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Inflammation: Cause or Consequence of Epilepsy?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jama.1909.02550020033007openalex-snapshot
A JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
inferredcites →https://doi.org/10.1002/brb3.348openalex-snapshot
Lipopolysaccharide potentiates hyperthermia‐induced seizures
inferredcites →https://doi.org/10.1007/s00401-018-1815-1openalex-snapshot
Functional morphology of the blood–brain barrier in health and disease
inferredcites →https://doi.org/10.1007/s00429-013-0528-4openalex-snapshot
MRI changes and complement activation correlate with epileptogenicity in a mouse model of temporal lobe epilepsy
inferredcites →https://doi.org/10.1007/s00540-016-2264-4openalex-snapshot
Preventive effects of dexmedetomidine on the development of cognitive dysfunction following systemic inflammation in aged rats
inferredcites →https://doi.org/10.1007/s11055-008-9089-zopenalex-snapshot
Caspase-3 activity in hippocampal slices reflects changes in synaptic plasticity
inferredcites →https://doi.org/10.1007/s11064-012-0771-8openalex-snapshot
The Anticonvulsant and Neuroprotective Effects of Baicalin on Pilocarpine-Induced Epileptic Model in Rats
inferredcites →https://doi.org/10.1007/s13311-014-0263-4openalex-snapshot
Origins of Temporal Lobe Epilepsy: Febrile Seizures and Febrile Status Epilepticus
inferredcites →https://doi.org/10.1016/0306-4522(85)90299-4openalex-snapshot
Limbic seizure and brain damage produced by kainic acid: Mechanisms and relevance to human temporal lobe epilepsy
inferredcites →https://doi.org/10.1016/b978-012078141-6/50014-7openalex-snapshot
Mechanisms of Fever and Febrile Seizures
inferredcites →https://doi.org/10.1016/j.bbi.2011.03.018openalex-snapshot
IL-1 receptor/Toll-like receptor signaling in infection, inflammation, stress and neurodegeneration couples hyperexcitability and seizures
inferredcites →https://doi.org/10.1016/j.bcp.2018.09.004openalex-snapshot
Rifampicin ameliorates lithium-pilocarpine-induced seizures, consequent hippocampal damage and memory deficit in rats: Impact on oxidative, inflammatory and apoptotic machineries
inferredcites →https://doi.org/10.1016/j.brainresbull.2012.04.007openalex-snapshot
Administration of docosahexaenoic acid before birth and until aging decreases kainate-induced seizures in adult zebrafish
inferredcites →https://doi.org/10.1016/j.ejphar.2018.01.023openalex-snapshot
Cerebellar oxidative stress and fine motor impairment in adolescent rats exposed to hyperthermia-induced seizures is prevented by maternal caffeine intake during gestation and lactation
inferredcites →https://doi.org/10.1016/j.ejphar.2018.08.020openalex-snapshot
Role of inflammation in epilepsy and neurobehavioral comorbidities: Implication for therapy
inferredcites →https://doi.org/10.1016/j.eplepsyres.2009.09.004openalex-snapshot
Contributions of peripheral inflammation to seizure susceptibility: Cytokines and brain excitability
inferredcites →https://doi.org/10.1016/j.eplepsyres.2017.11.003openalex-snapshot
Asiatic acid and maslinic acid attenuated kainic acid-induced seizure through decreasing hippocampal inflammatory and oxidative stress
inferredcites →https://doi.org/10.1016/j.expneurol.2011.09.033openalex-snapshot
