, corresponding to 3.97–4.37?g 100?g^?1 protein is adequate to optimize growth, feed conversion, protein productive value and improve carcass quality in fingerling H. fossilis.     

Dietary arginine requirement of Heteropneustes fossilis fry (Bloch) based on growth,nutrient retention and haematological parameters

Dietary arginine requirement of Heteropneustes fossilis fry (3.0 ± 0.5 cm; 5.1 ± 0.3 g) was determined by feeding casein‐gelatin‐based isonitrogenous (400 g kg^?1 crude protein) and isocaloric (17.97 kJ g^?1) amino acid test diets containing graded levels of l ‐arginine (15, 17, 19, 21, 23 and 25 g kg^?1 dry diet) for 12 weeks. Maximum absolute weight gain (AWG) (44.4), best feed conversion ratio (FCR) (1.22), highest protein retention efficiency (PRE%) (41%), energy retention efficiency (ERE%) (75%), best condition factor, hepatosomatic index and viscerosomatic index were noted at 21 g kg^?1 arginine of the dry diet. Maximum body protein (189.8 g kg^?1) was also obtained in fish fed above diet. Highest haematocrit value (35%), Hb concentration (9.54 g dL^?1), RBC count (3.44 × 10⁹ mL^?1) and lowest Erythrocyte sedimentation rate (ESR) (1.93 mm h^?1) were obtained at the above level of arginine in the diet. AWG, FCR, PRE% and ERE% data were analysed using broken‐line and an exponential fit to obtain more precise dietary arginine requirement. On the basis of broken‐line and exponential analyses of AWG, FCR, PRE and ERE data, inclusion of dietary arginine in the range of 20.4–22.6 g kg^?1 dry diet, corresponding to 51–56.5 g kg^?1 dietary protein, is recommended for formulating arginine‐balanced feeds for rearing H. fossilis fry.     

Dietary arginine requirement of fingerling Indian major carp, Cirrhinus mrigala (Hamilton)

Dietary arginine requirement of fingerling Indian major carp, Cirrhinus mrigala (4.20 ± 0.05 cm; 0.60 ± 0.02 g) was determined by conducting a 8‐week feeding trial with casein–gelatine‐based diets (400 g kg^?1 crude protein; 17.90 kJ g^?1, gross energy), containing crystalline amino acids with graded levels of l ‐arginine (10, 12.5, 15, 17.5, 20 and 22.5 g kg^?1, dry diet). Fish were randomly stocked, in triplicate groups, in 55‐L indoor polyvinyl flow through circular tanks and fed experimental diets at 5% of their body weight divided into two feedings at 08.00 and 16.00 hours. Live weight gain (321%) and feed conversion ratio (FCR 1.40) were significantly (P < 0.05) higher in fish fed diet containing 17.5 g kg^?1dietary arginine compared with other diets. Second‐degree polynomial regression analysis of live weight gain, FCR and protein efficiency ratio data indicated requirements for dietary arginine at 18.7, 18.4 and 18.3 g kg^?1 of the dry diet, respectively. Maximum carcass protein, and minimum moisture and fat contents were noticed at the requirement level. Carcass ash content remained insignificantly different among the treatments except at 17.5 g kg^?1 dietary arginine showing significantly higher ash content. Based on the above results, it is recommended that the diet for fingerling C. mrigala should contain arginine at 18.4 g kg^?1, dry diet, corresponding to 46 g kg^?1 dietary protein for optimum growth and efficient feed utilization.     

