Microglia and neuroinflammation: a pathological perspective

Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy

Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359

Inflammation and Alzheimer’s disease

Akiyama, H. (2000) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)00124-x · Cited by 4,514

Innate Immunity

Medzhitov, R. M., & Janeway, C. A. (2000) · New England Journal of Medicine · doi:10.1056/nejm200008033430506 · Cited by 1,827

Brain interleukin 1 and S-100 immunoreactivity are elevated in Down syndrome and Alzheimer disease.

Griffin, W. S., Stanley, L. C., Ling, C., White, L., MacLeod, V, Perrot, L. J., White, C. L., & Araoz, C. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.19.7611 · Cited by 1,777

Reactive microglia in patients with senile dementia of the Alzheimer type are positive for the histocompatibility glycoprotein HLA-DR

McGeer, P. L., Itagaki, S., Tago, H., & McGeer, E. G. (1987) · Neuroscience Letters · doi:10.1016/0304-3940(87)90696-3 · Cited by 836

APPSW Transgenic Mice Develop Age-related Aβ Deposits and Neuropil Abnormalities, but no Neuronal Loss in CA1

IRIZARRY, M. C., MCNAMARA, M., FEDORCHAK, K., HSIAO, K., & HYMAN, B. T. (1997) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-199709000-00002 · Cited by 649

Microglial response to amyloid plaques in APPsw transgenic mice.

Frautschy, S. A., Yang, F., Irrizarry, M., Hyman, B. T., Saido, T. C., Hsiao, K., & Cole, G. M. (1998) · Europe PMC (PubMed Central) · Cited by 592

Neuroinflammation in Alzheimer's disease and prion disease

Eikelenboom, P., Bate, C., van Gool, W. A., Hoozemans, J. J. M., Rozemüller, A. J. M., Veerhuis, R., & Williams, A. (2002) · Glia · doi:10.1002/glia.10146 · Cited by 412

Rats and mice exhibit distinct inflammatory reactions after spinal cord injury

Sroga, J. M., Jones, T. B., Kigerl, K. A., McGaughy, V. M., & Popovich, P. G. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10736 · Cited by 369

Fibrillar β-Amyloid Induces Microglial Phagocytosis, Expression of Inducible Nitric Oxide Synthase, and Loss of a Select Population of Neurons in the Rat CNS In Vivo

Weldon, D. T., Rogers, S. D., Ghilardi, J. R., Finke, M. P., Cleary, J. P., O’Hare, E., Esler, W. P., Maggio, J. E., & Mantyh, P. W. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-06-02161.1998 · Cited by 348

Neurovascular Dysfunction in Diverse Communities With Health Disparities—Contributions to Dementia and Alzheimer’s Disease

Saiyasit, N., Butlig, E.-A. R., Chaney, S. D., Traylor, M. K., Hawley, N. A., Randall, R. B., Bobinger, H. V., Frizell, C. A., Trimm, F., Crook, E. D., et al. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.915405 · Cited by 22

Changes in macrophage-like cells characterized by en face optical coherence tomography after retinal stroke

Zeng, Y., Wen, F., Mi, L., Ji, Y., & Zhang, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.987836 · Cited by 20

L-Type Ca2+ Channel Inhibition Rescues the LPS-Induced Neuroinflammatory Response and Impairments in Spatial Memory and Dendritic Spine Formation

Kim, J., Jeon, S. G., Jeong, H.-R., Park, H., Kim, J., & Hoe, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113606 · Cited by 20

Lipopolysaccharide-Initiated Rhinosinusitis Causes Neuroinflammation and Olfactory Dysfunction in Mice

Yeh, C., Huang, W.-H., Lan, M., & Hung, W. (2022) · American Journal of Rhinology and Allergy · doi:10.1177/19458924221140965 · Cited by 20

APOE genotype and sex modulate Alzheimer’s disease pathology in aged EFAD transgenic mice

Balu, D., Valencia‐Olvera, A. C., Islam, Z., Mielczarek, C., Hansen, A. L., Ramos, T. M. P., York, J. M., LaDu, M. J., & Tai, L. M. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1279343 · Cited by 20

A Comprehensive Review on Plant-Based Medications and Chemical Approaches for Autism Spectrum Disorders (ASDs) Psychopharmacotherapy

Ashwlayan, V. D., Ratnesh, R. K., Sharma, D., Sharma, A. K., Sangal, A., Saifi, A., & Singh, J. (2024) · Indian Journal of Microbiology · doi:10.1007/s12088-024-01265-y · Cited by 19

