Tumor necrosis factor ?; TTX: Tetrodotoxin; WNV: West Nile virus References ,
Immune Proteins in Brain Development and Synaptic Plasticity, Neuron, vol.64, issue.1, pp.93-109, 2009. ,
DOI : 10.1016/j.neuron.2009.09.001
URL : http://doi.org/10.1016/j.neuron.2009.09.001
Learning and memory ... and the immune system, Learning & Memory, vol.20, issue.10, pp.601-607, 2013. ,
DOI : 10.1101/lm.028357.112
Long-term depression in the CNS, Nature Reviews Neuroscience, vol.59, issue.7, pp.459-73, 2010. ,
DOI : 10.1007/BF00236625
Long-term potentiation: Peeling the onion, Neuropharmacology, vol.74, pp.18-22, 2013. ,
DOI : 10.1016/j.neuropharm.2013.02.010
The Spike-Timing Dependence of Plasticity, Neuron, vol.75, issue.4, pp.556-71, 2012. ,
DOI : 10.1016/j.neuron.2012.08.001
Neuropeptides in learning and memory, Neuropeptides, vol.47, issue.6, pp.439-50, 2013. ,
DOI : 10.1016/j.npep.2013.10.012
Neuropeptide Transmission in Brain Circuits, Neuron, vol.76, issue.1, pp.98-115, 2012. ,
DOI : 10.1016/j.neuron.2012.09.014
Regulators of synaptic transmission: Roles in the pathogenesis and treatment of epilepsy, Epilepsia, vol.245, issue.Suppl. 6, pp.41-58, 2012. ,
DOI : 10.1016/0922-4106(93)90162-3
Multiple cellular cascades participate in long-term potentiation and in hippocampus-dependent learning, Brain Research, vol.1621, pp.73-81, 2015. ,
DOI : 10.1016/j.brainres.2014.11.033
How does PKM? maintain long-term memory?, Nature Reviews Neuroscience, vol.16, issue.1, pp.9-15, 2011. ,
DOI : 10.1523/JNEUROSCI.3789-08.2009
Transcriptional regulation of long-term potentiation, neurogenetics, vol.324, issue.5924, pp.201-211, 2016. ,
DOI : 10.1126/science.1168978
The JAK/STAT Pathway Is Involved in Synaptic Plasticity, Neuron, vol.73, issue.2, pp.374-90, 2012. ,
DOI : 10.1016/j.neuron.2011.11.024
Pattern recognition receptors and central nervous system repair, Experimental Neurology, vol.258, pp.5-16, 2014. ,
DOI : 10.1016/j.expneurol.2014.01.001
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974939
Neural injury following stroke: are Toll-like receptors the link between the immune system and the CNS?, British Journal of Pharmacology, vol.23, issue.8, pp.1872-88, 2010. ,
DOI : 10.1097/01.WCB.0000078322.96027.78
Cytokine Signaling Modules in Inflammatory Responses, Immunity, vol.28, issue.4, pp.477-87, 2008. ,
DOI : 10.1016/j.immuni.2008.03.002
Interpreting mixed signals: the cell's cytokine conundrum, Current Opinion in Immunology, vol.23, issue.5, pp.632-640, 2011. ,
DOI : 10.1016/j.coi.2011.07.013
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3190023
Integration of cytokine and heterologous receptor signaling pathways, Nature Immunology, vol.54, issue.4, pp.333-342, 2009. ,
DOI : 10.4049/jimmunol.171.1.257
On the transplantation of the rat sarcoma in adult heterogenous animals, Jap Med World, vol.1, pp.14-19, 1921. ,
CONDITIONS DETERMINING THE TRANSPLANTABILITY OF TISSUES IN THE BRAIN, Journal of Experimental Medicine, vol.38, issue.2, pp.183-97, 1923. ,
DOI : 10.1084/jem.38.2.183
What is immune privilege (not)? Trends Immunol, pp.12-20, 2007. ,
DOI : 10.1016/j.it.2006.11.004
The movers and shapers in immune privilege of the CNS, Nature Immunology, vol.213, issue.2, pp.123-154, 2017. ,