Dietary arginine requirement of fingerling hybrid Clarias (Clarias gariepinus×Clarias macrocephalus)

The dietary arginine requirement of fingerling hybrid Clarias (Clarias gariepinus×Clarias macrocephalus) (4.2±0.03 cm, 0.56±0.04 g) was determined by feeding six isonitrogenous (400 g kg⁻¹ crude protein) and isocaloric (17.9 kJ g⁻¹) amino acid test diets containing casein, gelatin and l ‐crystalline amino acids with graded levels of arginine (10.0, 12.5, 15.0, 17.5, 20.0 and 22.5 g kg⁻¹) for 4 weeks to triplicate groups. Diets were fed twice a day at 09:00 and 16:00 hours at 8% body weight day⁻¹. Maximum weight gain (523%), best feed conversion ratio (FCR, 1.41), protein efficiency ratio (1.78) and specific growth rate (6.53%) were recorded in fish fed the diet containing arginine at 20.0gkg⁻¹ of the diet. Second‐degree polynomial regression analysis of live weight gain and FCR values indicated the dietary arginine requirement at 17.8 and 20.0 g kg⁻¹ of dry diet respectively. Significantly higher carcass protein and protein deposition values were recorded at the requirement level (20.0 g kg⁻¹). Higher fat and lower moisture values were obtained in carcass of fish fed the diet with 15.0g kg⁻¹ arginine. The maximum carcass ash value was noticed in the fish fed at 20.0 g kg⁻¹ dietary arginine. We recommend that the diet for hybrid Clarias (C. gariepinus×C. macrocephalus) should contain arginine in the range of 17.8–20.0 g kg⁻¹ of the dry diet, corresponding to 44.5 and 50 g kg⁻¹ of dietary protein respectively.     

Dietary isoleucine requirement of fingerling catla, Catla catla (Hamilton), based on growth, protein productive value, isoleucine retention efficiency and carcass composition

In order to determine the dietary isoleucine requirement of fingerling catla, Catla catla (4.25 ± 0.15 cm, 0.61 ± 0.04 g), six isonitrogenous (33.0 % crude protein) and isocaloric (13.7 kJ/g digestible energy) amino acid test diets containing casein, gelatin and l-crystalline amino acids with graded levels of isoleucine (0.5, 0.75, 1.0, 1.25, 1.5 and 1.75 % of the dry diet) were prepared. Triplicate groups of fish were randomly stocked in eighteen 70-l indoor polyvinyl circular troughs at a density of 25 fingerling per trough provided with a water flow-through system (1–1.5 l min^?1). The experimental diets were fed to fish to apparent satiation at 08:00, 12:30 and 17:30 h for 12 weeks. Growth of the fish was found to increase with the incremental levels of dietary isoleucine up to 1.25 % of the dry diet. Quadratic regression analysis at 95 % maximum response of absolute weight gain (6.18 g fish^?1), protein productive value (0.32), isoleucine retention efficiency (71.91 g fish^?1), RNA/DNA ratio (4.81) and carcass protein (15.7 %) yielded the optimum isoleucine requirement in the range of 1.13–1.18 % of the dry diet, corresponding to 3.42–3.58 % of dietary protein. Data generated in this experiment would be useful to formulate isoleucine-balanced, cost-effective quality feeds for fingerling catla.     

Quantitative dietary isoleucine requirement of juvenile Pacific white shrimp,Litopenaeus vannamei (Boone) reared in low-salinity water

This study was designed to determine the isoleucine requirement of juvenile Pacific white shrimp Litopenaeus vannamei (Boone) in low-salinity water (0.50–0.70 g L^?1). Six diets were formulated to contain 410 g kg^?1 crude protein with fish meal, peanut meal and pre-coated crystalline amino acids with different concentration of l-isoleucine (9.35, 11.85, 14.35, 16.85, 19.35, and 21.85 g kg^?1 dry diet, defined as diet I1, diet I2, diet I3, diet I4, diet I5 and diet I6, respectively.). Each diet was randomly assigned to triplicate treatments of 30 shrimps (0.43 ± 0.005 g), and the feed trial lasted for 8 weeks. The results indicated that the weight gain significantly increased with increasing isoleucine concentration up to 14.35 g kg^?1 (diet I3), whereas it was reduced in the treatments exceeding 16.85 g kg^?1 isoleucine (diet I4) significantly (P < 0.05). Moreover, the highest body protein deposition and protein efficiency ratio, and the lowest feed conversion ratio, haemolymph aspartate aminotransferase and alanine aminotransferase activities were also found at treatment I3–I4 (P < 0.05). And the haemolymph urea nitrogen concentration of shrimps-fed diet I6 was particularly higher than those fed with diets I1–I5 (P < 0.05). The results of polynomial regression based on weight gain, feed efficiency and body protein deposition indicated that the optimal dietary isoleucine requirement for L. vannamei reared in low-salinity water was 15.95 g kg^?1 isoleucine of dry diet, correspondingly 38.81 g kg^?1 of dietary protein.     

