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

Inhibition of extracellular signal-regulated kinase/calpain-2 pathway reduces neuroinflammation and necroptosis after cerebral ischemia-reperfusion injury in a rat model of cardiac arrest

Wang, W., Xie, L., Zou, X., Li, N., Yang, Y., Wu, Z.-J., Tian, X., Zhao, G., & Chen, M. (2021) · International Immunopharmacology · doi:10.1016/j.intimp.2021.107377 · Cited by 29

Microglia-Derived Interleukin 23: A Crucial Cytokine in Alzheimer's Disease?

Nitsch, L., Schneider, L. H., Zimmermann, J., & Müller, M. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.639353 · Cited by 27

Nicotinic Acetylcholine Receptors and Microglia as Therapeutic and Imaging Targets in Alzheimer’s Disease

Takata, K., Kimura, H., Yanagisawa, D., Harada, K., Nishimura, K., Kitamura, Y., Shimohama, S., & Tooyama, I. (2022) · Molecules · doi:10.3390/molecules27092780 · Cited by 29

Pyrrolidine Dithiocarbamate Prevents Neuroinflammation and Cognitive Dysfunction after Endotoxemia in Rats

Kan, M., Yang, T., Fu, H. Q., Fan, L., Wu, Y., Terrando, N., & Wang, T. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00175 · Cited by 29

Short-term effects of an endotoxin on substantia nigra dopamine neurons

Reinert, K. R. S., Umphlet, C. D., Quattlebaum, A., & Boger, H. A. (2014) · Brain Research · doi:10.1016/j.brainres.2014.02.005 · Cited by 28

Spatio-temporal dynamics of microglia phenotype in human and murine cSVD: impact of acute and chronic hypertensive states

Morton, L., Arndt, P., Garza, A. P., Henneicke, S., Mattern, H., Gonzalez, M., Dityatev, A. E., Yilmazer‐Hanke, D., Schreiber, S., & Dunay, I. R. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01672-0 · Cited by 28

Pathogenic synergy: dysfunctional mitochondria and neuroinflammation in neurodegenerative diseases associated with aging

Mani, S., Wasnik, S., Shandilya, C., Srivastava, V., Khan, S., & Singh, K. K. (2025) · Frontiers in Aging · doi:10.3389/fragi.2025.1615764 · Cited by 33

Pregabalin can prevent, but not treat, cognitive dysfunction following abdominal surgery in aged rats

Kawano, T., Eguchi, S., Iwata, H., Yamanaka, D., Tateiwa, H., Locatelli, F. M., & Yokoyama, M. (2016) · Life Sciences · doi:10.1016/j.lfs.2016.02.021 · Cited by 28

Natural Docosahexaenoic Acid in the Triglyceride Form Attenuates In Vitro Microglial Activation and Ameliorates Autoimmune Encephalomyelitis in Mice

Mancera, P., Wappenhans, B., Cordobilla, B., Virgili, N., Pugliese, M., Rueda, F., Espinosa‐Parrilla, J. F., & Domingo, J. C. (2017) · Nutrients · doi:10.3390/nu9070681 · Cited by 30

Rnf112 deletion protects brain against intracerebral hemorrhage (ICH) in mice by inhibiting TLR-4/NF-κB pathway

Zhang, F., & Zhang, C. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.10.141 · Cited by 28

A mathematical model of neuroinflammation in severe clinical traumatic brain injury

Vaughan, L. E., Ranganathan, P. R., Kumar, R. G., Wagner, A. K., & Rubin, J. E. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1384-1 · Cited by 30

What Is Autism Spectrum Disorder?

