Dietary Betaine Improves Intestinal Barrier Function and Ameliorates the Impact of Heat Stress in Multiple Vital Organs as Measured by Evans Blue Dye in Broiler Chickens

In a 2 × 2 factorial design, 60 male Ross-308 broilers were fed either a control or 1 g/kg betaine diet and housed under thermoneutral (TN) or heat stress (HS) conditions. Broilers were acclimated to diets for 1 week under TN (25 °C), then either kept at TN or HS, where the temperature increased 8 h...

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Veröffentlicht in:Animals (Basel) 2020-01, Vol.10 (1), p.38
Hauptverfasser: Shakeri, Majid, Cottrell, Jeremy James, Wilkinson, Stuart, Zhao, Weicheng, Le, Hieu Huu, McQuade, Rachel, Furness, John Barton, Dunshea, Frank Rowland
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Sprache:eng
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Zusammenfassung:In a 2 × 2 factorial design, 60 male Ross-308 broilers were fed either a control or 1 g/kg betaine diet and housed under thermoneutral (TN) or heat stress (HS) conditions. Broilers were acclimated to diets for 1 week under TN (25 °C), then either kept at TN or HS, where the temperature increased 8 h/day at 33 °C and 16 h/day at 25 °C for up to 10 days. Respiration rate (RR) was measured at four time points, and on each of 1, 2, 3, 7 and 10 days of HS, 12 broilers were injected with 0.5 mg/kg of Evans Blue Dye (EBD) solution to quantify regional changes in tissue damage. Betaine was quantified in tissues, and ileal damage was assessed via morphometry and transepithelial resistance (TER). Heat stress elevated RR ( < 0.001) and resulted in reduced villous height ( = 0.009) and TER ( < 0.001), while dietary betaine lowered RR during HS ( < 0.001), increased betaine distribution into tissues, and improved ileal villous height ( < 0.001) and TER ( = 0.006). Heat stress increased EBD in the muscle and kidney of chickens fed the control diet but not in those receiving betaine. Overall, these data indicate that supplemented betaine is distributed to vital organs and the gastrointestinal tract, where it is associated with improved tolerance of HS. Furthermore, EBD markers help reveal the effects of HS on organs dysfunction.
ISSN:2076-2615
2076-2615
DOI:10.3390/ani10010038