Growth performance and immune responses of gibel carp, <Emphasis Type="Italic">Carassius auratus gibelio</Emphasis>, fed with graded level of rare earth-chitosan chelate

A 12-week feeding trail was conducted to assess the effect of rare earth-chitosan chelate (RECC) on growth performance and immune responses of gibel carp, Carassius auratus gibelio. Isonitrogenous and isolipid experimental diets were supplemented with graded levels of rare earth-chitosan chelate (RECC 0, 0.8, 4 and 8 g Kg^?1). A total of 720 gibel carps (initial body weight about 14.32 g) were divided randomly into four groups with six replicates, respectively. Fish were fed with the experimental diets three times every day. At the end of the feeding trail, the survival rate was higher than 96 %. Weight gain rate and specific growth rate (SGR) significantly increased with RECC supplementation up to 0.8 g Kg^?1 (P < 0.05) and tended to decline at higher supplementation levels, while feed conversion ratio was not significantly different between groups (P > 0.05). Based on broken-line regression analysis of SGR, the optimum dietary RECC was estimated to be 0.71 g Kg^?1 of the diet. Condition factor and viscerosomatic index were not significantly affected by RECC (P > 0.05), while hepatosomatic index in the group fed with 0.8 g Kg^?1 RECC (3.45 ± 0.10 %) was significantly lower than in other groups (P < 0.05). Plasma ALT was significantly affected by RECC (P < 0.05), while AST was not. Plasma total protein and albumin were increased with RECC supplementation up to 0.8 g Kg^?1 and decreased significantly at higher supplementation levels (P < 0.05). RECC supplementation significantly decreased plasma urea and glucose concentration and increased plasma creatinine concentration significantly (P < 0.05). Respiratory burst activity of phagocytes and myeloperoxidase activity were not significantly different between groups, while superoxide dismutase activity and nitrogen monoxide concentration were increased with the increasing level of RECC in the diets. In conclusion, RECC could enhance growth performance and improve immunity of gibel carp.     

Dietary threonine requirement of fingerling Indian major carp,Labeo rohita (Hamilton)

An 8‐week feeding experiment was conducted in a water flow‐through system (26–28 °C) to determine the dietary threonine requirement of fingerling Labeo rohita (3.90±0.03 cm; 0.58±0.02 g). Growth, feed utilization and body composition of fish fed test diets (40% crude protein; 17.9 kJ g^?1 gross energy) with graded levels of l ‐threonine (0.75%, 1.0%, 1.25%, 1.50%, 1.75% and 2.0% dry diet) to apparent satiation were response variables used to assess threonine adequacy. Diets were made isonitrogenous and isoenergetic by adjusting the levels of glycine and dextrin. The amino acid profiles of the test diets were formulated to that of 40% whole chicken egg protein except for threonine. The performance of fish fed experimental diets was evaluated using calculated values for weight gain (g fish^?1), feed conversion ratio (FCR), protein efficiency ratio (PER) and protein productive value (PPV) data. Maximum weight gain (g fish^?1) (1.79), lowest FCR (1.39), highest PER (1.76) and PPV (0.33) were recorded at 1.50 g per 100 g dietary threonine. Statistical analysis of weight gain, FCR, PER and PPV data reflected significant differences (P<0.05) among treatments. Except for reduced growth performance in fish fed threonine‐deficient diets, no deficiency signs were noted. Weight gain, FCR, PER and PPV data were also analysed using second‐degree polynomial regression analysis to obtain a more accurate threonine requirement estimate, which was found, using each response variable, to be at 1.70, 1.63, 1.65 and 1.51 g per 100 g of dry diet, corresponding to 4.2, 4.07, 4.12 and 3.77 g per 100 g of dietary protein respectively. Based on the second‐degree polynomial regression analysis of the live weight gain, FCR, PER and PPV data, the optimum dietary level of threonine for fingerling L. rohita was found to be in the range of 1.51–1.70 g per 100 g of the dry diet, corresponding to 3.77–4.2 g per 100 g of dietary protein.     

