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水杨酸通过抑制皮脂细胞中的 AMPK/SREBP1 通路来治疗寻常痤疮。

Salicylic acid treats acne vulgaris by suppressing AMPK/SREBP1 pathway in sebocytes.

机构信息

Department of Dermatology, West China Hospital, Sichuan University, Chengdu, China.

State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy, Chengdu, China.

出版信息

Exp Dermatol. 2019 Jul;28(7):786-794. doi: 10.1111/exd.13934. Epub 2019 May 15.

Abstract

Acne vulgaris is a prevalent cutaneous disease characterized by a multifactorial pathogenic process including hyperseborrhea, inflammation, over-keratinization of follicular keratinocytes and Propionibacterium acnes (P acnes) overgrowth. Salicylic acid (SA), a beta-hydroxy acid, is frequently used in the treatment of acne. SA has been found to decrease skin lipids and to possess anti-inflammatory properties. However, few studies have elucidated the mechanisms and pathways involved in such treatment of acne. In this study, we initially investigated the anti-acne properties of SA in human SEB-1 sebocytes. Treatment with SA decreased sebocyte lipogenesis by downregulating the adenosine monophosphate-activated protein kinase (AMPK)/sterol response element-binding protein-1 (SREBP-1) pathway and reduced inflammation by suppressing the NF-κB pathway in these cells. Salicylic acid also decreased the cell viability of SEB-1 by increasing apoptosis via the death signal receptor pathway. Subsequently, histopathological analysis of a rabbit ear acne model after application of SA for three weeks confirmed that SA suppressed the levels of cytokines and major pathogenic proteins around acne lesions, which supports the mechanisms suggested by our in vitro experiments. These results initially clarified that therapeutic activities of SA in acne vulgaris treatment could be associated with the regulation of SREBP-1 pathway and NF-κB pathway in human SEB-1 sebocytes.

摘要

寻常痤疮是一种常见的皮肤疾病,其发病机制具有多因素性,包括皮脂过度分泌、炎症、毛囊角质形成细胞过度角化和痤疮丙酸杆菌过度生长。水杨酸(SA)是一种β-羟基酸,常用于治疗痤疮。已经发现 SA 可以减少皮肤油脂,并具有抗炎特性。然而,很少有研究阐明了这种治疗痤疮的机制和途径。在这项研究中,我们最初在人 SEB-1 皮脂腺细胞中研究了 SA 的抗痤疮特性。SA 通过下调腺苷单磷酸激活蛋白激酶(AMPK)/固醇调节元件结合蛋白-1(SREBP-1)途径来减少皮脂生成,并通过抑制这些细胞中的 NF-κB 途径来减少炎症。SA 还通过死亡信号受体途径增加细胞凋亡来降低 SEB-1 细胞的活力。随后,对应用 SA 治疗三周后的兔耳痤疮模型进行组织病理学分析证实,SA 抑制了痤疮病变周围细胞因子和主要致病蛋白的水平,这支持了我们体外实验提出的机制。这些结果初步阐明,SA 在寻常痤疮治疗中的治疗活性可能与调节人 SEB-1 皮脂腺细胞中的 SREBP-1 途径和 NF-κB 途径有关。

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