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pyruvic acid and BCKD Deficiency

pyruvic acid has been researched along with BCKD Deficiency in 5 studies

Pyruvic Acid: An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed)
pyruvic acid : A 2-oxo monocarboxylic acid that is the 2-keto derivative of propionic acid. It is a metabolite obtained during glycolysis.

Research Excerpts

ExcerptRelevanceReference
" In the present study, we evaluated the possible preventive effect of the co-administration of creatine plus pyruvate on the effects elicited by leucine administration to female Wistar rats during pregnancy and lactation on some oxidative stress parameters as well as the activities of some enzymes involved in the phosphoryltransfer network in the brain cortex and hippocampus of the offspring at 21 days of age."7.79Effect of leucine administration to female rats during pregnancy and lactation on oxidative stress and enzymes activities of phosphoryltransfer network in cerebral cortex and hippocampus of the offspring. ( Campos, AG; de Franceschi, ID; Feksa, LR; Rech, VC; Rieger, E; Rojas, DB; Vargas, AP; Wannmacher, CM, 2013)
" In the present study, we evaluated the possible preventive effect of the co-administration of creatine plus pyruvate on the effects elicited by leucine administration to female Wistar rats during pregnancy and lactation on some oxidative stress parameters as well as the activities of some enzymes involved in the phosphoryltransfer network in the brain cortex and hippocampus of the offspring at 21 days of age."3.79Effect of leucine administration to female rats during pregnancy and lactation on oxidative stress and enzymes activities of phosphoryltransfer network in cerebral cortex and hippocampus of the offspring. ( Campos, AG; de Franceschi, ID; Feksa, LR; Rech, VC; Rieger, E; Rojas, DB; Vargas, AP; Wannmacher, CM, 2013)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19903 (60.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ambrus, A1
de Franceschi, ID1
Rieger, E1
Vargas, AP1
Rojas, DB1
Campos, AG1
Rech, VC1
Feksa, LR1
Wannmacher, CM1
PICCARDO, MG1
LUZIETTI, L1
CAPURSO, L1
Cremer, JE1
Teal, HM1
Cunningham, VJ1
Kolodny, EH1
Yatziv, S1

Reviews

1 review available for pyruvic acid and BCKD Deficiency

ArticleYear
An Updated View on the Molecular Pathomechanisms of Human Dihydrolipoamide Dehydrogenase Deficiency in Light of Novel Crystallographic Evidence.
    Neurochemical research, 2019, Volume: 44, Issue:10

    Topics: Acidosis, Lactic; Amino Acid Oxidoreductases; Cytochrome-B(5) Reductase; Dihydrolipoamide Dehydrogen

2019

Other Studies

4 other studies available for pyruvic acid and BCKD Deficiency

ArticleYear
Effect of leucine administration to female rats during pregnancy and lactation on oxidative stress and enzymes activities of phosphoryltransfer network in cerebral cortex and hippocampus of the offspring.
    Neurochemical research, 2013, Volume: 38, Issue:3

    Topics: Animals; Antioxidants; Cerebral Cortex; Creatine; Female; Hippocampus; Lactation; Leucine; Male; Map

2013
[VARIOUS ASPECTS OF KETOACIDURIA AND KETOACIDEMIA IN DIABETICS: URINARY EXCRETION AND HEMATIC LEVELS OF ALPHA-KETOISOCAPROIC ACID, ALPHA-KETOISOVALERIC ACID, PYRUVIC ACID AND ALPHA-KETOGLUTARIC ACID].
    Il Policlinico. Sezione medica, 1963, Volume: 70

    Topics: Biomedical Research; Blood Chemical Analysis; Diabetes Mellitus; Hemiterpenes; Humans; Keto Acids; K

1963
Inhibition, by 2-oxo acids that accumulate in maple-syrup-urine disease, of lactate, pyruvate, and 3-hydroxybutyrate transport across the blood-brain barrier.
    Journal of neurochemistry, 1982, Volume: 39, Issue:3

    Topics: 3-Hydroxybutyric Acid; Animals; Blood-Brain Barrier; Brain; Humans; Hydroxybutyrates; Keto Acids; Ki

1982
Laboratory approaches for inherited neurometabolic diseases.
    Developmental medicine and child neurology, 1985, Volume: 27, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Galactosemias; Homocystinuria; Humans; Lactates; Lact

1985