Effect of dietary l‐lysine levels on growth,feed conversion,lysine retention efficiency and haematological indices of Heteropneustes fossilis (Bloch) fry

Effect of varying dietary lysine levels on growth, feed conversion, nutrient retention, lysine retention efficiency and haematological indices of Heteropneustes fossilis fry (2.97 ± 0.11 cm; 4.78 ± 0.31 g) was studied by conducting a 12‐week feeding trial. Isonitrogenous (450 g kg^?1 CP) and isocaloric (17.97 kJ g^?1 GE) amino acid test diets with graded concentrations of l ‐lysine (18, 20, 22, 24, 26, 28 g kg^?1 dry diet) were fed to triplicate groups of fish to apparent satiation twice daily at 17 and 17:30 h. Maximum thermal growth coefficient (TGC, 0.82), best feed conversion ratio (FCR, 1.28) highest protein retention efficiency (PRE, 36%), energy retention efficiency (ERE, 79%) and lysine retention efficiency (LRE, 75%) were noted at 24 g kg^?1 lysine of dry diet. Body protein was also found to be in line with growth data and peaked at 24 g kg^?1 lysine of dry diet. Similarly, superior somatic and haematological indices were exhibited by the groups fed dietary lysine at 24 g kg^?1 of the dry diet. However, exponential analysis of dietary lysine intake against TGC, lysine retention and protein retention indicated that inclusion of dietary lysine in the range of 13.24–14.14 g kg^?1 dry diet, corresponding to 29.42–31.42 g kg^?1 dietary protein, is essential for faster growth of this fish.     

Effect of dietary protein levels on growth,feed utilization and carcass composition of endangered bagrid catfish Horabagrus brachysoma (Gunther 1864) fingerlings

An 84‐day feeding trial was conducted to study the effect of different levels of dietary protein, 250 (P25), 300 (P30), 350 (P35), 400 (P40) and 450 g (P45) kg^?1 dry matter (DM) on growth, feed intake, feed utilization and carcass composition of bagrid catfish Horabagrus brachysoma fingerlings. Triplicate groups of fingerlings with mean initial body weight of 2.2 g were fed the experimental diets twice daily, till satiation, in 150‐L tanks supplied with flow‐through freshwater. Daily dry matter intake by the fingerlings decreased significantly (P < 0.05) when fed P25 diet, containing 250 g protein kg^?1. The highest body weight gain, specific growth rate (SGR) and protein efficiency ratio (PER), and the lowest feed conversion ratio (FCR) were observed in fish fed 350 g protein kg^?1 diet. The fish fed with P45 diet had the lowest (P < 0.05) carcass lipid content. The polynomial regression analysis indicates that H. brachysoma fingerlings require 391 g dietary crude protein kg^?1 diet.     