DOI : 10.1111/j.1600-065X.2006.00441.x
Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages, Science, vol.56, issue.2, pp.841-846, 2010. ,
DOI : 10.1016/S0301-0082(98)00035-5
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719181
ATP mediates rapid microglial response to local brain injury in vivo, Nature Neuroscience, vol.19, issue.6, pp.752-760, 2005. ,
DOI : 10.1523/JNEUROSCI.2294-04.2004
Resting Microglial Cells Are Highly Dynamic Surveillants of Brain Parenchyma in Vivo, Science, vol.308, issue.5726, pp.1314-1322, 2005. ,
DOI : 10.1126/science.1110647
Resting Microglia Directly Monitor the Functional State of Synapses In Vivo and Determine the Fate of Ischemic Terminals, Journal of Neuroscience, vol.29, issue.13, pp.3974-80, 2009. ,
DOI : 10.1523/JNEUROSCI.4363-08.2009
Microglial Interactions with Synapses Are Modulated by Visual Experience, PLoS Biology, vol.27, issue.Pt 17, p.1000527, 2010. ,
DOI : 10.1371/journal.pbio.1000527.s021
Neuron-Microglia Interaction in Neuroinflammation, Current Protein & Peptide Science, vol.14, issue.1, pp.16-20, 2013. ,
DOI : 10.2174/1389203711314010004
The Yin and Yang of Microglia, Developmental Neuroscience, vol.33, issue.3-4, pp.3-4199, 2011. ,
DOI : 10.1159/000328989
The Role of Microglia in the Healthy Brain, Journal of Neuroscience, vol.31, issue.45, pp.16064-16073, 2011. ,
DOI : 10.1523/JNEUROSCI.4158-11.2011
Astrocytes: Implications for Neuroinflammatory Pathogenesis of Alzheimers Disease, Current Alzheimer Research, vol.8, issue.1, pp.67-80, 2011. ,
DOI : 10.2174/156720511794604543
Astrocyte Reactivity and Reactive Astrogliosis: Costs and Benefits, Physiological Reviews, vol.94, issue.4, pp.1077-98, 2014. ,
DOI : 10.1152/physrev.00041.2013
Activation of microglial N-methyl-D-aspartate receptors triggers inflammation and neuronal cell death in the developing and mature brain, Annals of Neurology, vol.43, issue.4, pp.536-585, 2012. ,
DOI : 10.1016/S0304-3940(98)00029-9
The adaptive immune system in diseases of the central nervous system, Journal of Clinical Investigation, vol.122, issue.4, pp.1172-1181, 2012. ,
DOI : 10.1172/JCI58648
Mechanisms of the adaptive immune response inside the central nervous system during inflammatory and autoimmune diseases, Pharmacology & Therapeutics, vol.111, issue.3, pp.555-66, 2006. ,
DOI : 10.1016/j.pharmthera.2005.11.007
The anatomical and cellular basis of immune surveillance in the central nervous system, Nature Reviews Immunology, vol.130, issue.9, pp.623-658, 2012. ,
DOI : 10.1093/brain/awm038
Microglia and monocyte-derived macrophages: functionally distinct populations that act in concert in CNS plasticity and repair, Frontiers in Cellular Neuroscience, vol.7, p.34, 2013. ,
DOI : 10.3389/fncel.2013.00034
Structural and functional features of central nervous system lymphatic vessels, Nature, vol.14, issue.7560, pp.337-378, 2015. ,
DOI : 10.1097/00019052-200106000-00006
Revisiting the Mechanisms of CNS Immune Privilege, Trends in Immunology, vol.36, issue.10, pp.569-77, 2015. ,
DOI : 10.1016/j.it.2015.08.006
Innate immune activation in neurodegenerative disease, Nature Reviews Immunology, vol.87, issue.7, pp.463-77, 2014. ,
DOI : 10.1016/S0092-8674(00)81369-0
