نتایج جستجو برای: cuzn superoxide dismutase sod1

تعداد نتایج: 35610  

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2005
Sean P Didion Frank M Faraci

OBJECTIVE Ceramide is an important intracellular second messenger that may also increase superoxide. The goal of this study was to determine whether overexpression of CuZn superoxide dismutase (SOD) protects against ceramide-induced increases in vascular superoxide and endothelial dysfunction. METHODS AND RESULTS Carotid arteries from CuZnSOD-transgenic (CuZnSOD-Tg) and nontransgenic litterma...

Journal: :Neuron 2010
Adrian Israelson Nir Arbel Sandrine Da Cruz Hristelina Ilieva Koji Yamanaka Varda Shoshan-Barmatz Don W. Cleveland

Mutations in superoxide dismutase (SOD1) cause amyotrophic lateral sclerosis (ALS), a neurodegenerative disease characterized by loss of motor neurons. With conformation-specific antibodies, we now demonstrate that misfolded mutant SOD1 binds directly to the voltage-dependent anion channel (VDAC1), an integral membrane protein imbedded in the outer mitochondrial membrane. This interaction is fo...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2006
Alberto Ferri Mauro Cozzolino Claudia Crosio Monica Nencini Arianna Casciati Edith Butler Gralla Giuseppe Rotilio Joan Selverstone Valentine Maria Teresa Carrì

Recent studies suggest that the toxicity of familial amyotrophic lateral sclerosis mutant Cu, Zn superoxide dismutase (SOD1) arises from its selective recruitment to mitochondria. Here we demonstrate that each of 12 different familial ALS-mutant SOD1s with widely differing biophysical properties are associated with mitochondria of motoneuronal cells to a much greater extent than wild-type SOD1,...

2016
Soumaya Ferchichi Hamdi Trabelsi Inès Azzouz Amel Hanini Ahmed Rejeb Olfa Tebourbi Mohsen Sakly Hafedh Abdelmelek

The purpose of our study was the evaluation of toxicological effects of silica-coated gold nanoparticles (GNPs) and static magnetic fields (SMFs; 128 mT) exposure in rat lungs. Animals received a single injection of GNPs (1,100 µg/kg, 100 nm, intraperitoneally) and were exposed to SMFs, over 14 days (1 h/day). Results showed that GNPs treatment induced a hyperplasia of bronchus-associated lymph...

2013
Kenji Watanabe Shuichi Shibuya Hirofumi Koyama Yusuke Ozawa Toshihiko Toda Koutaro Yokote Takahiko Shimizu

Oxidative damages induced by a redox imbalance cause age-related changes in cells and tissues. Superoxide dismutase (SOD) enzymes play a major role in the antioxidant system and they also catalyze superoxide radicals (O2·-). Since the loss of cytoplasmic SOD (SOD1) resulted in aging-like phenotypes in several types of mouse tissue, SOD1 is essential for the maintenance of tissue homeostasis. To...

Journal: :International Journal of Secondary Metabolite 2021

Free radicals (FRs) are formed in the high amounts result of metabolic imbalance cells and tissue. These radicals-induced oxidative damages constitute basis many diseases. Organisms have antioxidant defence systems (ADS) to eliminate destructive effects damage. In addition these systems, dietary flavonoids effect protective role against present study, it was investigated whether a flavonoid der...

Journal: :Trends in biochemical sciences 2007
Bryan F Shaw Joan Selverstone Valentine

More than 100 different mutations in the gene encoding copper-zinc superoxide dismutase (SOD1) cause familial forms of amyotrophic lateral sclerosis (ALS)--a fatal neurodegenerative disease in which aggregation of the SOD1 protein is considered to be the primary mode of pathogenesis. Recent results show that these mutations have remarkably diverse and unexpected effects on the structure, activi...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Jae Keun Lee Jin Hee Shin Sang Gil Hwang Byoung Joo Gwag Ann C McKee Junghee Lee Neil W Kowall Hoon Ryu Dae-Sik Lim Eui-Ju Choi

Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disorder characterized by loss of motor neurons. Dominant mutations in the gene for superoxide dismutase 1 (SOD1) give rise to familial ALS by an unknown mechanism. Here we show that genetic deficiency of mammalian sterile 20-like kinase 1 (MST1) delays disease onset and extends survival in mice expressing the ALS-associate...

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