Rea, H. M., LaMotte, K., & Burrell, T. L. (2018) · Springer eBooks · doi:10.1007/978-3-030-03213-5_1 · Cited by 30

Anti-neuroinflammatory activity of 6,7-dihydroxy-2,4-dimethoxy phenanthrene isolated from Dioscorea batatas Decne partly through suppressing the p38 MAPK/NF-κB pathway in BV2 microglial cells

Lim, J. S., Oh, J., Yun, H. S., Lee, J. S., Hahn, D., & Kim, J. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.114633 · Cited by 28

Nuclear dynamics and stress responses in Alzheimer’s disease

Iatrou, A., Clark, E. M., & Wang, Y. (2021) · Molecular Neurodegeneration · doi:10.1186/s13024-021-00489-6 · Cited by 31

Looking to the Future of the Role of Macrophages and Extracellular Vesicles in Neuroinflammation in ALS

Carata, E., Muci, M., Giulio, S. D., Mariano, S., & Panzarini, E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241411251 · Cited by 30

Immunotherapy in Alzheimer's Disease: Where Do We Stand? Where Should We Go?

Rommy von Bernhardi, M. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-1248 · Cited by 28

Functional implication of BAFF synthesis and release in gangliosides-stimulated microglia

Kim, K. S., Park, J.-Y., Jou, I., & Park, S. M. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.1008659 · Cited by 28

Brain injury induces cholesterol 24-hydroxylase (Cyp46) expression in glial cells in a time-dependent manner

Smiljanić, K., Lavrnja, I. C., Mladenović, A., Ruždijić, S., Stojiljković, M., Peković, S., & Kanazir, S. (2010) · Histochemistry and Cell Biology · doi:10.1007/s00418-010-0718-6 · Cited by 28

miRNA 146A-5P-Loaded Poly( D , L -Lactic-Co-Glycolic Acid) Nanoparticles Impair Pain Behaviors by Inhibiting Multiple Inflammatory Pathways in Microglia

Phạm, T. L., Yin, Y., Kwon, H. H., Shin, N., Kim, S. I., Park, H., Shin, J., Shin, H. J., Hwang, J., Song, H., et al. (2020) · Nanomedicine · doi:10.2217/nnm-2019-0462 · Cited by 28

Tramadol: a Potential Neurotoxic Agent Affecting Prefrontal Cortices in Adult Male Rats and PC-12 Cell Line

Aghajanpour, F., Boroujeni, M. E., Jahanian, A., Soltani, R., Ezi, S., Khatmi, A., Abdollahifar, M., Mirbehbahani, S. H., Toreyhi, H., Aliaghaei, A., et al. (2020) · Neurotoxicity Research · doi:10.1007/s12640-020-00214-z · Cited by 29

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

Virus-induced brain pathology and the neuroinflammation-inflammation continuum: the neurochemists view

Sian‐Hülsmann, J., & Riederer, P. F. (2024) · Journal of Neural Transmission · doi:10.1007/s00702-023-02723-5 · Cited by 30

Hypothalamic NAD+-Sirtuin Axis: Function and Regulation

Roh, E., & Kim, M. (2020) · Biomolecules · doi:10.3390/biom10030396 · Cited by 30

A Review of the Application of Hyperbaric Oxygen Therapy in Alzheimer’s Disease

Somaa, F. A. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210157 · Cited by 26

Acute and Chronic Effects of Multiple Concussions on Midline Brain Structures

Churchill, N. W., Hutchison, M. G., Graham, S. J., & Schweizer, T. A. (2021) · Neurology · doi:10.1212/wnl.0000000000012580 · Cited by 29

Indoor VOCs exposure induced Parkinson-like behaviors through autophagy dysfunction and NLRP3 inflammasome-mediated neuroinflammation

Zheng, J., Pang, Y., Zhang, Y., Hu, W., Yang, P., Liu, Q., Ning, J., Du, Z., Jin, X., Tang, J., et al. (2022) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2022.129818 · Cited by 27

Cysteinyl leukotriene correlated with 8-isoprostane levels as predictive biomarkers for sensory dysfunction in autism