Microglia-Dependent Alteration of Glutamatergic Synaptic Transmission and Plasticity in the Hippocampus during Peripheral Inflammation, Journal of Neuroscience, vol.35, issue.12, pp.4942-52, 2015. ,
DOI : 10.1523/JNEUROSCI.4485-14.2015
Neuroinflammatory changes negatively impact on LTP: A focus on IL-1?, Brain Research, vol.1621, pp.197-204, 2015. ,
DOI : 10.1016/j.brainres.2014.08.040
Immune dysregulation and cognitive vulnerability in the aging brain: Interactions of microglia, IL-1?, BDNF and synaptic plasticity, Neuropharmacology, vol.96, pp.11-19, 2015. ,
DOI : 10.1016/j.neuropharm.2014.12.020
Inflammation Subverts Hippocampal Synaptic Plasticity in Experimental Multiple Sclerosis, PLoS ONE, vol.31, issue.1, p.54666, 2013. ,
DOI : 10.1371/journal.pone.0054666.g007
Cytokine Responses to LTP Induction in the Rat Hippocampus: A Comparison of In Vitro and In Vivo Techniques, Learning & Memory, vol.7, issue.6, pp.400-412, 2000. ,
DOI : 10.1101/lm.32600
Interleukin-6: a cytokine to forget, The FASEB Journal, vol.18, issue.14, pp.1788-90, 2004. ,
DOI : 10.1096/fj.04-1625fje
URL : https://lirias.kuleuven.be/bitstream/123456789/129134/2/Balschun_2004.pdf
Distribution of interleukin-1 receptor complex at the synaptic membrane driven by interleukin-1? and NMDA stimulation, Journal of Neuroinflammation, vol.8, issue.1, p.14, 2011. ,
DOI : 10.1186/1742-2094-8-14
Interleukin-1 beta modulates AMPA receptor expression and phosphorylation in hippocampal neurons, Journal of Neuroimmunology, vol.175, issue.1-2, pp.97-106, 2006. ,
DOI : 10.1016/j.jneuroim.2006.03.001
Neuromodulatory properties of inflammatory cytokines and their impact on neuronal excitability, Neuropharmacology, vol.96, pp.70-82, 2015. ,
DOI : 10.1016/j.neuropharm.2014.10.027
Selective Activation of Microglia Facilitates Synaptic Strength, Journal of Neuroscience, vol.35, issue.11, pp.4552-70, 2015. ,
DOI : 10.1523/JNEUROSCI.2061-14.2015
Microglial CR3 Activation Triggers Long-Term Synaptic Depression in the Hippocampus via NADPH Oxidase, Neuron, vol.82, issue.1, pp.195-207, 2014. ,
DOI : 10.1016/j.neuron.2014.01.043
The MHC class I antigen presentation pathway: strategies for viral immune evasion, Immunology, vol.2, issue.2, pp.163-172, 2003. ,
DOI : 10.1006/viro.2002.1365
Regulation of Class I MHC Gene Expression in the Developing and Mature CNS by Neural Activity, Neuron, vol.21, issue.3, pp.505-525, 1998. ,
DOI : 10.1016/S0896-6273(00)80562-0
Expression of nonclassical MHC class I (RT1-U) in certain neuronal populations of the central nervous system, European Journal of Neuroscience, vol.310, issue.12, pp.4468-72, 1999. ,
DOI : 10.1038/310688a0
Functional Requirement for Class I MHC in CNS Development and Plasticity, Science, vol.2, issue.1, pp.2155-2164, 2000. ,
DOI : 10.3109/02699058809150929
Regulation of CNS synapses by neuronal MHC class I, Proceedings of the National Academy of Sciences, vol.269, issue.5223, pp.6828-6861, 2007. ,
DOI : 10.1126/science.7624779
MHC class I molecules are present both pre- and postsynaptically in the visual cortex during postnatal development and in adulthood, Proceedings of the National Academy of Sciences, vol.104, issue.30, pp.16999-7004, 2010. ,
DOI : 10.1073/pnas.0705320104
