AI Article Synopsis

  • Single amino acids (AA) feeding is being studied for their effects beyond just nutrition, particularly their impact on endocrine and metabolic responses in sheep after fasting.
  • Fasted sheep were given a duodenal infusion of saline or specific AAs (glutamate, glutamine, lysine, threonine, valine) over four hours, while blood samples were collected to measure various metabolic markers.
  • Findings indicated that certain AAs enhanced ghrelin release, altered levels of plasma BHBA and NEFA, increased insulin and glucagon levels, and elevated IGF-1, suggesting that selective AA feeding can improve endocrine response and help manage fat mobilization during feed restriction.

Article Abstract

Single amino acids (AA) feeding is gaining more attention for their functional roles beyond nutritional needs. This study aimed to describe the endocrine and metabolic responses to a single AA administration (at 10% of MP for maintenance) in 48 hr fasted sheep (n = 4) receiving, over continued 4 hr, a duodenal infusate of saline (control), glutamate (Glu), glutamine (Gln), lysine HCl (Lys), threonine (Thr), or valine (Val) in a 4 by 6 Youden square design with weekly intervals. Blood samples were collected at 0, 15, 30, 60, 120, 180, and 240 min relative to the infusion onset, and plasma AA, glucose, β-hydroxybutyric acid (BHBA), nonesterified fatty acids (NEFA), ghrelin, insulin, glucagon, and insulin-like growth factor 1 (IGF-1) concentrations were measured. The results showed that the duodenal supply of Glu, Gln, Lys, Thr, and Val enhanced ghrelin release. Administration of Glu, Gln, and Val declined plasma BHBA concentrations, whereas plasma NEFA levels were decreased with Gln and Thr. Insulin concentration was greater with Thr, glucagon levels were increased with Lys, Thr, Val, and Glu, whereas IGF-1 levels were enhanced with Gln, Lys, and Thr supply. Thus, selective AA feeding can positively adjust the endocrine status and counteract the feed restriction-induced lipid mobilization.

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Source
http://dx.doi.org/10.1111/asj.13114DOI Listing

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