The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
Mitochondrial ROS govern the LPS-induced pro-inflammatory response in microglia cells by regulating MAPK and NF-κB pathways
Abstract
Activation of microglia cells in the brain contributes to neurodegenerative processes promoted by many neurotoxic factors such as pro-inflammatory cytokines and nitric oxide (NO). Reactive oxygen species (ROS) actively affect microglia-associated neurodegenerative diseases through their role as pro-inflammatory molecules and modulators of pro-inflammatory processes. Although the ROS which involved in microglia activation are thought to be generated primarily by NADPH oxidase (NOX) and involved in the immune response, mitochondrial ROS have also been proposed as important regulators of the inflammatory response in the innate immune system. However, the role of mitochondrial ROS in microglial activation has yet to be fully elucidated. In this study, we demonstrate that inhibition of mitochondrial ROS by treatment with Mito-TEMPO effectively suppressed the level of mitochondrial and intracellular ROS. Mito-TEMPO treatment also significantly prevented LPS-induced increase in the TNF-α, IL-1β, IL-6, iNOS and Cox-2 in BV-2 and primary microglia cells. Furthermore, LPS-induced suppression of mitochondrial ROS generation not only affected LPS-stimulated activation of MAPKs, including ERK, JNK, and p38, but also regulated IκB activation and NF-κB nuclear localization. These results indicate that mitochondria constitute a major source of ROS generation in LPS-mediated activated microglia cells. Additionally, suppression of LPS-induced mitochondrial ROS plays a role in modulating the production of pro-inflammatory mediators by preventing MAPK and NF-κB activation in microglia cells. Our findings suggest that a potential strategy in the development of therapy for inflammation-associated degenerative neurological diseases involves targeting the regulation of mitochondrial ROS in microglial cells.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Mitochondrial ROS (mROS), independent of NOX-generated ROS, are also involved in the inflammatory response of microglia by activating MAPKs.”
From ROS Generation in Microglia: Understanding Oxidative Stress and Inflammation in Neurodegenerative Disease (2020) · cites this paper as [158]
In the citing paper
“Therefore, MAPK and NFκB activation in microglial cells and the concurrent upregulation of pro-inflammatory mediators is facilitated, at least in part, by mROS.”
From ROS Generation in Microglia: Understanding Oxidative Stress and Inflammation in Neurodegenerative Disease (2020) · cites this paper as [158]
Citations
Cites
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
Bedard, K., & Krause, K.-H. (2007) · Physiological Reviews · doi:10.1152/physrev.00044.2005 · Cited by 6,989
A role for mitochondria in nlrp3 inflammasome activation
Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602
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
Nakahira, K., Haspel, J. A., Rathinam, V. A. K., Lee, S.-J., Dolinay, T., Lam, H. C., Englert, J. A., Rabinovitch, M., Cernadas, M., Kim, H. P., et al. (2011) · Nature Immunology · doi:10.1038/ni.1980 · Cited by 3,049
Tlr signalling augments macrophage bactericidal activity through mitochondrial ros
West, A. P., Brodsky, I. E., Rahner, C., Woo, D. K., Erdjument-Bromage, H., Tempst, P., Walsh, M. C., Choi, Y., Shadel, G. S., & Ghosh, S. (2011) · Nature · doi:10.1038/nature09973 · Cited by 1,659
