acetylcysteine and Electron Transport Chain Deficiencies, Mitochondrial

acetylcysteine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 17 studies

Research

Studies (17)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (5.88)29.6817
2010's13 (76.47)24.3611
2020's3 (17.65)2.80

Authors

AuthorsStudies
Anagnostou, F; Barzegari, A; Gueguen, V; Landon, R; Meddahi-Pellé, A; Omidi, Y; Parvizpour, S; Pavon-Djavid, G1
Bindoff, LA; Chen, A; Glover, JC; Ievglevskyi, O; Kondratskaya, E; Kristiansen, CK; Liang, KX; Sullivan, GJ; Vatne, GH1
Bennett, M; Falk, MJ; Guha, S; Konkwo, C; Kwon, YJ; Mathew, ND; Nakamaru-Ogiso, E; Ostrovsky, J; Polyak, E; Seiler, C; Xiao, R; Zhang, Z1
Bennett, M; Dingley, SD; Falk, MJ; Kwon, YJ; McCormack, SE; Ostrovsky, J; Peng, M; Polyak, E; Seiler, C; Tsukikawa, M; Xiao, R; Zhang, Z1
Andreu, AL; Barreiro, E; de Kier Joffé, ED; Fermoselle, C; García-Arumí, E; Puente-Maestu, L; Puig-Vilanova, E; Tejedor, A; Urtreger, AJ1
Baker, MJ; Herholz, D; Kladt, N; Kondadi, AK; Korwitz, A; Langer, T; Martinelli, P; Montagner, S; Rugarli, EI; Schauss, AC; Wang, S1
Dorko, K; Forster, J; Jaeschke, H; Kumer, SC; McGill, MR; Schmitt, TM; Xie, Y1
Cai, H; Gu, X; Qi, Y; Wei, X; Yang, J; Zhang, X; Zhang, Y1
Bastin, J; Bennett, MJ; Chen, J; Doulias, PT; Ischiropoulos, H; Tenopoulou, M1
Kaur, T; Sharma, M; Singla, SK1
Aguirre, MA; Barbarroja, N; Collantes-Estevez, E; Cuadrado, MJ; Jimenez-Gomez, Y; López-Pedrera, C1
Bartsakoulia, M; Boczonadi, V; Gomez-Duran, A; Horvath, R; Mϋller, JS; Yu-Wai-Man, P1
Berk, M; Pantelis, C; Wood, SJ; Yücel, M1
Frantz, MC; Wipf, P1
Basha, RH; Priscilla, DH1
Albayram, O; Beck, H; Bilkei-Gorzó, A; Drews, E; Filiou, MD; Frisch, P; Guerrero, C; Kudin, A; Kunz, WS; Otte, DM; Sommersberg, B; Turck, CW; Yilmaz, O; Zimmer, A1
Ahlqvist, KJ; Angers-Loustau, A; Forsström, S; Götz, A; Hämäläinen, RH; Kopra, OH; Larsson, NG; Prolla, T; Salven, P; Suomalainen, A; Terzioglu, M; Trifunovic, A; Tyynismaa, H; Uutela, M; Wartiovaara, K; Yatsuga, S1

Reviews

3 review(s) available for acetylcysteine and Electron Transport Chain Deficiencies, Mitochondrial

ArticleYear
Oxidative stress in the pathogenesis of atherothrombosis associated with anti-phospholipid syndrome and systemic lupus erythematosus: new therapeutic approaches.
    Rheumatology (Oxford, England), 2016, Volume: 55, Issue:12

    Topics: Acetylcysteine; Anticoagulants; Antioxidants; Antiphospholipid Syndrome; Atherosclerosis; Autoantibodies; beta 2-Glycoprotein I; Coagulants; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Inflammation; Lupus Erythematosus, Systemic; Mitochondrial Diseases; Oxidative Stress; Reactive Oxygen Species; Recurrence; Thrombosis; Ubiquinone

2016
Neurobiology of schizophrenia spectrum disorders: the role of oxidative stress.
    Annals of the Academy of Medicine, Singapore, 2009, Volume: 38, Issue:5

    Topics: Acetylcysteine; Glutathione; Humans; Magnetic Resonance Imaging; Mitochondrial Diseases; Nervous System; Oxidative Stress; Schizophrenia

