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Schwann cell autophagy counteracts the onset and chronification of neuropathic pain
Abstract
Axonal degeneration in peripheral nerves after injury is accompanied by myelin degradation initiated by Schwann cells (SCs). These cells activate autophagy, a ubiquitous cytoprotective process essential for degradation and recycling of cellular constituents. Concomitantly to nerve insult and axonal degeneration, neuropathic pain (NeP) arises. The role of SC autophagy in the mechanisms underlying NeP is still unknown. In this study, we examined the role of the autophagy during the early phase of Wallerian degeneration in NeP induction and chronification by using a murine model of peripheral nerve lesion (chronic constriction injury). We demonstrate that the autophagy inducer rapamycin, administered in the first week after nerve damage, induces long-lasting analgesic and antiinflammatory effects, facilitates nerve regeneration, and prevents pain chronification. Conversely, when autophagy is altered, by means of autophagic inhibitor 3-methyladenine administration or as occurs in activating molecule in Beclin-1-regulated autophagy transgenic mice (Ambra1(+/gt)), NeP is dramatically enhanced and prolonged. Immunohistochemical and ultrastructural evaluations show that rapamycin is able to increase autophagic flux in SCs, to accelerate myelin compaction, and to reduce inflammatory and immune reaction. Proteomic analysis combined with bioinformatic analysis suggests that a redox-sensitive mechanism could be responsible for SC autophagy activation. These data suggest that a deficiency of autophagic activity in SCs can be an early event in the origin of NeP chronification and that autophagy modulation may represent a powerful pharmacological approach to prevent the onset and chronification of NeP in the clinical setting.
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“Conversely, stimulating Schwann cell autophagy with rapamycin promotes myelination and improves peripheral nerve regeneration [465,466].”
From Autophagy and ALS: mechanistic insights and therapeutic implications (2022) · cites this paper as [466]
Citations
Cites
Ethical guidelines for investigations of experimental pain in conscious animals.
Zimmermann, M. (1983) · Pain · doi:10.1016/0304-3959(83)90201-4 · Cited by 7,762
Acute-Phase Proteins and Other Systemic Responses to Inflammation
Gabay, C., & Kushner, I. (1999) · New England Journal of Medicine · doi:10.1056/nejm199902113400607 · Cited by 6,734
Autophagy: Renovation of Cells and Tissues
Mizushima, N., & Komatsu, M. (2011) · Cell · doi:10.1016/j.cell.2011.10.026 · Cited by 6,615
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
Klionsky, D. J., Abdelmohsen, K., Abe, A., Abedin, M. J., Abeliovich, H., Acevedo Arozena, A., Adachi, H., Adams, C. M., Adams, P. D., Adeli, K., et al. (2016) · Autophagy · doi:10.1080/15548627.2015.1100356 · Cited by 5,894
A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man
Bennett, G. J., & Xie, Y.-K. (1988) · Pain · doi:10.1016/0304-3959(88)90209-6 · Cited by 5,376
Guidelines for the use and interpretation of assays for monitoring autophagy
Klionsky, D. J., Abdalla, F. C., Abeliovich, H., Abraham, R. T., Acevedo-Arozena, A., Adeli, K., Agholme, L., Agnello, M., Agostinis, P., Aguirre-Ghiso, J. A., et al. (2012) · Autophagy · doi:10.4161/auto.19496 · Cited by 3,996 · cited 1×
“Some evidence shows that the mTOR complex 1 (mTORC1, constituted by mTOR, Raptor, and GbL) positively regulates Notch signalling [29] and that Ras-ERK and PI3K-mTORC1 pathways cross-talk extensively and regulate each other both positively and negatively [34].”