Microglia in neurodegenerative disease
Perry, V. H., Nicoll, J. A. R., & Holmes, C. (2010) · Nature Reviews Neurology · doi:10.1038/nrneurol.2010.17 · Cited by 1,543
Bulua, A. C., Simon, A., Maddipati, R., Pelletier, M., Park, H., Kim, K.-Y., Sack, M. N., Kastner, D. L., & Siegel, R. M. (2011) · Journal of Experimental Medicine · doi:10.1084/jem.20102049 · Cited by 860
Mitochondrial reactive oxygen species drive proinflammatory cytokine production
Naik, E., & Dixit, V. M. (2011) · Journal of Experimental Medicine · doi:10.1084/jem.20110367 · Cited by 783
Redox regulation of glial inflammatory response to lipopolysaccharide and interferonγ
Pawate, S., Shen, Q., Fan, F., & Bhat, N. R. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20180 · Cited by 428
Kim, J.-H., Na, H.-J., Kim, C.-K., Kim, J.-Y., Ha, K.-S., Lee, H., Chung, H.-T., Kwon, H. J., Kwon, Y.-G., & Kim, Y.-M. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.06.019 · Cited by 273
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 530
Kim, Y. J., Park, S. Y., Koh, Y. J., & Lee, J. (2021) · Plants · doi:10.3390/plants10040688 · Cited by 14
Parasite worm antigens instruct macrophages to release immunoregulatory extracellular vesicles
Zakeri, A., Whitehead, B. J., Stensballe, A., de Korne, C. M., Williams, A. R., Everts, B., & Nejsum, P. L. (2021) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12131 · Cited by 14
Choi, B. R., Kim, H., Ko, W., Dong, L., Yoon, D., Oh, S. M., Lee, Y., Lee, D., Baek, N., & Lee, D. (2021) · Antioxidants · doi:10.3390/antiox10091334 · Cited by 14
Self-citationZhu, Y., Zhang, J., Li, C., Deng, G., Li, J., Liu, X., Wan, B., & Tian, Y. (2022) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.1c01571 · Cited by 14
Li, J., Bai, J., Tuerdi, N., & Liu, K. (2022) · Bioengineered · doi:10.1080/21655979.2022.2054501 · Cited by 14
Cao, L., Zhao, Y., Bai, M., Geliebter, D., Geliebter, J., Tiwari, R. K., He, H.-J., Wang, Z., Jia, X.-Y., Li, J., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.838261 · Cited by 16
Yu, Y., Li, W., Ren, L., Yang, C., Li, D., Han, X., Sun, Y., Lv, C., & Han, F. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.9209 · Cited by 14
Dexmedetomidine Reverses Postoperative Spatial Memory Deficit by Targeting Surf1 and Cytochrome c
Niu, K., Qin, J.-L., Lu, G., Guo, J., Williams, J. P., & An, J. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.04.009 · Cited by 13
Privitera, A., Cardaci, V., Weerasekara, D. B., Saab, M. W., Diolosà, L., Fidilio, A., Jolivet, R., Lazzarino, G., Amorini, A. M., Camarda, M., et al. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1161794 · Cited by 13
Abietane diterpenoids with anti-neuroinflammation activity from Rosmarinus officinalis
Tang, Z., Wang, J., Lin, Z., Zhu, H., Hu, W., Zhang, R., & Chen, X. (2024) · Fitoterapia · doi:10.1016/j.fitote.2024.105866 · Cited by 13
Yuchen-Zhang, Du, M., Zhang, Q.-Y., Yang, S., Chen, J., Dan, C.-M., Lian, L., & Wang, J. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.133035 · Cited by 13
NMDA receptor blockade attenuates Japanese encephalitis virus infection-induced microglia activation
Chang, C.-Y., Wu, C.-C., Tzeng, C., Li, J., Chen, Y., Chen, W., Kuan, Y., Liao, S., & Chen, C. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03288-0 · Cited by 14
IDH2 Deficiency in Microglia Decreases the Pro-inflammatory Response via the ERK and NF-κB Pathways
