Yokukansankachimpihange对sds诱导小鼠瘙痒相关反应的抑制作用及其潜在机制

Qun Zhang, Tomoyo Imamura, Shota Yoshida, Lili Han, Seiwa Michihara, Ryuji Takahashi
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引用次数: 0

摘要

Yokukansankachimpihange (YKSCH)是一种中国配方,在日本被证明是一种有效的治疗瘙痒的特应性皮炎或慢性荨麻疹和干性湿疹患者的精神神经症状,如失眠。十二烷基硫酸钠(SDS)可能引起人类和动物的皮肤刺激。在局部重复使用10% SDS后,出现皮肤干燥、屏障破坏、皮炎和瘙痒等不良反应。因此,本研究通过对反复SDS刺激小鼠皮肤的止痒作用进行了研究,并试图阐明其作用机制。用10% SDS刺激ICR小鼠,并与口服YKSCH提取物共处理4天。第5天仅口服YKSCH提取物。最后一次应用SDS后24 h观察抓痕行为。免疫荧光法观察表皮内神经生长情况。使用酶联免疫吸附法测定表皮中的NGF浓度。采用实时荧光定量PCR检测双调节蛋白(Areg)和信号蛋白3A (Sema3A)的表达。在sds处理小鼠中,口服YKSCH (200-400 mg/kg)剂量依赖性地抑制瘙痒,显著减少表皮内神经生长,下调表皮Areg mRNA表达。上述结果提示黄芪多糖对sds诱导的小鼠瘙痒具有抗瘙痒作用。YKSCH的作用机制可能是通过下调Areg的表达而降低表皮内神经密度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitory Effects and Potential Mechanism of Yokukansankachimpihange on SDS-induced Itch-associated Responses in Mice
Yokukansankachimpihange (YKSCH) is a Chinese formula proven in Japan to be an effective treatment for pruritus in patients with atopic dermatitis or chronic urticaria and dry eczema with psychoneurotic symptoms, such as insomnia. Sodium dodecyl sulfate (SDS) may cause skin irritation in both humans and animals. Adverse effects, such as skin dryness, barrier destruction, dermatitis, and pruritus, developed following the repeated application of 10% SDS to a local site. Therefore, the present study investigated the antipruritic effects of YKSCH on skin irritation induced by a repeated SDS stimulation in mice and attempted to elucidate the underlying mechanism of action. ICR mice were stimulated with 10% SDS and co-treated with oral YKSCH extract for four days. Only oral YKSCH extract was administered on the fifth day. Scratching behavior was observed 24 h after the last application of SDS. Intraepidermal nerve growth was investigated by an immunofluorescence analysis. NGF concentrations in the epidermis were measured using an enzyme-linked immunosorbent assay. The expression of amphiregulin (Areg) and semaphorin 3A (Sema3A) was assessed by quantitative real-time PCR. The oral administration of YKSCH (200-400 mg/kg) dose-dependently suppressed pruritus, significantly reduced intraepidermal nerve growth, and down-regulated epidermal Areg mRNA expression in SDS-treated mice. These results suggest that YKSCH exerts antipruritic effects against SDS-induced pruritus in mice. The mechanism of action of YKSCH may involve reductions in intraepidermal nerve density due to the down-regulated expression of Areg.
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