Plasticity of Hippocampal Excitatory-Inhibitory Balance: Missing the Synaptic Control in the Epileptic Brain

Epigenetic Regulations of GABAergic Neurotransmission: Relevance for Neurological Disorders and Epigenetic Therapy

Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,951

Glutamate neurotoxicity and diseases of the nervous system

Choi, D. W. (1988) · Neuron · doi:10.1016/0896-6273(88)90162-6 · Cited by 8,188

Modification of seizure activity by electrical stimulation: II. Motor seizure

Racine, R. J. (1972) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(72)90177-0 · Cited by 7,141

LTP and LTD

Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968

A permanent change in brain function resulting from daily electrical stimulation

Goddard, G. V., McIntyre, D., & Leech, C. K. (1969) · Experimental Neurology · doi:10.1016/0014-4886(69)90128-9 · Cited by 3,062

Excitatory actions of gaba during development: the nature of the nurture

Ben-Ari, Y. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn920 · Cited by 2,448

The metabotropic glutamate receptors: Structure and functions

Pin, J., & Duvoisin, R. M. (1995) · Neuropharmacology · doi:10.1016/0028-3908(94)00129-g · Cited by 2,273

Variations on an inhibitory theme: phasic and tonic activation of GABAA receptors

Farrant, M., & Nusser, Z. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1625 · Cited by 2,081

Epilepsy and Exacerbation of Brain Injury in Mice Lacking the Glutamate Transporter GLT-1

Tanaka, K., Watase, K., Manabe, T., Yamada, K., Watanabe, M., Takahashi, K., Iwama, H., Nishikawa, T., Ichihara, N., Kikuchi, T., et al. (1997) · Science · doi:10.1126/science.276.5319.1699 · Cited by 1,755

Molecular profile of reactive astrocytes—Implications for their role in neurologic disease

Eddleston, M., & Mucke, L. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90380-x · Cited by 1,441

Ionotropic Glutamate Receptors in Epilepsy: A Review Focusing on AMPA and NMDA Receptors

Hanada, T. (2020) · Biomolecules · doi:10.3390/biom10030464 · Cited by 252

Synaptic Plasticity Shapes Brain Connectivity: Implications for Network Topology

Bassi, M. S., Iezzi, E., Gilio, L., Centonze, D., & Buttari, F. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20246193 · Cited by 225

Astrocytes and the TGF-β1 Pathway in the Healthy and Diseased Brain: a Double-Edged Sword

Diniz, L. P., Matias, I. C. P., Siqueira, M., Stipursky, J., & Gomes, F. C. A. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1396-y · Cited by 169

Homeostatic plasticity and excitation-inhibition balance: The good, the bad, and the ugly

Chen, L., Li, X., Tjia, M., & Thapliyal, S. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102553 · Cited by 139

The effects of individualised intermittent theta burst stimulation in the prefrontal cortex: A TMS‐EEG study

Chung, S. W., Sullivan, C. M., Rogasch, N. C., Hoy, K. E., Bailey, N. W., Cash, R. F. H., & Fitzgerald, P. B. (2018) · Human Brain Mapping · doi:10.1002/hbm.24398 · Cited by 123

Neuronal pentraxins as biomarkers of synaptic activity: from physiological functions to pathological changes in neurodegeneration

Gómez de San José, N., Massa, F., Halbgebauer, S., Oeckl, P., Steinacker, P., & Otto, M. (2022) · Journal of Neural Transmission · doi:10.1007/s00702-021-02411-2 · Cited by 112

Colocalization of synapse marker proteins evaluated by STED-microscopy reveals patterns of neuronal synapse distribution in vitro

Dzyubenko, E., Rozenberg, A., Hermann, D. M., & Faissner, A. (2016) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2016.09.001 · Cited by 98

Homeostatic synaptic plasticity as a metaplasticity mechanism — a molecular and cellular perspective

Li, J., Park, E., Zhong, L. R., & Chen, L. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.08.010 · Cited by 84

Non-invasive ultrasonic neuromodulation of neuronal excitability for treatment of epilepsy

