Alterations in theta-gamma coupling and sharp wave-ripple, signs of prodromal hippocampal network impairment in the TgF344-AD rat model
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[1] Jordan S. Farrell,et al. A consensus statement on detection of hippocampal sharp wave ripples and differentiation from other fast oscillations , 2022, Nature Communications.
[2] Georgios A. Keliris,et al. Altered basal forebrain function during whole-brain network activity at pre- and early-plaque stages of Alzheimer’s disease in TgF344-AD rats , 2022, Alzheimer's Research & Therapy.
[3] D. Schwartz,et al. Theta Band-Power Shapes Amyloid-Driven Longitudinal EEG Changes in Elderly Subjective Memory Complainers At-Risk for Alzheimer’s Disease , 2022, Journal of Alzheimer's disease : JAD.
[4] H. Bimonte-Nelson,et al. Task-dependent learning and memory deficits in the TgF344-AD rat model of Alzheimer’s disease: three key timepoints through middle-age in females , 2022, Scientific Reports.
[5] J. McLaurin,et al. Parvalbumin neuroplasticity compensates for somatostatin impairment, maintaining cognitive function in Alzheimer’s disease , 2022, Translational neurodegeneration.
[6] Gabriel A. Devenyi,et al. Neurochemical and cognitive changes precede structural abnormalities in the TgF344-AD rat model , 2022, Brain communications.
[7] Z. Gu,et al. Cholinergic Regulation of Hippocampal Theta Rhythm , 2022, Biomedicines.
[8] L. McMahon,et al. Impairments in Fear Extinction Memory and Basolateral Amygdala Plasticity in the TgF344-AD Rat Model of Alzheimer’s Disease Are Distinct from Nonpathological Aging , 2022, eNeuro.
[9] D. Weinshenker,et al. Consequences of Hyperphosphorylated Tau in the Locus Coeruleus on Behavior and Cognition in a Rat Model of Alzheimer's Disease. , 2022, Journal of Alzheimer's disease : JAD.
[10] OUP accepted manuscript , 2022, Brain Communications.
[11] R. Robitsek,et al. Prodromal dysfunction of α5GABA-A receptor modulated hippocampal ripples occurs prior to neurodegeneration in the TgF344-AD rat model of Alzheimer's disease , 2021, Heliyon.
[12] S. Sakata,et al. Mutual Interactions between Brain States and Alzheimer’s Disease Pathology: A Focus on Gamma and Slow Oscillations , 2021, Biology.
[13] Jun-li Zhen,et al. Normal and Abnormal Sharp Wave Ripples in the Hippocampal-Entorhinal Cortex System: Implications for Memory Consolidation, Alzheimer's Disease, and Temporal Lobe Epilepsy , 2021, Frontiers in Aging Neuroscience.
[14] L. McMahon,et al. Heightened Hippocampal β-Adrenergic Receptor Function Drives Synaptic Potentiation and Supports Learning and Memory in the TgF344-AD Rat Model during Prodromal Alzheimer's Disease , 2021, The Journal of Neuroscience.
[15] Stephen R. Williams,et al. Prodromal neuroinflammatory, cholinergic and metabolite dysfunction detected by PET and MRS in the TgF344-AD transgenic rat model of AD: a collaborative multi-modal study , 2021, Theranostics.
[16] L. McMahon,et al. Dentate Granule Cells Are Hyperexcitable in the TgF344-AD Rat Model of Alzheimer's Disease , 2021, bioRxiv.
[17] A. Sánchez-Aguilera,et al. Sharp Wave Ripples in Alzheimer's Disease: In Search of Mechanisms , 2021, The Journal of Neuroscience.
[18] Matthew G. Buckley,et al. Individual differences in theta-band oscillations in a spatial memory network revealed by electroencephalography predict rapid place learning , 2021, Brain and neuroscience advances.
[19] György Buzsáki,et al. Subcircuits of Deep and Superficial CA1 Place Cells Support Efficient Spatial Coding across Heterogeneous Environments , 2020, Neuron.
[20] J. Brouillette,et al. Hyperactivity Induced by Soluble Amyloid-β Oligomers in the Early Stages of Alzheimer's Disease , 2021, Frontiers in Molecular Neuroscience.
[21] M. Valderrama,et al. Acute Effects of Two Different Species of Amyloid-β on Oscillatory Activity and Synaptic Plasticity in the Commissural CA3-CA1 Circuit of the Hippocampus , 2020, Neural plasticity.
