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