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aspartic acid and Mitochondrial Diseases

aspartic acid has been researched along with Mitochondrial Diseases in 20 studies

Aspartic Acid: One of the non-essential amino acids commonly occurring in the L-form. It is found in animals and plants, especially in sugar cane and sugar beets. It may be a neurotransmitter.
aspartic acid : An alpha-amino acid that consists of succinic acid bearing a single alpha-amino substituent
L-aspartic acid : The L-enantiomer of aspartic acid.

Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.

Research Excerpts

ExcerptRelevanceReference
"Semiquantitative analysis of NAA relative to creatine-containing compounds (Cr) and choline (Cho) was carried out from proton spectra obtained by means of chemical shift (CS) imaging and single-voxel (SV) methods in 25 patients with severe traumatic brain injuries (TBIs) (Glasgow Coma Scale scores < or = 8) using a 1."5.13Assessment of mitochondrial impairment in traumatic brain injury using high-resolution proton magnetic resonance spectroscopy. ( Aygok, GA; Bullock, RM; Fatouros, PP; Marmarou, A; Portella, G; Signoretti, S, 2008)
"Patients with mitochondrial disorders offer a unique window through which we can begin to understand the association between psychiatric symptoms and mitochondrial dysfunction in vivo."1.38Psychiatric symptoms correlate with metabolic indices in the hippocampus and cingulate in patients with mitochondrial disorders. ( Anglin, RE; Mazurek, MF; Noseworthy, MD; Rosebush, PI; Tarnopolsky, M, 2012)
"Recently, the clinical spectrum of dominant optic atrophy has been extended to frequent syndromic forms, exhibiting various degrees of neurological and muscle impairments frequently found in mitochondrial diseases."1.38The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse. ( Angebault, C; Bielicki, G; Boddaert, N; Brabet, P; Cazevieille, C; Chaix, B; Delettre, C; Gueguen, N; Hamel, CP; Lenaers, G; Mausset-Bonnefont, AL; Puel, JL; Renou, JP; Reynier, P; Rigau, V; Sarzi, E; Seveno, M; Wang, J, 2012)

Research

Studies (20)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's10 (50.00)29.6817
2010's10 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fukuda, M1
Nagao, Y1
Iannetti, EF1
Smeitink, JAM1
Willems, PHGM1
Beyrath, J1
Koopman, WJH1
Takanashi, J1
Nitta, N1
Iwasaki, N1
Saito, S1
Tanaka, R1
Barkovich, AJ1
Aoki, I1
Profilo, E1
Peña-Altamira, LE1
Corricelli, M1
Castegna, A1
Danese, A1
Agrimi, G1
Petralla, S1
Giannuzzi, G1
Porcelli, V1
Sbano, L1
Viscomi, C1
Massenzio, F1
Palmieri, EM1
Giorgi, C1
Fiermonte, G1
Virgili, M1
Palmieri, L1
Zeviani, M1
Pinton, P1
Monti, B1
Palmieri, F1
Lasorsa, FM1
Chandrashekar, KN1
Aygok, GA3
Marmarou, A3
Fatouros, P2
Kettenmann, B1
Bullock, RM2
Haller, RG1
Vissing, J1
Friedman, SD1
Shaw, DW1
Ishak, G1
Gropman, AL1
Saneto, RP1
Quintanilla, RA1
Dolan, PJ1
Jin, YN1
Johnson, GV1
Anglin, RE1
Rosebush, PI1
Noseworthy, MD1
Tarnopolsky, M1
Mazurek, MF1
Llorente-Folch, I1
Sahún, I1
Contreras, L1
Casarejos, MJ1
Grau, JM1
Saheki, T1
Mena, MA1
Satrústegui, J1
Dierssen, M1
Pardo, B1
Sarzi, E1
Angebault, C1
Seveno, M1
Gueguen, N1
Chaix, B1
Bielicki, G1
Boddaert, N1
Mausset-Bonnefont, AL1
Cazevieille, C1
Rigau, V1
Renou, JP1
Wang, J1
Delettre, C1
Brabet, P1
Puel, JL1
Hamel, CP1
Reynier, P1
Lenaers, G1
Haut, S1
de Villemeur, TB1
Brivet, M1
Guiochon-Mantel, A1
Boutron, A1
Rustin, P1
Legrand, A1
Slama, A1
Schweinsburg, BC1
Taylor, MJ1
Alhassoon, OM1
Gonzalez, R1
Brown, GG1
Ellis, RJ1
Letendre, S1
Videen, JS1
McCutchan, JA1
Patterson, TL1
Grant, I1
Dinopoulos, A1
Cecil, KM1
Schapiro, MB1
Papadimitriou, A1
Hadjigeorgiou, GM1
Wong, B1
deGrauw, T1
Egelhoff, JC1
Signoretti, S2
Bullock, R1
Correia, C1
Coutinho, AM1
Diogo, L1
Grazina, M1
Marques, C1
Miguel, T1
Ataíde, A1
Almeida, J1
Borges, L1
Oliveira, C1
Oliveira, G1
Vicente, AM1
Vielhaber, S1
Niessen, HG1
Debska-Vielhaber, G1
Kudin, AP1
Wellmer, J1
Kaufmann, J1
Schönfeld, MA1
Fendrich, R1
Willker, W1
Leibfritz, D1
Schramm, J1
Elger, CE1
Heinze, HJ1
Kunz, WS1
Fatouros, PP1
Portella, G1
Bizzi, A1
Castelli, G1
Bugiani, M1
Barker, PB1
Herskovits, EH1
Danesi, U1
Erbetta, A1
Moroni, I1
Farina, L1
Uziel, G1

