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quinolinic acid and Amino Acid Metabolism Disorders, Inborn

quinolinic acid has been researched along with Amino Acid Metabolism Disorders, Inborn in 6 studies

Quinolinic Acid: A metabolite of tryptophan with a possible role in neurodegenerative disorders. Elevated CSF levels of quinolinic acid are correlated with the severity of neuropsychological deficits in patients who have AIDS.
pyridinedicarboxylic acid : Any member of the class of pyridines carrying two carboxy groups.
quinolinic acid : A pyridinedicarboxylic acid that is pyridine substituted by carboxy groups at positions 2 and 3. It is a metabolite of tryptophan.

Research Excerpts

ExcerptRelevanceReference
"Quinolinic acid (QUIN) is an agonist of the neurotransmitter glutamate (Glu) capable of binding to N-methyl-D-aspartate receptors (NMDAR) increasing glutamatergic signaling."1.62Caenorhabditis elegans as a model for studies on quinolinic acid-induced NMDAR-dependent glutamatergic disorders. ( Antunes Soares, FA; Aschner, M; Bicca Obetine Baptista, F; Duarte Hartmann, D; Farina Gonçalves, D; Franzen da Silva, A; Lenz Dalla Corte, C; Limana da Silveira, T; Lopes Machado, M; Marafiga Cordeiro, L, 2021)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's1 (16.67)29.6817
2010's2 (33.33)24.3611
2020's2 (33.33)2.80

Authors

AuthorsStudies
Barbieri Caus, L1
Pasquetti, MV1
Seminotti, B3
Woontner, M1
Wajner, M3
Calcagnotto, ME1
Limana da Silveira, T1
Lopes Machado, M1
Bicca Obetine Baptista, F1
Farina Gonçalves, D1
Duarte Hartmann, D1
Marafiga Cordeiro, L1
Franzen da Silva, A1
Lenz Dalla Corte, C1
Aschner, M1
Antunes Soares, FA1
Amaral, AU1
da Silva, JC1
de Oliveira, FH1
Ribeiro, RT1
Vargas, CR1
Leipnitz, G2
Santamaría, A2
Souza, DO2
Colín-González, AL1
Paz-Loyola, AL1
Serratos, I1
Ribeiro, CA1
Goodman, SI1
Land, JM1
Goulder, P1
Johnson, A1
Hockaday, J1

Other Studies

6 other studies available for quinolinic acid and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Increased susceptibility to quinolinic acid-induced seizures and long-term changes in brain oscillations in an animal model of glutaric acidemia type I.
    Journal of neuroscience research, 2022, Volume: 100, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain; Brain Diseases, Metabolic; Disease Models, Ani

2022
Caenorhabditis elegans as a model for studies on quinolinic acid-induced NMDAR-dependent glutamatergic disorders.
    Brain research bulletin, 2021, Volume: 175

    Topics: 1-Octanol; Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Animals; Animals, Genetical

2021
Induction of Neuroinflammatory Response and Histopathological Alterations Caused by Quinolinic Acid Administration in the Striatum of Glutaryl-CoA Dehydrogenase Deficient Mice.
    Neurotoxicity research, 2018, Volume: 33, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic; CD3 Complex; Corpus Striat

2018
Toxic synergism between quinolinic acid and organic acids accumulating in glutaric acidemia type I and in disorders of propionate metabolism in rat brain synaptosomes: Relevance for metabolic acidemias.
    Neuroscience, 2015, Nov-12, Volume: 308

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain; Brain Diseases, Metabolic; Disease Models, Ani

2015
Development of pathogenic concepts in glutaryl-CoA dehydrogenase deficiency: the challenge.
    Journal of inherited metabolic disease, 2004, Volume: 27, Issue:6

    Topics: Amino Acid Metabolism, Inborn Errors; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Oxidoreductase

2004
Glutaric aciduria type 1 an atypical presentation together with some observations upon treatment and the possible cause of cerebral damage.
    Neuropediatrics, 1992, Volume: 23, Issue:6

    Topics: Amino Acid Metabolism, Inborn Errors; Aminocaproates; Brain; Glutarates; Humans; Infant; Quinolinic

1992