Synapse elimination and learning rules co-regulated by MHC class I H2-Db, Nature, vol.99, issue.7499, pp.195-200, 2014. ,
DOI : 10.1073/pnas.042693699
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4016165
MHC class I immune proteins are critical for hippocampus-dependent memory and gate NMDAR-dependent hippocampal long-term depression, Learning & Memory, vol.20, issue.9, pp.505-522, 2013. ,
DOI : 10.1101/lm.031351.113
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3744042
MHCI negatively regulates synapse density during the establishment of cortical connections, Nature Neuroscience, vol.23, issue.4, pp.442-51, 2011. ,
DOI : 10.1038/nn1677
MHC Class I Limits Hippocampal Synapse Density by Inhibiting Neuronal Insulin Receptor Signaling, Journal of Neuroscience, vol.34, issue.35, pp.11844-56, 2014. ,
DOI : 10.1523/JNEUROSCI.4642-12.2014
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468138
Altered cognitive performance and synaptic function in the hippocampus of mice lacking C3, Experimental Neurology, vol.253, pp.154-64, 2014. ,
DOI : 10.1016/j.expneurol.2013.12.013
A complement?microglial axis drives synapse loss during virus-induced memory impairment, Nature, vol.79, issue.7608, pp.538-581, 2016. ,
DOI : 10.1128/JVI.79.21.13350-13361.2005
Microglia: New Roles for the Synaptic Stripper, Neuron, vol.77, issue.1, pp.10-18, 2013. ,
DOI : 10.1016/j.neuron.2012.12.023
Neural activity and the dynamics of central nervous system development, Nature Neuroscience, vol.7, issue.4, pp.327-359, 2004. ,
DOI : 10.1038/nn1218
Distinct Roles for Spontaneous and Visual Activity in Remodeling of the Retinogeniculate Synapse, Neuron, vol.52, issue.2, pp.281-91, 2006. ,
DOI : 10.1016/j.neuron.2006.07.007
The postnatal development of the visual cortex and the influence of environment, Bioscience Reports, vol.185, issue.5, pp.351-77, 1982. ,
DOI : 10.1113/jphysiol.1975.sp010995
The Classical Complement Cascade Mediates CNS Synapse Elimination, Cell, vol.131, issue.6, pp.1164-78, 2007. ,
DOI : 10.1016/j.cell.2007.10.036
URL : http://doi.org/10.1016/j.cell.2007.10.036
Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner, Neuron, vol.74, issue.4, pp.691-705, 2012. ,
DOI : 10.1016/j.neuron.2012.03.026
Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex, Nature Communications, vol.10, pp.2-15, 2016. ,
DOI : 10.1016/S0896-6273(03)00286-1
URL : http://doi.org/10.1038/ncomms10905
Synaptic Pruning by Microglia Is Necessary for Normal Brain Development, Science, vol.107, issue.17, pp.1456-1464, 2011. ,
DOI : 10.1073/pnas.0913449107
Deficient neuron-microglia signaling results in impaired functional brain connectivity and social behavior, Nature Neuroscience, vol.19, issue.3, pp.400-406, 2014. ,
DOI : 10.1006/cbmr.1996.0014
CX3CR1 Deficiency Leads to Impairment of Hippocampal Cognitive Function and Synaptic Plasticity, Journal of Neuroscience, vol.31, issue.45, pp.16241-50, 2011. ,
DOI : 10.1523/JNEUROSCI.3667-11.2011
The Complement System: An Unexpected Role in Synaptic Pruning During Development and Disease, Annual Review of Neuroscience, vol.35, issue.1, pp.369-89, 2012. ,
DOI : 10.1146/annurev-neuro-061010-113810
Bidirectional Activity-Dependent Morphological Plasticity in Hippocampal Neurons, Neuron, vol.44, issue.5, pp.759-67, 2004. ,
