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Modulation of neuroinflammation and memory dysfunction using percutaneous vagus nerve stimulation in mice
Open accessAbstract
BACKGROUND: The vagus nerve is involved in regulating immunity and resolving inflammation. Current strategies aimed at modulating neuroinflammation and cognitive decline, in many cases, are limited and ineffective. OBJECTIVE: We sought to develop a minimally invasive, targeted, vagus nerve stimulation approach (pVNS), and we tested its efficacy with respect to microglial activation and amelioration of cognitive dysfunction following lipopolysaccharide (LPS) endotoxemia in mice. METHODS: We stimulated the cervical vagus nerve in mice using an ultrasound-guided needle electrode under sevoflurane anesthesia. The concentric bipolar needle electrode was percutaneously placed adjacent to the carotid sheath and stimulation was verified in real-time using bradycardia as a biomarker. Activation of vagal fibers was confirmed with immunostaining in relevant brainstem structures, including the dorsal motor nucleus and nucleus tractus solitarius. Efficacy of pVNS was evaluated following administration of LPS and analyses of changes in inflammation and behavior. RESULTS: pVNS enabled stimulation of the vagus nerve as demonstrated by changes in bradycardia and histological evaluation of c-Fos and choline acetyltransferase expression in brainstem nuclei. Following LPS administration, pVNS significantly reduced plasma levels of tumor necrosis factor-α at 3 h post-injection. pVNS prevented LPS-induced hippocampal microglial activation as analyzed by changes in Iba-1 immunoreactivity, including cell body enlargement and shortened ramifications. Cognitive dysfunction following endotoxemia was also restored by pVNS. CONCLUSION: Targeted cervical VNS using this novel percutaneous approach reduced LPS-induced systemic and brain inflammation and significantly improved cognitive responses. These results provide a novel therapeutic approach using bioelectronic medicine to modulate neuro-immune interactions that affect cognition.
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“Peripheral inflammation triggers central cytokine release via vagus nerve-mediated signal transduction, forming a vicious neuro-immune cycle [94].”
From Research Advances in the Pathogenesis of Sepsis-Associated Encephalopathy (2026) · cites this paper as [94]
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“Cholinergic system dysfunction is manifested by reduced ChAT-positive neurons and abnormal AChE activity, leading to dysregulated microglial activation thresholds and accelerated transformation towards neurotoxic phenotypes [94].”
From Research Advances in the Pathogenesis of Sepsis-Associated Encephalopathy (2026) · cites this paper as [94]
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“Cholinergic system dysfunction is manifested by reduced ChAT-positive neurons and abnormal AChE activity, leading to dysregulated microglial activation thresholds and accelerated transformation towards neurotoxic phenotypes [94].”
From Research Advances in the Pathogenesis of Sepsis-Associated Encephalopathy (2026) · cites this paper as [94]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Cholinergic system dysfunction is manifested by reduced ChAT-positive neurons and abnormal AChE activity, leading to dysregulated microglial activation thresholds and accelerated transformation towards neurotoxic phenotypes [94].”
From Research Advances in the Pathogenesis of Sepsis-Associated Encephalopathy (2026) · cites this paper as [94]
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Citations
Cites
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
Neuroinflammation in Alzheimer's disease
Heneka, M. T., Carson, M. J., Khoury, J. E., Landreth, G. E., Brosseron, F., Feinstein, D. L., Jacobs, A. H., Wyss-Coray, T., Vitorica, J., Ransohoff, R. M., et al. (2015) · The Lancet Neurology · doi:10.1016/s1474-4422(15)70016-5 · Cited by 6,226
Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin
Borovikova, L. V., Ivanova, S., Zhang, M., Yang, H., Botchkina, G. I., Watkins, L. R., Wang, H., Abumrad, N., Eaton, J. W., & Tracey, K. J. (2000) · Nature · doi:10.1038/35013070 · Cited by 4,211