BackgroundAutophagy as a Regulated Pathway of Cellular Degradation
Klionsky, D. J., & Emr, S. D. (2000) · Science · doi:10.1126/science.290.5497.1717 · Cited by 3,630
The Ras-ERK and PI3K-mTOR pathways: cross-talk and compensation
Mendoza, M. C., Er, E. E., & Blenis, J. (2011) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2011.03.006 · Cited by 1,817
Autophagy modulation as a potential therapeutic target for diverse diseases
Rubinsztein, D. C., Codogno, P., & Levine, B. (2012) · Nature Reviews Drug Discovery · doi:10.1038/nrd3802 · Cited by 1,464
The cellular and molecular basis of peripheral nerve regeneration
Fu, S. Y., & Gordon, T. (1997) · Molecular Neurobiology · doi:10.1007/bf02740621 · Cited by 1,203
Cited by
Sorted by citations
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
Klionsky, D. J., Abdelmohsen, K., Abe, A., Abedin, M. J., Abeliovich, H., Acevedo Arozena, A., Adachi, H., Adams, C. M., Adams, P. D., Adeli, K., et al. (2016) · Autophagy · doi:10.1080/15548627.2015.1100356 · Cited by 5,894
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1
Klionsky, D. J., Abdel-Aziz, A. K., Abdelfatah, S., Abdellatif, M., Abdoli, A., Abel, S., Abeliovich, H., Abildgaard, M. H., Abudu, Y. P., Acevedo-Arozena, A., et al. (2021) · Autophagy · doi:10.1080/15548627.2020.1797280 · Cited by 2,897
Self-citationLi, R., Li, D., Wu, C., Ye, L., Wu, Y., Yuan, Y., Yang, S., Xie, L., Mao, Y., Jiang, T., et al. (2020) · Theranostics · doi:10.7150/thno.40919 · Cited by 292
Autophagy and ALS: mechanistic insights and therapeutic implications
Chua, J. P., De Calbiac, H., Kabashi, E., & Barmada, S. J. (2022) · Autophagy · doi:10.1080/15548627.2021.1926656 · Cited by 189
“Conversely, stimulating Schwann cell autophagy with rapamycin promotes myelination and improves peripheral nerve regeneration [465,466].”
BackgroundEmerging Role of Schwann Cells in Neuropathic Pain: Receptors, Glial Mediators and Myelination
Wei, Z., Fei, Y., Su, W., & Chen, G. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00116 · Cited by 179
Yerra, V. G., Kalvala, A. K., & Kumar, A. (2017) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2017.05.001 · Cited by 122
Combination of autophagy and NFE2L2/NRF2 activation as a treatment approach for neuropathic pain
Li, J., Tian, M., Hua, T., Wang, H., Yang, M., Li, W., Zhang, X., & Yuan, H. (2021) · Autophagy · doi:10.1080/15548627.2021.1900498 · Cited by 123
Cianfanelli, V., Zio, D. D., Bartolomeo, S. D., Nazio, F., Strappazzon, F., & Cecconi, F. (2015) · Journal of Cell Science · doi:10.1242/jcs.168153 · Cited by 105
Self-citationWang, Y., Shi, Y., Huang, Y., Liu, W., Cai, G., Huang, S., Zeng, Y., Ren, S., Zhan, H., & Wu, W. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01991-2 · Cited by 80
Huang, H.-C., Chen, L., Zhang, H.-X., Li, S.-F., Liu, P., Zhao, T.-Y., & Li, C.-X. (2016) · Journal of Molecular Neuroscience · doi:10.1007/s12031-015-0672-9 · Cited by 80
Vacca, V., Marinelli, S., Pieroni, L., Urbani, A., Luvisetto, S., & Pavone, F. (2016) · Scientific Reports · doi:10.1038/srep18980 · Cited by 74
Self-citationThe Role of Autophagy and Apoptosis in Neuropathic Pain Formation
Liao, M., Lu, K., Hsu, J., Lee, C., Cheng, M.-Y., & Ro, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052685 · Cited by 82
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Klionsky, D. J., Abdelmohsen, K., Abe, A., Abedin, J., Abeliovich, H., Acevedo‐Arozena, A., Adachi, H., Adams, C. M., Adams, P. D., Adeli, K., et al. (2016) · Kölner Universitäts PublikationsServer (Universität zu Köln) · doi:10.5167/uzh-131237 · Cited by 69
mTOR Kinase: A Possible Pharmacological Target in the Management of Chronic Pain
Lisi, L., Aceto, P., Navarra, P., & Russo, C. D. (2015) · BioMed Research International · doi:10.1155/2015/394257 · Cited by 71
Spinal Autophagy is Differently Modulated in Distinct Mouse Models of Neuropathic Pain
Berliocchi, L., Maiarù, M., Varano, G. P., Russo, R., Corasaniti, M. T., Bagetta, G., & Tassorelli, C. (2015) · Molecular Pain · doi:10.1186/1744-8069-11-3 · Cited by 63