DOI : 10.1016/j.neuron.2004.11.016
Repetition of mGluR-dependent LTD causes slowly developing persistent reduction in synaptic strength accompanied by synapse elimination, Brain Research, vol.1042, issue.1, pp.99-107, 2005. ,
DOI : 10.1016/j.brainres.2005.02.028
Long-lasting synaptic loss after repeated induction of LTD: independence to the means of LTD induction, European Journal of Neuroscience, vol.436, issue.6, pp.1606-1622, 2006. ,
DOI : 10.1113/jphysiol.1978.sp012482
Long Lasting Protein Synthesis- and Activity-Dependent Spine Shrinkage and Elimination after Synaptic Depression, PLoS ONE, vol.7, issue.8, p.71155, 2013. ,
DOI : 10.1371/journal.pone.0071155.s001
Long-term depression triggers the selective elimination of weakly integrated synapses, Proceedings of the National Academy of Sciences, vol.272, issue.5262, pp.4510-4519, 2013. ,
DOI : 10.1126/science.272.5262.716
Dendritic spine dynamics leading to spine elimination after repeated inductions of LTD, Scientific Reports, vol.15, issue.1, pp.1-6, 2015. ,
DOI : 10.1016/S0165-0270(02)00152-8
Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain, Nature Communications, vol.20, p.4486, 2014. ,
DOI : 10.1016/j.jneumeth.2012.12.010
Microglia and neuroprotection, Journal of Neurochemistry, vol.120, issue.Suppl, pp.10-17, 2016. ,
DOI : 10.1172/JCI33144
Evidence for synaptic stripping by cortical microglia, Glia, vol.84, issue.4, pp.360-368, 2007. ,
DOI : 10.1093/jnen/61.1.23
The Role of Microglia in Synaptic Stripping and Synaptic Degeneration: A Revised Perspective, ASN Neuro, vol.962, issue.5, p.47, 2010. ,
DOI : 10.1111/j.1749-6632.2002.tb04061.x
Microglia in neuronal plasticity: Influence of stress, Neuropharmacology, vol.96, pp.19-28, 2015. ,
DOI : 10.1016/j.neuropharm.2014.12.034
Astrocyte response to motor neuron injury promotes structural synaptic plasticity via STAT3-regulated TSP-1 expression, Nature Communications, vol.45, p.4294, 2014. ,
DOI : 10.1002/cne.20822
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104454
Microglia Promote Learning-Dependent Synapse Formation through Brain-Derived Neurotrophic Factor, Cell, vol.155, issue.7, pp.1596-609, 2013. ,
DOI : 10.1016/j.cell.2013.11.030
URL : http://doi.org/10.1016/j.cell.2013.11.030
Microglia contact induces synapse formation in developing somatosensory cortex, Nature Communications, vol.34, p.12540, 2016. ,
DOI : 10.1523/JNEUROSCI.1346-14.2014
Activity-dependent scaling of quantal amplitude in neocortical neurons, Nature, vol.391, issue.6670, pp.892-898, 1998. ,
DOI : 10.1038/36103
The dialectic of Hebb and homeostasis, Philosophical Transactions of the Royal Society B: Biological Sciences, vol.41, issue.1715, p.20160258, 1715. ,
DOI : 10.1007/7854_2014_305
Synaptic scaling mediated by glial TNF-?, Nature, vol.37, issue.7087, pp.1054-1063, 2006. ,
DOI : 10.1016/0165-0270(91)90128-M
Activity-Dependent Regulation of Synaptic AMPA Receptor Composition and Abundance by ??3 Integrins, Neuron, vol.58, issue.5, pp.749-62, 2008. ,
DOI : 10.1016/j.neuron.2008.04.011
There's More Than One Way to Scale a Synapse, Neuron, vol.58, issue.5, pp.651-654, 2008. ,
DOI : 10.1016/j.neuron.2008.05.017
URL : http://doi.org/10.1016/j.neuron.2008.05.017
