Neuroimmune regulation of microglial activity involved in neuroinflammation and neurodegenerative diseases

Pattern Recognition Receptors and Inflammation

Takeuchi, O., & Akira, S. (2010) · Cell · doi:10.1016/j.cell.2010.01.022 · Cited by 8,895

α-Synuclein in Lewy bodies

Spillantini, M. G., Schmidt, M. L., Lee, V. M.-Y., Trojanowski, J. Q., Jakes, R., & Goedert, M. (1997) · Nature · doi:10.1038/42166 · Cited by 8,382

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

Foxp3 programs the development and function of CD4+CD25+ regulatory T cells

Fontenot, J. D., Gavin, M. A., & Rudensky, A. Y. (2003) · Nature Immunology · doi:10.1038/ni904 · Cited by 7,745

Macrophage plasticity and polarization: in vivo veritas

Sica, A., & Mantovani, A. (2012) · Journal of Clinical Investigation · doi:10.1172/jci59643 · Cited by 6,335

Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo

Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827

Astrocyte-endothelial interactions at the blood-brain barrier

Abbott, N. J., Rönnbäck, L., & Hansson, E. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1824 · Cited by 5,595

Synaptic Pruning by Microglia Is Necessary for Normal Brain Development

Paolicelli, R. C., Bolasco, G., Pagani, F., Maggi, L., Scianni, M., Panzanelli, P., Giustetto, M., Ferreira, T. A., Guiducci, E., Dumas, L., et al. (2011) · Science · doi:10.1126/science.1202529 · Cited by 4,244

Microglia-mediated neurotoxicity: uncovering the molecular mechanisms

Block, M. L., Zecca, L., & Hong, J.-S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2038 · Cited by 4,110

Mechanisms underlying inflammation in neurodegeneration

Glass, C. K., Saijo, K., Winner, B., Marchetto, M. C., & Gage, F. H. (2010) · Cell · doi:10.1016/j.cell.2010.02.016 · Cited by 3,580

Preclinical Evaluation of TSPO and MAO-B PET Radiotracers in an LPS Model of Neuroinflammation

Narayanaswami, V., Tong, J., Schifani, C., Bloomfield, P. M., Dahl, K., & Vasdev, N. (2021) · PET Clinics · doi:10.1016/j.cpet.2020.12.003 · Cited by 16

Bioactivity and safety profile of Daucus carota subsp. maximus essential oil

Valente, J., Resende, R., Zuzarte, M., Gonçalves, M. J., Lopes, M. C., Cavaleiro, C., Pereira, C., Salgueiro, L., & Cruz, M. T. (2015) · Industrial Crops and Products · doi:10.1016/j.indcrop.2015.08.037 · Cited by 16

A comprehensive review: neuroinflammation and immune communication between the central nervous system and the periphery

Kaur, R., Kumar, S., & Singh, L. (2025) · Cytokine · doi:10.1016/j.cyto.2025.156974 · Cited by 16

Regulation of Pain Perception by Microbiota in Parkinson Disease

Manjarres, Z., Calvo, M., & Pacheco, R. (2023) · Pharmacological Reviews · doi:10.1124/pharmrev.122.000674 · Cited by 15

Anti-inflammatory activity of Jatropha curcas L. in brain glial cells primary cultures

Bastos, E. M. S., da Silva, A. B., Coelho, P. L. C., Borges, J. M. P., da Silva, V. D. A., Moreau, V. H., & Costa, S. L. (2020) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2020.113201 · Cited by 15

Neuroprotective Effects of Low-Dose Statins in the Retinal Ultrastructure of Hypercholesterolemic Rabbits

Fernández-Navarro, J., Aldea, P., de Hoz, R., Salazar, J. J., Ramirez, A. I., Rojas, B., Gallego, B., Triviño, A., Tejerina, T., & Ramirez, J. M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0154800 · Cited by 15

Hirsutanol A Attenuates Lipopolysaccharide-Mediated Matrix Metalloproteinase 9 Expression and Cytokines Production and Improves Endotoxemia-Induced Acute Sickness Behavior and Acute Lung Injury

Jan, J., Yang, C., Wang, M.-H., Lin, F., Yen, J.-L., Hsieh, I., Khotimchenko, M., Lee, T., & Hsiao, G. (2019) · Marine Drugs · doi:10.3390/md17060360 · 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