Autophagy dysfunction in neuropathic pain
Liu, X., Zhu, M., Ju, Y., Li, A., & Sun, X. (2019) · Neuropeptides · doi:10.1016/j.npep.2019.03.005 · Cited by 63
Belgrad, J., Pace, R. D., & Fields, R. D. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1066-19.2019 · Cited by 63
ciRS-7 targeting miR-135a-5p promotes neuropathic pain in CCI rats via inflammation and autophagy
Cai, W., Zhang, Y., & Su, Z. (2020) · Gene · doi:10.1016/j.gene.2020.144386 · Cited by 56
Stress/cell death pathways, neuroinflammation, and neuropathic pain
Li, L., Li, T. X., Qu, X., Sun, G., Fu, Q., & Han, G. (2023) · Immunological Reviews · doi:10.1111/imr.13275 · Cited by 57
Potential Therapeutic Benefits of Maintaining Mitochondrial Health in Peripheral Neuropathies
Areti, A., Yerra, V. G., Komirishetty, P., & Kumar, A. (2016) · Current Neuropharmacology · doi:10.2174/1570159x14666151126215358 · Cited by 55
Visualizing Nerve Injury in a Neuropathic Pain Model with [18F]FTC-146 PET/MRI
Shen, B., Behera, D., James, M. L., Reyes, S. T., Andrews, L., Cipriano, P. W., Klukinov, M., Lutz, A. B., Mavlyutov, T. A., Rosenberg, J., et al. (2017) · Theranostics · doi:10.7150/thno.19378 · Cited by 53
Autophagy Inhibition Favors Survival of Rubrospinal Neurons After Spinal Cord Hemisection
Bisicchia, E., Latini, L., Cavallucci, V., Sasso, V., Nicolin, V., Molinari, M., D’Amelio, M., & Viscomi, M. T. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0031-z · Cited by 53
Self-citationProgranulin overexpression in sensory neurons attenuates neuropathic pain in mice: Role of autophagy
Altmann, C., Hardt, S., Fischer, C., Heidler, J., Lim, H., Häußler, A., Albuquerque, B., Zimmer, B., Möser, C. V., Behrends, C., et al. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.09.010 · Cited by 52
Gao, X., Gao, L., Kong, X., Zhang, Y.-N., Jia, S., & Meng, C. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109695 · Cited by 52
Connecting autophagy: AMBRA1 and its network of regulation
Cianfanelli, V., Nazio, F., & Cecconi, F. (2015) · Molecular & Cellular Oncology · doi:10.4161/23723548.2014.970059 · Cited by 49
Self-citationJin, G., Yue, R., He, S.-D., Hong, L.-M., Xu, Y., & Yu, C. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00989 · Cited by 48
Guo, J., Jing, P.-B., Wang, J., Zhang, R., Jiang, B., Gao, Y., & Zhang, Z. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.05.046 · Cited by 46
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Pieroni, L., Mortera, S. L., Greco, V., Sirolli, V., Ronci, M., Felaco, P., Fucci, G., Fulviis, S. D., Massoud, R., Sg, C., et al. (2015) · Molecular BioSystems · doi:10.1039/c5mb00058k · Cited by 44
Self-citationCoccurello, R., Nazio, F., Rossi, C., Angelis, F. D., Vacca, V., Giacovazzo, G., Procacci, P., Magnaghi, V., Ciavardelli, D., & Marinelli, S. (2018) · PLoS ONE · doi:10.1371/journal.pone.0208596 · Cited by 46
Self-citationReview: Myelin clearance is critical for regeneration after peripheral nerve injury
Yuan, Y., Wang, Y., Wu, S., & Zhao, M. Y. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.908148 · Cited by 49
Wu, L., Wang, X. J., Luo, X., Zhang, J., Zhao, X., & Qiu, C. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1427679 · Cited by 49
Schwann-Cell Autophagy, Functional Recovery, and Scar Reduction After Peripheral Nerve Repair
Ko, P., Yang, C.-C., Kuo, Y., Su, F., Hsu, T., Tu, Y., & Jou, I. (2018) · Journal of Molecular Neuroscience · doi:10.1007/s12031-018-1056-8 · Cited by 41
Electrical Muscle Stimulation Accelerates Functional Recovery After Nerve Injury
Fu, T., Jiang, L., Peng, Y., Li, Z., Liu, S., Lu, J., Zhang, F., & Zhang, J. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.10.052 · Cited by 41
Nazareth, L., John, J. A. S., Murtaza, M., & Ekberg, J. A. K. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.660259 · Cited by 42
Liu, Z., Chen, S., Qiu, C., Sun, Y., Li, W., Jiang, J., & Zhang, J. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00495 · Cited by 40
Autophagy: The missing link in diabetic neuropathy?