Epilepsy and brain inflammation
inferredcites →https://doi.org/10.1016/j.nbd.2003.08.001openalex-snapshot
Glia activation and cytokine increase in rat hippocampus by kainic acid-induced status epilepticus during postnatal development
inferredcites →https://doi.org/10.1016/j.nbd.2014.12.015openalex-snapshot
Effective termination of status epilepticus by rational polypharmacy in the lithium–pilocarpine model in rats: Window of opportunity to prevent epilepsy and prediction of epilepsy by biomarkers
inferredcites →https://doi.org/10.1016/j.neulet.2010.08.049openalex-snapshot
Reactive oxygen species generated by NADPH oxidase are involved in neurodegeneration in the pilocarpine model of temporal lobe epilepsy
inferredcites →https://doi.org/10.1016/j.neuro.2018.04.007openalex-snapshot
Forebrain glutamate uptake and behavioral parameters are altered in adult zebrafish after the induction of Status Epilepticus by kainic acid
inferredcites →https://doi.org/10.1016/j.neuron.2011.04.004openalex-snapshot
Nonapoptotic Function of BAD and BAX in Long-Term Depression of Synaptic Transmission
inferredcites →https://doi.org/10.1016/j.neuroscience.2003.08.043openalex-snapshot
The bacterial endotoxin lipopolysaccharide enhances seizure susceptibility in mice: involvement of proinflammatory factors: nitric oxide and prostaglandins
inferredcites →https://doi.org/10.1016/j.ntt.2009.02.005openalex-snapshot
Zebrafish provide a sensitive model of persisting neurobehavioral effects of developmental chlorpyrifos exposure: Comparison with nicotine and pilocarpine effects and relationship to dopamine deficits
inferredcites →https://doi.org/10.1016/j.pharep.2015.08.011openalex-snapshot
Pre- and post-exposure talampanel (GYKI 53773) against kainic acid seizures in neonatal rats
inferredcites →https://doi.org/10.1016/j.seizure.2010.01.010openalex-snapshot
Oxidative stress mediates hippocampal neuron death in rats after lithium–pilocarpine-induced status epilepticus
inferredcites →https://doi.org/10.1016/j.seizure.2014.09.018openalex-snapshot
Epilepsy research methods update: Understanding the causes of epileptic seizures and identifying new treatments using non-mammalian model organisms
inferredcites →https://doi.org/10.1016/j.seizure.2014.10.007openalex-snapshot
Increased interleukin-6 and high-sensitivity C-reactive protein levels in pediatric epilepsy patients with frequent, refractory generalized motor seizures
inferredcites →https://doi.org/10.1016/j.semcdb.2014.10.003openalex-snapshot
Blood–brain barrier dysfunction, seizures and epilepsy
inferredcites →https://doi.org/10.1016/j.yebeh.2011.08.016openalex-snapshot
Assessment of the convulsant liability of antidepressants using zebrafish and mouse seizure models
inferredcites →https://doi.org/10.1016/j.yebeh.2015.04.047openalex-snapshot
Status epilepticus, blood–brain barrier disruption, inflammation, and epileptogenesis
inferredcites →https://doi.org/10.1016/s0022-3565(24)37902-9openalex-snapshot
Peripheral Effects of Opioids in a Model of Chronic Intestinal Inflammation in Mice
inferredcites →https://doi.org/10.1016/s0022-3565(25)22374-6openalex-snapshot
Diarrhea associated with intestinal inflammation increases the potency of mu and delta opioids on the inhibition of gastrointestinal transit in mice.