ATP mediates rapid microglial response to local brain injury in vivo
Davalos, D., Grutzendler, J., Yang, G., Kim, J. V., Zuo, Y., Jung, S., Littman, D. R., Dustin, M. L., & Gan, W.-B. (2005) · Nature Neuroscience · doi:10.1038/nn1472 · Cited by 3,913
Nicotinic acetylcholine receptor α7 subunit is an essential regulator of inflammation
Wang, H., Yu, M., Ochani, M., Amella, C. A., Tanovic, M., Susarla, S., Li, J. H., Wang, H., Yang, H., Ulloa, L., et al. (2003) · Nature · doi:10.1038/nature01339 · Cited by 3,228
Microglia Function in the Central Nervous System During Health and Neurodegeneration
Colonna, M., & Butovsky, O. (2017) · Annual Review of Immunology · doi:10.1146/annurev-immunol-051116-052358 · Cited by 2,894
Acetylcholine-Synthesizing T Cells Relay Neural Signals in a Vagus Nerve Circuit
Rosas-Ballina, M., Olofsson, P. S., Ochani, M., Valdés-Ferrer, S. I., Levine, Y. A., Reardon, C., Tusche, M. W., Pavlov, V. A., Andersson, U., Chavan, S., et al. (2011) · Science · doi:10.1126/science.1209985 · Cited by 1,551
Control of microglial neurotoxicity by the fractalkine receptor
Cardona, A. E., Pioro, E. P., Sasse, M. E., Kostenko, V., Cardona, S. M., Dijkstra, I. M., Huang, D., Kidd, G., Dombrowski, S., Dutta, R., et al. (2006) · Nature Neuroscience · doi:10.1038/nn1715 · Cited by 1,531
Functional and chemical anatomy of the afferent vagal system
Berthoud, H.-R., & Neuhuber, W. L. (2000) · Autonomic Neuroscience · doi:10.1016/s1566-0702(00)00215-0 · Cited by 1,280
O'Connor, J. C., Lawson, M. A., André, C., Moreau, M., Lestage, J., Castanon, N., Kelley, K. W., & Dantzer, R. (2009) · Molecular Psychiatry · doi:10.1038/sj.mp.4002148 · Cited by 1,278
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Subramaniyan, S., & Terrando, N. (2019) · Anesthesia & Analgesia · doi:10.1213/ane.0000000000004053 · Cited by 462
Self-citationFarmer, A. D., Strzelczyk, A., Finisguerra, A., Gourine, A. V., Gharabaghi, A., Hasan, A., Burger, A. M., Jaramillo, A. M., Mertens, A., Majid, A., et al. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2020.568051 · Cited by 375
TREAT AF (Transcutaneous Electrical Vagus Nerve Stimulation to Suppress Atrial Fibrillation)
Stavrakis, S., Stoner, J. A., Humphrey, M. B., Morris, L. M., Filiberti, A., Reynolds, J. C., Elkholey, K., Javed, I., Twidale, N., Riha, P., et al. (2020) · JACC. Clinical electrophysiology · doi:10.1016/j.jacep.2019.11.008 · Cited by 247
Neuroprotection by dihydrotestosterone in LPS-induced neuroinflammation
Yang, L., Zhou, R., Tong, Y., Chen, P., Shen, Y., Miao, S., & Liu, X. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104814 · Cited by 249
Vagus nerve stimulation in brain diseases: Therapeutic applications and biological mechanisms
Wang, Y., Zhan, G., Cai, Z., Jiao, B., Zhao, Y., Li, S., & Luo, A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.04.018 · Cited by 211
Perioperative Neurocognitive Disorder
Eckenhoff, R. G., Maze, M., Xie, Z., Culley, D. J., Goodlin, S. J., Zuo, Z., Wei, H., Whittington, R. A., Terrando, N., Orser, B. A., et al. (2019) · Anesthesiology · doi:10.1097/aln.0000000000002956 · Cited by 181
Self-citationMicroglia and Neurodevelopmental Disorders
Lukens, J. R., & Eyo, U. B. (2022) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-110920-023056 · Cited by 171
Sepsis‐Induced Brain Dysfunction: Pathogenesis, Diagnosis, and Treatment
Pan, S., Lv, Z., Wang, R., Shu, H., Yuan, S., Yu, Y., & Shang, Y. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/1328729 · Cited by 169
Thompson, S. L., O’Leary, G. H., Austelle, C. W., Gruber, E., Kahn, A. T., Manett, A. J., Short, B., & Badran, B. W. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.709436 · Cited by 160
Inflammation in Neurological Disorders: The Thin Boundary Between Brain and Periphery
Cervellati, C., Trentini, A., Pecorelli, A., & Valacchi, G. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8076 · Cited by 140
Xiao, M., Liu, C. X., Zhou, L. G., Yang, Y., & Wang, Y. (2023) · Medicine · doi:10.1097/md.0000000000032991 · Cited by 140
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Narengaowa, Kong, W., Lan, F., Awan, M. U. F., Qing, H., & Ni, J. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.633735 · Cited by 134
Balasubramanian, R., Schneider, E., Gunnigle, E., Cotter, P. D., & Cryan, J. F. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105562 · Cited by 143