Qasem, H., AL-Ayadhi, L. Y., & El-Ansary, A. K. (2016) · Lipids in Health and Disease · doi:10.1186/s12944-016-0298-0 · Cited by 27

Cytokines IL-1β and IL-10 are required for Müller glia proliferation following light damage in the adult zebrafish retina

Lu, C., & Hyde, D. R. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1406330 · Cited by 27

Complement 3a induces the synapse loss via C3aR in mitochondria-dependent NLRP3 activating mechanisms during the development and progression of Alzheimer’s disease

Ge, T.-Q., Guan, P.-P., & Wang, P. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105868 · Cited by 28

Retinal neuroinflammatory induced neuronal degeneration - Role of toll-like receptor-4 and relationship with gliosis

Ghosh, F. K., Abdshill, H., Arnér, K. M., Voss, U., & Taylor, L. (2018) · Experimental Eye Research · doi:10.1016/j.exer.2018.02.002 · Cited by 26

Sceletium tortuosum may delay chronic disease progression via alkaloid-dependent antioxidant or anti-inflammatory action

Bennett, A. C., Camp, A. V., López, V., & Smith, C. (2018) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-018-0620-6 · Cited by 26

Brain Metabolites and Peripheral Biomarkers Associated with Neuroinflammation in Complex Regional Pain Syndrome Using [11C]-(R)-PK11195 Positron Emission Tomography and Magnetic Resonance Spectroscopy: A Pilot Study

Jung, Y.-H., Kim, H., Jeon, S. Y., Kwon, J. M., Lee, W. J., Kim, Y. C., Jang, J. H., Choi, S., Lee, J., & Kang, D. (2018) · Pain Medicine · doi:10.1093/pm/pny111 · Cited by 26

Late-life environmental enrichment preserves short-term memory and may attenuate microglia in male APP/PS1 mice

Stuart, K. E., King, A. E., King, N. E., Collins, J. M., Vickers, J. C., & Ziebell, J. M. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.04.015 · Cited by 27

Microglial HIV-1 Expression: Role in HIV-1 Associated Neurocognitive Disorders

Li, H., McLaurin, K. A., Illenberger, J. M., Mactutus, C. F., & Booze, R. M. (2021) · Viruses · doi:10.3390/v13050924 · Cited by 26

Retinal dendritic cell recruitment, but not function, was inhibited in MyD88 and TRIF deficient mice

Heuss, N. D., Pierson, M. J., Montaniel, K. R. C., McPherson, S. W., Lehmann, U., Hussong, S. A., Ferrington, D. A., Low, W. C., & Gregerson, D. S. (2014) · Journal of Neuroinflammation · doi:10.1186/s12974-014-0143-1 · Cited by 26

HDAC8 Inhibitor WK2-16 Therapeutically Targets Lipopolysaccharide-Induced Mouse Model of Neuroinflammation and Microglial Activation

Lin, F., Yen, J.-L., Kuo, Y.-C., Kang, J., Cheng, Y., Huang, W., & Hsiao, G. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20020410 · Cited by 26

Molecular Targets Involved in the Neuroprotection Mediated by Terpenoids

González‐Cofrade, L., Heras, B. D. L., Ticona, L. A., & Palomino, O. M. (2019) · Planta Medica · doi:10.1055/a-0953-6738 · Cited by 26

The Influence of Murine Genetic Background in Adeno-Associated Virus Transduction of the Mouse Brain

He, T., Itano, M. S., Earley, L. F., Hall, N. E., Riddick, N. V., Samulski, R. J., & Li, C. (2019) · Human Gene Therapy Clinical Development · doi:10.1089/humc.2019.030 · Cited by 26

Alterations of Glial Cells in the Mouse Hippocampus During Postnatal Development

Kimoto, H., Eto, R., Abe, M., Kato, H., & Araki, T. (2009) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-009-9412-4 · Cited by 26

The retinal environment induces microglia-like properties in recruited myeloid cells

