Alpha-Amino-n-butyric acid (A-ANB/α-Amino-N-butyric acid) is an intermediate occurring in the catabolism of two essential amino acids, methionine, and threonine.
Possible increased need for the nutrients which aid in threonine metabolism from which this AA is derived. These include α-KG and B6.
Possible treatment if low:
Supplement with vitamin B6 and alpha-ketoglutarate.
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Inadequate utilization of this amino acid for cellular energy generation. α-Amino-N-butyric acid is converted to succinyl Co-A for use in the citric acid cycle via mechanisms requiring biotin (Vit B7) and B12.
Elevated A-ANB can be secondary to elevations of either (methionine or threonine). No metabolic error specific to A-ANB is documented. Anecdotal evidence relates elevated A-ANB to vitamin B6 deficiency and adrenocortical excess or use of corticosteroid medications.
Via alpha-ketobutyric acid, A-ANB becomes propionic acid, and this transformation requires thiamin, vitamin B2 as FAD, B3 as NAD, lipoic acid, and magnesium. Deficiencies in these nutrients, as well as vitamin B6, could cause A-ANB to accumulate.
An elevated marker can also indicate alcoholism.
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1-Methylhistidine (Urine), 3-Methylhistidine (Urine), a-Amino-N-butyric Acid (Urine), a-Aminoadipic (Urine), Alanine (Urine), Anserine (dipeptide), Arginine (Urine), Asparagine (Urine), Aspartic Acid (Urine), b-Alanine (Urine), b-Aminoisobutyric Acid (Urine), Carnosine (dipeptide), Citrulline (Urine), Cystathionine (Urine), Cysteine (FMV urine), Cystine (FMV Urine), Ethanolamine (Urine), g-Aminobutyric Acid (Urine), Glutamic Acid (Urine), Glutamine (Urine), Glycine (Urine), Histidine (Urine), Isoleucine (Urine), Leucine (Urine), Lysine (Urine), Methionine (Urine), Ornithine (Urine), Phenylalanine (Urine), Phosphoethanolamine (Urine), Phosphoserine (Urine), Proline (Urine), Sarcosine (Urine), Serine (Urine), Taurine (Urine), Threonine (Urine), Tryptophan (Urine), Tyrosine (Urine), Urea (Urine), Valine (Urine)