inferredcites →https://doi.org/10.1016/s0165-3806(96)00190-3openalex-snapshot
Febrile seizures: an appropriate-aged model suitable for long-term studies
inferredcites →https://doi.org/10.1016/s0166-2236(00)01659-3openalex-snapshot
Kainate, a double agent that generates seizures: two decades of progress
inferredcites →https://doi.org/10.1021/jf203709qopenalex-snapshot
Fresh Green Tea and Gallic Acid Ameliorate Oxidative Stress in Kainic Acid-Induced Status Epilepticus
inferredcites →https://doi.org/10.1038/ncomms11153openalex-snapshot
CD8+ T-cell pathogenicity in Rasmussen encephalitis elucidated by large-scale T-cell receptor sequencing
inferredcites →https://doi.org/10.1038/nm.2127openalex-snapshot
Toll-like receptor 4 and high-mobility group box-1 are involved in ictogenesis and can be targeted to reduce seizures
inferredcites →https://doi.org/10.1073/pnas.0806682105openalex-snapshot
Microglial activation and TNFα production mediate altered CNS excitability following peripheral inflammation
inferredcites →https://doi.org/10.1080/01616412.2017.1379241openalex-snapshot
Anterior thalamic nuclei deep brain stimulation reduces disruption of the blood–brain barrier, albumin extravasation, inflammation and apoptosis in kainic acid-induced epileptic rats
inferredcites →https://doi.org/10.1093/brain/awl317openalex-snapshot
TGF- receptor-mediated albumin uptake into astrocytes is involved in neocortical epileptogenesis
inferredcites →https://doi.org/10.1097/wco.0b013e32833735feopenalex-snapshot
The growing recognition of immunotherapy-responsive seizure disorders with autoantibodies to specific neuronal proteins
inferredcites →https://doi.org/10.1111/cns.12352openalex-snapshot
In Rasmussen Encephalitis, Hemichannels Associated with Microglial Activation are linked to Cortical Pyramidal Neuron Coupling: A Possible Mechanism for Cellular Hyperexcitability
inferredcites →https://doi.org/10.1111/cns.12371openalex-snapshot
Inflammation and Epilepsy in the Developing Brain: Clinical and Experimental Evidence
inferredcites →https://doi.org/10.1111/epi.12042openalex-snapshot
Rasmussen encephalitis: Incidence and course under randomized therapy with tacrolimus or intravenous immunoglobulins
inferredcites →https://doi.org/10.1111/epi.13457openalex-snapshot
Transient and chronic seizure‐induced inflammation in human focal epilepsy
inferredcites →https://doi.org/10.1111/epi.13965openalex-snapshot
Commonalities in epileptogenic processes from different acute brain insults: Do they translate?
inferredcites →https://doi.org/10.1111/epi.14068openalex-snapshot
The primary prevention of epilepsy: A report of the Prevention Task Force of the International League Against Epilepsy
inferredcites →https://doi.org/10.1111/j.1472-8206.2009.0773.xopenalex-snapshot
Correlation of seizures and biochemical parameters of oxidative stress in experimentally induced inflammatory rat models
inferredcites →https://doi.org/10.1111/j.1528-1167.2012.03666.xopenalex-snapshot
Long‐lasting pro‐ictogenic effects induced in vivo by rat brain exposure to serum albumin in the absence of concomitant pathology
inferredcites →https://doi.org/10.1111/j.1749-6632.1998.tb08311.xopenalex-snapshot
Delineation of the Proinflammatory Cytokine Cascade in Fever Inductiona
inferredcites →https://doi.org/10.1111/jnc.12610openalex-snapshot
Triheptanoin partially restores levels of tricarboxylic acid cycle intermediates in the mouse pilocarpine model of epilepsy
inferredcites →https://doi.org/10.1146/annurev.immunol.13.1.437openalex-snapshot
Receptor-Dependent Mechanisms of Cell Stimulation by Bacterial Endotoxin
inferredcites →https://doi.org/10.1155/2011/765923openalex-snapshot
Blood-Brain Barrier Breakdown Following Traumatic Brain Injury: A Possible Role in Posttraumatic Epilepsy
inferredcites →https://doi.org/10.1155/2014/293689openalex-snapshot
Oxidative Stress Associated with Neuronal Apoptosis in Experimental Models of Epilepsy
inferredcites →https://doi.org/10.1159/000198104openalex-snapshot
Experimental Production of Diffuse Colitis in Rats
inferredcites →https://doi.org/10.1179/016164105x49526openalex-snapshot
Do pathogen exposure and innate immunity cause brain diseases?
