The present study was conducted to evaluate the effects of dietary marine-derived polysaccharides (MDP) from seaweed Enteromorpha on productive performance, egg quality, antioxidant capacity, and jejunal morphology in late-phase laying hens. A total of 240 Lohmann white laying hens (62 wk of age) were assigned to 4 dietary treatments that included MDP at concentrations of 0, 1,000, 2,500, and 5,000 mg/kg for 6 wk. Each treatment had 6 replicates with 5 cages (2 birds/cage). The results showed that dietary MDP quadratically improved egg production ( P < 0.05) during 5 to 6 wk and 1 to 6 wk. There was a linear reduction in cracked egg rate ( P < 0.05) with dietary MDP levels increased during 3 to 4 wk and 1 to 6 wk. After 4 wk of feeding trial, the egg shell thickness, yolk color, and Haugh unit showed a linear increase ( P < 0.05) in response to increasing dietary MDP levels. Besides, the egg shell breaking strength, egg shell thickness, yolk color, and Haugh unit were improved linearly ( P < 0.05) by dietary MDP at the end of the experiment. Moreover, dietary MDP showed a linear and quadratic reduction in serum malondialdehyde (MDA) content ( P < 0.05) at the end of third week. At the end of experiment, the activity of total superoxide dismutase in serum was increased quadratically ( P < 0.05) by dietary MDP, and dietary MDP quadratically improved the liver catalase (CAT) activity ( P < 0.05) and linearly enhanced jejunal CAT activity ( P < 0.05), whereas linearly decreased jejunal MDA concentration ( P < 0.05). Furthermore, supplemental MDP linearly improved the villus height ( P < 0.05) and quadratically increased villus height/crypt depth ratio ( P < 0.05) of jejunum. However, dietary MDP had no effect on jejunal trypsin, amylase, and protease activity ( P > 0.10). Taken together, these findings provided new insights into the role of MDP in improving the productive performance, egg quality, antioxidant capacity, and jejunal morphology of late-phase laying hens.
This study was done to evaluate the effects of heat stress (HS) on production performance, redox status, small intestinal barrier-related parameters, cecal microbiota, and metabolome of indigenous broilers. A total of forty female indigenous broilers (56-day-old) were randomly and equally divided into normal treatment group (NT group, 21.3 ± 1.2°C, 24 h/day) and HS group (32.5 ± 1.4°C, 8 h/day) with five replicates of each for 4 weeks feeding trial. The results showed that the body weight gain (BWG) of broilers in HS group was lower than those in NT group during 3–4 weeks and 1–4 weeks (p < 0.05). The HS exposure increased the abdominal fat rate (p < 0.05) but decreased the thigh muscle rate (p < 0.01). Besides, broilers in HS group had higher drip loss of breast muscle than NT group (p < 0.01). Broilers exposed to HS had lower total antioxidant capacity (T-AOC) in serum and jejunum, activities of total superoxide dismutase (T-SOD) in the jejunum, glutathione peroxidase (GSH-Px) in the thigh muscle, duodenum, and jejunum; and catalase (CAT) in breast muscle, duodenum, and jejunum (p < 0.05). Whereas the malondialdehyde (MDA) contents in breast muscle, duodenum, and jejunum was elevated by HS exposure (p < 0.05). Moreover, the relative mRNA expression of Occludin and ZO-1 in the duodenum, Occludin, Claudin-1, Claudin-4, ZO-1, Mucin-2 in the jejunum, and the Claudin-4 and Mucin-2 in the ileum was down-regulated by HS exposure (p < 0.05). The 16S rRNA sequencing results showed that the HS group increased the relative abundance of Anaerovorax in the cecum at the genus level (p < 0.05). Cecal metabolomics analysis indicated 19 differential metabolites between the two groups (p < 0.10, VIP >1). The Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis revealed that the differential metabolites mainly enriched in 10 signaling pathways such as the Citrate cycle (TCA cycle) (p < 0.01). In summary, chronic HS exposure caused a decline of production performance, reduced antioxidant capacity, disrupted intestinal barrier function, and negatively affected cecal microbiota and metabolome in indigenous broilers.
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