[22] N. Burgess,et al. Theta power and theta‐gamma coupling support long‐term spatial memory retrieval , 2020, Hippocampus.
[23] M. Munk,et al. Multimodal MRI analysis of basal forebrain structure and function across the Alzheimer’s disease spectrum , 2020, NeuroImage: Clinical.
[24] P. Millet,et al. Spatial reference learning deficits in absence of dysfunctional working memory in the TgF344‐AD rat model of Alzheimer's disease , 2020, Genes, brain, and behavior.
[25] B. Kolb,et al. Neural oscillations and brain stimulation in Alzheimer’s disease , 2020, Progress in Neurobiology.
[26] Yong Shen,et al. GABAergic dysfunction in excitatory and inhibitory (E/I) imbalance drives the pathogenesis of Alzheimer's disease , 2020, Alzheimer's & dementia : the journal of the Alzheimer's Association.
[27] C. B. Smith,et al. Behavioral Phenotype in the TgF344-AD Rat Model of Alzheimer’s Disease , 2020, Frontiers in Neuroscience.
[28] A. Draguhn,et al. Synchronicity of excitatory inputs drives hippocampal networks to distinct oscillatory patterns , 2020, Hippocampus.
[29] Biyu J He,et al. Neuromodulation of Brain State and Behavior. , 2020, Annual review of neuroscience.
[30] F. Cardenas,et al. Synaptic plasticity in Alzheimer’s disease and healthy aging , 2020, Reviews in the neurosciences.
[31] Shaomin Li,et al. A mechanistic hypothesis for the impairment of synaptic plasticity by soluble Aβ oligomers from Alzheimer’s brain , 2020, Journal of neurochemistry.
[32] Jian-Young Wu,et al. Inhibitory Parvalbumin Basket Cell Activity is Selectively Reduced during Hippocampal Sharp Wave Ripples in a Mouse Model of Familial Alzheimer's Disease , 2020, The Journal of Neuroscience.
[33] Blake A. Richards,et al. Optogenetic activation of parvalbumin and somatostatin interneurons selectively restores theta-nested gamma oscillations and oscillation-induced spike timing-dependent long-term potentiation impaired by amyloid β oligomers , 2020, BMC Biology.
[34] Blake A. Richards,et al. Optogenetic activation of parvalbumin and somatostatin interneurons selectively restores theta-nested gamma oscillations and oscillation-induced spike timing-dependent long-term potentiation impaired by amyloid β oligomers , 2020, BMC Biology.
[35] Sylvain Williams,et al. Optogenetic gamma stimulation rescues memory impairments in an Alzheimer’s disease mouse model , 2019, Nature Communications.
[36] Georgios A. Keliris,et al. Increased soluble amyloid-beta causes early aberrant brain network hypersynchronisation in a mature-onset mouse model of amyloidosis , 2019, Acta Neuropathologica Communications.
[37] Hovagim Bakardjian,et al. EEG EVIDENCE OF COMPENSATORY MECHANISMS IN PRECLINICAL ALZHEIMER’S DISEASE , 2019, Alzheimer's & Dementia.
[38] D. Lodge,et al. Modulation of extrasynaptic GABAA alpha 5 receptors in the ventral hippocampus normalizes physiological and behavioral deficits in a circuit specific manner , 2019, Nature Communications.
[39] Taylor W. Schmitz,et al. Basal forebrain volume reliably predicts the cortical spread of Alzheimer’s degeneration , 2019, bioRxiv.
[40] G. Buzsáki,et al. Long-duration hippocampal sharp wave ripples improve memory , 2019, Science.
[41] L. Frank,et al. Early Hippocampal Sharp-Wave Ripple Deficits Predict Later Learning and Memory Impairments in an Alzheimer’s Disease Mouse Model , 2019, bioRxiv.
[42] L. Frank,et al. Three brain states in the hippocampus and cortex , 2019, Hippocampus.
[43] Craig Kelley,et al. Altered Cortical and Hippocampal Excitability in TgF344-AD Rats Modeling Alzheimer's Disease Pathology. , 2018, Cerebral cortex.
[44] György Buzsáki,et al. Origin of Gamma Frequency Power during Hippocampal Sharp-Wave Ripples , 2018, Cell reports.
[45] T. Horvath,et al. Neurophysiological signals as predictive translational biomarkers for Alzheimer’s disease treatment: effects of donepezil on neuronal network oscillations in TgF344-AD rats , 2018, Alzheimer's Research & Therapy.