Lin, Z., Meng, L., Zou, J., Zhou, W., Huang, X., Xue, S. Y., Bian, T., Yuan, T., Niu, L., Guo, Y., et al. (2020) · Theranostics · doi:10.7150/thno.40520 · Cited by 88

Excitation/inhibition imbalance and impaired neurogenesis in neurodevelopmental and neurodegenerative disorders

Lopatina, O. L., Malinovskaya, N. A., Komleva, Y. K., Gorina, Y. V., Shuvaev, A. N., Olovyannikova, R. Y., Belozor, O. S., Belova, O. A., Higashida, H., & Salmina, A. B. (2019) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0014 · Cited by 74

Roles of N-Methyl-D-Aspartate Receptors (NMDARs) in Epilepsy

Chen, S., Xu, D., Liu, F., Fang, Z. H., Wang, X., & Li, M. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.797253 · Cited by 75

Interactions Between Epilepsy and Plasticity

Jarero-Basulto, J. J., Gasca-Martínez, Y., Rivera-Cervantes, M. C., Ureña‐Guerrero, M. E., Feria‐Velasco, A., & Beas‐Zárate, C. (2018) · Pharmaceuticals · doi:10.3390/ph11010017 · Cited by 73

Muscarinic Receptors, from Synaptic Plasticity to its Role in Network Activity

de Sevilla, D. F., Núñez, Á., & Buño, W. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.04.005 · Cited by 67

Presynaptic LRP4 promotes synapse number and function of excitatory CNS neurons

Mosca, T. J., Luginbuhl, D. J., Wang, I. E., & Luo, L. (2017) · eLife · doi:10.7554/elife.27347 · Cited by 65

Bestrophin1‐mediated tonic GABA release from reactive astrocytes prevents the development of seizure‐prone network in kainate‐injected hippocampi

Pandit, S., Neupane, C., Woo, J., Sharma, R., Nam, M., Lee, G., Yi, M., Shin, N., Kim, D. W., Cho, H., et al. (2019) · Glia · doi:10.1002/glia.23762 · Cited by 65

Epilepsy Mechanisms in Neurocutaneous Disorders: Tuberous Sclerosis Complex, Neurofibromatosis Type 1, and Sturge–Weber Syndrome

Stafstrom, C. E., Staedtke, V., & Comi, A. M. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00087 · Cited by 62

Role of Short Chain Fatty Acids in Epilepsy and Potential Benefits of Probiotics and Prebiotics: Targeting “Health” of Epileptic Patients

Kim, S., Park, S., Choi, T. G., & Kim, S. S. (2022) · Nutrients · doi:10.3390/nu14142982 · Cited by 62

The Glutamate System as a Crucial Regulator of CNS Toxicity and Survival of HIV Reservoirs

Górska, A. M., & Eugenín, E. A. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00261 · Cited by 57

Molecular Mechanisms Associated with Neurodegeneration of Neurotropic Viral Infection

Wongchitrat, P., Chanmee, T., & Govitrapong, P. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03761-6 · Cited by 65

Oxytocin and excitation/inhibition balance in social recognition

Lopatina, O. L., Komleva, Y. K., Gorina, Y. V., Olovyannikova, R. Y., Труфанова, Л. В., Hashimoto, T., Takahashi, T., Kikuchi, M., Minabe, Y., Higashida, H., et al. (2018) · Neuropeptides · doi:10.1016/j.npep.2018.09.003 · Cited by 53

Presynaptic α 2 δ-2 Calcium Channel Subunits Regulate Postsynaptic GABA A Receptor Abundance and Axonal Wiring

Geisler, S. M., Schöpf, C. L., Stanika, R. I., Kalb, M., Campiglio, M., Repetto, D., Traxler, L., Missler, M., & Obermair, G. J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2234-18.2019 · Cited by 56

Bidirectional Dysregulation of AMPA Receptor-Mediated Synaptic Transmission and Plasticity in Brain Disorders

Zhang, H., & Bramham, C. R. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00026 · Cited by 51

Synaptic Reshaping and Neuronal Outcomes in the Temporal Lobe Epilepsy

Ren, E., & Curia, G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22083860 · Cited by 51