Yerra, V. G., Gundu, C., Bachewal, P., & Kumar, A. (2015) · Medical Hypotheses · doi:10.1016/j.mehy.2015.11.004 · Cited by 37
Hydrogen-Rich Saline Activated Autophagy via HIF-1α Pathways in Neuropathic Pain Model
Wang, H., Huo, X., Chen, H., Лі, Б., Liu, J., Ma, W., Wang, X., Xie, K., Yu, Y., & Shi, K. (2018) · BioMed Research International · doi:10.1155/2018/4670834 · Cited by 34
Jiang, Y., Liang, J., Li, R., Peng, Y., Huang, J., & Huang, L. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16274 · Cited by 33
Wang, N., Zhang, Y., Wang, J., & Luo, F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052648 · Cited by 31
Schwann cells as a target cell for the treatment of cancer pain
Zhang, W.-J., Wu, C., & Liu, J. (2023) · Glia · doi:10.1002/glia.24391 · Cited by 30
Clarke, J.-P. W. E., & Mearow, K. M. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23733 · Cited by 30
Chai, Y., Liu, Y., Liu, Z., Wei, W., Dong, Y., Yang, C., & Chen, M. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-03960-9 · Cited by 28
Fu, S., Sun, H., Wang, J., Gao, S., Zhu, L., Cui, K., Liu, S., Qi, X., Guan, R.-Q., Fan, X., et al. (2024) · Autophagy · doi:10.1080/15548627.2024.2330038 · Cited by 25
Functional roles of lncRNAs and its potential mechanisms in neuropathic pain
Tang, S., Zhou, J., Jing, H., Liao, M., Lin, S., Huang, Z., Huang, T., Zhong, J., & HanbingWang (2019) · Clinical Epigenetics · doi:10.1186/s13148-019-0671-8 · Cited by 26
Liu, Y.-D., Wang, Z., Han, G., & Zhao, P. (2017) · Europe PMC (PubMed Central) · Cited by 25
Klein, D., Groh, J., Yuan, X., Berve, K., Stassart, R. M., Fledrich, R., & Martini, R. (2022) · Glia · doi:10.1002/glia.24158 · Cited by 23
Role of autophagy in the pathogenesis and regulation of pain
Zheng, G., Ren, J., Shang, L., & Bao, Y. (2023) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2023.175859 · Cited by 24
Marinelli, S., Vacca, V., Angelis, F. D., Pieroni, L., Orsini, T., Parisi, C., Soligo, M., Protto, V., Manni, L., Guerrieri, R., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-45037-x · Cited by 24
Self-citationAxonal Degeneration in Dental Pulp Precedes Human Primary Teeth Exfoliation
Suzuki, K., Lovera, M. P., Schmachtenberg, O., & Couve, E. (2015) · Journal of Dental Research · doi:10.1177/0022034515593055 · Cited by 24
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Angelis, F. D., Vacca, V., Tofanicchio, J., Strimpakos, G., Giacovazzo, G., Pavone, F., Coccurello, R., & Marinelli, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232314503 · Cited by 21
Self-citationFeng, X., Deng, H.-B., Wang, Z.-G., Wu, Y., Ke, J.-J., & Feng, X.-B. (2018) · Neurochemical Research · doi:10.1007/s11064-018-2698-1 · Cited by 21
Liu, Y.-D., Wang, Z., Han, G., Jin, L., & Zhao, P. (2019) · Journal of Pain Research · doi:10.2147/jpr.s189353 · Cited by 21
Liu, Y.-D., Kuai, S., Ding, M., Wang, Z., Zhao, L., & Zhao, P. (2022) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2022.891803 · Cited by 19
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Xiao, H., Wei, C., Liu, H., Li, Z., Zheng, C., & Luo, J. F. (2023) · Phytotherapy Research · doi:10.1002/ptr.7862 · Cited by 19
Novel Approaches to Apoptosis-Inducing Therapies
Westhoff, M., Marschall, N., & Debatin, K. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-39406-0_8 · Cited by 19
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Chen, Y., Deng, H., & Zhang, N. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01948 · Cited by 20
