Paeoniflorin suppressed IL-22 via p38 MAPK pathway and exerts anti-psoriatic effect

芍药苷 p38丝裂原活化蛋白激酶 银屑病 药理学 MAPK/ERK通路 免疫印迹 哈卡特 医学 脂多糖 化学 体外 免疫学 磷酸化 生物化学 色谱法 高效液相色谱法 基因
作者
Jinghong Yu,Zhicai Xiao,Ruizhi Zhao,Chuanjian Lu,Yuemei Zhang
出处
期刊:Life Sciences [Elsevier BV]
卷期号:180: 17-22 被引量:42
标识
DOI:10.1016/j.lfs.2017.04.019
摘要

The total glucosides of paeony (TGP) are used to treat psoriasis in the clinic. However, its active components and mechanisms are not clear. Paeoniflorin is the main constituent of TGP. Thus, the anti-psoriasis effect of paeoniflorin was studied, and its mechanism was explored.The effect of paeoniflorin was evaluated using a psoriasis-like model of guinea pigs. The levels of IL-6, IL-17A, IL-22, p38 MAPK, and ERK1/2 in HaCaT cells stimulated by lipopolysaccharide (LPS) were determined using RT-qPCR, enzyme linked immunosorbent assays (ELISAs) and western blot.Compared with the control group, the model group showed edema, redness, and lesions in the ear upon stimulation with propranolol hydrochloride, and the Baker Score increased by 7-fold. Paeoniflorin ameliorated the lesion and decreased the Baker Score by 37% (p<0.05). In vitro, paeoniflorin significantly inhibited the mRNA expression of IL-6, IL-17A and IL-22 at both 2.08 and 10.41μM (p<0.01), and paeoniflorin had a marginal effect on the protein expression of IL-17A and IL-6. However, it inhibited the protein expression of IL-22 significantly, with inhibition ratios of 48.5% and 47.8% at 2.08 and 10.41μM, respectively (p<0.05). This effect was achieved by inhibiting the phosphorylation of p38 MAPK.The results of this work demonstrated that paeoniflorin is the active components of TGP and support its use as a therapeutic compound for psoriasis therapy.

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