Distinct synaptic vesicle recycling in inhibitory nerve terminals is coordinated by SV2A

Bae, J. R., Lee, W., Jo, Y. O., Han, S., Koh, S., Song, W. K., & Kim, S. H. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101879 · Cited by 49

The Role of Neuronal Pentraxin 2 (NP2) in Regulating Glutamatergic Signaling and Neuropathology

Chapman, G., Shanmugalingam, U., & Smith, P. D. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00575 · Cited by 48

Functional connectivity discriminates epileptogenic states and predicts surgical outcome in children with drug resistant epilepsy

Rijal, S., Corona, L., Perry, M. S., Tamilia, E., Madsen, J. R., Stone, S. S. D., Bolton, J. B., Pearl, P. L., & Papadelis, C. L. (2023) · Scientific Reports · doi:10.1038/s41598-023-36551-0 · Cited by 47

Cannabinoid Actions on Neural Stem Cells: Implications for Pathophysiology

Rodrigues, R. S., Lourenço, D. M., Paulo, S. L., Mateus, J. M., Ferreira, M. F., Mouro, F. M., Moreira, J. B., Ribeiro, F. F., Sebastião, A. M., & Xapelli, S. (2019) · Molecules · doi:10.3390/molecules24071350 · Cited by 47

Defective Excitatory/Inhibitory Synaptic Balance and Increased Neuron Apoptosis in a Zebrafish Model of Dravet Syndrome

Brenet, A., Hassan-Abdi, R., Somkhit, J., Yanicostas, C., & Soussi‐Yanicostas, N. (2019) · Cells · doi:10.3390/cells8101199 · Cited by 45

Control of neuronal excitability by GSK-3beta: epilepsy and beyond.

Jaworski, T. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2020.118745 · Cited by 43

Synchronization and spatial patterns in a light-dependent neural network

Liu, Y., Xu, Y., & Ma, J. (2020) · Communications in Nonlinear Science and Numerical Simulation · doi:10.1016/j.cnsns.2020.105297 · Cited by 42

Preferential pruning of inhibitory synapses by microglia contributes to alteration of the balance between excitatory and inhibitory synapses in the hippocampus in temporal lobe epilepsy

Fan, J., Dong, X., Tang, Y., Wang, X., Lin, D., Gong, L., Chen, C., Jiang, J., Shen, W., Xu, A., et al. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14224 · Cited by 47

Astrocytic Ephrin-B1 Controls Excitatory-Inhibitory Balance in Developing Hippocampus

Nguyen, A. Q., Sutley-Koury, S. N., Koeppen, J., Mina, K., Woodruff, S., Hanna, S., Vengala, A., Hickmott, P. W., Obenaus, A., & Ethell, I. M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0413-20.2020 · Cited by 41

Rutin prevents seizures in kainic acid-treated rats: evidence of glutamate levels, inflammation and neuronal loss modulation

Chang, A., Chang, Y., & Wang, S. (2022) · Food & Function · doi:10.1039/d2fo01490d · Cited by 38

Neurotransmitters in Type 2 Diabetes and the Control of Systemic and Central Energy Balance

Al-Sayyar, A., Hammad, M. M., Williams, M. R., Al‐Onaizi, M., Abubaker, J. A., & Alzaïd, F. (2023) · Metabolites · doi:10.3390/metabo13030384 · Cited by 45

The broad-spectrum activity of perampanel: state of the art and future perspective of AMPA antagonism beyond epilepsy

Perversi, F., Costa, C., Labate, A., Lattanzi, S., Liguori, C., Maschio, M. C. E., Meletti, S., Nobili, L., Operto, F. F., Romigi, A., et al. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1182304 · Cited by 40

Human brain development through the lens of cerebral organoid models

Andrews, M. G., & Nowakowski, T. J. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146470 · Cited by 35

Inhibiting Epileptiform Activity in Cognitive Disorders: Possibilities for a Novel Therapeutic Approach

Horvath, A. A., Csernus, E. A., Lality, S., Kaminski, R. M., & Kamondi, A. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.557416 · Cited by 32

