Department of Dermatology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
The First Clinical Academy, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Bioengineered. 2022 Apr;13(4):11146-11155. doi: 10.1080/21655979.2022.2062090.
This study aimed to investigate whether shikonin combined with methotrexate could inhibit psoriasis progression by regulating the polarization of macrophages through and experiments. Imiquimod was administrated to the exposed skin of BALB/c mice, and shikonin and methotrexate suspension were also given by gavage. The erythema, scales and thickness were scored for mice lesions in each group, and the total score was obtained by adding the above three scores, and calculated as psoriasis area and severity index (PASI) score. The skin lesion tissue from mice was isolated and used for hematoxylin-eosin staining and immunohistochemistry assay. Drug-containing serum was prepared and administrated into mouse macrophage RAW264.7 cells, followed by simulation of LPS. The levels of tumor necrosis factor-α (TNF-α), Interleukin (IL)-1β, and IL-6 in cell supernatant were assessed using ELISA Kits and real-time PCR. In imiquimod-induced psoriasis mice, shikonin combined with methotrexate exerted protective effects by reducing erythema and PASI scores, decreasing backer score and epidermal thickness, and particularly regulating macrophage polarization. In LPS-stimulated RAW264.7 cells, shikonin combined with methotrexate regulated M1/M2 polarization and altered the levels of M1 markers. Shikonin combined with methotrexate inhibit psoriasis progression by regulating the polarization of macrophages, which may be useful in the treatment of psoriasis.
本研究旨在通过 和 实验,探讨紫草素联合甲氨蝶呤是否可以通过调节巨噬细胞的极化来抑制银屑病的进展。用咪喹莫特处理 BALB/c 小鼠的暴露皮肤,同时灌胃给予紫草素和甲氨蝶呤混悬液。对各组小鼠皮损进行红斑、鳞屑和厚度评分,将上述三项评分相加得到总评分,计算银屑病面积和严重程度指数(PASI)评分。分离小鼠皮损组织,进行苏木精-伊红染色和免疫组织化学检测。制备含药血清并给予小鼠巨噬细胞 RAW264.7 细胞,模拟 LPS。采用 ELISA 试剂盒和实时 PCR 检测细胞上清液中肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-1β和 IL-6 的水平。在咪喹莫特诱导的银屑病小鼠中,紫草素联合甲氨蝶呤通过降低红斑和 PASI 评分、减少背部评分和表皮厚度来发挥保护作用,特别调节了巨噬细胞极化。在 LPS 刺激的 RAW264.7 细胞中,紫草素联合甲氨蝶呤调节了 M1/M2 极化并改变了 M1 标志物的水平。紫草素联合甲氨蝶呤通过调节巨噬细胞的极化抑制银屑病的进展,这可能对银屑病的治疗有用。