[46] V. Kitchigina. Alterations of Coherent Theta and Gamma Network Oscillations as an Early Biomarker of Temporal Lobe Epilepsy and Alzheimer’s Disease , 2018, Front. Integr. Neurosci..
[47] Morten Mørup,et al. EEG Theta Power Is an Early Marker of Cognitive Decline in Dementia due to Alzheimer's Disease. , 2018, Journal of Alzheimer's disease : JAD.
[48] Alastair Flint,et al. Theta-Gamma Coupling and Working Memory in Alzheimer’s Dementia and Mild Cognitive Impairment , 2018, Front. Aging Neurosci..
[49] Paolo Bazzigaluppi,et al. Early‐stage attenuation of phase‐amplitude coupling in the hippocampus and medial prefrontal cortex in a transgenic rat model of Alzheimer's disease , 2018, Journal of neurochemistry.
[50] Boaz Styr,et al. Imbalance between firing homeostasis and synaptic plasticity drives early-phase Alzheimer’s disease , 2018, Nature Neuroscience.
[51] L. McMahon,et al. Deficits in synaptic function occur at medial perforant path-dentate granule cell synapses prior to Schaffer collateral-CA1 pyramidal cell synapses in the novel TgF344-Alzheimer's Disease Rat Model , 2018, Neurobiology of Disease.
[52] Laura E. Berkowitz,et al. Anxiety-like behavior as an early endophenotype in the TgF344-AD rat model of Alzheimer's disease , 2018, Neurobiology of Aging.
[53] J. Born,et al. Phase-Amplitude Coupling: A General Mechanism for Memory Processing and Synaptic Plasticity? , 2018, Neuron.
[54] J. Gordon,et al. Hippocampal-prefrontal theta-gamma coupling during performance of a spatial working memory task , 2017, Nature Communications.
[55] M. Reed,et al. Alterations in Hippocampal Activity and Alzheimer’s Disease , 2017, Translational issues in psychological science.
[56] John B. Trimper,et al. Gamma Oscillations in Rat Hippocampal Subregions Dentate Gyrus, CA3, CA1, and Subiculum Underlie Associative Memory Encoding. , 2017, Cell reports.
[57] D. Weinshenker,et al. Chemogenetic locus coeruleus activation restores reversal learning in a rat model of Alzheimer’s disease , 2017, Brain : a journal of neurology.
[58] Sylvain Baillet,et al. Time-resolved phase-amplitude coupling in neural oscillations , 2017, NeuroImage.
[59] Susumu Tonegawa,et al. Direct Medial Entorhinal Cortex Input to Hippocampal CA1 Is Crucial for Extended Quiet Awake Replay , 2017, Neuron.
[60] Huichao Yang,et al. Enhanced Gamma Activity and Cross-Frequency Interaction of Resting-State Electroencephalographic Oscillations in Patients with Alzheimer’s Disease , 2017, Front. Aging Neurosci..
[61] John G. Sled,et al. Early neurovascular dysfunction in a transgenic rat model of Alzheimer’s disease , 2017, Scientific Reports.
[62] E. Boyden,et al. Gamma frequency entrainment attenuates amyloid load and modifies microglia , 2016, Nature.
[63] L. Mucke,et al. Network abnormalities and interneuron dysfunction in Alzheimer disease , 2016, Nature Reviews Neuroscience.
[64] Annemie Van der Linden,et al. Early pathologic amyloid induces hypersynchrony of BOLD resting-state networks in transgenic mice and provides an early therapeutic window before amyloid plaque deposition , 2016, Alzheimer's & Dementia.
[65] Jonathan T. Brown,et al. Disrupted hippocampal sharp‐wave ripple‐associated spike dynamics in a transgenic mouse model of dementia , 2016, The Journal of physiology.
[66] Mattias P. Karlsson,et al. Apolipoprotein E4 Causes Age-Dependent Disruption of Slow Gamma Oscillations during Hippocampal Sharp-Wave Ripples , 2016, Neuron.
[67] L. Colgin. Rhythms of the hippocampal network , 2016, Nature Reviews Neuroscience.
[68] J. Mellor,et al. Sharp-Wave Ripples Orchestrate the Induction of Synaptic Plasticity during Reactivation of Place Cell Firing Patterns in the Hippocampus , 2016, Cell reports.
[69] Jihyeon Janel Lee,et al. Basal Forebrain Cholinergic Deficits Reduce Glucose Metabolism and Function of Cholinergic and GABAergic Systems in the Cingulate Cortex , 2015, Yonsei medical journal.
[70] M. Hajós,et al. Modulation of hippocampal neuronal network oscillations by α7 nACh receptors. , 2015, Biochemical pharmacology.
