Park Bo-Kyung, Park Yang-Chun, Jung In Chul, Kim Seung-Hyung, Choi Jeong June, Do Moonho, Kim Sun Yeou, Jin Mirim
Laboratory of Pharmacology, College of Korean Medicine, Daejeon University, Daejeon 300-706, Republic of Korea.
Department of Internal Medicine, Daejeon Korean Medicine Hospital of Daejeon University, Daejeon 301-724, Republic of Korea.
J Ethnopharmacol. 2015 May 13;165:54-60. doi: 10.1016/j.jep.2015.02.040. Epub 2015 Feb 23.
Gamisasangja-tang (GST) is a traditional herbal formula prescribed for patients with intractable pruritus in association with various inflammatory skin diseases. To evaluate the effects of GST on pruritic skin inflammation and investigate its cellular and molecular mechanisms.
We orally administered GST to NC/Nga (NC) mice, an animal model of atopic dermatitis. Scratching frequency and the dermatitis index were evaluated, and histological examination was performed using hematoxylin and eosin and toluidine blue staining. The levels of interleukin (IL)-31 and T-helper cell type 2 (TH2) cytokines were determined in both the dorsal skin and cultured splenocytes by real-time polymerase chain reaction (PCR) and enzyme-linked immunosorbent assay (ELISA), respectively. The serum levels of chemokines and immunoglobulin E (IgE) were determined by ELISA. Changes in the inflammatory cell population were analyzed by a hemocytometer.
GST significantly lowered scratching frequency and inhibited increases in dermatitis index, thickness of epidermis/dermis and infiltration of chemokine (C-C motif) receptor 3 (CCR3)(+) and cluster of differentiation (CD)117(+)/FcεRIα (Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide)(+) cells in atopic skin. Both IL-31 mRNA expression and production were significantly reduced by GST, which was accomrease in the levels of IL-4, IL-5, and IL-13. Further, GST treatment suppressed the secretion of eotaxin, TARC (thymus and activation-regulated chemokine), IgE, and increases in the number of basophils and eosinophils in the blood.
GST may have potential as an effective treatment for pruritic skin disease such as atopic dermatitis.
加味苍桑汤(GST)是一种传统草药配方,用于治疗伴有各种炎症性皮肤病的顽固性瘙痒患者。为了评估GST对瘙痒性皮肤炎症的影响并研究其细胞和分子机制。
我们对特应性皮炎动物模型NC/Nga(NC)小鼠口服给予GST。评估抓挠频率和皮炎指数,并使用苏木精和伊红以及甲苯胺蓝染色进行组织学检查。分别通过实时聚合酶链反应(PCR)和酶联免疫吸附测定(ELISA)测定背部皮肤和培养的脾细胞中白细胞介素(IL)-31和2型辅助性T细胞(TH2)细胞因子的水平。通过ELISA测定趋化因子和免疫球蛋白E(IgE)的血清水平。用血细胞计数器分析炎症细胞群体的变化。
GST显著降低了抓挠频率,并抑制了特应性皮肤中皮炎指数、表皮/真皮厚度以及趋化因子(C-C基序)受体3(CCR3)(+)和分化簇(CD)117(+)/FcεRIα(IgE的Fc片段,高亲和力I,受体;α多肽)(+)细胞浸润的增加。GST显著降低了IL-31 mRNA表达和产生,同时IL-4、IL-5和IL-13水平增加。此外,GST处理抑制了嗜酸性粒细胞趋化因子、胸腺和活化调节趋化因子(TARC)、IgE的分泌以及血液中嗜碱性粒细胞和嗜酸性粒细胞数量的增加。
GST可能有潜力作为治疗特应性皮炎等瘙痒性皮肤病的有效药物。