Chae, U., Kim, H. S., Kim, K., Lee, H., Lee, H., Park, J., & Lee, D. (2018) · Inflammation · doi:10.1007/s10753-018-0840-5 · Cited by 13
Self-citationJia, F., Zhang, X., Ma, W., Li, X., & Zhou, X. (2021) · Research in Veterinary Science · doi:10.1016/j.rvsc.2021.04.025 · Cited by 13
Lee, Y., Ju, X., Cui, J., Zhang, T., Hong, B., Kim, Y. H., Ko, Y., Park, J.-H., Choi, C. H., Heo, J. Y., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e28974 · Cited by 12
Self-citationChaubey, S., & Singh, L. (2024) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-024-03515-8 · Cited by 12
Mitochondrial reactive oxygen species regulate fungal protease-induced inflammatory responses
Kim, Y. H., & Lee, S. (2017) · Toxicology · doi:10.1016/j.tox.2017.01.008 · Cited by 12
Zonisamide Ameliorates Microglial Mitochondriopathy in Parkinson’s Disease Models
Tada, S., Choudhury, M. E., Kubo, M., Ando, R., Tanaka, J., & Nagai, M. (2022) · Brain Sciences · doi:10.3390/brainsci12020268 · Cited by 12
Wang, X., Deng, T., Zhou, X., Chu, L., Zeng, X., Zhang, S., Guan, W., & Chen, F. (2024) · Antioxidants · doi:10.3390/antiox13020246 · Cited by 12
Maiuolo, J., Bava, I., Carresi, C., Gliozzi, M., Musolino, V., Scicchitano, M., Macrì, R., Oppedisano, F., Scarano, F., Zito, M. C., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22157910 · Cited by 12
Xia, B., Meng, Q., Feng, X., Tang, X., Jia, A., Feng, J., Zhang, S., & Zhang, H. (2018) · Electrophoresis · doi:10.1002/elps.201700467 · Cited by 12
Zhang, H., Niu, Y., Qiu, L., Yang, J., Sun, J., & Xia, J. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.111210 · Cited by 11
Lei, S.-Y., Yang, Y.-Q., Liu, J., Zhang, D., Qu, Y., Sun, Y., Zhu, H.-J., Zhou, S., Yang, Y., & Guo, Z. (2024) · Journal of Tissue Engineering · doi:10.1177/20417314241237052 · Cited by 11
Hou, S.-K., Wang, C., Ma, X., Zhao, J., Wang, J., Fang, Y., Liu, H., Ding, H., Guo, J., & Lu, W. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26083603 · Cited by 11
1-O-alkyl glycerophosphate-induced CD36 expression drives oxidative stress in microglial cells
Tsukahara, T. (2019) · Cellular Signalling · doi:10.1016/j.cellsig.2019.109459 · Cited by 11
Lee, H., Liu, Z., Dong, L., Cheong, S. H., & Lee, D. (2022) · Antioxidants · doi:10.3390/antiox11040690 · Cited by 11
Self-citationLiu, S., Che, N., Ou, W., Yan, M., Liao, Y., & Cheng, Y. (2022) · Pharmaceutical Biology · doi:10.1080/13880209.2022.2121410 · Cited by 11
Hu, D., Huang, T., Shigeta, M., Ochi, Y., Kabayama, S., Watanabe, Y., & Cui, Y. (2022) · Nutrients · doi:10.3390/nu14214451 · Cited by 11
Thakuri, L. S., Park, C. M., Park, J., Kim, H., & Rhyu, D. Y. (2023) · ALGAE · doi:10.4490/algae.2023.38.12.26 · Cited by 11
Self-citationSun, X., Gao, S., Luo, S., Chang, R., Jia, H., Xu, Q., Jiang, Q., Loor, J. J., & Xu, C. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c07494 · Cited by 11
Tian, M., Wang, Q., Jia, X., Tian, Y., Hong, Y., & Zhou, Y. (2023) · Industrial Crops and Products · doi:10.1016/j.indcrop.2023.117353 · Cited by 11
Liu, S., Man, Y., & Zhao, L. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.02.086 · Cited by 11
RetractedBi, X., Jiang, B., Zhou, J., Luo, L., & Yin, Z. (2019) · Cell Biology International · doi:10.1002/cbin.11228 · Cited by 11
Dan, G. U. O., Zhao, G., Li, G., Wang, C., Wang, H., Liu, Z., Xu, B., & Guo, X. (2021) · Insect Molecular Biology · doi:10.1111/imb.12698 · Cited by 11
The role of PPARγ in chemotherapy-evoked pain