Long-term corticosteroid-induced chronic glaucoma model produced by intracameral injection of dexamethasone-loaded PLGA microspheres

Rodrigo, M. J., García-Herranz, D., Aragón-Navas, A., Subías, M., Martínez, T., Méndez-Martínez, S., Cardiel, M. J., García-Feijoo, J., Ruberte, J., Herrero‐Vanrell, R., et al. (2021) · Drug Delivery · doi:10.1080/10717544.2021.1998245 · Cited by 14

DiHuangYin decoction protects dopaminergic neurons in a Parkinson's disease model by alleviating peripheral inflammation

Wu, Y., Liu, H., Wang, Y., Sheng, H., Chen, Z., Xun, D., Wu, H., Xiao, S., Bi, Y., & Wang, Y. (2022) · Phytomedicine · doi:10.1016/j.phymed.2022.154357 · Cited by 14

Normal-Tension Glaucoma and Potential Clinical Links to Alzheimer’s Disease

Ho, K., Bodi, N. E., & Sharma, T. P. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13071948 · Cited by 15

Effects of epigallocatechin-3-gallate on systemic inflammation-induced cognitive dysfunction in aged rats

Yamanaka, D., Kawano, T., Nishigaki, A., Aoyama, B., Tateiwa, H., Shigematsu-Locatelli, M., Locatelli, F. M., & Yokoyama, M. (2017) · Journal of Anesthesia · doi:10.1007/s00540-017-2392-5 · Cited by 14

T-cell based immunotherapies for Parkinson’s disease

Pacheco, R. (2021) · Exploration of Neuroprotective Therapy · doi:10.37349/ent.2021.00007 · Cited by 13

Maternal Immune Activation and Neurodevelopmental Disorders: Integrating Molecular, Cellular and Systems Mechanisms

Yong, Q., Zhao, C., Xia, L., Zhu, T., & Xia, K. (2025) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s533813 · Cited by 14

High yield primary microglial cultures using granulocyte macrophage-colony stimulating factor from embryonic murine cerebral cortical tissue

Yu, A. C., Neil‐Sztramko, S., & Quandt, J. A. (2017) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2017.03.018 · Cited by 13

Triggering microglia through toll-like receptor 2 pathway induced interferon β expression in cell and animal model of Alzheimer’s disease

Heshmati-Fakhr, N., Sotoodehnejadnematalahi, F., Yousefi, N., Sayyah, M., Hosseini, S. M., & Pourbadie, H. G. (2018) · Neuroreport · doi:10.1097/wnr.0000000000001132 · Cited by 13

The atypical RhoGTPase RhoE/Rnd3 is a key molecule to acquire a neuroprotective phenotype in microglia

Neubrand, V. E., Forte‐Lago, I., Caro, M., & Delgado, M. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1386-z · Cited by 13

Neuroprotection by Abdominal Ultrasound in Lipopolysaccharide-Induced Systemic Inflammation

Song, W.-S., Hung, T., Liu, S., Zheng, Y., Lin, H.-M., & Yang, F. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119329 · Cited by 12

Excessive Alcohol Use as a Risk Factor for Alzheimer’s Disease: Epidemiological and Preclinical Evidence

Anton, P. E., Maphis, N. M., Linsenbardt, D. N., & Coleman, L. G. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-81908-7_10 · Cited by 12

JM-20 Treatment After Mild Traumatic Brain Injury Reduces Glial Cell Pro-inflammatory Signaling and Behavioral and Cognitive Deficits by Increasing Neurotrophin Expression

Furtado, A. B. V., Gonçalves, D. F., Hartmann, D. D., Courtes, A. A., Cassol, G., Núñez-Figueredo, Y., Argolo, D. S., do Nascimento, R. P., Costa, S. L., da Silva, V. D. A., et al. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02436-4 · Cited by 13

A Dual Anti-Inflammatory and Anti-Proliferative 3-Styrylchromone Derivative Synergistically Enhances the Anti-Cancer Effects of DNA-Damaging Agents on Colon Cancer Cells by Targeting HMGB1-RAGE-ERK1/2 Signaling

Tanuma, S., Oyama, T., Okazawa, M., Yamazaki, H., Takao, K., Sugita, Y., Amano, S., Abe, T., & Sakagami, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073426 · Cited by 11

Role of the Peli1–RIPK1 Signaling Axis in Methamphetamine-Induced Neuroinflammation

