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五味子甲素、乙素和丙素对痤疮相关炎症的比较影响。

Comparative Effects of Schisandrin A, B, and C on Acne-Related Inflammation.

机构信息

State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, People's Republic of China.

Technology Center, Shanghai Inoherb Co. Ltd, 121 Chengyin Road, Shanghai, 200083, People's Republic of China.

出版信息

Inflammation. 2017 Dec;40(6):2163-2172. doi: 10.1007/s10753-017-0656-8.

Abstract

Inflammatory responses induced by Propionibacterium acnes are a major etiological factor in the pathogenesis of acne vulgaris. Schisandrin A, schisandrin B, and schisandrin C are the representative lignans of Schisandra chinensis (Turcz.) Baill. extract. Although anti-inflammatory effects of the lignans have been shown, their effects on acne-related inflammation caused by P. acnes have not been investigated and compared. We pretreated THP-1 human monocytic cells with 5, 10, and 20 μM schisandrin A, B, and C, and stimulated the cells with P. acnes. Schisandrin B and C inhibited the release of inflammatory cytokines at a concentration of 5 μM, while schisandrin A required a concentration of 10 μM to exert the effects. All of the schisandrins decreased the levels of toll-like receptor 2, and schisandrin B and C reduced the intracellular mRNA expression of the receptor gene. We also studied the influence of schisandrins on the MAPK signaling pathway. Schisandrin A suppressed the P. acnes-induced activation of JNK, while exerting only a weak effect on ERK and p38. Schisandrin B exerted a strong effect on p38, a lesser effect on ERK, and almost no effect on JNK. Schisandrin C inhibited the phosphorylation of all three proteins, especially ERK. Furthermore, the three lignans also prevented the nuclear translocation of NF-κB. These results contribute to our understanding of the mechanisms underlying the effects of the three lignans on P. acnes-induced inflammation and suggest that schisandrins might be developed as pharmacological agents for acne therapy.

摘要

痤疮丙酸杆菌诱导的炎症反应是寻常痤疮发病机制的一个主要病因。五味子甲素、五味子乙素和五味子丙素是五味子提取物的代表性木脂素。虽然已经证明了木脂素有抗炎作用,但它们对痤疮丙酸杆菌引起的炎症的影响尚未得到研究和比较。我们用 5、10 和 20μM 的五味子甲素、乙素和丙素预处理 THP-1 人单核细胞,然后用痤疮丙酸杆菌刺激细胞。五味子乙素和丙素在 5μM 浓度下抑制炎症细胞因子的释放,而五味子甲素则需要 10μM 才能发挥作用。所有木脂素均降低了 Toll 样受体 2 的水平,五味子乙素和丙素降低了受体基因的细胞内 mRNA 表达。我们还研究了木脂素对 MAPK 信号通路的影响。五味子甲素抑制了痤疮丙酸杆菌诱导的 JNK 激活,而对 ERK 和 p38 的作用较弱。五味子乙素对 p38 有很强的作用,对 ERK 的作用较弱,对 JNK 的作用几乎没有。五味子丙素抑制了所有三种蛋白质的磷酸化,尤其是 ERK。此外,这三种木脂素还阻止了 NF-κB 的核转位。这些结果有助于我们理解这三种木脂素对痤疮丙酸杆菌诱导的炎症的作用机制,并表明五味子素可能被开发为治疗痤疮的药物。

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