Animal models of neuroinflammation secondary to acute insults originated outside the brain

Hamasaki, M. Y., Machado, M. C. C., & da Silva, F. P. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24184 · Cited by 21

Abnormal Cannabidiol Affects Production of Pro-Inflammatory Mediators and Astrocyte Wound Closure in Primary Astrocytic-Microglial Cocultures

von Widdern, J. C., Hohmann, T., & Dehghani, F. (2020) · Molecules · doi:10.3390/molecules25030496 · Cited by 19

Blockade of Microglial Kv1.3 Potassium Channels by the Peptide HsTX1[R14A] Attenuates Lipopolysaccharide-mediated Neuroinflammation

Nicolazzo, J. A., Pan, Y., Stefano, I. D., Choy, K. H. C., Reddiar, S. B., Low, Y. L., Wai, D. C. C., Norton, R. S., & Jin, L. (2021) · Journal of Pharmaceutical Sciences · doi:10.1016/j.xphs.2021.11.003 · Cited by 19

Investigating the microstructural and neurochemical environment within the basal ganglia of current methamphetamine abusers.

Lin, J. C., Jan, R. K., Kydd, R., & Russell, B. (2015) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2015.01.026 · Cited by 20

Retinal ischemia triggers early microglia activation in the optic nerve followed by neurofilament degeneration

Palmhof, M., Wagner, N., Nagel, C., Biert, N., Stute, G., Dick, H. B., & Joachim, S. C. (2020) · Experimental Eye Research · doi:10.1016/j.exer.2020.108133 · Cited by 18

Targeting the RNA-Binding Protein HuR as Potential Thera-Peutic Approach for Neurological Disorders: Focus on Amyo-Trophic Lateral Sclerosis (ALS), Spinal Muscle Atrophy (SMA) and Multiple Sclerosis

Borgonetti, V., Coppi, E., & Galeotti, N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910394 · Cited by 18

Potential natural products for the management of autism spectrum disorder

Sachdeva, P., Mehdi, I., Kaith, R., Ahmad, F., & Anwar, M. S. (2022) · Ibrain · doi:10.1002/ibra.12050 · Cited by 18

Blood circulating miR-28-5p and let-7d-5p associate with premature ageing in Down syndrome

Morsiani, C., Bacalini, M. G., Collura, S., Moreno‐Villanueva, M., Breusing, N., Bürkle, A., Grune, T., Franceschi, C., de Eguileor, M., & Capri, M. (2022) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2022.111691 · Cited by 18

Sugemule-7 alleviates oxidative stress, neuroinflammation, and cell death, promoting synaptic plasticity recovery in mice with postpartum depression

Fu, Q., Qiu, R., Liang, J., Wu, S., Huang, D., Qin, Y., Li, Q., Shi, X., Xiong, X., Jiang, Z., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-85276-9 · Cited by 18

Are Sigma Receptor Modulators a Weapon Against Multiple Sclerosis Disease?

Collina, S., Rui, M., Stotani, S., Bignardi, E., Rossi, D., Curti, D., Giordanetto, F., Malacrida, A., Scuteri, A., & Cavaletti, G. (2017) · Future Medicinal Chemistry · doi:10.4155/fmc-2017-0122 · Cited by 17

Tramadol administration induced hippocampal cells apoptosis, astrogliosis, and microgliosis in juvenile and adult male mice, histological and immunohistochemical study

Hussein, O. A., Mola, A. F. A., & Rateb, A. (2020) · Ultrastructural Pathology · doi:10.1080/01913123.2019.1711480 · Cited by 18

Overview of Brain-to-Gut Axis Exposed to Chronic CNS Bacterial Infection(s) and a Predictive Urinary Metabolic Profile of a Brain Infected by Mycobacterium tuberculosis

Isaiah, S., Loots, D. T., Solomons, R., van der Kuip, M., van Furth, A. M., & Mason, S. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00296 · Cited by 20

Minocycline attenuates oxycodone-induced positive subjective responses in non-dependent, recreational opioid users

Mogali, S., Askalsky, P., Madera, G., Jones, J. D., & Comer, S. D. (2021) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2021.173241 · Cited by 18

Interleukin-10/Ceftriaxone prevents E. coli-induced delays in sensorimotor task learning and spatial memory in neonatal and adult Sprague–Dawley rats

