**Background:** Poultry face various stressors that can disrupt redox balance. Modern fast-growing broiler strains are more susceptible to oxidative stress than slow-growing, more robust strains used in free-range production. While antioxidant system development during embryogenesis is well-described, post-hatch evolution remains unclear. This study aimed to provide a comprehensive weekly profile of metabolic and redox markers in two chicken strains differing in growth rate.
**Methods:** Fast-growing (FG) Ross 308 and slow-growing (SG) JA 657 male chicks (120 per strain) were reared under identical conditions with three feeding periods (starter D1–14, grower D15–28, finisher D29–42). Diets contained 20 ppm vitamin E. At D1, D7, D14, D21, D28, D35, and D42, 10 birds per strain were sacrificed after 8 h fasting. Blood, pectoralis major muscle, thigh muscle, and liver were collected. Plasma was analyzed for glucose, uric acid, triglycerides, free fatty acids (FFA), β-hydroxybutyrate (β-OH), total antioxidant status (TAS), hydroperoxides (HPO), α- and γ-tocopherol, and activities of SOD, GPx, GR, and peroxidase. Tissues were analyzed for TAS, TBARS (lipid peroxidation), and activities of SOD, GPx, GR, and catalase. Statistical analysis used two-way ANOVA (age, strain, interaction) with significance at p ≤ 0.05.
**Key Results:** Body weight increased from 51.6 g (D1) to 3134 g (D42) in FG and from 33.9 g to 1090 g in SG (p < 0.001). Plasma triglycerides dropped sharply from D1 to D7 (FG: 1061→266 mg/L; SG: 462→135 mg/L; p < 0.001). FFA increased from 217 to 877 μmol/L (D1→D21) in FG and from 96 to 643 μmol/L (D1→D7) in SG. β-OH peaked at D14 (FG: 737 μmol/L; SG: 821 μmol/L). Plasma hydroperoxides fell from 11.67 (FG) or 16.48 (SG) μmol/mL at D1 to ~2.2–2.6 μmol/mL at D14 (p < 0.001). α-tocopherol decreased from 53.99 (FG) or 34.15 (SG) ng/μL at D1 to ~6–7 ng/μL at D14 (p < 0.001). Plasma peroxidase activity declined from 3.68 (FG) or 4.69 (SG) mU/mL at D1 to ~2.2–2.6 mU/mL at D14 (p < 0.001). Plasma GR decreased from ~0.042–0.043 U/L at D1 to ~0.025–0.028 U/L at D7 (p < 0.001). In breast muscle, catalase dropped ~10-fold from ~9.5 U/μg proteins at D1 to ~0.9–1.3 U/μg proteins at D7 (p < 0.001). Liver TBARS increased from D1 to D7 (FG: 1.17→2.77; SG: 1.88→3.08 mg MDA/kg; p < 0.001) then declined. Strain differences: SG chicks had higher plasma uric acid at D1 (87.44 vs. 29.41 mg/L) but lower at D14–D28; FG uric acid peaked at D21 (91.78 mg/L). SOD activity was lower in FG plasma from D1–D21, in liver D1–D14, in thigh D7–D42, and in breast D14–D42 compared to SG (p < 0.05). FG had higher GR activity in breast muscle at D1 and D21–D42 (p < 0.05) and in plasma at D35–D42 (p < 0.05). Plasma TAS in SG decreased from 1.48 mmol/L (D1) to 0.88 mmol/L (D21), while FG TAS fluctuated (1.04→1.31→0.93→1.25 mmol/L).
**Clinical Implications:** The study confirms that the first week post-hatch is a period of intense oxidative stress, with rapid depletion of vitamin E and several antioxidant enzymes. The divergent antioxidant strategies between strains—SOD-dependent in SG chickens versus uric acid-dependent in FG chickens—suggest that nutritional or management interventions to support redox balance may need to be strain-specific. For slow-growing chickens, supporting SOD activity (e.g., through adequate manganese, zinc, and copper supplementation) may be beneficial, while for fast-growing chickens, managing protein metabolism and uric acid levels could be more relevant. The detailed temporal profiles provided can guide targeted antioxidant supplementation strategies at specific developmental stages to improve poultry health and robustness.