ALG13 participates in epileptogenesis via regulation of GABAA receptors in mouse models

Huo, J., Ren, S., Gao, P., Wan, D., Rong, S., Li, X., Liu, S., Xu, S., Sun, K., Guo, B., et al. (2020) · Cell Death Discovery · doi:10.1038/s41420-020-00319-6 · Cited by 30

Kainate and AMPA receptors in epilepsy: Cell biology, signalling pathways and possible crosstalk

Henley, J. M., Nair, J. D., Seager, R., Yucel, B. P., Woodhall, G. L., Henley, B. S., Talandyte, K., Needs, H. I., & Wilkinson, K. A. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108569 · Cited by 32

Potential causes of cognitive alterations in temporal lobe epilepsy

Chauvière, L. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112310 · Cited by 32

The Role of Phospholipase C in GABAergic Inhibition and Its Relevance to Epilepsy

Kim, H. Y., Suh, P., & Kim, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22063149 · Cited by 29

On the relationships between epilepsy, sleep, and Alzheimer’s disease: A narrative review

Hanke, J.-M., Schindler, K. A., & Seiler, A. (2022) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2022.108609 · Cited by 28

Central and Peripheral Inflammation: A Common Factor Causing Addictive and Neurological Disorders and Aging-Related Pathologies

Escobar, A. P., Bonansco, C., Cruz, G., Dagnino‐Subiabre, A., Fuenzalida, M., Negrón-Oyarzo, I., Sotomayor‐Zárate, R., Martínez-Pinto, J., & Jorquera, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210083 · Cited by 35

Cell injury and receptor expression in the epileptic human amygdala

Jafarian, M., Mousavi, S. M. M., Alipour, F., Aligholi, H., Noorbakhsh, F., Ghadipasha, M., Gharehdaghi, J., Kellinghaus, C., Kovac, S., Ghadiri, M. K., et al. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.12.017 · Cited by 26

A consistent map in the medial entorhinal cortex supports spatial memory

Malone, T. J., Tien, N.-W., Ma, Y., Cui, L., Lyu, S., Wang, G., Nguyen, D., Zhang, K., Myroshnychenko, M., Tyan, J., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-45853-4 · Cited by 26

Structural connectivity of the ANT region based on human ex-vivo and HCP data. Relevance for DBS in ANT for epilepsy

Majtanik, M., Gielen, F. L. H., Coenen, V. A., Lehtimäki, K. A., & Mai, J. K. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119551 · Cited by 24

Increased glutamate and glutamine levels and their relationship to astrocytes and dopaminergic transmissions in the brains of adults with autism

Oya, M., Matsuoka, K., Kubota, M., Fujino, J., Tei, S., Takahata, K., Tagai, K., Yamamoto, Y., Shimada, H., Seki, C., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-38306-3 · Cited by 26

Environmental enrichment restores impaired spatial memory and synaptic plasticity in prenatally stress exposed rats: The role of GABAergic neurotransmission

Aghighi, F., Salami, M., & Talaei, S. A. (2020) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.10052 · Cited by 23

Revealing the Precise Role of Calretinin Neurons in Epilepsy: We Are on the Way

Qi, Y., Cheng, H., Wang, Y., & Chen, Z. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00753-1 · Cited by 25

CBD enhances the cognitive score of adolescent rats prenatally exposed to THC and fine-tunes relevant effectors of hippocampal plasticity

Castelli, V., Lavanco, G., D’Amico, C., Feo, S., Tringali, G., Kuchař, M., Cannizzaro, C., & Brancato, A. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1237485 · Cited by 23

Gliotransmission: A Novel Target for the Development of Antiseizure Drugs

Riquelme, J., Wellmann, M., Sotomayor‐Zárate, R., & Bonansco, C. (2020) · The Neuroscientist · doi:10.1177/1073858420901474 · Cited by 23

Transgenic overexpression of furin increases epileptic susceptibility

Yang, Y., He, M., Tian, X., Guo, Y., Liu, F., Li, Y., Zhang, H., Lu, X., Xu, D., Zhou, R., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-1076-x · Cited by 22

