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Electroacupuncture at Auricular Vagus Nerve Inhibits Neuroinflammation in Rats with Cerebral Ischemia/ Reperfusion Injury via Downregulating the TLR4-Mediated NF-?B Signaling Pathway

Jiaen Yang, Zixuan Ou, Ning Jia, Jiaqi Feng

Abstract


Objective: To explore the inhibitory effect of auricular vagus nerve electroacupuncture (VNS) on neuroinflammation in rats
with cerebral ischemia/reperfusion (I/R) injury and its association with the TLR4-mediated NF-?B signaling pathway. Methods: Seventytwo SPF-grade rats (220~250g) were randomly divided into control, sham operation, model (I/R), and electroacupuncture (VNS) groups
(18 rats each). The middle cerebral artery occlusion (MCAO) model was established by the Longa method. The VNS group received
electroacupuncture at the auricular concha region 30 minutes after ischemia, with continuous treatment for 4 days. Modified Neurological
Severity Score (mNSS) was used to evaluate neurological function at 24h and 72h post-surgery. At 72h, ELISA detected IL-1?, IL-6, and
TNF-? levels in the ischemic cortex; immunohistochemistry observed brain pathological damage; Western blot measured TLR4 and NF-
?B protein expressions. Results: Compared with the model group, the VNS group had significantly higher mNSS scores at 72h (P<0.001),
reduced pro-inflammatory factors (IL-1?, TNF-?), upregulated anti-inflammatory IL-6 (all P<0.001), alleviated brain pathological damage,
and downregulated TLR4 and NF-?B protein expressions (P<0.05). Conclusion: Auricular vagus nerve electroacupuncture inhibits neuroinflammation and improves neurological deficits in I/R rats by downregulating the TLR4-mediated NF-?B pathway, providing experimental evidence for ischemic stroke treatment.

Keywords


Auricular Vagus Nerve Stimulation; Cerebral Ischemia/Reperfusion Injury; TLR4; NF-?B Signaling Pathway

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References


[1] Jayaraj R L, Azimullah S, Beiram R, et al. Neuroinflammation: friend and foe for ischemic stroke [J]. J Neuroinflammation, 2019,

16(1): 142.

[2] Kerr N, Dietrich D W, Bramlett H M, et al. Sexually dimorphic microglia and ischemic stroke [J]. CNS Neurosci Ther, 2019, 25(12):

1308-1317.

[3] Erfani S, Khaksari M, Oryan S, et al. Nampt/PBEF/visfatin exerts neuroprotective effects against ischemia/reperfusion injury via modulation of Bax/Bcl-2 ratio and prevention of caspase-3 activation [J]. J Mol Neurosci, 2015, 56(1): 237-243.

[4] Arle JE, Carlson KW, Mei L. Investigation of mechanisms of vagus nerve stimulation for seizure using finite element modeling [J]. Epilepsy Res, 2016, 126: 109-118.

[5] Ay I, Lu J, Ay H, et al. Vagus nerve stimulation reduces infarct size in rat focal cerebral ischemia [J]. Neurosci Lett, 2009, 459(3): 147-151.

[6] Medzhitov R, Preston-Hurlburt P, Janeway C A Jr. A human homologue of the Drosophila Toll protein signals activation of adaptive immunity [J]. Nature, 1997, 388(6640): 394-397.

[7] Buchanan M M, Hutchinson M, Watkins L R, et al. Toll-like receptor 4 in CNS pathologies [J]. J Neurochem, 2010, 114(1): 13-27.

[8] Taetzsch T, Levesque S, Mcgraw C, et al. Redox regulation of NF-?B p50 and M1 polarization in microglia [J]. Glia, 2015, 63(3): 423-440.

[9] Mravec B. The role of the vagus nerve in stroke [J]. Auton Neurosci, 2010, 158(1-2): 8-12.

[10] Borovikova LV, Ivanova S, Zhang M, et al. Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin [J]. Nature, 2000, 405(6785): 458-462.

[11] Ottani A, Giuliani D, Mioni C, et al. Vagus nerve mediates the protective effects of melanocortins against cerebral and systemic damage

after ischemic stroke [J]. J Cereb Blood Flow Metab, 2009, 29(3): 512-523.




DOI: http://dx.doi.org/10.70711/mhr.v3i1.9010

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