McPherson, S. W., Heuss, N. D., Lehmann, U., Roehrich, H., Abedin, M. J., & Gregerson, D. S. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1546-9 · Cited by 24

Design and synthesis of novel diosgenin-triazole hybrids targeting inflammation as potential neuroprotective agents

Huang, Y., Huang, W., Yang, G., Wang, R., & Ma, L. (2021) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2021.128092 · Cited by 26

Synthesis and Evaluation of a 18F-Labeled Ligand for PET Imaging of Colony-Stimulating Factor 1 Receptor

Lee, H., Park, J., Kim, H., Woo, S., Choi, J. Y., Lee, K.-H., & Choe, Y. S. (2022) · Pharmaceuticals · doi:10.3390/ph15030276 · Cited by 25

Neuroinflammation: A Common Pathway in Alzheimer’s Disease and Epilepsy

Liew, Y., Retinasamy, T., Arulsamy, A., Ali, I. Y., Jones, N. C., O'Brien, T. J., & Shaikh, M. F. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230059 · Cited by 28

Mouse Hepatitis Virus Infection Upregulates Genes Involved in Innate Immune Responses

Chatterjee, D., Addya, S., Khan, R. S., Kenyon, L. C., Choe, A., Cohrs, R. J., Shindler, K. S., & Sarma, J. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111351 · Cited by 25

Chronic treadmill running protects hippocampal neurons from hypobaric hypoxia-induced apoptosis in rats

Lin, C., Wu, C.-J., Wei, I., Tsai, M.-H., Chang, N.-W., Yang, T., & Kuo, Y. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.11.051 · Cited by 25

Nitric oxide/cyclic GMP signaling regulates motility of a microglial cell line and primary microglia in vitro

Scheiblich, H., Roloff, F., Singh, V., Stangel, M., Stern, M. K., & Bicker, G. (2014) · Brain Research · doi:10.1016/j.brainres.2014.03.048 · Cited by 25

Paeoniflorin attenuates the neuroinflammatory response in a rat model of chronic constriction injury

Zhou, J., Wang, J., Li, W., Wang, C., Li, W., & Zhang, J. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.6371 · Cited by 25

The attenuating effects of 1,2,3,4,6 penta-O-galloyl-β-d-glucose on pro-inflammatory responses of LPS/IFNγ-activated BV-2 microglial cells through NFƙB and MAPK signaling pathways

Mendonca, P., Taka, E., Bauer, D., Reams, R., & Soliman, K. F. A. (2018) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2018.09.004 · Cited by 25

Vitamin E increases S100B‐mediated microglial activation in an S100B‐overexpressing mouse model of pathological aging

Bialowas‐McGoey, L. A., Lesicka, A., & Whitaker‐Azmitia, P. M. (2008) · Glia · doi:10.1002/glia.20727 · Cited by 25

Combined analysis of the glia secretome and the CSF proteome: neuroinflammation and novel biomarkers

Suk, K. (2010) · Expert Review of Proteomics · doi:10.1586/epr.10.6 · Cited by 26

Chronic oral administration of minocycline to sheep with ovine CLN6 neuronal ceroid lipofuscinosis maintains pharmacological concentrations in the brain but does not suppress neuroinflammation or disease progression

Kay, G. W., & Palmer, D. N. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-97 · Cited by 24

Dexmedetomidine inhibits the lipopolysaccharide‐stimulated inflammatory response in microglia through the pathway involving TLR4 and NF‐κB

Zhou, X., Liu, J., Xu, Z., Fu, Q., Wang, P., & Zhang, H. (2019) · The Kaohsiung Journal of Medical Sciences · doi:10.1002/kjm2.12112 · Cited by 23

Minocycline restores spatial but not fear memory in olfactory bulbectomized rats

Borre, Y. E., Sir, V., de Kivit, S., Westphal, K. G. C., Olivier, B., & Oosting, R. S. (2012) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2012.09.005 · Cited by 24