Dietary amino acid l‐methionine requirement of fingerling Indian catfish,Heteropneustes fossilis (Bloch‐1974) estimated by growth and haemato‐biochemical parameters

An 8 weeks feeding trial was conducted to determine the dietary methionine requirement of fingerling Indian catfish, Heteropneustes fossilis (6.08 ± 0.95 cm; 4.33 ± 0.52 g). Six isonitrogenous (40%) and isoenergetic (17.90 kJ g^?1 GE) amino acid test diets were formulated with gradation of 0.25 g 100 g^?1containing graded levels of _L‐methionine (0.30, 0.55, 0.80, 1.05, 1.30 and 1.55 g 100 g^?1, dry diet) with 0.40 g 100 g^?1 constant level of cystine. Twenty fish were stocked in triplicate groups, in 75‐L circular trough with continuous flow‐through system and fed experimental diets at 4% BW/day twice daily, at 08:00 and 18:00 hours. Maximum live weight gain (296%), best feed conversion ratio (1.56) and protein efficiency ratio (1.60) were occurred at 1.05 g 100 g^?1 methionine, beyond which they showed declining tendency. However, quadratic regression analysis of weight gain, feed conversion ratio (FCR), protein efficiency ratio (PER) and body protein deposition (BPD) data indicated requirement for methionine at 1.15, 1.08, 1.06 and 1.05 g 100 g^?1 of dry diet respectively. Significantly (P < 0.05), higher whole body protein content, minimum moisture and intermediate fat contents were recorded at 1.05 g 100 g^?1 dietary methionine level. Ash content remained insignificantly (P > 0.05) low among all the treatments, excepting at diet I and diet II. Body protein deposition was also found to be significantly (P < 0.05) higher at 1.05 g 100 g^?1 methionine level. Best somatic and haematological indices values were also obtained at the requirement level. Based on above results, it is recommended that the diet for young H. fossilis should contain methionine at 1.09 g 100 g^?1 dry diet, corresponding to 2.73 g 100 g^?1 dietary protein with 0.40 g 100 g¹ cystine concentration for optimum growth and efficient feed utilization. Thus, the total sulphur amino acid requirement of H. fossilis would be (1.09 + 0.40) 1.49 g 100 g^?1 of dry diet, corresponding to 3.73 g 100 g^?1 of dietary protein.     

Dietary histidine requirement of fingerling Indian major carp, Cirrhinus mrigala (Hamilton)

An 8‐week growth trial was conducted to determine the dietary histidine requirement of the Indian major carp, Cirrhinus mrigala fingerling (length 4.22 ± 0.45 cm; weight 0.61 ± 0.08 g; n = 40). Isonitrogenous (400 g kg^?1 crude protein) and isoenergetic (17.90 kJ g^?1 gross energy) diets with graded levels of l ‐histidine (2.5, 5.0, 7.5, 10.0, 12.5 and 15.0 g kg^?1 dry diet) were formulated using casein and gelatin as a source of intact protein, supplemented with l ‐crystalline amino acids. Twenty fish were randomly stocked in 70‐L indoor polyvinyl circular fish tank (water volume 55‐L, water exchange rate 1–1.5 L min^?1) and fed experimental diets at the rate of 5% of their body weight/day divided over two feedings at 08:00 and 16:00 h. Maximum live weight gain (295%), best feed conversion ratio (FCR) (1.48) and protein efficiency ratio (PER) (1.69) occurred at 7.5 g kg^?1 of dietary histidine level. When live weight gain, FCR and PER data were analysed using second‐degree polynomial regression, the break points indicated histidine requirements at 9.4, 8.6 and 8.5 g kg^?1 of dry diet respectively. Significantly (P < 0.05) higher whole body protein and low moisture values were recorded at 7.5 g kg^?1 histidine level. Body fat increased significantly (P < 0.05) with increasing histidine levels. However, at 7.5 and 10 g kg^?1 histidine diets body fat did not differ (P > 0.05) to each other. Ash content of fish fed diets containing various levels of histidine did not differ except at 2.5 and 5.0 g kg^?1 inclusion levels where significantly (P < 0.05) higher ash was recorded. Protein deposition was also found to be significantly (P < 0.05) higher in the 7.5 g kg^?1 histidine diet. Based on the polynomial regression analysis of FCR and PER data, it is recommended that the diet for fingerling C. mrigala should contain histidine at 8.5 g kg^?1 of dry diet, corresponding to 21.25 g kg^?1 of dietary protein for optimum growth and efficient utilization of feed.     