Wallace, K. L., López, J. F., Shaffery, J. P., Wells, A., Paul, I. A., & Bennett, W. A. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2009.10.016 · Cited by 18

Crosstalk between SIRT1/Nrf2 signaling and NLRP3 inflammasome/pyroptosis as a mechanistic approach for the neuroprotective effect of linagliptin in Parkinson’s disease

Ghaith, W. Z., Wadie, W., & El-Yamany, M. F. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113716 · Cited by 19

Investigation on the mechanism of mafenide in inhibiting pyroptosis and the release of inflammatory factors

Han, C., Yang, Y., Yu, A., Guo, L., Guan, Q., Shen, H., & Jiao, Q. (2020) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2020.105303 · Cited by 18

Kinetic and protective role of autophagy in manganese-exposed BV-2 cells

Alcon, S. P., Gorojod, R. M., & Kotler, M. L. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2020.118787 · Cited by 17

Microglia activation linking amyloid-β drive tau spatial propagation in Alzheimer's disease

Wang, Q., & Xie, C. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.951128 · Cited by 20

Age‐dependent cyclooxygenase‐2 induction and neuronal damage after status epilepticus in the postnatal rat hippocampus

Järvelä, J. T., Lopez‐Picon, F. R., & Holopainen, I. E. (2008) · Epilepsia · doi:10.1111/j.1528-1167.2007.01454.x · Cited by 17

GM1 induces p38 and microtubule dependent ramification of rat primary microglia in vitro

Park, J., Kim, H. Y., Jou, I., & Park, S. M. (2008) · Brain Research · doi:10.1016/j.brainres.2008.09.072 · Cited by 17

MicroRNAs Modulating Neuroinflammation in Parkinson's disease

Saadh, M. J., Muhammad, F. A., Singh, A., Mustafa, M. A., Zuhairi, R. A. H. A., Ghildiyal, P., Hashim, G. M., Alsaikhan, F., Khalilollah, S., & Akhavan‐Sigari, R. (2024) · Inflammation · doi:10.1007/s10753-024-02125-z · Cited by 16

Long‐Term Neural Recording Performance of PEDOT/CNT/Dexamethasone‐Coated Electrode Array Implanted in Visual Cortex of Rats

Golabchi, A., Wu, B., Du, Z. J., & Cui, X. T. (2025) · Advanced NanoBiomed Research · doi:10.1002/anbr.202400114 · Cited by 16

Combined Therapy of A1AR Agonists and A2AAR Antagonists in Neuroinflammation

Marucci, G., Ben, D. D., Lambertucci, C., Navia, A. M., Spinaci, A., Volpini, R., & Buccioni, M. (2021) · Molecules · doi:10.3390/molecules26041188 · Cited by 16

Combined molecular, structural and memory data unravel the destructive effect of tramadol on hippocampus

Khatmi, A., Boroujeni, M. E., Ezi, S., Mirbehbahani, S. H., Aghajanpour, F., Soltani, R., Meftahi, G. H., Abdollahifar, M., Moghaddam, M. H., Toreyhi, H., et al. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136418 · Cited by 17

Pharmacological Inhibition of Spleen Tyrosine Kinase Suppressed Neuroinflammation and Cognitive Dysfunction in LPS-Induced Neurodegeneration Model

Kim, M. W., Choe, K., Park, J. S., Lee, H. J., Kang, M. H., Ahmad, R., & Kim, M. O. (2022) · Cells · doi:10.3390/cells11111777 · Cited by 17

Lithium Chloride Exerts Anti-Inflammatory and Neuroprotective Effects by Inhibiting Microglial Activation in LPS-Induced Retinal Injury

Wu, N., Luo, Q., Huang, Y., Wan, L., Hou, X., Jiang, Z., Li, Y., Qiu, J., Chen, P., Yu, K., et al. (2023) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.64.3.35 · Cited by 16

PNA5, A Novel Mas Receptor Agonist, Improves Neurovascular and Blood-Brain-Barrier Function in a Mouse Model of Vascular Cognitive Impairment and Dementia

Hoyer-Kimura, C. H., Hay, M., Konhilas, J. P., Morrison, H. W., Methajit, M., Strom, J. G., Polt, R. L., Salcedo, V., Fricks, J. P., Kalya, A., et al. (2023) · Aging and Disease · doi:10.14336/ad.2023.0928 · Cited by 17