Xu, W., Yang, T., Lou, X., Chen, J., Wang, X., Hu, M., An, D., Gao, R., Wang, J., & Chen, X. (2023) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.2c00623 · Cited by 12

Anti-neuroinflammatory effect of Iresine celosia on lipopolysaccharide-stimulated microglial cells and mouse

Kim, N., Martínez, C. C., Jang, D. S., Lee, J. K., & Oh, M. S. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.01.017 · Cited by 12

Two Rationally Identified Novel Glitazones Reversed the Behavioral Dysfunctions and Exhibited Neuroprotection Through Ameliorating Brain Cytokines and Oxy-Radicals in ICV-LPS Neuroinflammatory Rat Model

Justin, A., Ashwini, P., Jose, J. A., Jeyarani, V., Dhanabal, S. P., Manisha, C., Mandal, S. P., Bhavimani, G., Prabhakaran, P., Yuvaraj, S., et al. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.530148 · Cited by 12

Ginkgolide B alleviates the inflammatory response and attenuates the activation of LPS‑induced BV2 cells in vitro and in vivo

Sun, M.-X., Sheng, Y., & Zhu, Y. (2021) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2021.10018 · Cited by 12

Inter-Organ Crosstalk in Neurodegenerative Disease

Carata, E., Destino, M., Tenuzzo, B. A., & Panzarini, E. (2025) · Life · doi:10.3390/life15101499 · Cited by 14

Costunolide normalizes neuroinflammation and improves neurogenesis deficits in a mouse model of depression through inhibiting microglial Akt/mTOR/NF-κB pathway

Zhang, S.-Q., Deng, Q., Tian, C. L., Zhao, H., Yang, L.-Y., Cheng, X.-W., Wang, G., & Liu, D. (2025) · Acta Pharmacologica Sinica · doi:10.1038/s41401-025-01506-w · Cited by 11

Infiltrating T helper 17 cells in the paraventricular nucleus are pathogenic for stress-induced hypertension

Wu, Q. J., Mi, Y., Cheng, W., Xia, C., Zhu, D., & Du, D. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.05.121 · Cited by 11

MicroRNA-451 Attenuates the Inflammatory Response of Activated Microglia by Downregulating Nucleotide Binding Oligomerization Domain-Like Receptor Protein 3

Hong, Z., Cheng, J., Ye, Y., Chen, X., & Zhang, F. (2022) · World Neurosurgery · doi:10.1016/j.wneu.2022.08.139 · Cited by 11

Novel Indications for Benzodiazepine Antagonist Flumazenil in GABA Mediated Pathological Conditions of the Central Nervous System

Hulse, G. K., Kelty, E. A., Hood, S. D., Norman, A. F., Basso, M., & Reece, A. S. (2015) · Current Pharmaceutical Design · doi:10.2174/1381612821666150619092720 · Cited by 11

Neuroimmune Signaling: Cytokines and the Central Nervous System

Kennedy, R. H., & Silver, R. (2016) · Springer eBooks · doi:10.1007/978-1-4614-6434-1_174-2 · Cited by 11

Acupuncture at ST36 Exerts Neuroprotective Effects via Inhibition of Reactive Astrogliosis in Infantile Rats with Hydrocephalus

Tida, J. A., Catalão, C. H. R., Garcia, C. A. B., dos Santos, A. C., Salmón, C. E. G., & Lopes, L. D. S. (2018) · Acupuncture in Medicine · doi:10.1136/acupmed-2017-011515 · Cited by 11

Vanillic acid ameliorates diethyl phthalate and bisphenol S‐induced oxidative stress and neuroinflammation in the hippocampus of experimental rats

Eteng, O. E., Ugwor, E. I., James, A. S., Moses, C. A., Ogbonna, C. U., Iwara, I. A., Akamo, A. J., Akintunde, J. K., Blessing, O. A., Tola, Y. M., et al. (2024) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.70017 · Cited by 9

Effects of Interleukin-1β in Glycinergic Transmission at the Central Amygdala

Solorza, J., Oliva, C. A., Castillo, K., Amestica, G., Maldifassi, M. C., López-Cortés, X. A., Barra, R., Stehberg, J., Piesche, M., Sáez‐Briones, P., et al. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.613105 · Cited by 9

Mesenchymal stem cells and their conditioned medium as potential therapeutic strategies in managing comorbid anxiety in rat sepsis induced by cecal ligation and puncture.

