Fumie Shiba, Shiiko Maekawara, Atsuko Inoue, Koji Ohta, Mutsumi Miyauchi
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The wound area was harvested 10 h after stomatitis induction, and gene expression associated with pain and inflammation was analyzed using qPCR. The dorsal root ganglia of the rat spinal cord were isolated, dispersed, and cultured to examine the inhibitory effect of EA on the K+-evoked release of neurotransmitter substance P. In the stomatitis/100*EA group, a significant reduction in wound size was observed compared with the stomatitis/physiological saline (PS) group, and the weight gain rate was considerably higher. The stomatitis/EA group revealed similar histological changes in the wound and wound size as the stomatitis/PS group; however, the weight gain rate was considerably higher on day 7. The stomatitis/EA group suppressed the expression of inflammatory cytokine mRNA, such as Tnf-α and Il-6, and Cox-2 mRNA in the wound area compared with the stomatitis/PS group. EA treatment reduced the upregulated substance P release from the dorsal root ganglia following high-concentration K+ stimulation. EA alleviates pain in a stomatitis model by suppressing inflammatory cytokine expression in the wound area and substance P release from primary sensory neurons. 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引用次数: 0
摘要
复发性口腔炎会导致溃疡,引起剧烈疼痛,给患者带来沉重负担。马钱子提取物(EA)是一种粗制药物,可促进分娩时会阴切开引起的粘膜伤口愈合并减轻疼痛。在此,我们在口腔炎仓鼠模型中阐明了马钱子提取物对伤口愈合和疼痛的影响。在诱导口腔炎后,通过在颊囊内注射醋酸,在伤口处持续施加两种不同剂量的 EA(口腔炎/100*EA 组和口腔炎/EA 组)。在诱导口腔炎后测量体重和伤口面积,并进行组织学评估。诱导口腔炎 10 小时后采集伤口面积,并使用 qPCR 分析与疼痛和炎症相关的基因表达。分离、分散和培养大鼠脊髓背根神经节,研究 EA 对 K+诱发的神经递质 P 物质释放的抑制作用。与口腔炎/生理盐水(PS)组相比,口腔炎/100*EA 组的伤口面积明显缩小,体重增加率也显著提高。口腔炎/EA 组的伤口组织学变化和伤口大小与口腔炎/生理盐水组相似,但第 7 天的体重增加率要高得多。与口腔炎/PS 组相比,口腔炎/EA 组抑制了伤口区域炎性细胞因子 mRNA(如 Tnf-α 和 Il-6)和 Cox-2 mRNA 的表达。在高浓度 K+ 刺激下,EA 可减少背根神经节上调的 P 物质释放。EA 可抑制伤口区域炎性细胞因子的表达和初级感觉神经元的 P 物质释放,从而减轻口腔炎模型中的疼痛。因此,使用含有 EA 的口腔护理产品有望抑制口腔炎疼痛。
Antinociceptive effect of Equisetum arvense extract on the stomatitis hamster model.
Recurrent aphthous stomatitis leads to ulcers that cause severe pain, which is a substantial burden on patients. Equisetum arvense extract (EA) is a crude drug that promotes wound healing of mucous membranes caused by perineal incision during childbirth and alleviates pain. Here, we elucidated the effects of EA on wound healing and pain in a stomatitis hamster model. After stomatitis induction, two different EA doses were continuously applied to the wound area through the intramucosal injection of acetic acid into the cheek pouch (stomatitis/100*EA group and stomatitis/EA group). The body weight and wound area were measured over time, and histological evaluation was performed after stomatitis induction. The wound area was harvested 10 h after stomatitis induction, and gene expression associated with pain and inflammation was analyzed using qPCR. The dorsal root ganglia of the rat spinal cord were isolated, dispersed, and cultured to examine the inhibitory effect of EA on the K+-evoked release of neurotransmitter substance P. In the stomatitis/100*EA group, a significant reduction in wound size was observed compared with the stomatitis/physiological saline (PS) group, and the weight gain rate was considerably higher. The stomatitis/EA group revealed similar histological changes in the wound and wound size as the stomatitis/PS group; however, the weight gain rate was considerably higher on day 7. The stomatitis/EA group suppressed the expression of inflammatory cytokine mRNA, such as Tnf-α and Il-6, and Cox-2 mRNA in the wound area compared with the stomatitis/PS group. EA treatment reduced the upregulated substance P release from the dorsal root ganglia following high-concentration K+ stimulation. EA alleviates pain in a stomatitis model by suppressing inflammatory cytokine expression in the wound area and substance P release from primary sensory neurons. Therefore, using oral care products containing EA is expected to suppress stomatitis pain.
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