Xu, X., Chen, R., Yu, Y., Yang, J., Lin, C., & Liu, R. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.111419 · Cited by 19
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Rita, A. D., & Strappazzon, F. (2016) · International review of cytology · doi:10.1016/bs.ircmb.2016.09.002 · Cited by 18
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Kim, H. W., Wang, S., Davies, A. J., & Oh, S. B. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2023.05.008 · Cited by 19
Osman, A. A. M., Dahlin, L. B., Thomsen, N., & Mohseni, S. (2014) · Diabetologia · doi:10.1007/s00125-014-3477-4 · Cited by 18
Angelis, F. D., Vacca, V., Pavone, F., & Marinelli, S. (2019) · European Journal of Pain · doi:10.1002/ejp.1493 · Cited by 17
Self-citationTchetina, E. V., Pivanova, A. N., Markova, G. A., Lukina, G. V., Aleksandrova, E. N., Aleksankin, A. P., Makarov, S. A., & Kuzin, A. N. (2016) · Arthritis · doi:10.1155/2016/4963950 · Cited by 17
Xiao, P., Chen, J.-Y., Zeng, Q., Huang, Z., Huang, B.-X., Yu, J., & Liao, S. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02861-z · Cited by 17
Safari, M. B., Nozad, A., Ghaffari, F., Ghavamzadeh, S., Alijaniha, F., & Naseri, M. (2020) · The Journal of Alternative and Complementary Medicine · doi:10.1089/acm.2019.0360 · Cited by 16
Levitan, D. M., Hitt, M. E., Geiser, D. R., & Lyman, R. (2021) · Journal of Small Animal Practice · doi:10.1111/jsap.13356 · Cited by 15
Chen, R., Xu, X., Yu, Y., Chen, Y., Lin, C., & Liu, R. (2024) · Scientific Reports · doi:10.1038/s41598-024-55095-5 · Cited by 15
Sampaolo, S., Esposito, T., Gianfrancesco, F., Napolitano, F., Lombardi, L., Lucà, R., Roperto, F. P., & Iorio, G. D. (2014) · Neuromuscular Disorders · doi:10.1016/j.nmd.2014.11.006 · Cited by 15
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Ronci, M., Leporini, L., Felaco, P., Sirolli, V., Pieroni, L., Greco, V., Aceto, A., Urbani, A., & Bonomini, M. (2018) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.201700140 · Cited by 15
Self-citationHu, B., Zhang, H., Xu, M., Li, L., Wu, M., Zhang, S., Liu, X., Xia, W., Xu, K., Xiao, J., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.778680 · Cited by 14
AMBRA1-regulated autophagy in vertebrate development
Antonioli, M., Albiero, F., Fimia, G. M., & Piacentini, M. (2015) · The International Journal of Developmental Biology · doi:10.1387/ijdb.150057mp · Cited by 16
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Inada, T., Sato, H., Hayashi, Y., Hitomi, S., Furukawa, A., Ando, M., Oshima, E., Otsuji, J., Taguchi, N., Shibuta, I., et al. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.05.033 · Cited by 13
Wang, Z., Liu, Y.-D., Wang, S., & Zhao, P. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.317989 · Cited by 13
Gao, N., Ma, B., Jia, H., Hao, C., Jin, T., & Liu, X. (2023) · Diabetic Medicine · doi:10.1111/dme.15090 · Cited by 13
Liao, M., Yeh, S.-R., Lu, K., Hsu, J., Chao, P.-K., Hsu, H., Peng, C.-H., Lee, Y.-L., Hung, Y.-H., & Ro, L. (2021) · Biomedicines · doi:10.3390/biomedicines9050542 · Cited by 14
Liu, J., & Wong, S. S. C. (2022) · Anesthesia & Analgesia · doi:10.1213/ane.0000000000006289 · Cited by 12
Qiu, X.-T., Guo, C., Ma, L., Li, X.-N., Zhang, Q.-Y., Huang, F., Zhang, M.-M., Bai, Y., Liang, G., & Li, Y.-Q. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1164426 · Cited by 11