Reviews

1 review available for aspartic acid and Mitochondrial Diseases

ArticleYear
The use of neuroimaging in the diagnosis of mitochondrial disease.
    Developmental disabilities research reviews, 2010, Volume: 16, Issue:2

    Topics: Adenosine Triphosphate; Aspartic Acid; Brain; Child; Developmental Disabilities; Diagnosis, Differen

2010

Trials

3 trials available for aspartic acid and Mitochondrial Diseases

ArticleYear
Brain mitochondrial injury in human immunodeficiency virus-seropositive (HIV+) individuals taking nucleoside reverse transcriptase inhibitors.
    Journal of neurovirology, 2005, Volume: 11, Issue:4

    Topics: Adult; Aspartic Acid; Brain; Cell Respiration; Didanosine; Female; HIV Infections; Humans; Lamivudin

2005
Mitochondrial injury measured by proton magnetic resonance spectroscopy in severe head trauma patients.
    Acta neurochirurgica. Supplement, 2005, Volume: 95

    Topics: Adult; Aspartic Acid; Biomarkers; Brain; Brain Ischemia; Choline; Craniocerebral Trauma; Creatine; F

2005
Assessment of mitochondrial impairment in traumatic brain injury using high-resolution proton magnetic resonance spectroscopy.
    Journal of neurosurgery, 2008, Volume: 108, Issue:1

    Topics: Adolescent; Adult; Aspartic Acid; Brain Injuries; Choline; Creatine; Female; Follow-Up Studies; Huma

2008

Other Studies

16 other studies available for aspartic acid and Mitochondrial Diseases

ArticleYear
Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report.
    Journal of medical case reports, 2019, Oct-21, Volume: 13, Issue:1

    Topics: Arginine; Aspartic Acid; Biomarkers; Deafness; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Growth

2019
Rescue from galactose-induced death of Leigh Syndrome patient cells by pyruvate and NAD
    Cell death & disease, 2018, 11-14, Volume: 9, Issue:11

    Topics: Adenosine Triphosphate; Aspartic Acid; Cell Death; Culture Media; Electron Transport Complex I; Fibr

2018
Neurochemistry in shiverer mouse depicted on MR spectroscopy.
    Journal of magnetic resonance imaging : JMRI, 2014, Volume: 39, Issue:6