Khasabova, I. A., Seybold, V. S., & Simone, D. A. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135845 · Cited by 11
Corydecumine G inhibits microglia activation via MAPK pathway in a rat model of neuropathic pain
Tan, L., Hu, Y., Zhang, X., Zhang, C., Xi, C., Yang, Z., Cao, Z., & Zhao, F. (2022) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2022.102124 · Cited by 11
Le, D. D., Jang, Y. S., Truong, V., Dinh, T., Dang, T., Yu, S., & Lee, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252211965 · Cited by 10
Marchesi, L. T., Stockholm, D., Esteves, T., Leblanc, M., Auger, N., Branchu, J., Hachimi, K. H. E., & Stévanin, G. (2025) · Scientific Reports · doi:10.1038/s41598-025-86337-9 · Cited by 10
Temviriyanukul, P., Lertmongkolaksorn, T., Supasawat, P., Pitchakarn, P., Thiyajai, P., Nusuetrong, P., Phochantachinda, S., Chansawhang, A., & Chantong, B. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.115440 · Cited by 10
Pan, P., Chen, J., Xie, F., Guo, Y., Liu, X., Zhang, D., Xie, L., & Su, L. (2023) · The FASEB Journal · doi:10.1096/fj.202202144rrr · Cited by 10
Kim, M.-J., Chaudhary, S. C., Kim, B., & Kim, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242115603 · Cited by 10
Self-citationParker, L. M., Sayyadi, N., Staikopoulos, V., Shrestha, A., Hutchinson, M. R., & Packer, N. H. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1451-2 · Cited by 10
Zhao, C., Chen, J., Ye, J., Li, Z., Su, L., Wang, J., Zhang, Y., Chen, J., Yang, H., Shi, J., et al. (2021) · Angewandte Chemie · doi:10.1002/ange.202100873 · Cited by 10
Jiang, S., Wang, Y.-Q., Tang, Y., Lu, X., & Guo, D. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/6208872 · Cited by 10
Fock, E. M., Bachteeva, V. T., Lavrova, E. A., & Parnova, R. G. (2018) · Journal of Lipids · doi:10.1155/2018/5745790 · Cited by 10
Hao, X., Liu, M., Zhang, X., Yu, H., Fang, Z., Gao, X., Chen, M., Shao, Q., Gao, W., Lei, L., et al. (2024) · Journal of Dairy Science · doi:10.3168/jds.2023-23465 · Cited by 9
Zhang, D., He, J., Hua, S. Y., Li, Y., & Zhou, M. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c00564 · Cited by 10
Cui, J. R., Lai, Q. F., & Li, Y. (2025) · Reviews in Aquaculture · doi:10.1111/raq.70118 · Cited by 9
Jiang, M., Su, X., Liu, J., Zheng, C., & Li, X. (2020) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2020/4858201 · Cited by 9
Chunchai, T., Apaijai, N., Benjanuwattra, J., Pintana, H., Singhanat, K., Arunsak, B., Chattipakorn, N., & Chattipakorn, S. C. (2022) · Current Research in Pharmacology and Drug Discovery · doi:10.1016/j.crphar.2022.100124 · Cited by 9
Kondo, T., Kakinuma, H., Fujimura, K., Ambo, S., Otake, K., Sato, Y., & Egusa, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24129861 · Cited by 9
Gao, L., Gao, Y.-Q., Liu, W.-Y., Stadler, M., Zhu, Y.-T., Qi, J., Han, W., & Gao, J. (2024) · Journal of Natural Products · doi:10.1021/acs.jnatprod.4c00334 · Cited by 9
Selection signatures in candidate genes and QTL for reproductive traits in Nellore heifers
Montes-Vergara, D. E., Braz, C. U., Ribeiro, A. M. F., Cavani, L., Barbero, M. M. D., de Albuquerque, L. G., Curi, R. A., & de Oliveira, H. N. (2019) · Animal Reproduction Science · doi:10.1016/j.anireprosci.2019.06.004 · Cited by 9
Glial Purinergic Signaling‐Mediated Oxidative Stress (GPOS) in Neuropsychiatric Disorders
Huang, L., Tang, Y., & Sperlágh, B. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/1075440 · Cited by 9