Ranjbaran, M., Kianian, F., Kadkhodaee, M., Seifi, B., Ashabi, G., Akhondzadeh, F., Adelipour, M., Izad, M. H., & Abdolmohammadi, K. (2022) · PubMed Central · doi:10.22038/ijbms.2022.61860.13690 · Cited by 9

Trehalose: A promising new treatment for traumatic brain injury? A systematic review of animal evidence

Ghorbani, M., Mehrizi, M. A. A., Tajvidi, M., Habibi, M. A., Mohammadi, M., Esmaeilian, S., Torabi, P., Rahmanipour, E., Daskareh, M., & Mohammadi, A. (2023) · Interdisciplinary Neurosurgery · doi:10.1016/j.inat.2023.101947 · Cited by 9

Bridging the Gap: The Neuro-immune Axis as a Key Player in Neurodegenerative Disorders

Liu, T., Wu, H., & Wei, J. (2025) · Neuroscience Bulletin · doi:10.1007/s12264-025-01439-8 · Cited by 9

Single-nucleus transcriptomics reveals sepsis-related neurovascular dysfunction in the human hippocampus

Liu, L., Li, P., Wilkerson, B. A., Wu, Y., Liu, M., Jiang, W., Hamlett, E. D., Carroll, S. L., & Fan, H. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1648278 · Cited by 9

Enantioselective Synthesis and Pharmacological Evaluation of Aza-CGP37157–Lipoic Acid Hybrids for the Treatment of Alzheimer’s Disease

Cores, Á., Michalska, P., Pérez, J. M., Crisman, E., Gómez, C., Villacampa, M., Menéndez, J. C., & Leon, R. M. (2022) · Antioxidants · doi:10.3390/antiox11010112 · Cited by 8

Prior exposure to stress exacerbates neuroinflammation and causes long-term behavior changes in sepsis

Miyao, M., Hirotsu, A., Tatsumi, K., & Tanaka, T. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e16904 · Cited by 8

Engraftment of Human Glioblastoma Cells in Immunocompetent Rats through Acquired Immunosuppression

Huszthy, P. C., Sakariassen, P. Ø., Espedal, H., Brokstad, K. A., Bjerkvig, R., & Miletić, H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136089 · Cited by 8

Kaolin-induced hydrocephalus causes acetylcholinesterase activity dysfunction following hypothalamic damage in infant rats

Catalão, C. H. R., Souza, A. D. O., Santos-Júnior, N. N., da Silva, S. C., da Costa, L. H. A., Alberici, L. C., Rocha, M. J. A., & Lopes, L. D. S. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146408 · Cited by 8

Sepsis-associated Encephalopathy

Siami, S., Polito, A., & Sharshar, T. (2009) · Springer eBooks · doi:10.1007/978-3-540-92276-6_74 · Cited by 8

The Role of NO/cGMP Signaling on Neuroinflammation: A New Therapeutic Opportunity

Peixoto, C. A., Nunes, A. K. S., & Rapôso, C. (2017) · InTech eBooks · doi:10.5772/intechopen.68990 · Cited by 8

Citicoline and Coenzyme Q10: Therapeutic Agents for Glial Activation Reduction in Ocular Hypertension

Matamoros, J. A., Rubio‐Casado, S., Fernández‐Albarral, J. A., Martínez‐López, M. A., Ramirez, A. I., Salobrar‐García, E., Marco, E. M., Paleo‐García, V., de Hoz, R., López‐Cuenca, I., et al. (2025) · Pharmaceuticals · doi:10.3390/ph18050694 · Cited by 7

Analyzing Facial Asymmetry in Alzheimer’s Dementia Using Image-Based Technology

Chien, C., Sung, J.-L., Wang, C.-P., Yen, C., & Yang, Y. (2023) · Biomedicines · doi:10.3390/biomedicines11102802 · Cited by 7

Anti-Neuroinflammatory Effects of Arecae pericarpium on LPS-Stimulated BV2 Cells

Cho, H.-G., Kim, D.-U., Oh, J.-Y., Park, S., Kweon, B., & Bae, G. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46010056 · Cited by 7

Inflammation and the Brain Disorders: A Review

Bargi, R., Salmani, H., Yazdi, F. A., & Hosseini, M. (2017) · The Neuroscience Journal of Shefaye Khatam · doi:10.18869/acadpub.shefa.5.3.68 · Cited by 7

