Poultry

Heat stress poses a considerable challenge to the modern poultry industry by negatively impacting immune system maturation and eliciting inflammatory responses. Peroxisome proliferators-activated receptors α (PPARα), predominantly expressed in metabolically active tissues such as skeletal muscle, are essential for regulating the inflammatory process. Moreover, our recent research has found that heat stress down-regulates the transcription of PPARα in broiler chickens. To study if PPARα regulation is involved in heat-stress-induced skeletal muscle inflammatory response in broiler chickens, 180 male Arbor Acres (AA) broilers aged 22 days were randomly assigned to three experimental groups: a thermoneutral condition group at 21 °C, a heat stress group at 31 °C and a heat stress group at 31 °C supplemented with the PPARα activator fenofibrate. After 7 days of adaptive feeding, the broilers were subjected to a 14-day formal experimental phase. Results demonstrated that heat stress decreased the spleen and thymus index and increased serum and breast muscle inflammatory factor concentrations (p < 0.05). Moreover, heat-stress-induced abnormal breast muscle fiber morphology in broiler chickens. Furthermore, heat stress significantly up-regulated nuclear factor kappa-B (NF-κB) expression in boiler chickens (p < 0.05). However, activating PPARα through fenofibrate improved the growth performance (p < 0.05), enhanced immune organ indexes (p < 0.05), reduced inflammatory factor concentrations (p < 0.05), alleviated breast muscle fiber morphology damage and suppressed NF-κB expression (p < 0.05) in the breast muscle of broiler chickens. Based on our previous research, these results collectively underscore that heat stress induced inflammation and up-regulated NF-κB in the breast muscle of broiler chickens by inhibiting PPARα.

This study aimed to evaluate the performance, nutrient digestibility, intestinal health, and duodenum gene expression of broilers challenged with Eimeria spp. supplemented with or without monensin sodium. A total of 144 male chicks were used, distributed in a completely randomized design with three treatments: unchallenged control (UN), challenged control (CC), and CC + 100 mg/kg of monensin sodium (MON). Six replicates of eight birds each were used. At 14 days of age, the challenged groups were inoculated with a mixture of Eimeria oocysts, 12,500 E. maxima, 62,500 E. acervulina, and 12,500 E. tenella oocysts/chick. Coccidial challenge impaired growth performance and nutrient digestibility and induced intestinal damage, as evidenced by reduced body weight gain and feed intake (p < 0.001), lower apparent digestibility coefficients (p < 0.001), and altered intestinal morphometry and ISI score in the jejunum and cecum (p < 0.001). Monensin supplementation partially alleviated these negative effects, improving performance and nutrient digestibility (p < 0.001) and delaying oocyst excretion (p = 0.006) when compared with the CC group. However, the duodenal expression of tight junction-related genes, as well as intestinal integrity and health parameters, remained impaired despite monensin supplementation. It is concluded that monensin preserves nutrient digestibility and attenuates performance loss in broilers challenged with Eimeria spp. but not reduced intestinal damage.

In most countries, male siblings of laying hybrids are culled immediately after hatching because their rearing is economically unfeasible due to low growth performance, poor feed efficiency, and a body composition unacceptable to consumers. In Germany, however, culling male day-old chicks has been prohibited for animal welfare reasons since 2022, making their rearing mandatory. Currently, no recommendations exist for protein and amino acid supply for these birds. This study aimed to determine the requirements for standardized ileal digestible (SID) methionine + cysteine (Met + Cys) and SID lysine (Lys) during the starter period (days 1–21) in male LSL Classic chicks by a dose–response approach. Two trials were conducted with 120 male chicks each, fed six diets containing SID Met + Cys concentrations ranging from 0.36% to 0.71% (Trial 1) or SID Lys concentrations ranging from 0.50% to 0.89% (Trial 2). Optimal concentrations were estimated using broken-line and exponential models based on body weight gain, feed intake, and feed conversion ratio. Considering all criteria, the optimal SID Met + Cys concentration was 0.58% (0.42 g/MJ AME_N), and the optimal SID Lys concentration was 0.74% (0.56 g/MJ AME_N). The calculated optimum SID Met + Cys:SID Lys ratio when standardized to an identical energy level was 74:100. These findings provide a basis for adjusting SID Met + Cys and SID Lys levels in starter diets for male chicks of a layer breed, supporting more efficient and sustainable rearing practices under current animal welfare regulations.