Jiao, W., Lin, J., Deng, Y., Ji, Y., Liang, C., Wei, S., Xi, J., & Yan, F. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03312-3 · Cited by 132
Stavrakis, S., Elkholey, K., Morris, L. M., Niewiadomska, M., Asad, Z. U. A., & Humphrey, M. B. (2022) · Journal of the American Heart Association · doi:10.1161/jaha.121.023582 · Cited by 111
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Shi, Y., Wei, B., Li, L., Wang, B., & Sun, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.932152 · Cited by 108
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Singh, A., Dawson, T. M., & Kulkarni, S. (2021) · Journal of Clinical Investigation · doi:10.1172/jci143775 · Cited by 104
Forte, N. R., Fernández-Rilo, A. C., Palomba, L., Marzo, V. D., & Cristino, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21051554 · Cited by 105
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Fang, Y., Lin, Y.-T., Tseng, W.-L., Tseng, P. H., Hua, G.-L., Chao, Y., & Wu, Y. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1173987 · Cited by 102
Chang, E. H., Chavan, S. S., & Pavlov, V. A. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00263 · Cited by 98
Xin, Y., Tian, M., Deng, S., Li, J., Yang, M., Gao, J., Pei, X., Wang, Y., Tan, J., Zhao, F., et al. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-03148-z · Cited by 102
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Chen, Q.-Q., Haikal, C., Li, W., & Li, J. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00218 · Cited by 88
Pavlov, V. A., Chavan, S. S., & Tracey, K. J. (2019) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a034140 · Cited by 85
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Alexaki, V. I. (2021) · Cells · doi:10.3390/cells10071584 · Cited by 84
Yang, H., Shi, W., Fan, J., Wang, T., Song, Y., Lian, Y., Shan, W., & Wang, Q. (2023) · Neurotherapeutics · doi:10.1007/s13311-023-01353-9 · Cited by 76
Wang, Y., Tan, Q., Pan, M., Yu, J., Wu, S., Tu, W., Li, M., & Jiang, S. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112030 · Cited by 63
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Ge, T., Yao, X., Zhao, H., Yang, W., Zou, X., Peng, F., Li, B., & Cui, R. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105909 · Cited by 62
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Namgung, U., Kim, K.-J., Jo, B.-G., & Park, J.-M. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02396-z · Cited by 59
Chen, H., Feng, Z., Min, L., Deng, W., Tan, M., Hong, J., Gong, Q., Zhang, D., Liu, H., & Hou, J. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.813472 · Cited by 56
Borsom, E. M., Lee, K., & Cope, E. K. (2020) · Brain Sciences · doi:10.3390/brainsci10110814 · Cited by 56
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Ma, J., Qiao, P., Li, Q., Wang, Y., Zhang, L., Yan, L., & Cai, Z. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104539 · Cited by 53
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Wang, X., Wen, X., Yuan, S., & Zhang, J. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106499 · Cited by 47
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Slater, C. L., & Wang, Q. (2021) · Clinical and Translational Medicine · doi:10.1002/ctm2.397 · Cited by 47
Zhang, Z., Ma, Q., Velagapudi, R., Barclay, W. E., Rodriguiz, R. M., Wetsel, W. C., Yang, T., Shinohara, M. L., & Terrando, N. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.856254 · Cited by 44
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Xin, Y., Wang, J.-X., & Xu, A. (2022) · Acupuncture in Medicine · doi:10.1177/09645284221076515 · Cited by 46
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Xia, X., Duan, Y., Wang, Y., Han, R.-X., Dong, Y., Jiang, S.-Y., Zheng, Y., Qiao, C., Cao, L., Xiao, L., et al. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-024-01245-4 · Cited by 45
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Vázquez-Oliver, A., Brambilla-Pisoni, C., Domingo-Gainza, M., Maldonado, R., Ivorra, A., & Ozaita, A. (2019) · Brain Stimulation · doi:10.1016/j.brs.2019.12.024 · Cited by 34
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Lai, I. K., Valdearcos, M., Morioka, K., Saxena, S., Feng, X., Li, R., Uchida, Y., An, L., Li, W., Pan, J. Z., et al. (2020) · British Journal of Anaesthesia · doi:10.1016/j.bja.2020.05.018 · Cited by 37