Risk Factors for Epilepsy: A National Cross-Sectional Study from National Health and Nutrition Examination Survey 2013 to 2018

Yang, L., Wang, Y., Chen, X., Zhang, C., Chen, J., Cheng, H., & Zhang, L. (2021) · International Journal of General Medicine · doi:10.2147/ijgm.s323209 · Cited by 21

Excitation and Inhibition Balance Underlying Epileptiform Activity

Liu, Y., Grigorovsky, V., & Bardakjian, B. L. (2020) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2019.2963430 · Cited by 19

Delayed effective connectivity characterizes the epileptogenic zone during stereo-EEG

Feys, O., Wens, V., Rovaï, A., Schuind, S., Rikir, E., Legros, B., Tiège, X. D., & Gaspard, N. (2023) · Clinical Neurophysiology · doi:10.1016/j.clinph.2023.12.013 · Cited by 18

Event‐Driven Neuroplasticity and Spiking Modulation in a Photoelectric Neuristor Configured by Threshold Switching Memristor and Optoelectronic Transistor

Chen, K., Lin, P., Huang, Y., Chen, S. C., Liao, Z., & Chen, J. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202412452 · Cited by 18

Variability of cortico‐cortical evoked potentials in the epileptogenic zone is related to seizure occurrence

Feys, O., Wens, V., Schuind, S., Rikir, E., Legros, B., Tiège, X. D., & Gaspard, N. (2024) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.52179 · Cited by 17

Dynamic Transitions in Neuronal Network Firing Sustained by Abnormal Astrocyte Feedback

Yu, Y., Yuan, Z., Fan, Y., Li, J., & Wu, Y. (2020) · Neural Plasticity · doi:10.1155/2020/8864246 · Cited by 16

VIPergic neuroprotection in epileptogenesis: challenges and opportunities

Cunha‐Reis, D., Caulino‐Rocha, A., & Correia‐de‐Sá, P. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105356 · Cited by 16

Therapeutic Potential of Astrocyte Purinergic Signalling in Epilepsy and Multiple Sclerosis

Nobili, P., Shen, W., Milicevic, K. D., Pristov, J. B., Audinat, É., & Nikolic, L. M. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.900337 · Cited by 17

Investigation of the mechanism of tanshinone IIA to improve cognitive function via synaptic plasticity in epileptic rats

Chen, J., Zhang, R., Wei, L., Xie, J., Suqin, Z., Yin, W., Hua, X., Xiao, N., Ma, M., & Jiao, H. (2022) · Pharmaceutical Biology · doi:10.1080/13880209.2022.2157843 · Cited by 16

Few, Activity-Dependent, and Ubiquitous VGLUT1/VGAT Terminals in Rat and Mouse Brain

Fattorini, G., Ciriachi, C., & Conti, F. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00229 · Cited by 16

Deep brain stimulation restores the glutamatergic and GABAergic synaptic transmission and plasticity to normal levels in kindled rats

Ghafouri, S., Fathollahi, Y., Semnanian, S., Shojaei, A., Asgari, A., Amini, A. E., & Mirnajafi‐Zadeh, J. (2019) · PLoS ONE · doi:10.1371/journal.pone.0224834 · Cited by 15

Inhibitory synaptic transmission is impaired at higher extracellular Ca2+ concentrations in Scn1a+/− mouse model of Dravet syndrome

Uchino, K., Kawano, H., Tanaka, Y., Adaniya, Y., Asahara, A., Deshimaru, M., Kubota, K., Watanabe, T., Katsurabayashi, S., Iwasaki, K., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-90224-4 · Cited by 15

Pharmacological perspectives and mechanisms involved in epileptogenesis

Marques, F. V. B. S., Kawamura, L. R. D. S. M., Quintanilha, M. V. T., Mota, I. F. L., Vasconcelos, A. S., da Silva, J. F. F., & Mortari, M. R. (2022) · Beni-Suef University Journal of Basic and Applied Sciences · doi:10.1186/s43088-022-00278-0 · Cited by 15