Effects of practical dietary protein to lipid levels on growth,digestive enzyme activities and body composition of juvenile rice field eel (Monopterus albus)

A 10-week feeding experiment was conducted to evaluate the effects of dietary protein to lipid ratios (P/L) on growth, intestinal digestive enzyme activities and body composition in juvenile rice field eel (Monopterus albus) (initial mean body weight of 65.76 ± 1.07 g, mean ± SEM). Nine test diets were formulated in a 3 × 3 factorial design to contain three protein levels (350, 400 and 450 g kg^?1) for each of three lipid levels (40, 80 and 120 g kg^?1), respectively. Each diet was randomly assigned to triplicate groups of 60 fish per net cage (1.5 × 2.0 × 1.5 m). Results showed the survival was above 96 % and was not affected by dietary treatments. Fish fed the diet with 450 g kg^?1 protein and 40 g kg^?1 lipid showed the best weight gain (WG) (103.95 %) and feed conversion ratio (1.60) (P < 0.05). WG, protein efficiency ratio and energy retention increased with the increasing in lipid at 350 g kg^?1 protein level (P < 0.05). However, WG showed a little decline with increasing dietary lipid when fish fed the diets with 400 and 450 g kg^?1 protein level, but no significant difference was observed (P < 0.05). Hepatosomatic index, visceralsomatic index and intestinal lipase activity increased with the increasing of dietary lipid level irrespective protein level. Intestinal trypsin activity increased with the increasing of dietary lipid level when fish fed the diets with 350 g kg^?1 protein, but showed converse trend when fish fed the diets with 400 and 450 g kg^?1 protein. Serum triglyceride, body lipid and energy were positively correlated with the dietary lipid. Results of the present study showed that the dietary protein/lipid ratio of 450/40 g kg^?1 is considered optimum for rice field eel under culture conditions, and the increase in dietary lipid level has no efficient protein-sparing effect when fish fed the diets with 400 and 450 g kg^?1 protein level.     

Effect of dietary garlic supplementation on lipid peroxidation and protein oxidation biomarkers of tissues as well as some serum biochemical parameters in common carp Cyprinus carpio

This study aims to investigate the effects of dietary garlic powder (25 and 50 g kg^?1 feed) supplementation for 6 weeks on lipid and protein oxidation biomarkers in various tissues as well as some blood biochemical parameters in common carp. Based on the present study results, serum malondialdehyde (MDA) concentrations were decreased following garlic supplementation, but the decrease was only significant (P < 0.05) in the group that received 50 g kg^?1 dietary garlic compared with the control group. Moreover, garlic at 50 g kg^?1 diet caused significant decrease in MDA values of liver and kidney. Additionally, the decreasing effect of garlic at 25 g kg^?1 diet on MDA values was only significant in liver. Protein carbonyl contents were only decreased significantly in muscle following garlic administration at 25 g kg^?1 diet. Serum aspartate aminotransferase activity decreased significantly in carp that received 25 g kg^?1 dietary garlic. Moreover, alkaline phosphatase activity decreased significantly in carp fed diets containing 25 and 50 g kg^?1 garlic. On the other hand, garlic supplementation had no significant effect on gamma-glutamyl transferase activity and total protein, albumin, and creatinine concentrations. The results of the present study indicate that garlic powder has potential to decrease oxidative stress to some extent by reducing lipid and protein oxidation in some tissues of common carp.     