Tumor Necrosis Factor-?? Mediates One Component of Competitive, Experience-Dependent Plasticity in Developing Visual Cortex, Neuron, vol.58, issue.5, pp.673-80, 2008. ,
DOI : 10.1016/j.neuron.2008.04.023
Understanding brain dysfunction in sepsis, Annals of Intensive Care, vol.3, issue.1, p.15, 2013. ,
DOI : 10.1097/CCM.0b013e31823779ca
URL : https://hal.archives-ouvertes.fr/pasteur-00830839
Acute encephalopathy and encephalitis caused by influenza virus infection, Current Opinion in Neurology, vol.23, issue.3, pp.305-316, 2010. ,
DOI : 10.1097/WCO.0b013e328338f6c9
Infectious Agents and Neurodegeneration, Molecular Neurobiology, vol.105, issue.Suppl 2, pp.614-652, 2012. ,
DOI : 10.1371/journal.pone.0020495
Influenza Infection Induces Neuroinflammation, Alters Hippocampal Neuron Morphology, and Impairs Cognition in Adult Mice, Journal of Neuroscience, vol.32, issue.12, pp.3958-68, 2012. ,
DOI : 10.1523/JNEUROSCI.6389-11.2012
Changes in calcium currents and GABAergic spontaneous activity in cultured rat hippocampal neurons after a neurotropic influenza A virus infection, Brain Research Bulletin, vol.55, issue.3, pp.421-430, 2001. ,
DOI : 10.1016/S0361-9230(01)00536-6
Effects on synaptic activity in cultured hippocampal neurons by influenza A viral proteins, Journal of Neurovirology, vol.76, issue.4, pp.395-402, 2005. ,
DOI : 10.1080/13550280500186916
HSV-1 promotes Ca2+ ?mediated APP phosphorylation and Abeta accumulation in rat cortical neurons, Neurobiol Aging, vol.32, issue.12, pp.2323-2336, 2011. ,
DOI : 10.1016/j.neurobiolaging.2010.06.009
To die or not to die for neurons in ischemia, traumatic brain injury and epilepsy: a review on the stress-activated signaling pathways and apoptotic pathways, Progress in Neurobiology, vol.69, issue.2, pp.103-145, 2003. ,
DOI : 10.1016/S0301-0082(03)00005-4
Traumatic Brain Injury and NADPH Oxidase: A Deep Relationship, Oxidative Medicine and Cellular Longevity, vol.24, issue.2, p.370312, 2015. ,
DOI : 10.1523/jneurosci.2246-12.2012
URL : http://doi.org/10.1155/2015/370312
Strategies for CNS repair following TBI, Experimental Neurology, vol.275, pp.411-437, 2016. ,
DOI : 10.1016/j.expneurol.2015.01.008
Inflammation and Neuroprotection in Traumatic Brain Injury, JAMA Neurology, vol.72, issue.3, pp.355-62, 2015. ,
DOI : 10.1001/jamaneurol.2014.3558
Traumatic Brain Injury and the Neuronal Microenvironment: A Potential Role for Neuropathological Mechanotransduction, Neuron, vol.85, issue.6, pp.1177-92, 2015. ,
DOI : 10.1016/j.neuron.2015.02.041
Epilepsy and brain inflammation, Experimental Neurology, vol.244, pp.11-21, 2013. ,
DOI : 10.1016/j.expneurol.2011.09.033
The role of inflammation in epilepsy, Nature Reviews Neurology, vol.36, issue.1, pp.31-40, 2011. ,
DOI : 10.1016/S0165-0173(01)00102-3
Epileptogenesis due to glia-mediated synaptic scaling, Journal of The Royal Society Interface, vol.71, issue.4, pp.655-68, 2009. ,
DOI : 10.1128/IAI.71.4.2288-2291.2003
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839938
Tumor necrosis factor-?? potentiates long-term potentiation in the rat dentate gyrus after acute hypoxia, Journal of Neuroscience Research, vol.46, issue.5, pp.815-844, 2015. ,
DOI : 10.1021/jm030152f