NaV1.5 sodium channels in a human microglial cell line

Nicholson, E., & Randall, A. D. (2009) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2009.07.009 · Cited by 16

Gambogic amide, a selective TrkA agonist, does not improve outcomes from traumatic brain injury in mice

Johnstone, M. R., Sun, M., Taylor, C. J., Brady, R. D., Grills, B. L., Church, J. E., Shultz, S. R., & McDonald, S. J. (2017) · Brain Injury · doi:10.1080/02699052.2017.1394492 · Cited by 16

Association of TNF-α rs1799964 and IL-1β rs16944 polymorphisms with multiple system atrophy in Chinese Han population

Zhou, X. H., Wang, C., Chen, Z., Peng, Y., Peng, H., Hou, X., Ye, W., Qiu, R., Xia, K., Tang, B., et al. (2017) · International Journal of Neuroscience · doi:10.1080/00207454.2017.1418346 · Cited by 14

A unified model of dementias and age‐related neurodegeneration

Fossel, M. (2020) · Alzheimer s & Dementia · doi:10.1002/alz.12012 · Cited by 16

Attenuation of Inflammatory Symptoms by Icariside B2 in Carrageenan and LPS-Induced Inflammation Models via Regulation of MAPK/NF-κB Signaling Cascades

Alam, M. B., Kwon, Y.-G., Simu, S. Y., Shahriyar, S. A., & Lee, S. (2020) · Biomolecules · doi:10.3390/biom10071037 · Cited by 17

Age-related loss of recognition memory and its correlation with hippocampal and perirhinal cortex changes in female Sprague Dawley rats

Canatelli-Mallat, M., Chiavellini, P., Lehmann, M., Goya, R. G., & Morel, G. R. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.114026 · Cited by 16

Vespa tropica venom suppresses lipopolysaccharide-mediated secretion of pro-inflammatory cyto-chemokines by abrogating nuclear factor-κ B activation in microglia

Kaushik, D. K., Thounaojam, M. C., Mitra, A., & Basu, A. (2014) · Inflammation Research · doi:10.1007/s00011-014-0738-0 · Cited by 16

Preventive effects of multisensory rehabilitation on development of cognitive dysfunction following systemic inflammation in aged rats

Kawano, T., Morikawa, A., Imori, S., Waki, S., Tamura, T., Yamanaka, D., Yamazaki, F., & Yokoyama, M. (2014) · Journal of Anesthesia · doi:10.1007/s00540-013-1786-2 · Cited by 16

Neuroinflammation and excitatory symptoms in bipolar disorder

Sani, G., Panaccione, I., & Spalletta, G. (2015) · Neuroimmunology and Neuroinflammation · doi:10.4103/2347-8659.167304 · Cited by 17

SMYD proteins in immunity: dawning of a new era

Doughan, M., Spellmon, N., Li, C., & Yang, Z. (2016) · AIMS Biophysics · doi:10.3934/biophy.2016.4.450 · Cited by 16

Energy homeostasis deregulation is attenuated by TUDCA treatment in streptozotocin-induced Alzheimer’s disease mice model

Zangerolamo, L., Solon, C., Soares, G. M., Engel, D. F., Velloso, L. A., Boschero, A. C., Carneiro, E. M., & Barbosa, H. C. L. (2021) · Scientific Reports · doi:10.1038/s41598-021-97624-6 · Cited by 15

Corticosterone potentiates ochratoxin A-induced microglial activation

Chansawhang, A., Phochantachinda, S., Temviriyanukul, P., & Chantong, B. (2022) · BioMolecular Concepts · doi:10.1515/bmc-2022-0017 · Cited by 15

Effects of a nutritional intervention on impaired behavior and cognitive function in an emphysematous murine model of COPD with endotoxin-induced lung inflammation

Pelgrim, C. E., van Ark, I., van Berkum, R. E., Schuitemaker-Borneman, A. M., Flier, I., Leusink-Muis, T., Janbazacyabar, H., Diks, M. A. P., Gosker, H. R., KELDERS, M. C. J. M., et al. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1010989 · Cited by 15

Cancer treatment induces neuroinflammation and behavioral deficits in mice

Demos-Davies, K. M., Lawrence, J., Rogich, A., Lind, E. B., & Seelig, D. M. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.1067298 · Cited by 15

Associations Between Systemic and Cerebral Inflammation in an Ovine Model of Cardiopulmonary Bypass