2009
Mitochondria as a target in treatment.
    Environmental and molecular mutagenesis, 2010, Volume: 51, Issue:5

    Topics: Acetylcysteine; Antioxidants; Benzodiazepines; Glutathione; Gramicidin; Humans; Mitochondria; Mitochondrial Diseases; Prodrugs; Reactive Oxygen Species; Sulfonylurea Compounds

2010

Other Studies

14 other study(ies) available for acetylcysteine and Electron Transport Chain Deficiencies, Mitochondrial

ArticleYear
The protective effect of N-acetylcysteine on antimycin A-induced respiratory chain deficiency in mesenchymal stem cells.
    Chemico-biological interactions, 2022, Jun-01, Volume: 360

    Topics: Acetylcysteine; Antimycin A; Antioxidants; Apoptosis; Humans; Mesenchymal Stem Cells; Mitochondrial Diseases; Oxidative Stress

2022
N-acetylcysteine amide ameliorates mitochondrial dysfunction and reduces oxidative stress in hiPSC-derived dopaminergic neurons with POLG mutation.
    Experimental neurology, 2021, Volume: 337

    Topics: Acetylcysteine; Action Potentials; Antioxidants; Cellular Senescence; DNA Polymerase gamma; DNA, Mitochondrial; Dopaminergic Neurons; Electron Transport Complex I; Excitatory Postsynaptic Potentials; Humans; Induced Pluripotent Stem Cells; Membrane Potential, Mitochondrial; Mitochondrial Diseases; Oxidative Stress; Sodium Channels

2021
Combinatorial glucose, nicotinic acid and N-acetylcysteine therapy has synergistic effect in preclinical C. elegans and zebrafish models of mitochondrial complex I disease.
    Human molecular genetics, 2021, 05-12, Volume: 30, Issue:7

    Topics: Acetylcysteine; Animals; Caenorhabditis elegans; Disease Models, Animal; Drug Synergism; Electron Transport Complex I; Free Radical Scavengers; Glucose; Humans; Longevity; Membrane Potential, Mitochondrial; Mitochondria; Mitochondrial Diseases; Mutation; Niacin; Oxidative Stress; Zebrafish

2021
N-acetylcysteine and vitamin E rescue animal longevity and cellular oxidative stress in pre-clinical models of mitochondrial complex I disease.
    Molecular genetics and metabolism, 2018, Volume: 123, Issue:4

    Topics: Acetylcysteine; Animals; Animals, Genetically Modified; Antioxidants; Caenorhabditis elegans; Cells, Cultured; Drug Evaluation, Preclinical; Electron Transport Complex I; Fibroblasts; Free Radical Scavengers; Humans; Longevity; Mitochondria; Mitochondrial Diseases; Mutant Proteins; Mutation; Oxidative Stress; Vitamin E

2018
Mitochondrial dysfunction and therapeutic approaches in respiratory and limb muscles of cancer cachectic mice.
    Experimental physiology, 2013, Volume: 98, Issue:9

    Topics: Acetylcysteine; Animals; Antioxidants; Boronic Acids; Bortezomib; Cachexia; Diaphragm; Electron Transport Chain Complex Proteins; Female; Lung Neoplasms; MAP Kinase Signaling System; Mice; Mitochondria; Mitochondrial Diseases; Mitogen-Activated Protein Kinases; Muscle Strength; Muscle, Skeletal; NF-kappa B; Oxidative Stress; Pyrazines

2013
Loss of the m-AAA protease subunit AFG₃L₂ causes mitochondrial transport defects and tau hyperphosphorylation.
    The EMBO journal, 2014, May-02, Volume: 33, Issue:9

    Topics: Acetylcysteine; Animals; ATP-Dependent Proteases; ATPases Associated with Diverse Cellular Activities; Biological Transport; Cells, Cultured; Cyclic AMP-Dependent Protein Kinases; Embryo, Mammalian; MAP Kinase Signaling System; Metalloproteases; Mice; Mice, Inbred C57BL; Mice, Knockout; Mitochondria; Mitochondrial Diseases; Mitochondrial Proteins; Neurons; Phosphorylation; Reactive Oxygen Species; tau Proteins

2014
Mechanisms of acetaminophen-induced cell death in primary human hepatocytes.
    Toxicology and applied pharmacology, 2014, Sep-15, Volume: 279, Issue:3

    Topics: Acetaminophen; Acetylcysteine; Adult; Aged; Analgesics, Non-Narcotic; Antidotes; Cell Death; Enzyme Activation; Female; Glutathione; Hepatocytes; Humans; JNK Mitogen-Activated Protein Kinases; Male; Middle Aged; Mitochondria, Liver; Mitochondrial Diseases; Necrosis; Primary Cell Culture; Proteins; Subcellular Fractions; Young Adult

