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Fermentation strategy is well documented to improve the nutritional value of agricultural waste by-products such olive cake (OC), which, in turn, provides healthy, safe, and affordable feedstuff. This study assessed the combined impact of Aspergillus oryzae-fermented OC (AFOC) on the growth performance, intestinal morphometry, blood biochemistry, lysozyme activity, gut immune-related genes, and flesh quality of Nile tilapia. We divided 225 fish into five groups and further subdivided into three replicates (n = 15 each) and fed them five diets (Control, AFOC5, AFOC10, AFOC15, AFOC20) to determine AFOC nutritional value and its optimized incorporation level in the diet. The trial continued for 3 months. The crude protein content of OC improved by 7.77% after A. oryzae fermentation, while lipid content decreased by 14.19%. In addition, growth and feed utilization significantly improved at (10.8–11.2) % AFOC dietary level. High-density lipoprotein (HDL) significantly improved, and the serum lysozyme level was significantly higher in the AFOC10 group compared to other groups. Interestingly, gut-related inflammatory cytokines tumor necrosis factor alpha (TNF- α) and interleukin 1 beta (IL-1β) revealed higher relative mRNA expression in the AFOC10 group compared to other groups. The histomorphometric parameters was greatly influenced by the AFOC incorporation level (10%–20%). These findings suggested that A. orzae fermentation modifies the nutritional quality of OC, as seen through its positive impact on the growth performance, local and systemic immunity, and intestinal absorptive capacity of Nile tilapia. The recommended dose for dietary AFOC was around 11%

The present investigation aimed to evaluate the effect of dietary chitosan supplementation on growth performance, body composition, immune response and histopathology of Nile tilapia, and also the in vitro antibacterial activity of chitosan against Streptococcus agalactiae (S. agalactiae). About 180 fish (average body weight 39.3 ± 0.3 g) were randomly divided into three groups according to chitosan supplementation: control group (basal diet without chitosan), Ch3 group (3 g chitosan/kg diet) and Ch5 group (5 g chitosan/kg diet). Growth performance parameters and body proximate composition were measured before infection but biochemical parameters and lysozyme and antibacterial activities before and after experimental infection. Results of the present investigation showed dietary chitosan (5 g chitosan/kg diet) significantly (p

The present study aimed to assess the in ovo administration of clenbuterol on chick fertility, growth performance, muscle growth, myogenic gene expression, fatty acid, amino acid profile, intestinal morphology, and hepatic lipid-related gene expressions. In this study, 750 healthy fertile eggs from the local chicken breed Dokki-4 strain were analyzed. Fertile eggs were randomly divided into five experimental groups (150 eggs/3 replicates for each group). On day 14 of incubation, in addition to the control group, four other groups were established where 0.5 mL of worm saline (30 °C) was injected into the second group of eggs. In the third, fourth, and fifth groups, 0.5 mL of worm saline (30 °C), 0.9% of NaCl, and 10, 15, and 20 ppm of clenbuterol were injected into the eggs. Results suggested that clenbuterol increased growth efficiency up to 12 weeks of age, especially at 15 ppm, followed by 10 ppm, decreased abdominal body fat mass, and improved hatchability (p &lt, 0.01). Clenbuterol also modulated saturated fatty acid levels in the breast muscles and improved essential amino acids when administered at 10 and 15 ppm. Additionally, clenbuterol at 15 ppm significantly decreased myostatin gene expression (p &lt, 0.01) and considerably increased IGF1r and IGF-binding protein (IGFBP) expression. Clenbuterol administration led to a significant upregulation of hepatic PPARα, growth hormone receptor, and Lipoprotein lipase (LPL) mRNA expression with a marked decrease in fatty acid synthase (FAS) and sterol regulatory element-binding protein 1 (SREBP-1c) expression. In conclusion, the current study revealed that in ovo injection of clenbuterol showed positive effects on the growth of hatched chicks through reduced abdominal fat deposition, improved intestinal morphology, and modulation of hepatic gene expressions in myogenesis, lipogenesis, and lipolysis.