[71] G. Buzsáki. Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning , 2015, Hippocampus.
[72] N. Axmacher,et al. Neuronal Network Oscillations in Neurodegenerative Diseases , 2015, NeuroMolecular Medicine.
[73] Caroline L. Speck,et al. Response of the medial temporal lobe network in amnestic mild cognitive impairment to therapeutic intervention assessed by fMRI and memory task performance , 2015, NeuroImage: Clinical.
[74] Stefan Klöppel,et al. Basal Forebrain and Hippocampus as Predictors of Conversion to Alzheimer's Disease in Patients with Mild Cognitive Impairment - A Multicenter DTI and Volumetry Study. , 2015, Journal of Alzheimer's disease : JAD.
[75] Eran Stark,et al. Excitation and Inhibition Compete to Control Spiking during Hippocampal Ripples: Intracellular Study in Behaving Mice , 2014, The Journal of Neuroscience.
[76] Stefan J. Teipel,et al. Basal forebrain atrophy and cortical amyloid deposition in nondemented elderly subjects , 2014, Alzheimer's & Dementia.
[77] L. Colgin,et al. Slow and Fast Gamma Rhythms Coordinate Different Spatial Coding Modes in Hippocampal Place Cells , 2014, Neuron.
[78] Li Lu,et al. Coordination of entorhinal–hippocampal ensemble activity during associative learning , 2014, Nature.
[79] Ehren L. Newman,et al. Cholinergic Blockade Reduces Theta-Gamma Phase Amplitude Coupling and Speed Modulation of Theta Frequency Consistent with Behavioral Effects on Encoding , 2013, The Journal of Neuroscience.
[80] Matt Stead,et al. Network oscillations modulate interictal epileptiform spike rate during human memory. , 2013, Brain : a journal of neurology.
[81] Jesse Jackson,et al. Alterations in hippocampal network oscillations and theta–gamma coupling arise before Aβ overproduction in a mouse model of Alzheimer's disease , 2013, The European journal of neuroscience.
[82] H. Tanila,et al. Increased cortical and thalamic excitability in freely moving APPswe/PS1dE9 mice modeling epileptic activity associated with Alzheimer's disease. , 2013, Cerebral cortex.
[83] Pasko Rakic,et al. A Transgenic Alzheimer Rat with Plaques, Tau Pathology, Behavioral Impairment, Oligomeric Aβ, and Frank Neuronal Loss , 2013, The Journal of Neuroscience.
[84] Margaret F. Carr,et al. Transient Slow Gamma Synchrony Underlies Hippocampal Memory Replay , 2012, Neuron.
[85] Liam Scott,et al. Age-dependent disruption in hippocampal theta oscillation in amyloid-β overproducing transgenic mice , 2012, Neurobiology of Aging.
[86] Bert Sakmann,et al. Critical role of soluble amyloid-β for early hippocampal hyperactivity in a mouse model of Alzheimer’s disease , 2012, Proceedings of the National Academy of Sciences.
[87] R. Schmidt,et al. Cross-Frequency Phase–Phase Coupling between Theta and Gamma Oscillations in the Hippocampus , 2012, The Journal of Neuroscience.
[88] E. Klann,et al. Amyloid β: linking synaptic plasticity failure to memory disruption in Alzheimer’s disease , 2012, Journal of neurochemistry.
[89] Dietmar R. Thal,et al. Stages of the Pathologic Process in Alzheimer Disease: Age Categories From 1 to 100 Years , 2011, Journal of neuropathology and experimental neurology.
[90] Michaël Zugaro,et al. Hippocampal ripples and memory consolidation , 2011, Current Opinion in Neurobiology.
[91] Denise C. Park,et al. Toward defining the preclinical stages of Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease , 2011, Alzheimer's & Dementia.
[92] Richard M. Leahy,et al. Brainstorm: A User-Friendly Application for MEG/EEG Analysis , 2011, Comput. Intell. Neurosci..
[93] J. Fell,et al. The role of phase synchronization in memory processes , 2011, Nature Reviews Neuroscience.
[94] Margaret F. Carr,et al. Hippocampal replay in the awake state: a potential substrate for memory consolidation and retrieval , 2011, Nature Neuroscience.
[95] Robert Oostenveld,et al. FieldTrip: Open Source Software for Advanced Analysis of MEG, EEG, and Invasive Electrophysiological Data , 2010, Comput. Intell. Neurosci..