Binge Drinking in Adolescents: A Review of Neurophysiological and Neuroimaging Research, Alcohol and Alcoholism, vol.49, issue.2, pp.198-206, 2014. ,
DOI : 10.1093/alcalc/agt172
Glutamate receptor function in learning and memory, Behavioural Brain Research, vol.140, issue.1-2, pp.1-47, 2003. ,
DOI : 10.1016/S0166-4328(02)00272-3
Biochemical and Neurotransmitter Changes Implicated in Alcohol-Induced Brain Damage in Chronic or 'Binge Drinking' Alcohol Abuse, Alcohol and Alcoholism, vol.44, issue.2, pp.128-163, 2009. ,
DOI : 10.1093/alcalc/agn100
URL : http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.695.779
Mechanisms involved in the neurotoxic, cognitive, and neurobehavioral effects of alcohol consumption during adolescence, Alcohol, vol.44, issue.1, pp.15-26, 2010. ,
DOI : 10.1016/j.alcohol.2009.10.003
Increased receptor for advanced glycation end product expression in the human alcoholic prefrontal cortex is linked to adolescent drinking, Neurobiology of Disease, vol.59, pp.52-62, 2013. ,
DOI : 10.1016/j.nbd.2013.07.002
Developmental Differences in the Accumbal Dopaminergic Response to Repeated Ethanol Exposure, Annals of the New York Academy of Sciences, vol.7, issue.1, pp.422-428, 2004. ,
DOI : 10.1196/annals.1308.056
Serotonin and alcohol intake, abuse, and dependence: Findings of animal studies, Biological Psychiatry, vol.36, issue.6, pp.395-421, 1994. ,
DOI : 10.1016/0006-3223(94)91215-7
Variations in GABRA2, Encoding the ?2 Subunit of the GABAA Receptor, Are Associated with Alcohol Dependence and with Brain Oscillations, The American Journal of Human Genetics, vol.74, issue.4, pp.705-719, 2004. ,
DOI : 10.1086/383283
Aberrant NMDA-dependent LTD after perinatal ethanol exposure in young adult rat hippocampus, Hippocampus, vol.34, issue.8, pp.912-935, 2015. ,
DOI : 10.1111/j.1460-9568.2011.07776.x
Neurotoxic Effects of Alcohol in Adolescence, Annual Review of Clinical Psychology, vol.9, issue.1, pp.703-724, 2013. ,
DOI : 10.1146/annurev-clinpsy-050212-185610
Longitudinal Changes in White Matter Integrity Among Adolescent Substance Users, Alcoholism: Clinical and Experimental Research, vol.194, pp.181-190, 2013. ,
DOI : 10.1007/s00213-007-0823-y
Structural Magnetic Resonance Imaging of the Adolescent Brain, Annals of the New York Academy of Sciences, vol.11, issue.1 ,
DOI : 10.1001/archneur.1994.00540210046012
The Teen Brain: Insights from Neuroimaging, Journal of Adolescent Health, vol.42, issue.4, pp.335-378, 2008. ,
DOI : 10.1016/j.jadohealth.2008.01.007
Foetal Alcohol Spectrum Disorders and Alterations in Brain and Behaviour, Alcohol and Alcoholism, vol.44, issue.2, pp.108-122, 2009. ,
DOI : 10.1093/alcalc/agn105
Gender differences in alcohol-induced neurotoxicity and brain damage, Toxicology, vol.311, issue.1-2, pp.27-34, 2013. ,
DOI : 10.1016/j.tox.2013.03.001
The link between inflammation, synaptic transmission and neurodegeneration in multiple sclerosis, Cell Death and Differentiation, vol.80, issue.7, pp.1083-91, 2010. ,
DOI : 10.1093/hmg/ddm189
Inflammation in neurodegenerative diseases?-?an update, Immunology, vol.15, issue.2, pp.151-66, 2014. ,
DOI : 10.1038/nn.3163
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008224
Targeting Synaptic Dysfunction in Alzheimer???s Disease Therapy, Molecular Neurobiology, vol.21, issue.3, pp.572-87, 2012. ,