Microcirculation of the brain: morphological assessment in degenerative diseases and restoration processes

Kolinko, Y., Krakorová, K., Cendelín, J., Tonar, Z., & Králíčková, M. (2014) · Reviews in the Neurosciences · doi:10.1515/revneuro-2014-0049 · Cited by 28

Nurr1 and PPARγ protect PC12 cells against MPP+ toxicity: involvement of selective genes, anti-inflammatory, ROS generation, and antimitochondrial impairment

Farshbaf, M. J., Forouzanfar, M., Ghaedi, K., Kiani-Esfahani, A., Peymani, M., Shoaraye-nejati, A., Izadi, T., Karbalaie, K., Noorbakhshnia, M., Rahgozar, S., et al. (2016) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-016-2764-4 · Cited by 26

A standardized randomized 6-month aerobic exercise-training down-regulated pro-inflammatory genes, but up-regulated anti-inflammatory, neuron survival and axon growth-related genes

Iyalomhe, O., Chen, Y., Allard, J. S., Ntekim, O. E., Johnson, S. M., Bond, V., Goerlitz, D. S., Li, J., & Obisesan, T. O. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2015.05.005 · Cited by 25

Inhibitory effect of 9-hydroxy-6,7-dimethoxydalbergiquinol from Dalbergia odorifera on the NF-κB-related neuroinflammatory response in lipopolysaccharide-stimulated mouse BV2 microglial cells is mediated by heme oxygenase-1

Lee, D., Li, B., Keo, S., Kim, K.-S., Jeong, G., Oh, H., & Kim, Y. (2013) · International Immunopharmacology · doi:10.1016/j.intimp.2013.08.024 · Cited by 24

Persistent Borna Disease Virus (BDV) infection activates microglia prior to a detectable loss of granule cells in the hippocampus

Ovanesov, M. V., Moldovan, K., Smith, K., Vogel, M. W., & Pletnikov, M. V. (2008) · Journal of Neuroinflammation · doi:10.1186/1742-2094-5-16 · Cited by 24

Selective transfer of exosomes from oligodendrocytes to microglia by macropinocytosis

Schnaars, M. (2011) · doi:10.53846/goediss-919 · Cited by 25

Anti-neuroinflammatory effect of 6,8,1′-tri- O -methylaverantin, a metabolite from a marine-derived fungal strain Aspergillus sp., via upregulation of heme oxygenase-1 in lipopolysaccharide-activated microglia

Kim, K.-W., Kim, H. J., Sohn, J. H., Yim, J. H., Kim, Y., & Oh, H. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.11.010 · Cited by 23

Anti-neuroinflammatory effect of oxaline, isorhodoptilometrin, and 5-hydroxy-7-(2′-hydroxypropyl)-2-methyl-chromone obtained from the marine fungal strain Penicillium oxalicum CLC-MF05

Kim, D., Quang, T. H., Tiên, N. T., Kim, K.-W., Kim, Y., Ngân, N. T. T., Cường, N. X., Nam, N. H., & Oh, H. (2022) · Archives of Pharmacal Research · doi:10.1007/s12272-022-01370-w · Cited by 24

Age-Associated Glia Remodeling and Mitochondrial Dysfunction in Neurodegeneration: Antioxidant Supplementation as a Possible Intervention

Picca, A., Ferri, E., Calvani, R., Coelho‐Júnior, H. J., Marzetti, E., & Arosio, B. (2022) · Nutrients · doi:10.3390/nu14122406 · Cited by 24

Selective GSK3β Inhibition Mediates an Nrf2-Independent Anti-inflammatory Microglial Response

Yousef, M. H., Salama, M., El‐Fawal, H. A. N., & Abdelnaser, A. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02923-2 · Cited by 23

BAY-117082-driven NLRP3 inflammasome inhibition resolves nitro-glycerine (NTG) neuronal damage in in vivo model of migraine