Elsaafien, K., Sloan, J. M., Evans, R. G., Cochrane, A. D., Marino, B., McCall, P., Hood, S. G., Yao, S. T., Korim, W. S., Bailey, S. R., et al. (2023) · Anesthesia & Analgesia · doi:10.1213/ane.0000000000006379 · Cited by 15

A vaccine with Aβ oligomer-specific mimotope attenuates cognitive deficits and brain pathologies in transgenic mice with Alzheimer’s disease

Wang, S.-W., Liu, D., Zhang, L. L., Ji, M., Zhang, Y., Dong, Q.-X., Liu, S., Xie, X.-X., & Liu, R. (2017) · Alzheimer s Research & Therapy · doi:10.1186/s13195-017-0267-5 · Cited by 15

Longer Repetition Time Proton MR Spectroscopy Shows Increasing Hippocampal and Parahippocampal Metabolite Concentrations with Aging

Sporn, L., MacMillan, E. L., Ge, R., Greenway, K. T., Vila‐Rodriguez, F., & Laule, C. (2019) · Journal of Neuroimaging · doi:10.1111/jon.12648 · Cited by 15

Alterations of neuroimmune cell density and pro-inflammatory cytokines in response to thimerosal in prefrontal lobe of male rats

Afsordeh, K., Sadeghi, Y., Amini, A., Namvarpour, Z., Abdollahifar, M., Abbaszadeh, H., & Aliaghaei, A. (2018) · Drug and Chemical Toxicology · doi:10.1080/01480545.2018.1465949 · Cited by 15

Therapeutic effects of human umbilical cord mesenchymal stem cell on sepsis-associated encephalopathy in mice by regulating PI3K/AKT pathway

Zhang, Z., Wang, L., Li, F., Qian, X., Hong, Z., Wu, L.-C., Jiang, Y., & Hu, H. (2022) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2101038 · Cited by 14

Sesamin protects against neurotoxicity via inhibition of microglial activation under high glucose circumstances through modulating p38 and JNK signaling pathways

Kongtawelert, P., Kaewmool, C., Phitak, T., Phimphilai, M., Pothacharoen, P., & Shwe, T. H. (2022) · Scientific Reports · doi:10.1038/s41598-022-15411-3 · Cited by 15

Sinapic Acid Attenuates the Neuroinflammatory Response by Targeting AKT and MAPK in LPS-Activated Microglial Models

Huang, T., Zhao, D. F., Lee, S., Keum, G., & Yang, H. O. (2022) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2022.092 · Cited by 14

Microglial morphology in the somatosensory cortex across lifespan. A quantitative study

Godeanu, S., Clarke, D., Stopper, L., Deftu, A., Popa‐Wagner, A., Bălşeanu, T. A., Scheller, A., & Cătălin, B. (2023) · Developmental Dynamics · doi:10.1002/dvdy.582 · Cited by 15

Possible Implications of Obesity-Primed Microglia that Could Contribute to Stroke-Associated Damage

Carreto, R. J. R., Rodríguez-Cortés, Y. M., Guerrero, H. T., & Chavarría, A. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01329-5 · Cited by 15

Methylprednisolone alleviates cognitive functions through the regulation of neuroinflammation in Alzheimer’s disease

Sun, Y., Li, J., Nan, A., Li, Z., Zhong, W., Chen, L., Liu, S., Zhang, B., Zhu, Z., & Li, X. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1192940 · Cited by 13

Optimization and evaluation of pyridinyl vinyl sulfones as Nrf2 activator for the antioxidant and anti-inflammatory effects

Kim, B., Kim, R., Kim, H. J., Kim, Y., Park, S. J., Lee, E. H., Kim, J., Kim, J., Choi, J. W., Park, J., et al. (2023) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2023.115433 · Cited by 14

The effect of SARS-CoV-2 on the development of Parkinson's disease: the role of α-synuclein

Iravanpour, F., Farrokhi, M. R., Jafarinia, M., & Oliaee, R. T. (2023) · Human Cell · doi:10.1007/s13577-023-00988-2 · Cited by 14

Carvedilol attenuates inflammatory reactions of lipopolysaccharide-stimulated BV2 cells and modulates M1/M2 polarization of microglia via regulating NLRP3, Notch, and PPAR-γ signaling pathways

Foumani, M. K., Amirshahrokhi, K., Namjoo, Z., & Niapour, A. (2023) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-023-02914-7 · Cited by 15

Physiologically normal 5% O2 supports neuronal differentiation and resistance to inflammatory injury in neural stem cell cultures