This study aimed to elucidate the response of broiler chickens to the dietary nano-zinc supplementation in terms of immune response and antioxidant activity. Ninety-one-day-old chicks (Ross 308) were randomly assigned to one of three dietary treatments in three replicates, in a feeding trial that lasted for 5 weeks. Birds were fed a basal diet supplemented with inorganic zinc oxide at 40 mg/kg diet (control), zinc oxide nanoparticles (ZnONPs) at 40 mg/kg diet (ZN1), or ZnONPs at 80 mg/kg diet (ZN2). Birds were injected with DNP-KLH at the 7th and 21st days from the beginning of the experiment, and blood samples were collected on days 7, 14, 21, 28, and 35 to determine the levels of immunoglobulin Y (IgY) and malondialdehyde as well as the antioxidant enzyme activities. Cellular immunity was assayed by estimation of phagocytic percentage and index of peripheral monocytes of blood and estimation of the T lymphocyte activity using a lymphocyte transformation test. The results showed that feeding broiler chickens a diet supplemented with ZnONPs increased (p

The study aimed to investigate the effect of Se sources and concentrations on performance, thyroid activity, antioxidant defense, and functional egg quality of Japanese quail. One hundred and twenty, 8-week-old birds were randomly assigned to 1 of 4 dietary treatments in 3 replicates (10 birds/replicate). The treatments contained inorganic sodium selenite (SS) at 0.2 mg/kg diet (SS1 = control) or 0.4 mg/kg diet (SS2) or selenomethionine (SM) at 0.2 mg/kg diet (SM1) or 0.4 mg/kg diet (SM2). Egg production (%) and feed intake were daily recorded, and feed conversion ratio (FCR) was calculated. Blood samples were collected and analyzed for glucose, thyroxine (T4), triiodothyronine (T3), glutathione peroxidase (GPX), and superoxide dismutase (SOD) enzymes. Egg quality was determined in terms of Se content and concentrations of triglycerides, LDL, HDL, and cholesterol. Dietary supplementation of SM2 increased (P 0.05) egg production (%) and egg mass and decreased FCR compared to the other groups, which showed no significant differences (P 0.05) in between. It is the first study reporting that the eggs from the quail fed SM2 diet had lower concentrations (P 0.05) of triglycerides, LDL, and cholesterol than those fed SS. Feeding SM increased (P 0.05) blood glucose, T4, and T3 levels. Moreover, feeding SM increased the activity of GPX and SOD with a higher significance (P 0.05) for SM2 than SM1. In conclusion, no adverse effects from supplementation of SM up to 0.4 mg/kg were observed and could improve their performance, antioxidant defense, thyroid activity, and functional egg quality.

This study explored the impact of supplementation of L- carnitine on the performance of broiler chicken, biochemical parameters and expression of cationic amino acid transporter ( CAT2 ), myogenic determining factor ( MYOD ) and myogenic factor 5 ( MYF5 ) genes. This study included two groups; the first one is the control group and the second one received L-carnitine at a dose 50 mg/kg/day in drinking water. After 35 day, the sera and muscle tissue were obtained for biochemical and real time polymerase chain reaction (qPCR) analysis. The obtained results revealed a significant increase in the body weight, total body weight gain and a significant decrease in food consumption, food conversion rate in L-carnitine-supplemented group as compared to the control group. Moreover, there was no significant changes in serum cholesterol, triacylglycerol, AST, ALT, total protein and uric acid levels which showed a slight decrease in L-carnitine-supplemented group in comparison with the control group. This study also revealed a significant up regulation for the expression of CAT2 , MYOD and MYF5 genes in muscles of broiler chicken-supplemented with L- carnitine as compared to the control one. The present study concluded that supplementation of L- carnitine to broiler chicken was useful to increase the total body weight gain and muscle mass and this beneficial effect was associated with up regulation of CAT2 , MYOD , and MYF5 genes. Key words : L-carnitine; broiler chicken; growth traits; CAT2; MYOD; MYF5