Synaptic Development in Diverse Olfactory Neuron Classes Uses Distinct Temporal and Activity-Related Programs

Aimino, M. A., DePew, A. T., Restrepo, L., & Mosca, T. J. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0884-22.2022 · Cited by 16

Ceftriaxone Relieves Trigeminal Neuropathic Pain Through Suppression of Spatiotemporal Synaptic Plasticity via Restoration of Glutamate Transporter 1 in the Medullary Dorsal Horn

Luo, X. L., He, T., Wang, Y., Wang, J., Yan, X., Zhou, H., Wang, R., Du, R., Wang, X., Chen, J., et al. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00199 · Cited by 13

Mechanism of Anti-seizure Medications and Emerging Trends in Epilepsy Treatment

Rana, Z. S., Suman, R., Veleri, S., & Punnakkal, P. (2023) · International Journal of Drug Discovery and Pharmacology · doi:10.53941/ijddp.2023.100001 · Cited by 14

Monaural 40-Hz auditory steady-state magnetic responses can be useful for identifying epileptic focus in mesial temporal lobe epilepsy

Matsubara, T., Ogata, K., Hironaga, N., Uehara, T., Mitsudo, T., Shigeto, H., Maekawa, T., & Tobimatsu, S. (2018) · Clinical Neurophysiology · doi:10.1016/j.clinph.2018.11.026 · Cited by 14

Autonomic dysfunction in epilepsy mouse models with implications for SUDEP research

Bauer, J., Devinsky, O., Rothermel, M., & Koch, H. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2022.1040648 · Cited by 13

Supplementation of n-3 PUFAs in Adulthood Attenuated Susceptibility to Pentylenetetrazol Induced Epilepsy in Mice Fed with n-3 PUFAs Deficient Diet in Early Life

Zhao, Y., Wang, C., Li, X., Wang, D., Wang, Y., Xue, C., Wen, M., & Zhang, T. (2023) · Marine Drugs · doi:10.3390/md21060354 · Cited by 12

Recent Advances in Bioactive Flavonoids-based Nanotherapeutics as Promising Neuroprotectants in Epilepsy

Pradhan, P., Jana, K., Ghosh, S., Debnath, B., Rout, S. K., Rai, V. K., Kar, B., Kar, D. M., Ghosh, G., & Rath, G. (2025) · Current Aging Science · doi:10.2174/0118746098369369250119112935 · Cited by 12

miR-146a/KLF4 axis in epileptic mice: A novel regulator of synaptic plasticity involving STAT3 signaling

Chen, Y., Chen, Y., Chen, Y., & Li, Y. (2022) · Brain Research · doi:10.1016/j.brainres.2022.147988 · Cited by 13

Enhanced Astrocyte Activity and Excitatory Synaptic Function in the Hippocampus of Pentylenetetrazole Kindling Model of Epilepsy

Díaz, F., Aguilar, F., Wellmann, M., Martorell, A., González‐Arancibia, C., Chacana-Véliz, L., Negrón-Oyarzo, I., Chávez, A. E., Fuenzalida, M., Nualart, F., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914506 · Cited by 11

Effect of Osteopathic Cranial Manipulative Medicine on an Aged Rat Model of Alzheimer Disease

Tobey, H., Lucas, T., Bledsoe, D., Mykins, M., Campbell, C., Berr, S. S., Sasser, T. A., Helm, R. F., Brolinson, P. G., Klein, B. G., et al. (2019) · Journal of Osteopathic Medicine · doi:10.7556/jaoa.2019.121 · Cited by 11

Dynamic structural neuroplasticity during and after epileptogenesis in a pilocarpine rat model of epilepsy

Heysieattalab, S., & Sadeghi, L. (2021) · Acta Epileptologica · doi:10.1186/s42494-020-00037-7 · Cited by 12

Current Understanding of the Roles of Gut–Brain Axis in the Cognitive Deficits Caused by Perinatal Stress Exposure

Rubinstein, M. R., Burgueño, A. L., Quiroga, S., Wald, M. R., & Genaro, A. M. (2023) · Cells · doi:10.3390/cells12131735 · Cited by 11