Naloxone Protects against Lipopolysaccharide-Induced Neuroinflammation and Microglial Activation via Inhibiting ATP-Sensitive Potassium Channel

Tang, Z., Shao, X., Wu, J., Chen, H., Zhang, A., Xu, F., Ping, H., Li, S., Liu, C., Li, Y., et al. (2021) · Computational and Mathematical Methods in Medicine · doi:10.1155/2021/7731528 · Cited by 7

Exacerbated immune response of the brain to peripheral immune challenge in post-septic mice

Salmani, H., Hosseini, M., Nabi, M. M., Noshahr, Z. S., Baghcheghi, Y., & Sadeghi, M. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.04.013 · Cited by 6

Neuroimmune Signaling: Cytokines and the Central Nervous System

Kennedy, R. H., & Silver, R. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_174 · Cited by 7

Green Tea Polyphenol Epigallocatechine Gallate (EGCG) Prevented LPS-induced BV-2 Micoglial Cell Activation

Park, E., & Chun, H. S. (2016) · Journal of Life Science · doi:10.5352/jls.2016.26.6.640 · Cited by 7

A Unique Anti-Cancer 3-Styrylchromone Suppresses Inflammatory Response via HMGB1-RAGE Signaling

Abe, H., Okazawa, M., Oyama, T., Yamazaki, H., Yoshimori, A., Kamiya, T., Tsukimoto, M., Takao, K., Sugita, Y., Sakagami, H., et al. (2021) · Medicines · doi:10.3390/medicines8040017 · Cited by 8

Using Single-Cell RNA sequencing with Drosophila, Zebrafish, and mouse models for studying Alzheimer’s and Parkinson’s disease

Lau, F., Binacchi, R., Brugnara, S., Cumplido-Mayoral, A., Savino, S. D., Khan, I., Orso, A., Sartori, S., Bellosta, P., Carl, M., et al. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.03.042 · Cited by 6

Bacillus Calmette–Guérin Tokyo-172 vaccine provides age-related neuroprotection in actively induced and spontaneous experimental autoimmune encephalomyelitis models

Cossu, D., Yokoyama, K., Sakanishi, T., Sechi, L. A., & Hattori, N. (2023) · Clinical & Experimental Immunology · doi:10.1093/cei/uxad015 · Cited by 6

The Effect of Pentoxifylline on Passive Avoidance Learning and Expression of Tumor Necrosis Factor-Alpha and Caspase-3 in the Rat Hippocampus Following Lipopolysaccharide-Induced Inflammation

Farahmandfar, M., Akbari, Z., Reisi, P., & Torkaman‐Boutorabi, A. (2019) · Advanced Biomedical Research · doi:10.4103/abr.abr_33_19 · Cited by 6

Faim knockout leads to gliosis and late‐onset neurodegeneration of photoreceptors in the mouse retina

Sires, A. M., Turch, M., Bogdanov, P. M., Sampedro, J., Ramos, H., Ruiz, A., Huo, J., Xu, S., Lam, K., López‐Soriano, J., et al. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24978 · Cited by 6

Impact of imipramine on proteome of rat primary glial cells

Kędracka–Krok, S., Świderska, B., Bielecka, A., Pruś, G., Skupień-Rabian, B., Jankowska, U., & Obuchowicz, E. (2018) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2018.04.008 · Cited by 6

Neuroimmune Signaling: Cytokines and the Central Nervous System

Kennedy, R. H., & Silver, R. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3474-4_174 · Cited by 6

Therapeutic Effects of Physical Exercise and the Mesenchymal Stem Cell Secretome by Modulating Neuroinflammatory Response in Multiple Sclerosis

Hurtado, J. C., González, L. M., Ospina, L., Sperling, L. E., & Chaparro, O. (2021) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x16666211209155333 · Cited by 5

Mesenchymal Stem Cell—Macrophage Crosstalk Provides Specific Exosomal Cargo to Direct Immune Response Licensing of Macrophages during Inflammatory Responses

Naaldijk, Y., Sherman, L. S., Turrini, N., Kenfack, Y., Ratajczak, M. Z., Souayah, N., Rameshwar, P., & Ulrich, H. (2023) · Stem Cell Reviews and Reports · doi:10.1007/s12015-023-10612-3 · Cited by 5