Ma, P., Ding, Y., Xuan, L., Wang, L., Shi, J., Bai, J., Lin, M., Zheng, W., & Hou, Q. (2016) · Journal of Asian Natural Products Research · doi:10.1080/10286020.2016.1181622 · Cited by 9
Yun, H. K., Park, J., Chae, U., Lee, H., Huh, J., Lee, S., Bae, Y. C., & Lee, D. (2019) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2019.577044 · Cited by 9
Self-citationSadiq, N. B., Ryu, D. H., Cho, J. Y., Lee, A.-H., Song, D., Dorjsembe, B., Kim, J., Jung, J.-H., Nho, C. W., Hamayun, M., et al. (2021) · Molecules · doi:10.3390/molecules26154484 · Cited by 9
Cai, Y., Fan, Y., Wu, W., & Chen, W. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2025.1508661 · Cited by 8
The NF ‐ κB Signalling Pathway: Mechanisms, Consequences and Therapeutic Targets
Pourdad, B., & Pourdad, A. (2026) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.71229 · Cited by 8
Wei, X. L., Wang, D., Liu, J., Zhu, Q., Xu, Z., Niu, J., & Xu, W. (2024) · Nutrients · doi:10.3390/nu16081167 · Cited by 8
From immune response to mental health: neutrophils in schizophrenia
Obeagu, E. I., & Obeagu, G. U. (2024) · Annals of Medicine and Surgery · doi:10.1097/ms9.0000000000002744 · Cited by 8
Mining Complex Genetic Patterns Conferring Multiple Sclerosis Risk
Briggs, F. B. S., & Sept, C. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18052518 · Cited by 9
Bi, J., Li, J., Chen, S., Rao, J.-K., Xie, Y., Yang, H., Wang, L., & Cheng, B. (2019) · Journal of Functional Foods · doi:10.1016/j.jff.2019.05.050 · Cited by 8
Imipramine and Venlafaxine Differentially Affect Primary Glial Cultures of Prenatally Stressed Rats
Obuchowicz, E., Bielecka, A., Zielinski, M. W., Machnik, G., Gołyszny, M. J., & Ludyga, T. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01687 · Cited by 8
Colaço, M., Duarte, A., Zuzarte, M., Costa, B. F. O., & Borges, O. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.110500 · Cited by 8
Du, G., Zheng, K., Sun, C., Sun, M., Pan, J., Meng, D., Guan, W., & Zhao, H. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1522294 · Cited by 7
Prayoga, D. K., Aulifa, D. L., Budiman, A., Levita, J., & Jiranusornkul, S. (2025) · Journal of Experimental Pharmacology · doi:10.2147/jep.s524517 · Cited by 7
Xu, Q., Teng, Y., Huang, Y., Mu, J., Teng, L. A., Qian, H., Huang, Q., Liu, M., Zou, Y., Zhang, L., et al. (2025) · Advanced Science · doi:10.1002/advs.202506107 · Cited by 7
Akhmetzyanova, E. R., Rizvanov, A. A., & Mukhamedshina, Y. O. (2025) · Experimental Neurology · doi:10.1016/j.expneurol.2025.115523 · Cited by 8
Li, Y., Yin, S., Chen, X., Shi, F., Wang, J., & Yang, H. (2022) · Microbiology · doi:10.1099/mic.0.001210 · Cited by 7
Li, Q., Liu, X., Xing, R., & Sui, R. (2022) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.22-0060 · Cited by 7
The Emerging Role of Microglial Hv1 as a Target for Immunomodulation in Myelin Repair
Tang, Y., Wu, X., Li, J., Li, Y., Xu, X., Li, G., Zhang, P., Qin, C., Wu, L., Tang, Z., et al. (2023) · Aging and Disease · doi:10.14336/ad.2023.1107 · Cited by 7
Pb induces the release of CXCL10 and CCL2 chemokines via mtROS/NF-κB activation in BV-2 cells
Jiang, C., Li, X., Cui, X., & Ye, F. (2023) · Toxicology Letters · doi:10.1016/j.toxlet.2023.12.001 · Cited by 7
Trang, N. M., Vinh, L. B., Phong, N. V., & Yang, S. Y. (2024) · Planta Medica · doi:10.1055/a-2440-5166 · Cited by 7