DOI : 10.3233/JAD-2010-100225
Synaptic Plasticity as a Therapeutic Target in the Treatment of Autism-related Single-gene Disorders, Current Pharmaceutical Design, vol.19, issue.36, pp.6480-90, 2013. ,
DOI : 10.2174/1381612811319360008
Synaptic plasticity in multiple sclerosis and in experimental autoimmune encephalomyelitis, Philosophical Transactions of the Royal Society B: Biological Sciences, vol.46, issue.3, p.20130162, 1633. ,
DOI : 10.1007/s12035-012-8302-9
Multiple sclerosis: a complicated picture of autoimmunity, Nature Immunology, vol.96, issue.9, pp.913-922, 2007. ,
DOI : 10.1016/j.jns.2005.03.011
Interleukin-1?? Promotes Long-Term Potentiation in Patients with Multiple Sclerosis, NeuroMolecular Medicine, vol.90, issue.5, pp.38-51, 2014. ,
DOI : 10.1038/labinvest.2010.6
Inflammation-mediated memory dysfunction and effects of a ketogenic diet in a murine model of multiple sclerosis, PLoS ONE, vol.7, issue.5, p.35476, 2012. ,
Microglial activation in early stages of amyloid ?? protein deposition, Acta Neuropathologica, vol.94, issue.4, pp.316-338, 1997. ,
DOI : 10.1007/s004010050713
Inflammatory markers and the risk of Alzheimer disease: The Framingham Study, Neurology, vol.68, issue.22, pp.1902-1910, 2007. ,
DOI : 10.1212/01.wnl.0000263217.36439.da
?-amyloid inhibition of long-term potentiation is mediated via tumor necrosis factor, European Journal of Neuroscience, vol.274, issue.11, pp.2827-2859, 2005. ,
DOI : 10.4049/jimmunol.168.6.2644
The effects of IL-1 receptor antagonist on beta amyloid mediated depression of LTP in the rat CA1 in vivo, Hippocampus, vol.78, issue.7, pp.670-676, 2009. ,
DOI : 10.1002/hipo.20542
Cyclooxygenase-2 inhibition improves amyloid-??-mediated suppression of memory and synaptic plasticity, Brain, vol.131, issue.3, pp.651-64, 2008. ,
DOI : 10.1093/brain/awn008
How dependent is synaptic plasticity on microglial phenotype?, Neuropharmacology, vol.96, pp.3-10, 2015. ,
DOI : 10.1016/j.neuropharm.2014.08.012
Complement and microglia mediate early synapse loss in Alzheimer mouse models, Science, vol.509, issue.6152, pp.712-718, 2016. ,
DOI : 10.1038/nature13154
Extracellular Alpha-Synuclein Oligomers Modulate Synaptic Transmission and Impair LTP Via NMDA-Receptor Activation, Journal of Neuroscience, vol.32, issue.34, pp.11750-62, 2012. ,
DOI : 10.1523/JNEUROSCI.0234-12.2012
URL : http://goedoc.uni-goettingen.de/goescholar/bitstream/handle/1/9413/11750.full.pdf?sequence=1
Neuroinflammation in Parkinson's disease: a target for neuroprotection?, The Lancet Neurology, vol.8, issue.4, pp.382-97, 2009. ,
DOI : 10.1016/S1474-4422(09)70062-6
Neuroinflammatory processes in Parkinson's disease, Annals of Neurology, vol.374, issue.S3 ,
DOI : 10.1002/ana.10481
Baicalein ameliorated the upregulation of striatal glutamatergic transmission in the mice model of Parkinson's disease, Brain Research Bulletin, vol.103, pp.54-63, 2014. ,
DOI : 10.1016/j.brainresbull.2014.02.004
Neuroinflammation and synaptic plasticity: theoretical basis for a novel, immune-centred, therapeutic approach to neurological disorders, Trends in Pharmacological Sciences, vol.29, issue.8, pp.402-414, 2008. ,
DOI : 10.1016/j.tips.2008.06.005