Modulation of appetite,lipid and glucose metabolism of juvenile grass carp (<Emphasis Type="Italic">Ctenopharyngodon idellus</Emphasis>) by different dietary protein levels

This study was undertaken to explore the systemic metabolic strategies of juvenile grass carp (Ctenopharyngodon idellus) to maintain growth when fed with different dietary protein levels. The optimal growth group and two growing discomfort groups were selected through the basic data, to explain the growth difference from appetite regulation and lipid and glucose metabolism perspective. Three experimental diets were formulated with three dietary protein levels at 200.3, 296.1 and 442.9 g kg^?1, named P1, P2 and P3, respectively. Juvenile grass carp (initial body weight 12.28 ± 0.14 g) were fed with three diets with 3 replications per dietary treatment in an indoor recirculation system for an 8-week feeding trial. Fish fed with diet P2 dietary group showed significantly higher WG, SGR, FI and PER than other groups. Compared with other groups, mRNA expressions of NPY, Y8a and Y8b in fish fed with P2 significantly down-regulated, while the expressions of CCK and CART in fish fed with P3 significantly down-regulated (P < 0.05). With increasing dietary protein levels, G6Pase, GK, PK and PEPCK were all significantly inhibited (P < 0.05). For lipid metabolism, the mRNA expression of ACC in P1 dietary group was significantly higher than P3 dietary group; besides, LPL expression in P3 group was significantly higher than other two groups (P < 0.05). PPARα expression in P2 was significantly lower than other groups (P < 0.05). These results suggested that grass carp fed with P2 (296.1 g kg^?1 protein level) showed highest weight gain, contributed to more balanced nutrient metabolism and appetite regulation. Too high dietary protein (442.9 g kg^?1) should be avoided because it induced lowest PER, body lipid and liver lipid, and inhibited glucose and lipid metabolism in juvenile grass carp.     

Dietary l‐lysine requirement of fingerling stinging catfish,Heteropneustes fossilis (Bloch) for optimizing growth,feed conversion,protein and lysine deposition

Dietary lysine requirement of fingerling Heteropneustes fossilis (6.96 ± 0.05 g) was quantified by conducting 12‐week feeding trial in a flow‐through system at 28°C. Casein–gelatin based isonitrogenous (38% CP) and isocaloric (14.7 kJ g^?1 DE) amino acid test diets with six levels of dietary lysine (1.5%, 1.75%, 2.0%, 2.25%, 2.5%, 3.0% dry diet) were fed to apparent satiation in triplicates. Broken‐line and second‐degree polynomial regression analyses at 95% plateau of absolute weight gain (AWG; g fish^?1), feed conversion ratio (FCR), protein deposition (PD; g fish^?1) and lysine deposition (LD; g fish^?1) exhibited lysine requirement between 2.0% to 2.3% of the dry diet, corresponding to 5.3–6.1% protein.     

Dietary protein and carbohydrate requirement of juvenile Hawaiian limpet (<Emphasis Type="Italic">Cellana sandwicensis</Emphasis> Pease, 1861) fed practical diet

This study was conducted to evaluate dietary protein and carbohydrate requirement of juvenile Hawaiian limpets Cellana sandwincensis. A total of 64 juvenile limpets (3.12 ± 0.86 g) were fed five different dietary protein levels ranging from 270 to 470 g kg^?1 for 90 days. Carbohydrate and lipid levels were held constant at 180 and 49.7 g kg^?1, respectively. Weight gain and growth rates of the animals did not differ significantly (P > 0.05) among the protein levels ranging from 270 g kg^?1 (0.30 % day^?1) to 470 g kg^?1 (0.23 % day^?1). Next, opihi were fed four diets with protein levels from 210 to 500 g kg^?1 with a constant carbohydrate level at 120 g kg^?1. Weight gain and specific growth rates of opihi increased with increasing dietary protein from 210 to 350 g kg^?1, and significantly (P < 0.05) decreased at the 500 g kg^?1 diet. Highest weight gain, growth rates, and protein efficiency ratio were achieved at 350 g kg^?1. Elevated carbohydrate levels (180–370 g kg^?1) produced a significant difference (P < 0.05) in growth. The fastest growth rates of animals were obtained with 270 g kg^?1 (0.27 % day^?1) and 320 g kg^?1 (0.26 % day^?1). The weight gain of animals fed 180 and 370 g kg^?1 carbohydrate diets were significantly (P < 0.05) lower than those of animals fed 270 and 320 g kg^?1. We conclude that about 350 g kg^?1 protein and 320 g kg^?1 carbohydrate levels could be used for opihi.     