Integrated computational approaches for identification of potent pyrazole-based glycogen synthase kinase-3β (GSK-3β) inhibitors: 3D-QSAR, virtual screening, docking, MM/GBSA, EC, MD simulation studies

Niharika, D. G., Salaria, P., & Amarendar Reddy, M. (2024) · Molecular Diversity · doi:10.1007/s11030-024-11026-0 · Cited by 12

Molecular mechanisms mediating involvement of glial cells in brain plastic remodeling in epilepsy

Хаспеков, Л. Г., & Frumkina, L. E. (2017) · Biochemistry (Moscow) · doi:10.1134/s0006297917030178 · Cited by 10

Hippocampal neurodegeneration and rhythms mirror each other during acute spinal cord injury in male rats

Zangbar, H. S., Shahabi, P., Vafaee, M. S., Ghadiri, T., Kalan, A. E., Fallahi, S., Ghorbani, M., & Jafarzadehgharehziaaddin, M. (2021) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2021.04.004 · Cited by 9

An aqueous extract of Syzygium cumini protects against kainate-induced status epilepticus and amnesia: evidence for antioxidant and anti-inflammatory intervention

Kandeda, A. K., Nodeina, S., & Mabou, S. T. (2022) · Metabolic Brain Disease · doi:10.1007/s11011-022-01052-y · Cited by 9

Retrograde activation of CB1R by muscarinic receptors protects against central organophosphorus toxicity

Hoffman, K. M., Eisen, M. R., Chandler, J. K., Nelson, M. R., Johnson, E. A., & McNutt, P. M. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.05.028 · Cited by 8

SynLight: a bicistronic strategy for simultaneous active zone and cell labeling in the Drosophila nervous system

Aimino, M. A., Humenik, J., Parisi, M. J., Duhart, J. C., & Mosca, T. J. (2023) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkad221 · Cited by 10

Vasoactive intestinal peptide (VIP) conducts the neuronal activity during absence seizures: GABA seems to be the main mediator of VIP

Korkmaz, O. T., Arkan, S., Öncü-Kaya, E. M., Ateş, N., & Tunçel, N. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136268 · Cited by 8

Bioelectronic tools for understanding the universal language of electrical signaling across species and kingdoms

Shukla, S., Comerci, C. J., Süel, G. M., & Jahed, Z. (2024) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2024.116843 · Cited by 7

Agomelatine alleviates neuronal loss through BDNF signaling in the post-status epilepticus model induced by kainic acid in rat

Tchekalarova, J. D., Atanasova, D., Kortenska, L., Lazarov, N., Shishmanova-Doseva, M., Galchev, T., & Marinov, P. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.01.017 · Cited by 7

Unilateral optogenetic kindling of hippocampus leads to more severe impairments of the inhibitory signaling in the contralateral hippocampus

Tescarollo, F. C., Valdivia, D. J., Chen, S. C., & Sun, H. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1268311 · Cited by 6

Effect of conventional transcranial direct current stimulation devices and electrode sizes on motor cortical excitability of the quadriceps muscle

Gardi, A. Z., Vogel, A. K., Dharia, A. K., & Krishnan, C. (2021) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-211210 · Cited by 6

Glial cells inhibition affects the incidence of metaplasticity in the hippocampus of Pentylentetrazole-induced kindled rats

Tavassoli, Z., Giahi, M., Janahmadi, M., & Hosseinmardi, N. (2022) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2022.108907 · Cited by 5

Anti-seizure medication eslicarbazepine affects the synaptic transmission and plasticity in the rat hippocampal synapses

Rana, Z. S., Pathania, C., Modgil, A., & Punnakkal, P. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.04.016 · Cited by 5

Effects of HCN2 Mutations on Dendritic Excitability and Synaptic Plasticity: A Computational Study

Thomas, M., Ranjith, G., Radhakrishnan, A., & Anirudhan, V. A. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.10.019 · Cited by 5

Amygdaloid complex anatomopathological findings in animal models of status epilepticus

Tilelli, C. Q., Flôres, L. R., Cota, V. R., de Castro, O. W., & Garcia‐Cairasco, N. (2019) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2019.106831 · Cited by 5

