Induction of a Proinflammatory Response in Cortical Astrocytes by the Major Metabolites Accumulating in HMG-CoA Lyase Deficiency: the Role of ERK Signaling Pathway in Cytokine Release
暂无分享,去创建一个
M. Wajner | C. Fernandes | B. Seminotti | André Quincozes-Santos | A. Santamaría | A. L. Colín-González | M. Rodrigues
[1] M. Brenner. Role of GFAP in CNS injuries , 2014, Neuroscience Letters.
[2] A. Santamaría,et al. Comparing the effects of two neurotoxins in cortical astrocytes obtained from rats of different ages: involvement of oxidative damage , 2014, Journal of applied toxicology : JAT.
[3] G. Leipnitz,et al. In vivo experimental evidence that the major metabolites accumulating in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency induce oxidative stress in striatum of developing rats: a potential pathophysiological mechanism of striatal damage in this disorder. , 2013, Molecular genetics and metabolism.
[4] Jialin C. Zheng,et al. IL‐1β and TNF‐α induce neurotoxicity through glutamate production: a potential role for neuronal glutaminase , 2013, Journal of neurochemistry.
[5] André Quincozes-Santos,et al. Characterization of Adult Rat Astrocyte Cultures , 2013, PloS one.
[6] D. Souza,et al. Resveratrol Prevents Ammonia Toxicity in Astroglial Cells , 2012, PloS one.
[7] A. Quintana,et al. Interleukin-6, a Major Cytokine in the Central Nervous System , 2012, International journal of biological sciences.
[8] M. Norenberg,et al. Primary Cultures of Astrocytes: Their Value in Understanding Astrocytes in Health and Disease , 2012, Neurochemical Research.
[9] Peter W Zandstra,et al. Systematic engineering of 3D pluripotent stem cell niches to guide blood development. , 2012, Biomaterials.
[10] Pierre J Magistretti,et al. Brain energy metabolism: focus on astrocyte-neuron metabolic cooperation. , 2011, Cell metabolism.
[11] O. Kozawa,et al. Midazolam suppresses interleukin-1β-induced interleukin-6 release from rat glial cells , 2011, Journal of Neuroinflammation.
[12] M. Santello,et al. TNFα Controls Glutamatergic Gliotransmission in the Hippocampal Dentate Gyrus , 2011, Neuron.
[13] M. Wajner,et al. Neurochemical evidence that 3-methylglutaric acid inhibits synaptic Na+,K+-ATPase activity probably through oxidative damage in brain cortex of young rats , 2011, International Journal of Developmental Neuroscience.
[14] T. Kensler,et al. When NRF2 talks, who's listening? , 2010, Antioxidants & redox signaling.
[15] Yu Tian Wang,et al. Depletion of GSH in glial cells induces neurotoxicity: relevance to aging and degenerative neurological diseases , 2010, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[16] O. Kozawa,et al. Mechanisms of tumor necrosis factor-α-induced interleukin-6 synthesis in glioma cells , 2010, Journal of Neuroinflammation.
[17] J. O'Callaghan,et al. Astrogliosis in CNS Pathologies: Is There A Role for Microglia? , 2010, Molecular Neurobiology.
[18] M. Sofroniew,et al. Astrocytes: biology and pathology , 2009, Acta Neuropathologica.
[19] J. Ezekowitz,et al. A Case of Dilated Cardiomyopathy Associated with 3-Hydroxy-3-Methylglutaryl-Coenzyme A (HMG CoA) Lyase Deficiency , 2009, Case reports in medicine.
[20] G. Leipnitz,et al. Striatum is more vulnerable to oxidative damage induced by the metabolites accumulating in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency as compared to liver , 2009, International Journal of Developmental Neuroscience.
[21] C. Gottfried,et al. The Janus Face of Resveratrol in Astroglial Cells , 2009, Neurotoxicity Research.
[22] S. Reimão,et al. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: Initial presentation in a young adult , 2009, Journal of Inherited Metabolic Disease.
[23] A. Bordey,et al. The astrocyte odyssey , 2008, Progress in Neurobiology.
[24] S. Heales,et al. Astrocytes Protect Against Copper-Catalysed Loss of Extracellular Glutathione , 2008, Neurochemical Research.
[25] G. Leipnitz,et al. Induction of oxidative stress by the metabolites accumulating in 3-methylglutaconic aciduria in cerebral cortex of young rats. , 2008, Life sciences.
[26] G. Leipnitz,et al. Evidence that 3‐hydroxy‐3‐methylglutaric acid promotes lipid and protein oxidative damage and reduces the nonenzymatic antioxidant defenses in rat cerebral cortex , 2008, Journal of neuroscience research.
[27] B. Puisac,et al. Molecular genetics of HMG-CoA lyase deficiency. , 2007, Molecular genetics and metabolism.
[28] D. Zafeiriou,et al. 3-Hydroxy-3-methylglutaryl coenzyme a lyase deficiency with reversible white matter changes after treatment. , 2007, Pediatric neurology.
[29] Sang Won Suh,et al. Hypoglycemic neuronal death is triggered by glucose reperfusion and activation of neuronal NADPH oxidase. , 2007, The Journal of clinical investigation.
[30] G. Burckhardt,et al. 3-Hydroxyglutaric acid is transported via the sodium-dependent dicarboxylate transporter NaDC3 , 2007, Journal of Molecular Medicine.
[31] C. Farina,et al. Astrocytes are active players in cerebral innate immunity. , 2007, Trends in immunology.
[32] S. Legrand-Poels,et al. NF-κB activation by reactive oxygen species: Fifteen years later , 2006 .
[33] C. Gottfried,et al. Resveratrol increases glutamate uptake and glutamine synthetase activity in C6 glioma cells. , 2006, Archives of biochemistry and biophysics.
