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丁酸钠局部应用可恢复银屑病皮肤中 G 蛋白偶联受体 GPR43 和 GPR109a 的表达减少。

Decreased expression of G-protein-coupled receptors GPR43 and GPR109a in psoriatic skin can be restored by topical application of sodium butyrate.

机构信息

Department of Histology and Embryology, Medical University of Warsaw, Warsaw, Poland.

Department of Dermatology, University Medical Center Schleswig-Holstein, Campus Kiel, Rosalind-Franklin-Str. 7, Kiel, Germany.

出版信息

Arch Dermatol Res. 2018 Nov;310(9):751-758. doi: 10.1007/s00403-018-1865-1. Epub 2018 Sep 12.

Abstract

The G-protein-coupled receptors GPR43 and GPR109a are known to play an important role in mediating anti-inflammatory and anti-cancer functions in the gut. Short-chain fatty acids, such as sodium butyrate (SB), are activators of GPR43 and GPR109a and thereby promote anti-inflammatory effects. The present study aimed to examine the expression of these receptors and their reaction to SB in psoriasis. Lesional and non-lesional biopsies of 6 psoriasis patients and of 4 controls were obtained and stained for GPR109a and GPR43. Ex vivo stimulation with SB was performed on fresh biopsy material. Lesional and non-lesional psoriatic skin showed a decreased expression of GPR109a and GPR43 on keratinocytes in comparison with control skin. Topical application of SB was able to increase the low-level expression of both receptors. The data suggest that SB by restoring the impaired expression of GPR109a and GPR43 might exert anti-inflammatory effects and may be utilized as a topical tool for the treatment of psoriasis, which has to be proven in future clinical trials.

摘要

G 蛋白偶联受体 GPR43 和 GPR109a 已知在介导肠道中的抗炎和抗癌功能方面发挥重要作用。短链脂肪酸,如丁酸钠 (SB),是 GPR43 和 GPR109a 的激活剂,从而促进抗炎作用。本研究旨在研究这些受体在银屑病中的表达及其对 SB 的反应。从 6 名银屑病患者和 4 名对照者的皮损和非皮损活检组织中获取标本并进行 GPR109a 和 GPR43 染色。对新鲜活检组织进行 SB 的体外刺激。与对照皮肤相比,皮损和非皮损银屑病皮肤的角质形成细胞中 GPR109a 和 GPR43 的表达降低。SB 的局部应用能够增加这两种受体的低水平表达。这些数据表明,SB 通过恢复 GPR109a 和 GPR43 的受损表达可能发挥抗炎作用,并可作为治疗银屑病的局部工具,这需要在未来的临床试验中证明。

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