    Topics: Amino Acid Transport Systems, Acidic; Analysis of Variance; Animals; Antiporters; Aspartic Acid; Bra

2014
Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cells.
    Biochimica et biophysica acta. Molecular basis of disease, 2017, Volume: 1863, Issue:6

    Topics: Amino Acid Transport Systems; Amino Acid Transport Systems, Acidic; Antiporters; Aspartic Acid; Cell

2017
D-Aspartic acid induced oxidative stress and mitochondrial dysfunctions in testis of prepubertal rats.
    Amino acids, 2010, Volume: 38, Issue:3

    Topics: Animals; Aspartic Acid; Biomarkers; Calcium Signaling; Dose-Response Relationship, Drug; Lipid Perox

2010
Assessment of mitochondrial impairment and cerebral blood flow in severe brain injured patients.
    Acta neurochirurgica. Supplement, 2008, Volume: 102

    Topics: Aspartic Acid; Blood Flow Velocity; Brain Injuries; Cerebrovascular Circulation; Diffusion Magnetic

2008
Drilling for energy in mitochondrial disease.
    Archives of neurology, 2009, Volume: 66, Issue:8

    Topics: Adenosine Triphosphate; Animals; Apoptosis; Aspartic Acid; Cell Survival; Cells, Cultured; DNA Mutat

2009
Truncated tau and Aβ cooperatively impair mitochondria in primary neurons.
    Neurobiology of aging, 2012, Volume: 33, Issue:3

    Topics: Alzheimer Disease; Amyloid beta-Peptides; Animals; Aspartic Acid; Cell Line, Transformed; Down-Regul

2012
Psychiatric symptoms correlate with metabolic indices in the hippocampus and cingulate in patients with mitochondrial disorders.
    Translational psychiatry, 2012, Nov-13, Volume: 2

    Topics: Adult; Aged; Anxiety; Aspartic Acid; Case-Control Studies; Caudate Nucleus; Creatine; Female; Glutam

2012
AGC1-malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway.
    Journal of neurochemistry, 2013, Volume: 124, Issue:3

    Topics: Amino Acid Transport Systems, Acidic; Animals; Antiporters; Aspartic Acid; Corpus Striatum; Dopamine

2013
The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse.
    Brain : a journal of neurology, 2012, Volume: 135, Issue:Pt 12

    Topics: Acoustic Stimulation; Age Factors; Aging, Premature; Animals; Aspartic Acid; Chi-Square Distribution

2012
The deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriers.
    European journal of human genetics : EJHG, 2004, Volume: 12, Issue:3

    Topics: Amino Acid Sequence; Aspartic Acid; Child, Preschool; Cytochromes b; DNA, Mitochondrial; Electron Tr

2004
Brain MRI and proton MRS findings in infants and children with respiratory chain defects.
    Neuropediatrics, 2005, Volume: 36, Issue:5

    Topics: Aspartic Acid; Brain; Brain Chemistry; Brain Mapping; Child; Child, Preschool; Female; Humans; Infan

2005
Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene.
    Journal of autism and developmental disorders, 2006, Volume: 36, Issue:8

    Topics: Aspartic Acid; Autistic Disorder; Chromosome Mapping; DNA Mutational Analysis; DNA Primers; DNA, Mit

2006
Subfield-specific loss of hippocampal N-acetyl aspartate in temporal lobe epilepsy.
    Epilepsia, 2008, Volume: 49, Issue:1

    Topics: Aconitate Hydratase; Adult; Aged; Aspartic Acid; Cell Count; Electroencephalography; Epilepsy, Tempo

2008
Classification of childhood white matter disorders using proton MR spectroscopic imaging.
    AJNR. American journal of neuroradiology, 2008, Volume: 29, Issue:7

    Topics: Adrenoleukodystrophy; Adult; Alexander Disease; Aspartic Acid; Brain; Child; Child, Preschool; Choli

2008