The aim of current study was to determine the effect of dietary omega 3 fatty acids (FA) mainly eicosapentaenoic (EPA) and docosahexaenoic (DHA) on inflammatory response of post calving cows during transition to lactation. Twenty Holstein lactating cows were assigned into two groups (10 each). The two groups fed on the basal diet while one of them was supplemented with 70 g of omega-3 FA per cow. The supplement was added to the diet from the 1 ST day of calving till the 60 th days of lactation. Blood samples were taken 3 times weekly from the 2 nd to the 4 th week post calving. The blood samples were analyzed for glucose, insulin, non-esterified fatty acids (NEFA), beta hydroxyl butyric acid (BHBA), C- reactive protein (CRP), haptoglobin, albumin and globulin. Feeding omega-3 FAs significantly increased (P

The present study investigated the influence of altering omega 6 to omega 3 fatty acids (FA) ratio on growth, hemato- biochemical parameters and absorptive capacity of Nile tilapia. One hundred and fifty fingerlings (25.1±0.3 g), were assigned into 3 groups (5 replicates each) and fed on iso-caloric and iso-nitrogenous diets. Diets were supplemented with fish and soy oil to create 3 different ratio of omega 6 to omega 3 FA, namely, 0.91, 2.85 and 9.3 parts of omega 6 to 1 part of omega 3 (R1, R3 and R9, respectively). Increasing the ratio from R1 to R9 significantly decreased average daily gain and increased feed conversion ratio. Also this alteration decreased ash content in the carcass on the expense of ether extract. Number of erythrocytes, packed cell volume, hemoglobin concentration were significantly increased in fish fed R1. Feeding R9 increased heterophils and decreased lymphocytes as compared with R1 and R3. Fish fed R1 significantly had high serum protein and serum antibacterial activity (47.6%) than R9 (43.5%) and R3 (44.9%). Feeding R1 significantly decreased serum triglycerides, cholesterol and creatinine. Feeding R3 and R1 enhanced absorptive capacity of jejunum villi more than the group fed R9. Increasing the ratio of omega 6 to omega 3 FA from R1 to R9 decreased growth performance through decreasing absorptive capacity of jejunum villi. However, Feeding R3 had a positive effect on growth performance and absorptive capacity of the intestine of Nile tilapia. Key words : fish oil; growth performance; intestinal villi; Nile tilapia; soybean oil

The experiment designed to study the influences of nutritional eicosapentaenoic (EPA) and docosahexaenoic (DHA) fatty acids (FA) on performance, egg yolk fat characteristics and FA profile in laying hens. From 30 to 36 weeks of age, 180 laying hens were allotted randomly to 2 dietary treatments, each of 6 replicates (15 birds for each replicate). The control diet was supplied with soy oil while the experimental diet was supplied with EPA and DHA to create 2 different ratio of n-6 to n-3 FA (18.8:1 and 5:1, respectively). The egg production % was recorded daily. The eggs were weighed to estimate egg mass. Also, feed consumption was recorded daily and the feed conversion ratio (FCR) was estimated. The FA profile of egg yolk was determined in the last week of the experiment. The dietary EPA and DHA resulted in significantly higher egg production (76.89 versus 67.23%), weightier egg mass (42.46 versus 37. 72 g) and lower FCR (2.49 versus 2.72) than the control. Also, supplying the dietary EPA and DHA was reflected in increasing of total polyunsaturated and n-3 FA in the eggs. Moreover, reducing the ratio of n-6 to n-3 FA to 5:1 decreased egg triglycerides, total cholesterol and cholesterol associated with low density lipoprotein and very low density lipoprotein. In conclusion, supplying EPA and DHA in the diet of laying hens positively influences performance, egg yolk FA profile and cholesterol. Practically, EPA and DHA could be used in laying hen diets to improve their performance and enhance public health of egg consumers.