Wagner, L. E., Melnyk, O., Muncy, A. N., Turner, A., Duffett, B. E., Muralidharan, C., Irizarry, M. M. M., Arvin, M. C., Orr, K. S., Wu, W., et al. (2026) · Science Translational Medicine · doi:10.1126/scitranslmed.adx7770 · Cited by 7
Shao, Q., Jiang, C., Xia, Y., Zhao, M., Zhang, Q., Jin, B., & Liu, J. (2019) · Europe PMC (PubMed Central) · Cited by 7
He, S.-F., Xue, J., Cao, P., Hou, J., Cui, Y. T., Chang, J., Huang, L., Han, Y., Duan, X., Tan, K., et al. (2021) · Inflammation · doi:10.1007/s10753-021-01603-y · Cited by 7
Zhang, J., Lai, Y., Zhu, L.-J., Lu, Z., Hu, C., Zhou, H., Lu, Z., Tang, Z., He, Z., & Tang, F. (2022) · Disease Markers · doi:10.1155/2022/2651105 · Cited by 7
Rubinstein, L., Kiffer, F. C., Puukila, S., Lowe, M. G., Goo, B., Luthens, A., Schreurs, A., Torres, S. M., Steczina, S., Tahimic, C. G. T., et al. (2022) · Life · doi:10.3390/life12111838 · Cited by 7
Badawy, M. M., Sayed-Ahmed, M. Z., Almoshari, Y., Alqahtani, S. S., Alshahrani, S., Mabrouk, H. A. A., Abd-Elsalam, M. M., Alkashif, K., Ahmad, S., El‐Sebaey, A. M., et al. (2023) · Toxics · doi:10.3390/toxics11040381 · Cited by 7
Tran, T. H. M., Lee, S., Huh, J., Perumalsamy, H., Balusamy, S. R., & Kim, Y.-J. (2023) · Journal of Functional Foods · doi:10.1016/j.jff.2023.105752 · Cited by 7
Abdelkader, G. S., El-Naenaeey, E.-S. Y., Abdallah, H. M., Zeid, E. H. A., Rehan, I. F., Zigo, F., & Elmowalid, G. A. (2025) · Frontiers in Veterinary Science · doi:10.3389/fvets.2025.1557671 · Cited by 6
Mohanta, O., Das, P. K., Panda, S. S., Sahoo, A., Jena, S., Ray, A., Nayak, S., & Panda, P. C. (2025) · Scientific Reports · doi:10.1038/s41598-025-17480-6 · Cited by 6
Ngo, T. H., Mishra, S. K., Kil, Y., Chen, Z., Choi, H., Chang, J., & Nam, J. (2025) · Phytochemical Analysis · doi:10.1002/pca.70032 · Cited by 6
Su, H., Tan, Y., Zhou, Z., Wang, C., Chen, W., Wang, J., & Sun, H. (2023) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2023.12068 · Cited by 6
Zhou, X. E., Lv, M., Duan, Z., Liu, W., Yan, F., Liu, J., & Cui, Y. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2300572 · Cited by 6
Trinh, T. T., Fadriquela, A., Lee, K., Bajgai, J., Sharma, S., Rahman, M. H., Kim, C.-S., Youn, S. H., & Jeon, H.-T. (2021) · Processes · doi:10.3390/pr9111928 · Cited by 6
Chronic allergy signaling: is it all stressed-out mitochondria?
Hussain, S.-R. A., & Grayson, M. H. (2022) · Faculty Reviews · doi:10.12703/r/11-37 · Cited by 6
Yanar, K. E., Gür, C., Değirmençay, Ş., Aydın, Ö., Aktaş, M. S., & Baysal, S. (2023) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2023.110706 · Cited by 6
Zhang, Y., Pang, X., & Yang, Y. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116454 · Cited by 6
Hua, Y., Dong, M., Xu, Y., He, N., Dai, X., & Li, K. (2015) · RSC Advances · doi:10.1039/c5ra16739f · Cited by 6
Jia, X., Yang, Y., Wang, Q., Tian, Y., Hong, Y., Tian, M., & Tang, D. (2023) · Arabian Journal of Chemistry · doi:10.1016/j.arabjc.2023.104952 · Cited by 6
Activated protein C inhibits lung injury induced by LPS via downregulating MAPK signaling
Zhou, J., Hu, R., Jing, S., Xue, X., & Tang, W. (2018) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2018.6228 · Cited by 6
Zhang, C., Yu, P., Ma, J., Zhu, L., Xu, A., & Zhang, J. (2019) · Inflammation · doi:10.1007/s10753-019-01089-9 · Cited by 6
Liu, J., Li, Z., Peng, X., Zhao, W., Chu, T., Ju, J., Ren, J., & Gao, F. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.106208 · Cited by 6
Kakkalide promotes spinal cord injury repair by regulating microglial M2 polarization via mitophagy.