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Menden, A., Hall, D., Hahn-Townsend, C., Broedlow, C. A., Joshi, U., Pearson, A., Crawford, F., Evans, J. E., Klatt, N. R., Crynen, S., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-08840-7 · Cited by 22
Hosomoto, K., Sasaki, T., Yasuhara, T., Kameda, M., Sasada, S., Kin, I., Kuwahara, K., Kawauchi, S., Okazaki, Y., Yabuno, S., et al. (2023) · Brain stimulation · doi:10.1016/j.brs.2023.03.003 · Cited by 22
Rodenkirch, C., & Wang, Q. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/ab6b84 · Cited by 21
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Levine, Y. A., Faltys, M. A., & Chernoff, D. (2019) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a034330 · Cited by 22
Zhou, Q., Zheng, Z., Wang, X., Li, W., Wang, L., Yin, C., Zhang, Q., & Wang, Q. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03871-6 · Cited by 20
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Ji, M., Gao, Y.-Z., Shi, C., Wu, X., & Yang, J. (2023) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2023.2250917 · Cited by 22
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Adler, B. L., Chung, T., Rowe, P. C., & Aucott, J. N. (2024) · Frontiers in Neurology · doi:10.3389/fneur.2024.1344862 · Cited by 21
Sun, Y., Jiang, X., Lü, B., Gao, Q., Chen, Y.-F., Wu, D., Zeng, W., Yang, L., Li, H.-H., & Yu, B. (2020) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-020-3274-5 · Cited by 20
Luo, Q., Ma, H., Guo, E., Yu, L., Jia, L., Zhang, B., Feng, G., & Liu, R. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.909828 · Cited by 18
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Bonfante, S., Netto, M. B., de Oliveira, A. N., Mathias, K., Machado, R. S., Joaquim, L. D. S., Cidreira, T., da Silva, M. G., Daros, G. C., Danielski, L. G., et al. (2024) · Metabolic Brain Disease · doi:10.1007/s11011-024-01425-5 · Cited by 19
Li, T., Guo, M., Xie, P., Liu, S., & Luan, G. (2022) · Current Neuropharmacology · doi:10.2174/1570159x20666220706100136 · Cited by 19
Yan, Q., Chen, J., Ren, X., Song, Y., Xu, J., Xuan, S., Jiang, X., Kuang, Z., & Tang, Z. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.08.026 · Cited by 19
Park, E. Y., Lyon, J. G., Alvarado‐Velez, M., Betancur, M. I., Mokarram, N., Shin, J. H., & Bellamkonda, R. V. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24834 · Cited by 17
Venkatasamy, L., Nizamutdinov, D., Jenkins, J., & Shapiro, L. A. (2021) · Neuroscience Insights · doi:10.1177/26331055211018456 · Cited by 18
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Xiong, J., Wang, H., Bao, Y., Guo, Y., & Sun, Y. (2019) · BMC Anesthesiology · doi:10.1186/s12871-019-0885-5 · Cited by 17
Veiz, E., Kieslich, S.-K., Czesnik, D., Herrmann‐Lingen, C., Meyer, T., & Staab, J. (2022) · NeuroImmunoModulation · doi:10.1159/000524646 · Cited by 16
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Metadata
- Authors
- Huffman, W. J., Subramaniyan, S., Rodriguiz, R. M., Wetsel, W. C., Grill, W. M., & Terrando, N.
- Affiliations
- Duke University (US)
- Corresponding author
- Terrando, Niccolò
- ORCID
- Venue
- Brain Stimulation
- Publisher
- Elsevier BV
- Published
- 2019-01
- Volume
- 12
- Issue
- 1
- Pages
- 19-29
- ISSN
- 1876-4754 (ISSN-L)
- 1935-861X
- PMC
- PMC6301148
- OpenAlex
- W2897533172
- Cited by
- 181
- References
- 49
- Citations by year
- 2026: 17 · 2025: 27 · 2024: 22 · 2023: 29 · 2022: 33 · 2021: 24 · 2020: 18 · 2019: 11
- FWCI
- 5.94
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Brain stimulation (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Institute on Aging (R21AG055877, R01AG057525)
- Topics
- Life Sciences › Neuroscience › Neurology › Vagus Nerve Stimulation Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Keywords
- neuroinflammation, memory impairment, microglial activation, hippocampus, bioelectronic medicine, neuroimmune interactions, TNF-α, dorsal motor nucleus of the vagus, nucleus tractus solitarius, cognitive impairment
- MeSH terms
- Animals, Inflammation, Lipopolysaccharides, Male, Cytokines, Solitary Nucleus, Endotoxemia, Mice, Vagus Nerve Stimulation, Cognitive Dysfunction
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