Page 166 - GHES-2-3
P. 166
Global Health Economics and
Sustainability
Vagal tone restoration for LC
Disorders, 16:eCollection 2023. Tan Qi Hui, C., et al. (2024). Direct vagus nerve stimulation:
A new tool to control allergic airway inflammation through
https://doi.org/10.1177/17562864231180711
α7 nicotinic acetylcholine receptor. British Journal of
Pendse, M., De Selle, H., Vo, N., Quinn, G., Dende, C., Li, Y., Pharmacology, 181(13):1916-1934.
et al. (2023). Macrophages regulate gastrointestinal motility
through complement component 1q. Elife, 12:e78558. https://doi.org/10.1111/bph.16334
Siopi, E., Galerne, M., Rivagorda, M., Saha, S., Moigneu, C.,
https://doi.org/10.7554/eLife.78558
Moriceau, S., et al. (2023). Gut microbiota changes require
Petrisko, T.J., Gargus, M., Chu, S.H., Selvan, P., Whiteson, K.L., vagus nerve integrity to promote depressive-like behaviors
& Tenner, A.J. (2023). Influence of complement protein in mice. Molecular Psychiatry, 28(7):3002-3012.
C1q or complement receptor C5aR1 on gut microbiota
composition in wildtype and Alzheimer’s mouse models. https://doi.org/10.1038/s41380-023-02071-6
Journal of Neuroinflammation, 20(1):211. Van Westerloo, D.J., Giebelen, I.A.J., Meijers, J.C.M., Daalhuisen, J.,
De Vos, A.F., Levi, M., et al. (2006). Vagus nerve stimulation
https://doi.org/10.1186/s12974-023-02885-9
inhibits activation of coagulation and fibrinolysis during
Rangon, C.M. (2024). VNS in Long COVID. In: Vagus Nerve endotoxemia in rats. Journal of Thrombosis and Haemostasis,
Stimulation. United States: Academic Press Inc. 4(9):1997-2002.
Rangon, C.M., & Staats, P. (2024). Benefit of noninvasive vagus https://doi.org/10.1111/j.1538-7836.2006.02112.x
nerve stimulation in vaccine optimization for young Yang, Y., Yang, L.Y., Orban, L., Cuylear, D., Thompson, J., Simon, B.,
children. Microbes and Immunity, 1(1):2598.
et al. (2018). Non-invasive vagus nerve stimulation reduces
https://doi.org/10.36922/mi.2598 blood-brain barrier disruption in a rat model of ischemic
stroke. Brain Stimulation, 11(4):689-698.
Rangon, C.M., Barruet, R., Mazouni, A., Le Cossec, C., Thevenin, S.,
Guillaume, J., et al. (2021). Auricular neuromodulation for https://doi.org/10.1016/j.brs.2018.01.034
mass vagus nerve stimulation: Insights from SOS COVID-19 Zhang, D., Zhou, Y., Ma, Y., Chen, P., Tang, J., Yang, B., et al.
a multicentric, randomized, controlled, double-blind French (2023). Gut microbiota dysbiosis correlates with Long
pilot study. Frontiers in Physiology, 12:704599.
COVID-19 at one-year after discharge. Journal of Korean
https://doi.org/10.3389/fphys.2021.704599 Medical Science, 38(15):e120.
Rangon, C.M., Krantic, S., Moyse, E., & Fougère, B. (2020). The https://doi.org/10.3346/jkms.2023.38.e120
vagal autonomic pathway of COVID-19 at the crossroad Zheng, Z.S., Simonian, N., Wang, J., & Rosario, E.R. (2024),
of Alzheimer’s Disease and aging: A review of knowledge. Transcutaneous vagus nerve stimulation improves Long
Journal of Alzheimers Disease Reports, 4(1):537-551.
COVID symptoms in a female cohort: A pilot study.
https://doi.org/10.3233/ADR-200273 Frontiers in Neurology, 15:1393371.
Schedel, A., Thornton, S., Schloss, P., Klüter, H., & Bugert, P. https://doi.org/10.3389/fneur.2024.1393371
(2011). Human platelets express functional Alpha7-nicotinic Zhou, H., Liang, H., Li, Z.F., Xiang, H., Liu, W., & Li, J.G. (2013).
acetylcholine receptors. Arteriosclerosis, Thrombosis, and Vagus nerve stimulation attenuates intestinal epithelial
Vascular Biology, 31(4):928-934.
tight junctions disruption in endotoxemic mice through α7
https://doi.org/10.1161/ATVBAHA.110.218297 nicotinic acetylcholine receptors. Shock, 40(2):144-151.
Sévoz‐Couche, C., Liao, W., Foo, H.Y.C., Bonne, I., Lu, T.B., https://doi.org/10.1097/SHK.0b013e318299e9c0
Volume 2 Issue 3 (2024) 3 https://doi.org/10.36922/ghes.3556