[96] R. Knight,et al. The functional role of cross-frequency coupling , 2010, Trends in Cognitive Sciences.
[97] G. Caravaglios,et al. Theta power responses in mild Alzheimer’s disease during an auditory oddball paradigm: lack of theta enhancement during stimulus processing , 2010, Journal of Neural Transmission.
[98] P. Dutar,et al. Decreased Rhythmic GABAergic Septal Activity and Memory-Associated θ Oscillations after Hippocampal Amyloid-β Pathology in the Rat , 2010, The Journal of Neuroscience.
[99] H. Eichenbaum,et al. Measuring phase-amplitude coupling between neuronal oscillations of different frequencies. , 2010, Journal of neurophysiology.
[100] Craig E. L. Stark,et al. High-resolution structural and functional MRI of hippocampal CA3 and dentate gyrus in patients with amnestic Mild Cognitive Impairment , 2010, NeuroImage.
[101] Gustavo Puras,et al. Medial septal β-amyloid 1-40 injections alter septo-hippocampal anatomy and function , 2010, Neurobiology of Aging.
[102] M. Wilson,et al. Disruption of ripple‐associated hippocampal activity during rest impairs spatial learning in the rat , 2009, Hippocampus.
[103] Adriano B. L. Tort,et al. Theta–gamma coupling increases during the learning of item–context associations , 2009, Proceedings of the National Academy of Sciences.
[104] T. Hafting,et al. Frequency of gamma oscillations routes flow of information in the hippocampus , 2009, Nature.
[105] Adriano B. L. Tort,et al. Dynamic cross-frequency couplings of local field potential oscillations in rat striatum and hippocampus during performance of a T-maze task , 2008, Proceedings of the National Academy of Sciences.
[106] D. Katz,et al. Behavioral states, network states, and sensory response variability. , 2008, Journal of neurophysiology.
[107] J. Fell,et al. Ripples in the medial temporal lobe are relevant for human memory consolidation. , 2008, Brain : a journal of neurology.
[108] M. Høydal,et al. Running speed and maximal oxygen uptake in rats and mice: practical implications for exercise training , 2007, European journal of cardiovascular prevention and rehabilitation : official journal of the European Society of Cardiology, Working Groups on Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology.
[109] Brian Litt,et al. Gamma Oscillations Distinguish True From False Memories , 2007, Psychological science.
[110] Peter Boesiger,et al. Enhanced brain activity may precede the diagnosis of Alzheimer's disease by 30 years. , 2006, Brain : a journal of neurology.
[111] M. Berger,et al. High Gamma Power Is Phase-Locked to Theta Oscillations in Human Neocortex , 2006, Science.
[112] J. Born,et al. Hippocampal sharp wave-ripples linked to slow oscillations in rat slow-wave sleep. , 2006, Journal of neurophysiology.
[113] R. Verwer,et al. Increased Metabolic Activity in Nucleus Basalis of Meynert Neurons in Elderly Individuals With Mild Cognitive Impairment as Indicated by the Size of the Golgi Apparatus , 2006, Journal of neuropathology and experimental neurology.
[114] G. Buzsáki. Rhythms of the brain , 2006 .
[115] H. Eichenbaum,et al. Age-Associated Alterations of Hippocampal Place Cells Are Subregion Specific , 2005, The Journal of Neuroscience.
[116] Joshua A. Gordon,et al. State-Dependent Alterations in Hippocampal Oscillations in Serotonin 1A Receptor-Deficient Mice , 2005, The Journal of Neuroscience.
[117] J. Fell,et al. Phase/amplitude reset and theta–gamma interaction in the human medial temporal lobe during a continuous word recognition memory task , 2005, Hippocampus.
[118] H. Braak,et al. Neuropathological stageing of Alzheimer-related changes , 2004, Acta Neuropathologica.
[119] G. Buzsáki,et al. Hippocampal network patterns of activity in the mouse , 2003, Neuroscience.
[120] G. Buzsáki. Theta Oscillations in the Hippocampus , 2002, Neuron.
[121] L. Bianchi,et al. Effects of novelty and habituation on acetylcholine, GABA, and glutamate release from the frontal cortex and hippocampus of freely moving rats , 2001, Neuroscience.
[122] G. Buzsáki,et al. Gamma (40-100 Hz) oscillation in the hippocampus of the behaving rat , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[123] C. H. Vanderwolf,et al. Two types of hippocampal rhythmical slow activity in both the rabbit and the rat: Relations to behavior and effects of atropine, diethyl ether, urethane, and pentobarbital , 1975, Experimental Neurology.