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硫酸镁给药对大鼠慢性术后疼痛的影响。

Effects of magnesium sulfate administration in attenuating chronic postsurgical pain in rats.

机构信息

Department of Anesthesiology, Kanagawa Dental University Hospital, Yokosuka, Kanagawa, Japan.

Department of Anesthesiology, Kanagawa Dental University Hospital, Yokosuka, Kanagawa, Japan.

出版信息

Biochem Biophys Res Commun. 2021 Jan 1;534:395-400. doi: 10.1016/j.bbrc.2020.11.069. Epub 2020 Nov 25.

Abstract

Chronic postsurgical pain (CPSP) is a serious issue for many postoperative patients. Though there are numerous treatment options for the prevention of CPSP, none of them is optimal as the mechanisms of the transition from acute to chronic postoperative pain have not been elucidated. Ketamine and opioids have been administered for chronic postoperative pain treatment but induce severe adverse reactions and/or physical dependency. Here, we examined whether pre-administration of the nonselective N-methyl-d-aspartate (NMDA) receptor antagonist magnesium sulfate attenuates CPSP behavior and alters the expression of glutamate ionotropic receptor NMDA type subunit 1a (Grin1 mRNA) in a rat skin/muscle incision and retraction (SMIR) model. We assessed the effects of a single subcutaneous magnesium sulfate injection on nociceptive behaviors including guarding pain, mechanical hyperalgesia, and heat hypersensitivity in rats after SMIR surgery. We used reverse transcription-quantitative PCR (RT-qPCR) to evaluate Grin1 mRNA expression in the dorsal horn of the spinal cord on postoperative day 14. Compared with the vehicle, magnesium sulfate administration before SMIR surgery reduced mechanical hyperalgesia for 17 d Grin1 gene expression was significantly higher on the ipsilateral side than the contralateral side (P = 0.001) on postoperative day 14. The magnesium sulfate injection prevented Grin1 mRNA upregulation in the spinal cord dorsal horn. A single magnesium sulfate injection mitigated SMIR-induced mechanical hyperalgesia possibly by modulating Grin1 expression. Preoperative magnesium sulfate administration could prove to be a simple and safe CPSP treatment.

摘要

慢性术后疼痛(CPSP)是许多术后患者的严重问题。尽管有许多预防 CPSP 的治疗选择,但由于急性向慢性术后疼痛的转变机制尚未阐明,因此没有一种是最佳选择。氯胺酮和阿片类药物已被用于治疗慢性术后疼痛,但会引起严重的不良反应和/或身体依赖性。在这里,我们研究了预先给予非选择性 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂硫酸镁是否可以减轻 CPSP 行为,并改变谷氨酸离子型受体 NMDA 1a 亚基(Grin1 mRNA)在大鼠皮肤/肌肉切开和回缩(SMIR)模型中的表达。我们评估了单次皮下硫酸镁注射对 SMIR 手术后大鼠疼痛行为(包括保护疼痛、机械性痛觉过敏和热敏感)的影响。我们使用逆转录定量 PCR(RT-qPCR)评估术后第 14 天脊髓背角的 Grin1 mRNA 表达。与载体相比,SMIR 手术前给予硫酸镁可减轻机械性痛觉过敏 17 天 Grin1 基因表达在术后第 14 天明显高于同侧(P=0.001)。硫酸镁注射可防止脊髓背角 Grin1 mRNA 的上调。单次硫酸镁注射可减轻 SMIR 引起的机械性痛觉过敏,可能是通过调节 Grin1 表达。术前硫酸镁给药可能被证明是一种简单而安全的 CPSP 治疗方法。

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