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右美托咪定预处理对功能性慢性内脏痛大鼠脊髓镇痛的机制

Mechanism of dexmedetomidine preconditioning on spinal cord analgesia in rats with functional chronic visceral pain.

作者信息

Li Jun, Tang Huizhong, Tu Weifeng

机构信息

Graduate student. Southern Medical University - Guangzhou, China.

MD. Department of Radiology - People's Hospital of Guangxi Zhuang Autonomous Region - Nanning, China.

出版信息

Acta Cir Bras. 2022 May 2;37(2):e370203. doi: 10.1590/acb370203. eCollection 2022.

Abstract

PURPOSE

To analyze the effect and mechanism of dexmedetomidine (DEX) analgesia pretreatment on functional chronic visceral pain in rats.

METHODS

Rats were divided into six groups: W1, W2, W3, W4, W5, and W6. The behavioral changes and electrophysiological indexes of rats in each group before and after DEX treatment were detected.

RESULTS

The levels of abdominal withdrawal reflex (AWR) in W5 and W6 groups were significantly lower than those in group W3, while the levels of thermal withdrawal latency (TWL) and mechanical withdrawal threshold (MWT) were significantly higher than those in group W3 (p < 0.05). The electromyographic signals of W1, W5, and W6 groups showed little fluctuation, while those of groups W2, W3, and W4 showed obvious fluctuation. TLR4 mRNA expression, IRF3, P65, and phosphorylation levels in W4, W5, and W6 groups were significantly lower than those in group W2 (p < 0.05).

CONCLUSIONS

Dexmedetomidine epidural anesthesia pretreatment could significantly inhibit visceral pain response in rats with functional chronic visceral pain, and its mechanism was related to the activation of TLR4 in spinal dorsal horn tissue of rats and the activation inhibition of IRF3 and P65 in the downstream key signals.

摘要

目的

分析右美托咪定(DEX)镇痛预处理对大鼠功能性慢性内脏痛的影响及机制。

方法

将大鼠分为六组:W1、W2、W3、W4、W5和W6。检测各组大鼠在DEX处理前后的行为变化和电生理指标。

结果

W5组和W6组的腹部退缩反射(AWR)水平显著低于W3组,而热退缩潜伏期(TWL)和机械退缩阈值(MWT)水平显著高于W3组(p<0.05)。W1、W5和W6组的肌电信号波动较小,而W2、W3和W4组的肌电信号波动明显。W4、W5和W6组的TLR4 mRNA表达、IRF3、P65及磷酸化水平显著低于W2组(p<0.05)。

结论

右美托咪定硬膜外麻醉预处理可显著抑制功能性慢性内脏痛大鼠的内脏痛反应,其机制与大鼠脊髓背角组织中TLR4的激活及下游关键信号中IRF3和P65的激活抑制有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8417/9064187/78654ca46a11/1678-2674-acb-37-2-e370203-gf01.jpg

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