2018
DOI: 10.21037/atm.2018.12.12
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Amino acid disorders

Abstract: Amino acids serve as key building blocks and as an energy source for cell repair, survival, regeneration and growth. Each amino acid has an amino group, a carboxylic acid, and a unique carbon structure. Human utilize 21 different amino acids; most of these can be synthesized endogenously, but 9 are "essential" in that they must be ingested in the diet. In addition to their role as building blocks of protein, amino acids are key energy source (ketogenic, glucogenic or both), are building blocks of Kreb's (aka T… Show more

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Cited by 93 publications
(64 citation statements)
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“…With increasing national income and advancements in poultry production and genetics, the national rate of chicken breast consumption has increased as a desired dietary protein source providing all 9 essential amino acids (histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine) required in the human diet ( USDA, 2015 ; Aliu et al., 2018 ). The essential amino acids are required in the diet to maintain vital physiological functions and cannot be produced de novo .…”
Section: Resultsmentioning
confidence: 99%
“…With increasing national income and advancements in poultry production and genetics, the national rate of chicken breast consumption has increased as a desired dietary protein source providing all 9 essential amino acids (histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine) required in the human diet ( USDA, 2015 ; Aliu et al., 2018 ). The essential amino acids are required in the diet to maintain vital physiological functions and cannot be produced de novo .…”
Section: Resultsmentioning
confidence: 99%
“…Glutamate, methionine, glycine, isoleucine, leucine, lysine, and phenylalanine were found in significantly lower concentrations in severe hypospadias. These metabolites are associated with inborn errors of metabolism (32)(33)(34)(35)(36)(37)(38). Some examples of inborn errors of metabolism diseases are phenylketonuria, maple syrup urine disease, tyrosinemia type I, glycine encephalopathy, which involve the deficiency or accumulation of these amino acids (32).…”
Section: Discussionmentioning
confidence: 99%
“…These metabolites are associated with inborn errors of metabolism (32)(33)(34)(35)(36)(37)(38). Some examples of inborn errors of metabolism diseases are phenylketonuria, maple syrup urine disease, tyrosinemia type I, glycine encephalopathy, which involve the deficiency or accumulation of these amino acids (32). Moreover, Carmichael and colleagues (38) investigated whether hypospadias is associated with maternal dietary intake of nutrients related to one-carbon metabolism, including methionine.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, a high reduction of 2-hydroxyisovalerate and 2-hydroxyisocaproate concentrations after the ulcer treatment with probiotics was also detected. These molecules are hydroxyderivate of the alpha-ketoacid catabolites respectively produced by transamination of valine and leucine [38, 39]. Valine and leucine catabolism may proceed toward propionate synthesis or may shift to 2-hydroxyisovalerate and 2-hydroxyisocaproate production.…”
Section: Discussionmentioning
confidence: 99%