Diao Ruohan, Duan Xingwu, L I Lingling, Q U Tiange, Feng Huishang, Chen Guangshan
{"title":"Intervention and mechanism of Xiaoyin Anshen Yin in treatment of psoriasis combined with sleep disorders.","authors":"Diao Ruohan, Duan Xingwu, L I Lingling, Q U Tiange, Feng Huishang, Chen Guangshan","doi":"10.19852/j.cnki.jtcm.2025.03.004","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To explore the therapeutic mechanisms of Xiaoyin Anshen Yin (, XYAS) in treating psoriasis associated with sleep focusing on melatonin and the regulation of the nuclear factor kappa-B (NF-κB) pathway.</p><p><strong>Methods: </strong>Forty Sprague-Dawley rats were randomly divided into four groups, and administered distilled water, XYAS and its two different disassembly prescriptions by gavage respectively. Four types of drug-containing serums corresponding to the four groups were then prepared. Tumor necrosis factor (TNF)-α stimulated HaCaT was used to establish a psoriasis cell model, and the serums and the retinoid related orphan receptor alpha (RORα) inverse agonist were used respectively to intervene in the model. Enzyme-linked immunosorbent assay was used to detect the levels of interleukin (IL)-6 and melatonin in each group; flow cytometry was used to detect the levels of reactive oxygen species (ROS), mitochondrial membrane potential, and apoptosis; Western blot was used to evaluate the levels of superoxide dismutase 2 (SOD2), cytochrome-c (Cyt-c), inhibitor of kappa-B alpha (IκBα), p65 and phosphorylated p65.</p><p><strong>Results: </strong>XYAS and its disassembly prescriptions inhibited the secretion of inflammatory factors such as IL-6, reduced the ROS content and Cyt-c expression, increased the mitochondrial membrane potential and SOD2 content, promoted the apoptosis in HaCaT cells and inhibited the activation of the NF-κB pathway. XYAS was also found increase the melatonin content. The above effects are beneficial in the treatment of psoriasis combined with sleep disorders. Meanwhile, XYAS no longer had a significant ameliorative effect after applying the RORα inverse agonist, suggesting that the therapeutic effect of XYAS is related to RORα.</p><p><strong>Conclusions: </strong>The results of this study confirm that XYAS can be utilized for the treatment of psoriasis combined with sleep disorders <i>via</i> inhibiting the NF-κB pathway, anti-inflammatory, antioxidant and pro-apoptotic, which is in part related to the regulatory role of melatonin and its receptor RORα.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"45 3","pages":"552-560"},"PeriodicalIF":0.0000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12134322/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19852/j.cnki.jtcm.2025.03.004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: To explore the therapeutic mechanisms of Xiaoyin Anshen Yin (, XYAS) in treating psoriasis associated with sleep focusing on melatonin and the regulation of the nuclear factor kappa-B (NF-κB) pathway.
Methods: Forty Sprague-Dawley rats were randomly divided into four groups, and administered distilled water, XYAS and its two different disassembly prescriptions by gavage respectively. Four types of drug-containing serums corresponding to the four groups were then prepared. Tumor necrosis factor (TNF)-α stimulated HaCaT was used to establish a psoriasis cell model, and the serums and the retinoid related orphan receptor alpha (RORα) inverse agonist were used respectively to intervene in the model. Enzyme-linked immunosorbent assay was used to detect the levels of interleukin (IL)-6 and melatonin in each group; flow cytometry was used to detect the levels of reactive oxygen species (ROS), mitochondrial membrane potential, and apoptosis; Western blot was used to evaluate the levels of superoxide dismutase 2 (SOD2), cytochrome-c (Cyt-c), inhibitor of kappa-B alpha (IκBα), p65 and phosphorylated p65.
Results: XYAS and its disassembly prescriptions inhibited the secretion of inflammatory factors such as IL-6, reduced the ROS content and Cyt-c expression, increased the mitochondrial membrane potential and SOD2 content, promoted the apoptosis in HaCaT cells and inhibited the activation of the NF-κB pathway. XYAS was also found increase the melatonin content. The above effects are beneficial in the treatment of psoriasis combined with sleep disorders. Meanwhile, XYAS no longer had a significant ameliorative effect after applying the RORα inverse agonist, suggesting that the therapeutic effect of XYAS is related to RORα.
Conclusions: The results of this study confirm that XYAS can be utilized for the treatment of psoriasis combined with sleep disorders via inhibiting the NF-κB pathway, anti-inflammatory, antioxidant and pro-apoptotic, which is in part related to the regulatory role of melatonin and its receptor RORα.
目的:探讨消阴安神饮(XYAS)治疗睡眠相关性银屑病的作用机制,重点探讨褪黑激素及核因子κ b (NF-κB)通路的调控作用。方法:将40只sd大鼠随机分为4组,分别灌胃蒸馏水、XYAS及其2种不同拆装方。然后制备四组对应的四种含药血清。采用肿瘤坏死因子(TNF)-α刺激HaCaT建立银屑病细胞模型,分别用血清和类视黄醇相关孤儿受体α (RORα)逆激动剂干预该模型。采用酶联免疫吸附法检测各组白细胞介素(IL)-6、褪黑素水平;流式细胞术检测活性氧(ROS)水平、线粒体膜电位和细胞凋亡;Western blot检测大鼠血清超氧化物歧化酶2 (SOD2)、细胞色素c (Cyt-c)、κ b α抑制剂(IκBα)、p65及磷酸化p65的表达水平。结果:XYAS及其分解方能抑制IL-6等炎症因子的分泌,降低ROS含量和Cyt-c表达,提高线粒体膜电位和SOD2含量,促进HaCaT细胞凋亡,抑制NF-κB通路的激活。XYAS还能增加褪黑素的含量。以上效果对银屑病合并睡眠障碍的治疗有益。同时,应用RORα逆转录激动剂后,XYAS不再有明显的改善作用,提示XYAS的治疗作用与RORα有关。结论:本研究结果证实XYAS可通过抑制NF-κB通路、抗炎、抗氧化、促凋亡等作用治疗银屑病合并睡眠障碍,其作用机制与褪黑激素及其受体RORα的调控作用有关。