Amino acid pool
- Describes all free amino acids in the body
- Amino acids: body’s primary source of nitrogen
AMINO ACID STRUCTURE
- Central carbon bound to: -H, -COOH, -NH3, R-group
- R-group: acidic (-), basic (+), branched, etc.
AMINO ACID POOL: INPUTS AND OUTPUTS
Input
- Dietary proteins: absorbed as amino acids/peptides in small intestine
– Pass through hepatic portal vein and immediately enter liver
– Liver plays central role in fates of free amino acids - De novo amino acid synthesis: use C-skeletons & alpha-amino group of other amino acids to synthesize new ones
- Protein turnover: breakdown of cellular proteins
Output
- Oxidation: excess amino acids degraded to alpha amino group & C-skeleton
– Urea cycle: liver rids body of nitrogen waste
– Energy production: C-skeletons enter glycolysis or citric acid cycle
– Gluconeogenesis: occurs in liver
– Storage: amino acids can’t be stored –> C-skeletons stored as glycogen/fats - Synthesis of nitrogen-containing molecules
– Amino acids
– Neurotransmitters
– Nucleotides (purines and pyrimidines)
– Creatine, etc. - Protein turnover: synthesis of new proteins
Protein turnover
Cyclic synthesis and breakdown of proteins in the body
- Produces and consumes free amino acids
- Protein synthesis: depletes pool of free amino acids
- Protein breakdown: replenishes pool
ESSENTIAL AMINO ACIDS
Must be obtained from diet
- “My Tall Vegan Friend Is Watering Kale Leaves” – M, T, V, F, I, W, K, L
- Glucogenic: Methionine, threonine, valine
- Glucogenic & ketogenic: Phenylalanine, isoleucine, tryptophan
- Ketogenic: lysine & leucine
Branched chain amino acids (BCAA)
- Valine, leucine, isoleucine
- Immediately shunt from liver to circulation
- Liver lacks an aminotransferase that muscle, adipose, kidney & brain have
Aminotransferases: family of enzymes involved in amino acid breakdown
NONESSENTIAL AMINO ACIDS
Synthesized endogenously (The rest of the amino acids)
- Glucogenic: alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, histidine*, proline & serine
- Glucogenic and ketogenic: tyrosine
- Histidine is often considered essential because it is essential during the first 5 years of life but later becomes nonessential.
Note that there are many ways to categorize essential/nonessential amino acids
CLINICAL CORRELATION
Conditionally essential amino acids
- Cannot be synthesized under certain physiologic conditions
- Infants < 5 years old can’t synthesize: arginine, cysteine, histidine, tyrosine
- Immunosuppressed patients/postoperative infections: treat w/ arginine & glutamine supplements