Cerebellar Cortex Neurons and Microglia Reaction to Sevoflurane Anesthesia

Yukina, G. Y., Sukhorukova, E. G., Владимировна, Б. И., Polushin, Y. S., Викторович, Т. В., & Polushin, A. Y. (2019) · Cell and Tissue Biology · doi:10.1134/s1990519x19060105 · Cited by 5

Inhibitory effect ofPetalonia binghamiaeon neuroinflammation in LPS-stimulated microglial cells

Park, J. H., Kim, S. H., & Lee, S. R. (2017) · Journal of Nutrition and Health · doi:10.4163/jnh.2017.50.1.25 · Cited by 5

Curcumin modulates long term potentiation in lipopolysaccharide-treated rats

Ardeshiri, M. R., Beheshti, S. A., Beheshti, F., Hosseini, M., & Akbari, E. (2020) · PharmaNutrition · doi:10.1016/j.phanu.2020.100195 · Cited by 5

Intracerebellar injection of monocytic immature myeloid cells prevents the adverse effects caused by stereotactic surgery in a model of cerebellar neurodegeneration

del Pilar, C., Garrido-Matilla, L., del Pozo-Filíu, L., Lebrón‐Galán, R., Arias, R. F., Clemente, D., Alonso, J. R., Weruaga, E., & Díaz, D. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-023-03000-8 · Cited by 4

PMA treatment fosters rat retinal ganglion cell survival via TNF signaling

Ferreira, É. C., Oliveira, A. C. D. R., Garcia, C. G., Cossenza, M., Gonçalves-de-Albuquerque, C. F., Castro-Faria-Neto, H. C., Giestal‐de‐Araujo, E., & dos Santos, A. A. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136197 · Cited by 4

Anti‐inflammatory and antioxidative actions of tacrolimus ( FK506 ) on human microglial HMC3 cell line

Koçancı, F. G., & Erol, A. Y. G. (2023) · Scandinavian Journal of Immunology · doi:10.1111/sji.13339 · Cited by 4

Effects of eldepryl on glial cell proliferation and activation in the substantia nigra and striatum in a rat model of Parkinson’s disease

Liu, B., Lv, C., Zhang, J., Liu, Y., Sun, J., Cheng, X., Mao, W., Ma, Y., & Li, S. (2017) · Neurological Research · doi:10.1080/01616412.2017.1297911 · Cited by 4

Advances in Neuroimmunology

Gruol, D. L. (2017) · Brain Sciences · doi:10.3390/brainsci7100124 · Cited by 4

Neurological complications during HIV infection

Martinez-Navío, J. M. (2021) · Exploration of Neuroprotective Therapy · doi:10.37349/ent.2021.00004 · Cited by 4

Hyperactivity of the non-canonical inflammasome in SPG11 and SPG48

Afzal, M. A., Ghait, M., Hussain, A., Siegmund, A., Tuchscherr, L. P. N., Babic, P., Press, A. T., Hardt, R., Winter, D., Rödiger, A., et al. (2025) · EBioMedicine · doi:10.1016/j.ebiom.2025.105985 · Cited by 3

Anti-neuroinflammatory effects of the KIOM -patented Polygonum multiflorum maximized root tuber against LPS-stimulated BV2 Cells

Oh, T. W., Ban, Y., & Kang, Y. (2024) · Applied Biological Chemistry · doi:10.1186/s13765-024-00928-0 · Cited by 3

A REVIEW ON MICROGLIA: ROLE IN NEUROINFLAMMATION, SCREENING MODELS AND THERAPEUTIC STRATEGIES FOR TREATMENT

Choudhury, S., & Vellapandian, C. (2019) · International Research Journal of Pharmacy · doi:10.7897/2230-8407.10013 · Cited by 2

MICROGLIA OF THE HUMAN SUBSTANTIA NIGRA

Korzhevsky, D. E., Kirik, O. V., Sukhorukova, E. G., & Syrszova, M. A. (2014) · Medical academic journal · doi:10.17816/maj14468-72 · Cited by 3

Neuroinflammation: From Target Selection to Preclinical and Clinical Studies

Zinnhardt, B., Barca, C., Foray, C., Fricke, I. B., Viel, T., Winkeler, A., Windhorst, A. D., & Jacobs, A. H. (2020) · Springer eBooks · doi:10.1007/978-3-030-53176-8_17 · Cited by 3

Exercise Attenuates Sickness Behavior And Protects Against Dopaminergic Impairment Induced By NeuroinflammationPreprint

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