Hypoxia-Induced Neuroinflammation and Learning–Memory Impairments in Adult Zebrafish Are Suppressed by Glucosamine

[1]  D. Souza,et al.  Brain zinc chelation by diethyldithiocarbamate increased the behavioral and mitochondrial damages in zebrafish subjected to hypoxia , 2016, Scientific Reports.

[2]  S. Kida,et al.  Functional roles of CREB as a positive regulator in the formation and enhancement of memory , 2014, Brain Research Bulletin.

[3]  D. Souza,et al.  Evaluation of spontaneous recovery of behavioral and brain injury profiles in zebrafish after hypoxia , 2013, Behavioural Brain Research.

[4]  B. Prakken,et al.  Cerebral ischemia initiates an immediate innate immune response in neonates during cardiac surgery , 2013, Journal of Neuroinflammation.

[5]  M. Higley,et al.  Acetylcholine as a Neuromodulator: Cholinergic Signaling Shapes Nervous System Function and Behavior , 2012, Neuron.

[6]  J. Walsh,et al.  Hypoxia/Reoxygenation Impairs Memory Formation via Adenosine-Dependent Activation of Caspase 1 , 2012, The Journal of Neuroscience.

[7]  T. Osaki,et al.  Suppressive Effects of N-Acetyl-d-Glucosamine on Rheumatoid Arthritis Mouse Models , 2012, Inflammation.

[8]  Ji-Sun Hwang,et al.  Glucosamine exerts a neuroprotective effect via suppression of inflammation in rat brain ischemia/reperfusion injury , 2010, Glia.

[9]  M. Jung,et al.  Scopolamine-induced learning impairment reversed by physostigmine in zebrafish , 2010, Neuroscience Research.

[10]  A. Lazarowski,et al.  Intermittent hypoxia during sleep induces reactive gliosis and limited neuronal death in rats: implications for sleep apnea , 2010, Journal of neurochemistry.

[11]  Allan V. Kalueff,et al.  Understanding behavioral and physiological phenotypes of stress and anxiety in zebrafish , 2009, Behavioural Brain Research.

[12]  Ryoichiro Kageyama,et al.  Roles of continuous neurogenesis in the structural and functional integrity of the adult forebrain , 2008, Nature Neuroscience.

[13]  B. Kosofsky,et al.  Enhanced CREB and DARPP‐32 phosphorylation in the nucleus accumbens and CREB, ERK, and GluR1 phosphorylation in the dorsal hippocampus is associated with cocaine‐conditioned place preference behavior , 2008, Journal of neurochemistry.

[14]  A. Roach,et al.  Zebrafish: an emerging technology for in vivo pharmacological assessment to identify potential safety liabilities in early drug discovery , 2008, British journal of pharmacology.

[15]  R. Marchase,et al.  Glucosamine protects neonatal cardiomyocytes from ischemia-reperfusion injury via increased protein O-GlcNAc and increased mitochondrial Bcl-2. , 2008, American journal of physiology. Cell physiology.

[16]  Li Zhang,et al.  [Neuroglobin and hypoxic-ischemic brain bamage]. , 2008, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

[17]  Michael Brand,et al.  Proliferation, neurogenesis and regeneration in the non-mammalian vertebrate brain , 2008, Philosophical Transactions of the Royal Society B: Biological Sciences.

[18]  C. Farina,et al.  Astrocytes are active players in cerebral innate immunity. , 2007, Trends in immunology.

[19]  J. Frey,et al.  The late maintenance of hippocampal LTP: Requirements, phases, ‘synaptic tagging’, ‘late-associativity’ and implications , 2007, Neuropharmacology.

[20]  M. Bogo,et al.  In vitro effect of zinc and cadmium on acetylcholinesterase and ectonucleotidase activities in zebrafish (Danio rerio) brain. , 2006, Toxicology in vitro : an international journal published in association with BIBRA.

[21]  J. Kaslin,et al.  Neural stem cells and neurogenesis in the adult zebrafish brain: origin, proliferation dynamics, migration and cell fate. , 2006, Developmental biology.

[22]  Gernot Riedel,et al.  Foreground contextual fear memory consolidation requires two independent phases of hippocampal ERK/CREB activation. , 2006, Learning & memory.

[23]  R. Marchase,et al.  Increased hexosamine biosynthesis and protein O-GlcNAc levels associated with myocardial protection against calcium paradox and ischemia. , 2006, Journal of molecular and cellular cardiology.