Estradiol Regulates Polysialylated Form of the Neural Cell Adhesion Molecule Expression and Connectivity of O-LM Interneurons in the Hippocampus of Adult Female Mice

Pérez-Rando, M., Guirado, R., Tellez-Merlo, G., Carceller, H., & Nácher, J. (2021) · Neuroendocrinology · doi:10.1159/000515052 · Cited by 4

Deep brain stimulation effects on learning, memory and glutamate and GABAA receptor subunit gene expression in kindled rats

Faraz, M., Kosarmadar, N., Rezaei, M., Zare, M., Javan, M., Barkley, V., Shojaei, A., & Mirnajafi‐Zadeh, J. (2021) · Acta Neurobiologiae Experimentalis · doi:10.21307/ane-2021-006 · Cited by 5

Fatal Epileptic Seizures in Mice Having Compromised Glutathione and Ascorbic Acid Biosynthesis

Chen, Y., Holland, K. D., Shertzer, H. G., Nebert, D. W., & Dalton, T. P. (2023) · Antioxidants · doi:10.3390/antiox12020448 · Cited by 4

Gender‐related variation expressions of neuroplastin TRAF6, GluA1, GABA(A) receptor, and PMCA in cortex, hippocampus, and brainstem in an experimental epilepsy model

Doğanyiğit, Z., Okan, A., Yılmaz, S., Uğuz, A. C., & Akyüz, E. (2024) · Synapse · doi:10.1002/syn.22289 · Cited by 4

The Role of Epileptic Activity in Alzheimer’s Disease

Chen, T., Lai, M., Hong, W., & Huang, C. (2024) · American Journal of Alzheimer s Disease & Other Dementias® · doi:10.1177/15333175241303569 · Cited by 4

Neuronal pentraxin-2 (NPTX2) serum levels during an acute psychotic episode in patients with schizophrenia

Göverti, D., Büyüklüoğlu, N., Kaya, H., Yüksel, R. N., Yücel, Ç., & Göka, E. (2022) · Psychopharmacology · doi:10.1007/s00213-022-06147-z · Cited by 5

The adhesion GPCR ADGRV1 controls glutamate homeostasis in hippocampal astrocytes supporting neuron development: first insights into to pathophysiology of ADGRV1 -associated epilepsyPreprint

Güler, B. E., Zorin, M., Linnert, J., Nagel‐Wolfrum, K., & Uwe Wolfrum, B. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.25.591120 · Cited by 4

Socrates: A Novel N-Ethyl-N-nitrosourea-Induced Mouse Mutant with Audiogenic Epilepsy

Varlamova, E. G., Borisova, E., Evstratova, Y. A., Newman, A., Kuldaeva, V. P., Gavrish, M., Kondakova, E., Tarabykin, V. S., Babaev, A., & Turovsky, E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242317104 · Cited by 2

Molecular mechanisms mediating involvement of glial cells in brain plastic remodeling in epilepsy

Хаспеков, Л. Г., & Frumkina, L. E. (2017) · Biochemistry (Moscow) · doi:10.1134/s0006297917030178 · Cited by 10

P2Y1 receptor inhibition rescues impaired synaptic plasticity and astroglial Ca2+-dependent activity in the epileptic hippocampus

Martorell, A., Wellmann, M., Guiffa, F., Fuenzalida, M., & Bonansco, C. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105132 · Cited by 32

Astrocyte-neuron circuits in epilepsy

Purnell, B. S., Alves, M., & Boison, D. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106058 · Cited by 83

Synaptic Dysfunction in Epilepsy

Zaitsev, A. V., Amakhin, D. V., Dyomina, A. V., Zakharova, M. V., Ergina, J. L., Postnikova, T. Y., Diespirov, G. P., & Magazanik, L. G. (2021) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s002209302103008x · Cited by 29

Rapid plasticity at inhibitory and excitatory synapses in the hippocampus induced by ictal epileptiform discharges

Lopantsev, V., Both, M., & Draguhn, A. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06663.x · Cited by 48