World Journal of Emergency Medicine ›› 2023, Vol. 14 ›› Issue (6): 462-470.doi: 10.5847/wjem.j.1920-8642.2023.102
• Original Article • Previous Articles Next Articles
Shuang Xu1, Lang Guo2, Weijing Shao1, Licai Liang3, Tingting Shu4, Yuhan Zhang5, He Huang6, Guangqi Guo1, Qing Zhang7(), Peng Sun1()
Received:
2023-03-09
Accepted:
2023-06-20
Online:
2023-11-10
Published:
2023-11-01
Contact:
Qing Zhang, Email: Shuang Xu, Lang Guo, Weijing Shao, Licai Liang, Tingting Shu, Yuhan Zhang, He Huang, Guangqi Guo, Qing Zhang, Peng Sun. Vagus nerve stimulation protects against cerebral injury after cardiopulmonary resuscitation by inhibiting inflammation through the TLR4/NF-κB and α7nAChR/JAK2 signaling pathways[J]. World Journal of Emergency Medicine, 2023, 14(6): 462-470.
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URL: http://wjem.com.cn/EN/10.5847/wjem.j.1920-8642.2023.102
Figure 1.
Vagus nerve stimulation (VNS) treatment improved 72-hour survival and neurological recovery in mice after cardiac arrest/cardiopulmonary resuscitation (CA/CPR). (A) experimental procedure. The GTS-21 (α7nAChR agonist) (4 mg/kg) was injected 30 min before CA. The methyllycaconitine citrate (MLA, inhibitor of α7nAChR) (4 mg/kg) was given 30 min before CA. (B) Kaplan-Meier curves of cumulative survival 72 h after CA and CPR in the five groups. VNS significantly improves neurological deficit score (NDS) at 24 h (C), 48 h (D), and 72 h (E) after CA/CPR. Black points indicate values for individual mice; horizontal bars indicate mean with range values (**P < 0.01 vs. Sham group; *P < 0.05 vs. Sham group; #P < 0.05 vs. CPR group). ROSC: return of spontaneous circulation.
Figure 2.
Vagus nerve stimulation (VNS) markedly reduced pathological damage in mice after cardiac arrest/cardiopulmonary resuscitation (CA/CPR). (A) HE staining in hippocampal CA1 region of mice at the 72 h after return of spontaneous circulation (ROSC). Red square shows the hippocampus CA1 region (magnification 40×). Right panels are 10× magnification photomicrographs from the red square of left panel. Black arrows indicate the nuclear pyknosis. Scale bar is 25 μm. The serum concentrations of interleukin-6 (IL-6) (B), and tumor necrosis factor-α (TNF-α) (C) at 72 h after resuscitation. (n=3, *P<0.05 vs. Sham group, **P<0.01 vs. Sham group, ***P<0.001 vs. Sham group; #P< 0.05 vs. CPR group, ##P<0.01 vs. CPR group, ###P < 0.001 vs. CPR group; &P< 0.05 vs. MLA+VNS group, &&P< 0.01 vs. MLA+VNS group).
Figure 4.
Nicotine inhibited TLR4/NF-κB pathway by activating α7nAChR/JAK2 axis in BV-2 cell after ischemia/reperfusion (I/R). (A) Representative immunoblots of TLR4, α7nAChR, NF-κB p65, and p-NF-κB p65. (B) Quantitative analysis of TLR4, α7nAChR, NF-κB p65, and p-NF-κB p65 expression. The protein amount was normalized to GAPDH. (C) Representative immunoblots of TLR4, p-JAK2, JAK2, and α7nAChR. Quantitative analysis of TLR4, α7nAChR (D) and p-JAK2 (E) expression. (F) Immunostaining of TLR4 in BV-2 cells. TLR4 (red), DAPI (blue). **P < 0.01; ns: not significantly different.
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