[24]  S. Josselyn,et al.  CREB, synapses and memory disorders: past progress and future challenges. , 2005, Current drug targets. CNS and neurological disorders.

[25]  F. Gage,et al.  Proliferation, migration, neuronal differentiation, and long‐term survival of new cells in the adult zebrafish brain , 2005, The Journal of comparative neurology.

[26]  E. Nestler,et al.  The many faces of CREB , 2005, Trends in Neurosciences.

[27]  D. Ferriero.  Neonatal brain injury. , 2004, The New England journal of medicine.

[28]  J. Groswasser,et al.  Clinicopathological correlation between brainstem gliosis using GFAP as a marker and sleep apnea in the sudden infant death syndrome. , 2003, Early human development.

[29]  A. Privat.  Astrocytes as support for axonal regeneration in the central nervous system of mammals , 2003, Glia.

[30]  T. Myhrer.  Neurotransmitter systems involved in learning and memory in the rat: a meta-analysis based on studies of four behavioral tasks , 2003, Brain Research Reviews.

[31]  Marietta F. Wright,et al.  Immunosuppressive Effects of Glucosamine* , 2002, The Journal of Biological Chemistry.

[32]  T. Nabeshima,et al.  CREB phosphorylation as a molecular marker of memory processing in the hippocampus for spatial learning , 2002, Behavioural Brain Research.

[33]  G. Zupanc.  Adult Neurogenesis and Neuronal Regeneration in the Central Nervous System of Teleost Fish , 2001, Brain, Behavior and Evolution.

[34]  D. Gozal,et al.  Behavioral and Anatomical Correlates of Chronic Episodic Hypoxia during Sleep in the Rat , 2001, The Journal of Neuroscience.

[35]  Erry,et al.  Longitudinal assessment of neurocognitive function after coronary-artery bypass surgery. , 2001, The New England journal of medicine.

[36]  I. Izquierdo,et al.  Learning-associated activation of nuclear MAPK, CREB and Elk-1, along with Fos production, in the rat hippocampus after a one-trial avoidance learning: abolition by NMDA receptor blockade. , 2000, Brain research. Molecular brain research.

[37]  Michael Schroeter,et al.  Inflammation and glial responses in ischemic brain lesions , 1998, Progress in Neurobiology.

[38]  S. K. Malhotra,et al.  Reactive astrocytes: cellular and molecular cues to biological function , 1997, Trends in Neurosciences.

[39]  B. Shukitt-Hale,et al.  Tyrosine administration prevents hypoxia-induced decrements in learning and memory , 1996, Physiology & Behavior.

[40]  M. Ross,et al.  Inducible Nitric Oxide Synthase Gene Expression in Brain following Cerebral Ischemia , 1995, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[41]  I. Zupanets,et al.  [Antihypoxic effect of glucosamine in acute hypoxic states in mice]. , 1992, Fiziologicheskii zhurnal.

[42]  C. Petito,et al.  The Two Patterns of Reactive Astrocytosis in Postischemic Rat Brain , 1990, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[43]  D. Salmon,et al.  Procedural learning in a patient with amnesia due to hypoxia , 1987, Brain and Cognition.

[44]  A. Hamberger,et al.  Ischemia-Induced Shift of Inhibitory and Excitatory Amino Acids from Intra- to Extracellular Compartments , 1985, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[45]  M. Johnston.  Neurotransmitter alterations in a model of perinatal hypoxic‐ischemic brain injury , 1983, Annals of neurology.

[46]  J. Altman.  Autoradiographic and histological studies of postnatal neurogenesis. IV. Cell proliferation and migration in the anterior forebrain, with special reference to persisting neurogenesis in the olfactory bulb , 1969, The Journal of comparative neurology.

[47]  Yang V. Li,et al.  Zebrafish as an alternative model for hypoxic-ischemic brain damage. , 2011, International journal of physiology, pathophysiology and pharmacology.

[48]  R. Marchase,et al.  Glucosamine protects neonatal cardiomyocytes from ischemia-reperfusion injury via increased protein-associated O-GlcNAc. , 2007, American journal of physiology. Cell physiology.

[49]  A. Shaywitz,et al.  CREB: a stimulus-induced transcription factor activated by a diverse array of extracellular signals. , 1999, Annual review of biochemistry.

[50]  G. Lynch,et al.  Selective impairment of learning and blockade of long-term potentiation by an N-methyl-D-aspartate receptor antagonist, AP5 , 1986, Nature.