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Chronic lung inflammation affects plasma amino acid concentrations in pigs
D Melchior1, B Sève, N Le Floc'h
1Institut National de la Recherche Agronomique, Unité Mixte de Recherche sur le Veau et le Porc, 35590 Saint Gilles, France.
Journal of Animal Science
|April 15, 2004
Summary
Chronic lung inflammation alters amino acid (AA) metabolism in piglets, decreasing plasma tryptophan and increasing utilization of certain AAs. This highlights potential nutritional interventions for immune support and growth during inflammation.
Area of Science:
- Animal Nutrition
- Immunology
- Biochemistry
Background:
- Inflammatory processes and immune responses significantly impact protein and amino acid (AA) requirements.
- Understanding these metabolic shifts is crucial for developing nutritional strategies to support growth and immune function simultaneously.
Purpose of the Study:
- To identify specific amino acids (AAs) whose metabolism is altered by chronic lung inflammation in a piglet model.
- To investigate the impact of inflammation on plasma AA concentrations and their utilization.
Main Methods:
- Six pairs of littermate piglets were used, with one receiving complete Freund's adjuvant (CFA) to induce inflammation and the other a saline control (CON).
- Piglets were pair-fed to control for feed intake variations.
- Plasma AA concentrations were measured in both fasted and fed states over 9 days, alongside body temperature, weight gain, and haptoglobin levels.
Main Results:
- CFA injection led to decreased food intake, increased body temperature, and elevated plasma haptoglobin.
- Plasma concentrations of tryptophan, glutamine, proline, glycine, tyrosine, ornithine, and total AAs were lower in CFA than CON pigs.
- Histidine levels were higher in CFA pigs, while serine, arginine, alanine, and asparagine were lower in the fed state only.
- Tryptophan was the only essential AA significantly lower in CFA pigs under both fasted and fed conditions.
Conclusions:
- Chronic lung inflammation differentially affects individual AA metabolism in piglets.
- Results suggest an increased utilization of certain AAs, potentially including tryptophan, during inflammation.
- Activation of tryptophan catabolism via indoleamine 2,3-dioxygenase is a plausible explanation for increased tryptophan utilization.