inferredcites →https://doi.org/10.1186/1742-2094-10-53openalex-snapshot
Hippocampal gene expression dysregulation of Klotho, nuclear factor kappa B and tumor necrosis factor in temporal lobe epilepsy patients
inferredcites →https://doi.org/10.1186/s12929-015-0157-8openalex-snapshot
Peripheral inflammation increases seizure susceptibility via the induction of neuroinflammation and oxidative stress in the hippocampus
inferredcites →https://doi.org/10.1186/s12974-018-1192-7openalex-snapshot
The role of inflammation in the development of epilepsy
inferredcites →https://doi.org/10.1189/jlb.0304127openalex-snapshot
Endogenous ligands of Toll-like receptors
inferredcites →https://doi.org/10.1189/jlb.0306164openalex-snapshot
DAMPs, PAMPs and alarmins: all we need to know about danger
inferredcites →https://doi.org/10.1248/bpb.b14-00633openalex-snapshot
Protective Effects of Bupivacaine against Kainic Acid-Induced Seizure and Neuronal Cell Death in the Rat Hippocampus
inferredcites →https://doi.org/10.1523/jneurosci.0430-09.2009openalex-snapshot
Transcriptome Profiling Reveals TGF- Signaling Involvement in Epileptogenesis
inferredcites →https://doi.org/10.1523/jneurosci.0551-10.2010openalex-snapshot
Epileptogenesis Provoked by Prolonged Experimental Febrile Seizures: Mechanisms and Biomarkers
inferredcites →https://doi.org/10.1523/jneurosci.2323-09.2009openalex-snapshot
Astrocytic Dysfunction in Epileptogenesis: Consequence of Altered Potassium and Glutamate Homeostasis?
inferredcites →https://doi.org/10.2174/1871527314666150317225945openalex-snapshot
Dynamic Expression of MicroRNAs (183, 135a, 125b, 128, 30c and 27a) in the Rat Pilocarpine Model and Temporal Lobe Epilepsy Patients
inferredcites →https://doi.org/10.3389/fphar.2017.00515openalex-snapshot
Zebrafish as a Model for Epilepsy-Induced Cognitive Dysfunction: A Pharmacological, Biochemical and Behavioral Approach
inferredcites →https://doi.org/10.3389/fphar.2018.00655openalex-snapshot
A Systematic Review on Non-mammalian Models in Epilepsy Research
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4622275openalex-extracted
Peripheral Blood Regulatory B and T Cells are Decreased in Patients with Focal Epilepsy
inferred← citeshttps://doi.org/10.1007/s11033-021-06896-8openalex-snapshot
Pharmacological modulation of cytokines correlating neuroinflammatory cascades in epileptogenesis
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2021.05.001openalex-snapshot
A literature overview on epilepsy and inflammasome activation
inferred← citeshttps://doi.org/10.1016/j.seizure.2020.03.017openalex-snapshot
Effects of the ketogenic diet on platelet counts and global coagulation tests in childhood epilepsy
inferred← citeshttps://doi.org/10.1016/j.yebeh.2020.107707openalex-snapshot
Pergularia daemia alters epileptogenesis and attenuates cognitive impairment in kainate-treated mice: Insight into anti-inflammatory mechanisms
inferred← citeshttps://doi.org/10.1136/bcr-2022-252637openalex-snapshot
Inflammatory epilepsy (FIRES) and haemophagocytic lymphohistiocytosis (HLH): an adult case
inferred← citeshttps://doi.org/10.34172/jhp.54007openalex-snapshot
Antiepileptic potential of the aqueous extract of Crassocephalum bauchiense (Hutch.) Milne-Redh. (Asteraceae) in a kainate induced mouse model of temporal lobe epilepsy
inferred← citeshttps://doi.org/10.70675/0a82ed6ez6595z4366z832fz70cbe839c7ffopenalex-snapshot
In vitro and in vivo study of the effects of Levetiracetam on activated microglia during sepsis
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