[34] G. Ekinci,et al. Corticospinal tract involvement in a patient with 3-HMG coenzyme A lyase deficiency. , 2006, Pediatric neurology.
[35] C. Harding,et al. Intracerebral accumulation of glutaric and 3‐hydroxyglutaric acids secondary to limited flux across the blood–brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl‐CoA dehydrogenase deficiency , 2006, Journal of neurochemistry.
[36] C. Darlington. Astrocytes as targets for neuroprotective drugs. , 2005, Current opinion in investigational drugs.
[37] Leif Hertz,et al. Astrocytic control of glutamatergic activity: astrocytes as stars of the show , 2004, Trends in Neurosciences.
[38] Stefan Kahlert,et al. Glial perspectives of metabolic states during cerebral hypoxia--calcium regulation and metabolic energy. , 2004, Cell calcium.
[39] G. Kaur,et al. Impact of hypoglycemia and diabetes on CNS: Correlation of mitochondrial oxidative stress with DNA damage , 2004, Molecular and Cellular Biochemistry.
[40] Toshio Matsuda,et al. Astrocyte apoptosis: implications for neuroprotection , 2004, Progress in Neurobiology.
[41] S. Goldman,et al. New roles for astrocytes: Redefining the functional architecture of the brain , 2003, Trends in Neurosciences.
[42] J. Zeman,et al. Biochemical and molecular analyses in three patients with 3-hydroxy-3-methylglutaric aciduria , 2003, Journal of Inherited Metabolic Disease.
[43] Robert M Friedlander,et al. Apoptosis and caspases in neurodegenerative diseases. , 2003, The New England journal of medicine.
[44] J. Saudubray,et al. Branched-chain organic acidurias. , 2002, Seminars in neonatology : SN.
[45] N. Urgancı,et al. A rare cause of hepatomegaly: 3-hydroxy-3-methylglutaryl coenzyme-a lyase deficiency. , 2001, Journal of pediatric gastroenterology and nutrition.
[46] C. Scriver,et al. The Metabolic and Molecular Bases of Inherited Disease, 8th Edition 2001 , 2001, Journal of Inherited Metabolic Disease.
[47] R. Dringen,et al. Metabolism and functions of glutathione in brain , 2000, Progress in Neurobiology.
[48] R. Swanson,et al. Astrocyte glutamate transport: Review of properties, regulation, and physiological functions , 2000, Glia.
[49] T. Nakahata,et al. Cerebral infarction and pancreatitis: possible complications of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency , 2000, Journal of Inherited Metabolic Disease.
[50] C. Heizmann,et al. Evaluation of urinary acylglycines by electrospray tandem mass spectrometry in mitochondrial energy metabolism defects and organic acidurias. , 2000, Molecular genetics and metabolism.
[51] A. Dinçer,et al. MRI and MRS in HMG-CoA lyase deficiency. , 1999, Pediatric neurology.
[52] J. Lai,et al. Functional studies in cultured astrocytes. , 1998, Methods.
[53] J. Valk,et al. MR imaging and proton spectroscopy in 3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency. , 1998, AJNR. American journal of neuroradiology.
[54] M. Robert,et al. Molecular prenatal diagnosis of 3‐hydroxy−3‐methylglutaryl coa lyase deficiency , 1995, Prenatal diagnosis.
[55] M. Tsai,et al. Differences in the disposition and toxicity of 1‐methyl‐4‐phenylpyridinium in cultured rat and mouse astrocytes , 1994, Glia.
[56] R. Wanders,et al. Fatal cardiomyopathy associated with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency , 1994, Journal of Inherited Metabolic Disease.
[57] J. T. Clarke,et al. Pancreatitis in patients with organic acidemias. , 1994, The Journal of pediatrics.
[58] T. Coşkun,et al. 3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency , 1993, Journal of Inherited Metabolic Disease.
[59] R. Surtees,et al. Physiology and pathophysiology of organic acids in cerebrospinal fluid , 1993, Journal of Inherited Metabolic Disease.
[60] K. Gibson,et al. 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients , 1988, European Journal of Pediatrics.
[61] S. Wysocki,et al. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: A review , 1986, Journal of Inherited Metabolic Disease.
[62] A. Beaudet,et al. Atypical presentation and neuropathological studies in 3‐hydroxy‐3‐methylglutaryl–CoA lyase deficiency , 1986, Annals of neurology.
[63] O. Søvik,et al. A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency , 1984, European Journal of Pediatrics.
[64] E. Owles,et al. 3‐HYDROXY‐3‐METHYLGLUTARYL COENZYME A LYASE DEFICIENCY , 1981, Acta paediatrica Scandinavica.
[65] Oliver H. Lowry,et al. Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.
[66] C. B. Ransom,et al. Astrocytes: multitalented stars of the central nervous system. , 2012, Methods in molecular biology.
[67] B. Nehru,et al. Modulatory effects of N-acetylcysteine on cerebral cortex and cerebellum regions of ageing rat brain. , 2007, Nutricion hospitalaria.
[68] S. Legrand-Poels,et al. NF-kappaB activation by reactive oxygen species: fifteen years later. , 2006, Biochemical pharmacology.
[69] H. Bremer,et al. Neurological manifestations of organic acid disorders , 2005, European Journal of Pediatrics.
[70] M. Durán,et al. Group tests for selective screening of inborn errors of metabolism , 2005, European Journal of Pediatrics.
[71] A. Castoldi,et al. Biological markers of neurotoxic diseases. , 2001, Functional neurology.
[72] D. Bredesen,et al. Cellular resistance to methylmercury. , 1996, Neurotoxicology.
[73] M. Durán,et al. Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase. , 1979, The Journal of pediatrics.