Sun, X., Voloboueva, L. A., Stary, C. M., & Giffard, R. G. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23615 · Cited by 14

Does the Interplay Between Aging and Neuroinflammation Modulate Alzheimer’s Disease Clinical Phenotypes? A Clinico-Pathological Perspective

Taipa, R. J. F., Sousa, A. L., Pires, M. M., & Sousa, N. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-160121 · Cited by 15

Protective Effect of Human-Neural-Crest-Derived Nasal Turbinate Stem Cells against Amyloid-β Neurotoxicity through Inhibition of Osteopontin in a Human Cerebral Organoid Model of Alzheimer’s Disease

Lim, J. Y., Lee, J. E., Park, S. A., Park, S., Yon, J.-M., Park, J.-A., Jeun, S., Kim, S. J., Lee, H. J., Kim, S. W., et al. (2022) · Cells · doi:10.3390/cells11061029 · Cited by 15

Inhibition of microglial neurotoxicity by ethanol extract of Artemisia asiatica Nakai

Lim, B. O., Chung, H. G., Lee, W., Lee, H., & Suk, K. (2007) · Phytotherapy Research · doi:10.1002/ptr.2304 · Cited by 14

Critical Contribution of Adenosine A2AReceptors in Bone Marrow–Derived Cells to White Matter Lesions Induced by Chronic Cerebral Hypoperfusion

Ran, H., Duan, W., Gong, Z., Xu, S., Zhu, H., Hou, X., Jiang, L., He, Q., & Zheng, J. (2015) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0000000000000174 · Cited by 14

Phytochemical, pharmacological and clinical studies of petasites hybridus (l.) P. Gaertn., B. Mey. & Scherb. A review /

Ożarowski, M., Przystanowicz, J., & Adamczak, A. (2013) · Herba Polonica · doi:10.2478/hepo-2013-0028 · Cited by 14

A Cytokine-based model for the pathophysiology of Long COVID symptomsPreprint

Low, R. N., Low, R. J., & Akrami, A. (2020) · doi:10.31219/osf.io/7gcnv · Cited by 14

Extracellular vesicles released from macrophages modulates interleukin-1β in astrocytic and neuronal cells

Kodidela, S., Sinha, N., Kumar, A., Zhou, L., Godse, S., & Kumar, S. (2023) · Scientific Reports · doi:10.1038/s41598-023-29746-y · Cited by 13

Effects of Caloric Restriction on Spatial Object Recognition Memory, Hippocampal Neuron Loss and Neuroinflammation in Aged Rats

Tresserra, M. P., Galofré-López, N., Pallares, E., Gimenez-Montes, C., Barcia, C., Granero, R., Rojic-Becker, D., Vale-Martı́nez, A., Martí‐Nicolovius, M., & Guillazo‐Blanch, G. (2023) · Nutrients · doi:10.3390/nu15071572 · Cited by 16

Microglial Phagocytosis/Cell Health High‐Content Assay

Mason, E. R., Soni, D. M., & Chu, S. (2023) · Current Protocols · doi:10.1002/cpz1.724 · Cited by 14

Pathological mechanisms of glial cell activation and neurodegenerative and neuropsychiatric disorders caused by Toxoplasma gondii infection

Yang, Z., Chen, J., Zhang, C., & Peng, H. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1512233 · Cited by 13

Neuroinflammation in cognitive decline post-cardiac surgery (the FOCUS study): an observational study protocol

van Ton, A. M. P., Duindam, H. B., van Tuijl, J., Li, W. W. L., Dieker, H.-J., Riksen, N. P., Meijer, F. J. A., Kessels, R. P. C., Kohn, N., van der Hoeven, J. G., et al. (2021) · BMJ Open · doi:10.1136/bmjopen-2020-044062 · Cited by 13

Brain white matter extracellular free-water increases are related to reduced neurocognitive function in systemic lupus erythematosus

Qian, X., Ji, F., Ng, K. K., Koh, A. J., Loo, B. R. Y., Townsend, M. C., Pasternak, O., Tay, S. H., Zhou, J. H., & Mak, A. (2021) · Rheumatology · doi:10.1093/rheumatology/keab511 · Cited by 13

A Breakdown of Immune Tolerance in the Cerebellum

Hampe, C. S., & Mitoma, H. (2022) · Brain Sciences · doi:10.3390/brainsci12030328 · Cited by 15

Central Nervous System

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