2014
ROS act as an upstream signal to mediate cadmium-induced mitophagy in mouse brain.
    Neurotoxicology, 2015, Volume: 46

    Topics: Acetylcarnitine; Acetylcysteine; Analysis of Variance; Animals; Brain; Cadmium; Collagenases; Dose-Response Relationship, Drug; Male; Mice; Mice, Inbred Strains; Microscopy, Electron, Transmission; Microtubule Proteins; Microtubule-Associated Proteins; Mitochondrial Diseases; Reactive Oxygen Species; Signal Transduction; Ubiquitin-Protein Ligases

2015
Strategies for correcting very long chain acyl-CoA dehydrogenase deficiency.
    The Journal of biological chemistry, 2015, Apr-17, Volume: 290, Issue:16

    Topics: Acetylcysteine; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Amino Acid Sequence; Carnitine; Congenital Bone Marrow Failure Syndromes; Cysteine; Dose-Response Relationship, Drug; Fatty Acids; Fibroblasts; Genetic Therapy; Humans; Kinetics; Lipid Metabolism, Inborn Errors; Mitochondrial Diseases; Molecular Sequence Data; Muscular Diseases; Mutation; Oxidation-Reduction; Primary Cell Culture; Skin

2015
Protective effects of N-acetylcysteine against hyperoxaluria induced mitochondrial dysfunction in male wistar rats.
    Molecular and cellular biochemistry, 2015, Volume: 405, Issue:1-2

    Topics: Acetylcysteine; Animals; Calcium; Citric Acid Cycle; Creatinine; Glutathione; Glutathione Peroxidase; Glutathione Reductase; Hyperoxaluria; Kidney; L-Lactate Dehydrogenase; Lipid Peroxidation; Male; Mitochondria; Mitochondrial Diseases; Nephrolithiasis; Oxidative Stress; Protective Agents; Rats; Rats, Wistar; Superoxide Dismutase

2015
Cysteine Supplementation May be Beneficial in a Subgroup of Mitochondrial Translation Deficiencies.
    Journal of neuromuscular diseases, 2016, 08-30, Volume: 3, Issue:3

    Topics: Acetylcysteine; Carrier Proteins; Cyclooxygenase 2; Cysteine; Dietary Supplements; Fibroblasts; Humans; In Vitro Techniques; MELAS Syndrome; MERRF Syndrome; Mitochondria; Mitochondrial Diseases; Mitochondrial Proteins; Mutation; Neoplasm Proteins; Oxygen Consumption; Protein Biosynthesis; RNA-Binding Proteins; tRNA Methyltransferases

2016
An in vivo and in vitro study on the protective effects of N-acetylcysteine on mitochondrial dysfunction in isoproterenol treated myocardial infarcted rats.
    Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie, 2013, Volume: 65, Issue:1-2

    Topics: Acetylcysteine; Animals; Antioxidants; Creatine Kinase; Data Interpretation, Statistical; Disease Models, Animal; In Vitro Techniques; Isoproterenol; Lipid Peroxidation; Male; Microscopy, Electron, Transmission; Mitochondria, Heart; Mitochondrial Diseases; Myocardial Infarction; Rats; Rats, Wistar

2013
N-acetyl cysteine treatment rescues cognitive deficits induced by mitochondrial dysfunction in G72/G30 transgenic mice.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Volume: 36, Issue:11

    Topics: Acetylcysteine; Animals; Carrier Proteins; Cognition Disorders; Electron Transport Complex I; Humans; Intracellular Signaling Peptides and Proteins; Male; Mice; Mice, Transgenic; Mitochondrial Diseases; Reactive Oxygen Species; Treatment Outcome

2011
Somatic progenitor cell vulnerability to mitochondrial DNA mutagenesis underlies progeroid phenotypes in Polg mutator mice.
    Cell metabolism, 2012, Jan-04, Volume: 15, Issue:1

    Topics: Acetylcysteine; Animals; Cell Differentiation; DNA, Mitochondrial; Electron Transport; Erythropoiesis; Hematopoietic Stem Cells; Lymphopoiesis; Mice; Mice, Mutant Strains; Mitochondrial Diseases; Mutagenesis; Neural Stem Cells; Oxidation-Reduction; Phenotype; Reactive Oxygen Species

2012