نتایج جستجو برای: mitochondrial respiratory chain complex i

تعداد نتایج: 2265450  

Journal: :The Journal of clinical investigation 1984
R W Moreadith M L Batshaw T Ohnishi D Kerr B Knox D Jackson R Hruban J Olson B Reynafarje A L Lehninger

We report the case of an infant with hypoglycemia, progressive lactic acidosis, an increased serum lactate/pyruvate ratio, and elevated plasma alanine, who had a moderate to profound decrease in the ability of mitochondria from four organs to oxidize pyruvate, malate plus glutamate, citrate, and other NAD+-linked respiratory substrates. The capacity to oxidize the flavin adenine dinucleotide-li...

2014
Rafał Kozieł Christoph Ruckenstuhl Eva Albertini Michael Neuhaus Christine Netzberger Maria Bust Frank Madeo Rudolf J Wiesner Pidder Jansen-Dürr

Methionine restriction (MetR) extends lifespan in animal models including rodents. Using human diploid fibroblasts (HDF), we report here that MetR significantly extends their replicative lifespan, thereby postponing cellular senescence. MetR significantly decreased activity of mitochondrial complex IV and diminished the accumulation of reactive oxygen species. Lifespan extension was accompanied...

Journal: :Journal of medical genetics 2004
D M Kirby R McFarland A Ohtake C Dunning M T Ryan C Wilson D Ketteridge D M Turnbull D R Thorburn R W Taylor

C omplex I is the largest of the mitochondrial respiratory chain enzyme complexes, consisting of at least 46 subunits, seven of which are encoded by mtDNA. Deficiency of complex I is the most common respiratory chain defect, and can be caused by mutations in both nuclear and mtDNA encoded genes. It has a wide range of clinical presentations, from lethal infantile mitochondrial disease to isolat...

2004
D M Kirby D M Turnbull D R Thorburn R W Taylor

C omplex I is the largest of the mitochondrial respiratory chain enzyme complexes, consisting of at least 46 subunits, seven of which are encoded by mtDNA. Deficiency of complex I is the most common respiratory chain defect, and can be caused by mutations in both nuclear and mtDNA encoded genes. It has a wide range of clinical presentations, from lethal infantile mitochondrial disease to isolat...

Journal: :The Journal of biological chemistry 2004
Alexei P Kudin Nana Yaw-B Bimpong-Buta Stefan Vielhaber Christian E Elger Wolfram S Kunz

Mitochondrial respiratory chain complexes I and III have been shown to produce superoxide but the exact contribution and localization of individual sites have remained unclear. We approached this question investigating the effects of oxygen, substrates, inhibitors, and of the NAD+/NADH redox couple on H2O2 and superoxide production of isolated mitochondria from rat and human brain. Although rat...

2018
Karen M. Davies Thorsten B. Blum Werner Kühlbrandt

We used electron cryo-tomography and subtomogram averaging to investigate the structure of complex I and its supramolecular assemblies in the inner mitochondrial membrane of mammals, fungi, and plants. Tomographic volumes containing complex I were averaged at ∼4 nm resolution. Principal component analysis indicated that ∼60% of complex I formed a supercomplex with dimeric complex III, while ∼40...

Journal: :The Biochemical journal 2012
Margarida Duarte Arnaldo Videira

Respiratory chain deficiency can result from alterations in mitochondrial and/or cytosolic protein synthesis due to the dual genetic origin of mitochondrial oxidative phosphorylation. In the present paper we report a point mutation (D750G) in the bifunctional VARS (valyl-tRNA synthetase) of the fungus Neurospora crassa, associated with a temperature-sensitive phenotype. Analysis of the mutant s...

Journal: :The Journal of biological chemistry 2002
Anastasios E Damdimopoulos Antonio Miranda-Vizuete Markku Pelto-Huikko Jan-Ake Gustafsson Giannis Spyrou

Thioredoxins (Trx) are a class of small multifunctional redox-active proteins found in all organisms. Recently, we reported the cloning of a mitochondrial thioredoxin, Trx2, from rat heart. To investigate the biological role of Trx2 we have isolated the human homologue, hTrx2, and generated HEK-293 cells overexpressing Trx2 (HEK-Trx2). Here, we show that HEK-Trx2 cells are more resistant toward...

2015
Liang Zhang Song Zhang Izumi Maezawa Sergey Trushin Paras Minhas Matthew Pinto Lee-Way Jin Keshar Prasain Thi D.T. Nguyen Yu Yamazaki Takahisa Kanekiyo Guojun Bu Benjamin Gateno Kyeong-Ok Chang Karl A. Nath Emirhan Nemutlu Petras Dzeja Yuan-Ping Pang Duy H. Hua Eugenia Trushina

Development of therapeutic strategies to prevent Alzheimer's Disease (AD) is of great importance. We show that mild inhibition of mitochondrial complex I with small molecule CP2 reduces levels of amyloid beta and phospho-Tau and averts cognitive decline in three animal models of familial AD. Low-mass molecular dynamics simulations and biochemical studies confirmed that CP2 competes with flavin ...

2010
Pilar del Hoyo Alberto García-Redondo Fernando de Bustos José Antonio Molina Youssef Sayed Hortensia Alonso-Navarro Luis Caballero Joaquín Arenas José AG Agúndez Félix Javier Jiménez-Jiménez

BACKGROUND In the substantia nigra of Parkinson's disease (PD) patients, increased lipid peroxidation, decreased activities of the mitochondrial complex I of the respiratory chain, catalase and glutathione-peroxidase, and decreased levels of reduced glutathione have been reported. These observations suggest that oxidative stress and mitochondrial dysfunction play a role in the neurodegeneration...

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