You, T., Dai, B., Ding, X., He, Z., Peng, J.-F., Tao, S., Ye, L., Song, T., Fan, Z.-H., & Chen, N. (2026) · Phytomedicine · doi:10.1016/j.phymed.2026.157985 · Cited by 5
Microglial fructose metabolism is essential for glioblastoma growth
Billingham, L. K., DeLay, S. L., Eshac, Y., Chia, T.-Y., Tripathi, S., Olson, I. E., Zilinger, K., Subbiah, J., Wang, Z., Sadagopan, N. S., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2521256123 · Cited by 5
Brain mitochondria as key drivers of cognition and behaviour
Sandi, C., Lobo, M. K., Hollis, F., Hirabayashi, Y., de Juan‐Sanz, J., & Bolaños, J. P. (2026) · Nature reviews. Neuroscience · doi:10.1038/s41583-026-01061-1 · Cited by 5
Inhibitory Potential of the Drimane Sesquiterpenoids Isotadeonal and Polygodial in the NF-kB Pathway
Marín, V., Villegas, C., Ogundele, A. V., Cabrera‐Pardo, J. R., Schmidt, B., Paz, C., & Burgos, V. (2025) · Molecules · doi:10.3390/molecules30071555 · Cited by 5
Coordinated Transcriptional Waves Define the Inflammatory Response of Primary Microglial Culture
Zohar, K., Lezmi, E., Reichert, F., Eliyahu, T., Rotshenker, S., Weinstock, M., & Linial, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310928 · Cited by 5
Metadata
- Authors
- Park, J., Min, J.-S., Kim, B., Chae, U.-B., Yun, J. W., Choi, M.-S., Kong, I.-K., Chang, K.-T., & Lee, D.-S.
- Affiliations
- Kyungpook National University (KR)
- Daegu University (KR)
- Gyeongsang National University (KR)
- Korea Research Institute of Bioscience and Biotechnology (KR)
- Corresponding author
- Lee, Dong-Seok
- ORCID
- Venue
- Neuroscience Letters
- Publisher
- Elsevier BV
- Published
- 2015-01
- Volume
- 584
- Pages
- 191-196
- ISSN
- 0304-3940 (ISSN-L)
- OpenAlex
- W2042183116
- Cited by
- 529
- References
- 26
- Citations by year
- 2026: 53 · 2025: 37 · 2024: 59 · 2023: 64 · 2022: 64 · 2021: 47 · 2020: 51 · 2019: 54 · 2018: 43 · 2017: 23 · 2016: 18 · 2015: 15
- FWCI
- 9.69
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience Letters (publishedVersion)
- PubMed (publishedVersion)
- KRIBB Repository (submittedVersion)
- Funders
- National Research Foundation of Korea (NRF-2012R1A1A2008880, 112020-03-2-SB020)
- Korea Institute of Planning & Evaluation for Technology in Food, Agriculture, Forestry and Fisheries (2008-0062618)
- Korea Research Institute of Bioscience and Biotechnology (KGM4611411)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Keywords
- mitochondrial reactive oxygen species, microglial activation, lipopolysaccharide, pro-inflammatory response, MAPK signaling, NF-κB signaling, MitoTEMPO, ERK, JNK, p38 MAPK, TNF-α, IL-1β, interleukin-6, inducible nitric oxide synthase, cyclooxygenase-2, neuroinflammation, neurodegenerative diseases
- MeSH terms
- Animals, Cell Line, Inflammation, Lipopolysaccharides, Mitochondria, Organophosphorus Compounds, Piperidines, Signal Transduction, NF-kappa B, Reactive Oxygen Species, Microglia, Mitogen-Activated Protein Kinases, Extracellular Signal-Regulated MAP Kinases, p38 Mitogen-Activated Protein Kinases, MAP Kinase Kinase 4, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review