Filippone, A., Scuderi, S. A., Basilotta, R., Lanza, M., Casili, G., Bova, V., Paterniti, I., & Esposito, E. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113851 · Cited by 25

Neural cell membrane-coated DNA nanogels as a potential target-specific drug delivery tool for the central nervous system

Lin, P. H., Huang, C., Hu, Y., Vaibavi, S. R., Lee, E. S., Singh, R., Milbreta, U., Cheung, C., Ying, J. Y., & Chew, S. Y. (2023) · Biomaterials · doi:10.1016/j.biomaterials.2023.122325 · Cited by 22

Multiple Sclerosis: Implications of Obesity in Neuroinflammation

Novo, A. M., & Batista, S. (2017) · Advances in neurobiology · doi:10.1007/978-3-319-63260-5_8 · Cited by 22

Anti-neuroinflammatory effects of cudraflavanone A isolated from the chloroform fraction of Cudrania tricuspidata root bark

Kim, K.-W., Quang, T. H., Ko, W., Kim, D., Yoon, C., Oh, H., & Kim, Y. (2018) · Pharmaceutical Biology · doi:10.1080/13880209.2018.1447972 · Cited by 23

Direct and indirect pro-inflammatory cytokine response resulting from TC-83 infection of glial cells

Keck, F., Kortchak, S., Bakovic, A., Roberts, B., Agrawal, N., & Narayanan, A. (2018) · Virulence · doi:10.1080/21505594.2018.1509668 · Cited by 23

Brain tocopherol levels are associated with lower activated microglia density in elderly human cortex

de Leeuw, F. A., Schneider, J. A., Agrawal, S., Leurgans, S. E., & Morris, M. C. (2020) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1002/trc2.12021 · Cited by 23

Breaking a dogma: acute anti-inflammatory treatment alters both post-lesional functional recovery and endogenous adaptive plasticity mechanisms in a rodent model of acute peripheral vestibulopathy

Mahmoudi, N. E., Rastoldo, G., Marouane, E., Péricat, D., Watabe, I., Tonetto, A., Hautefort, C., Chabbert, C., Sargolini, F., & Tighilet, B. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02222-y · Cited by 24

Parecoxib is neuroprotective in spontaneously hypertensive rats after transient middle cerebral artery occlusion: a divided treatment response?

Kelsen, J., Kjær, K., Chen, G., Pedersen, M., Røhl, L., Frøkiær, J., Nielsen, S. U., Nyengaard, J. R., & Rønn, L. C. B. (2006) · Journal of Neuroinflammation · doi:10.1186/1742-2094-3-31 · Cited by 23

Neuroinflammation and Alzheimer's disease: Unravelling the molecular mechanisms

Kakkar, A., Singh, H., Singh, B. K., Kumar, A., Mishra, A. K., & Chopra, H. (2025) · Journal of Alzheimer s Disease · doi:10.1177/13872877251374353 · Cited by 26

Inflammatory mediator release from primary rhesus microglia in response to Borrelia burgdorferi results from the activation of several receptors and pathways

Parthasarathy, G., & Philipp, M. T. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0274-z · Cited by 22

LncRNA AK148321 alleviates neuroinflammation in LPS-stimulated BV2 microglial cell through regulating microRNA-1199-5p/HSPA5 axis

Gao, S., Cheng, Q., Hu, Y., Tan, Z., Chen, L., Liu, S., Kang, Q., & Wei, T. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118863 · Cited by 22

Ketogenic Diet: A Promising Neuroprotective Composition for Managing Alzheimer’s Diseases and its Pathological Mechanisms

Sridharan, B., & Lee, M. (2021) · Current Molecular Medicine · doi:10.2174/1566524021666211004104703 · Cited by 22

Exploring the management approaches of cytokines including viral infection and neuroinflammation for neurological disorders

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