Effects of dietary protein levels on growth,feed utilization,protein retention efficiency and body composition of young <Emphasis Type="Italic">Heteropneustes fossilis</Emphasis> (Bloch)

An 8-week growth trial was conducted to assess the effect of dietary protein on growth, feed utilization, protein retention efficiency, and body composition of young Heteropneustes fossilis (10.02 ± 0.09 g; 9.93 ± 0.07 cm). Isocaloric (4.15 kcal g⁻¹, GE) diets with varying levels of protein (25, 30, 35, 40, 45, and 50% of the diet) were fed near to satiation to triplicate groups of fish. Optimum dietary protein was determined by analyzing live weight gain (LWG%), feed conversion ratio (FCR), protein efficiency ratio (PER), specific growth rate (SGR%), and protein retention efficiency (PRE%) data. Maximum LWG% (167), best FCR (1.42), PER (1.75), SGR (1.76), and PRE (31.7%) were evident in fish fed 40% protein diet (Diet 4). Body protein data also supported the above level. However, second-degree polynomial regression analysis of the above data indicated that inclusion of dietary protein in the range of 40–43% is optimum for the growth of young H. fossilis.     

Dietary tryptophan requirement of fingerling Indian major carp, Cirrhinus mrigala (Hamilton)

An 8‐week feeding trial was conducted to evaluate the effects of dietary tryptophan concentration on weight gain and feed efficiencies of fingerling Indian major carp, Cirrhinus mrigala. Six isonitrogenous (40% crude protein) and isocaloric (17.90 kJ g^?1) amino acid test diets containing casein, gelatin and l ‐crystalline amino acids with graded levels of l ‐tryptophan (0.06, 0.16, 0.26, 0.36, 0.46 and 0.56 g 100 g^?1 dry diet) were formulated. Fish (4.25±0.30 cm, 0.62±0.02 g) were randomly stocked in triplicate groups in 70 L (water volume 55 L) flow‐through (1–1.5 L min^?1) indoor circular tanks and fed experimental diets at 5% of their body weight/day in two feedings at 08:00 and 16:00 hours. Maximum live weight gain (277%), lowest feed conversion ratio (FCR) (1.50) and highest protein efficiency ratio (PER) (1.66) were measured at 0.36% dietary tryptophan. The relationship between dietary tryptophan levels and weight gain, FCR and PER data were described using second‐degree polynomial regression analysis indicating the tryptophan requirement at 0.42, 0.39 and 0.38 g 100 g^?1 of dry diet respectively. Whole body moisture decreased with increasing tryptophan up to 0.36%. Significantly (P<0.05) higher protein content was evident in fish fed diet containing 0.36% tryptophan. Body fat increased significantly (P<0.05) in fish fed with different tryptophan concentrations except those fed 0.36% tryptophan where a significantly lower fat content was noted. Significantly (P<0.05) higher ash content was reported at 0.06% and 0.16% tryptophan levels. Survival was 100% in fish fed all the diets except those fed 0.06% tryptophan. Based on the results, diets for fingerling C. mrigala should contain tryptophan at 0.38 g 100 g^?1 dry diet, corresponding to 0.95 g 100 g^?1 dietary protein for optimum growth and efficient feed utilization.