Li, S., Guan, S., Wang, Y., Cheng, L., Yang, Q., Tian, Z., Zhao, M., Wang, X., & Feng, B. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.04.016 · Cited by 11
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Liu, X., Zhao, S., Zhao, Q., Chen, Y., Jia, S., Xiang, R., Zhang, J., Sun, J., Xu, Y., & Zhao, M. (2023) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2023.116570 · Cited by 10
Marinelli, S. (2025) · Toxicon · doi:10.1016/j.toxicon.2025.108250 · Cited by 9
Self-citationMaiarù, M., Petrini, A., Angelis, F. D., Nazio, F., & Marinelli, S. (2025) · Neurobiology of Pain · doi:10.1016/j.ynpai.2025.100200 · Cited by 10
Self-citationCheng, K., Chang, Y., Chu, L., Hsieh, S., An, L., Dai, Z., & Wu, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415873 · Cited by 9
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Schmitd, L. B., Hafner, H., Ward, A. L., Adib, E. A., Biscola, N. P., Kohen, R., Athaiya, M., Tuttle, M., Patel, M., Williamson, R. E., et al. (2025) · Science Translational Medicine · doi:10.1126/scitranslmed.adp9155 · Cited by 10
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Valek, L., Tran, B. N., & Tegeder, I. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.09.010 · Cited by 8
He, J., Wei, X., Wu, M., Song, Z.-B., Jiang, L., & Zhang, W. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03893-0 · Cited by 8
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Narasimhan, K. K. S., Chettiar, P. B., Kiritoshi, T., Ji, G., Neugebauer, V., & Dravid, S. M. (2025) · Autophagy · doi:10.1080/15548627.2025.2574968 · Cited by 9
Haynes, J., Joshi, A., Larue, R. C., Eisenmann, E. D., & Govindarajan, R. (2024) · Pharmaceutics · doi:10.3390/pharmaceutics16121592 · Cited by 9
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Metadata
- Authors
- Marinelli, S., Nazio, F., Tinari, A., Ciarlo, L., D'Amelio, M., Pieroni, L., Vacca, V., Urbani, A., Cecconi, F., Malorni, W., & Pavone, F.
- Affiliations
- University of Rome Tor Vergata (IT)
- Fondazione Santa Lucia (IT)
- Istituto Superiore di Sanità (IT)
- Corresponding author
- Pavone, Flaminia
- ORCID
- Venue
- Pain
- Published
- 2014-01
- Volume
- 155
- Issue
- 1
- Pages
- 93-107
- ISSN
- 0304-3959 (ISSN-L)
- OpenAlex
- W2078852360
- Cited by
- 119
- References
- 68
- Citations by year
- 2026: 3 · 2025: 11 · 2024: 11 · 2023: 16 · 2022: 15 · 2021: 11 · 2020: 9 · 2019: 9 · 2018: 8 · 2017: 3 · 2016: 12 · 2015: 9 · 2014: 2
- FWCI
- 5.32
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Pain (publishedVersion)
- PubMed (publishedVersion)
- Cineca Institutional Research Information System (Tor Vergata University) (submittedVersion)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Pain Mechanisms and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Keywords
- Schwann cells, autophagy, neuropathic pain, pain chronification, Wallerian degeneration, chronic constriction injury, rapamycin, myelin degradation, axonal degeneration, nerve regeneration, Beclin-1, 3-methyladenine, redox signaling, neuroinflammation, peripheral nerve injury
- MeSH terms
- Adenine, Animals, Autophagy, Disease Models, Animal, Gene Expression Regulation, Glial Fibrillary Acidic Protein, Immunosuppressive Agents, Mice, Transgenic, Microtubule-Associated Proteins, Pain Measurement, Schwann Cells, Sciatic Nerve, Sciatica, Time Factors, Sirolimus, CD11b Antigen, Adaptor Proteins, Signal Transducing, Green Fluorescent Proteins, Mice
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