Lee Do Yeon, Hwang Chul Ju, Choi Ji Yeon, Park Mi Hee, Song Min Ji, Oh Ki Wan, Son Dong Ju, Lee Seung Hwa, Han Sang Bae, Hong Jin Tae
College of Pharmacy and Medical Research Center, Chungbuk National University, Cheongju 28160, Republic of Korea.
Department of Industrial Cosmetics, Chungbuk National University, Cheongju 28160, Republic of Korea.
Biomol Ther (Seoul). 2017 Sep 1;25(5):535-544. doi: 10.4062/biomolther.2017.006.
Carnosol is a phenolic antioxidant present in rosemary (). It is known for anti-inflammatory effects, analgesic activity and anti-cancer effects. However, no study has been dedicated yet to its effect on atopic dermatitis (AD). Here, we show that carnosol effectively inhibited LPS-induced nitric oxide (NO) generation and expression of inflammatory marker proteins (iNOS and COX-2) in RAW 264.7 cells. In addition, carnosol effectively inhibits the phosphorylation of STAT3 and DNA binding activity in RAW 264.7 cells. Pull down assay and docking model analysis showed that carnosol directly binds to the DNA binding domain (DBD) of STAT3. We next examined the anti-atopic activity of carnosol (0.05 µg/cm) using 5% Phthalic anhydride (PA)-induced AD model in HR1 mice. Carnosol treatment significantly reduced 5% PA-induced AD like skin inflammation in skin tissues compared with control mice. Moreover, carnosol treatment inhibits the expression of iNOS and COX-2 in skin tissue. In addition, the levels of TNF-α, IL-1β, and Immunoglobulin-E in blood serum was significantly decreased in carnosol treated mice compared with those of 5% PA treated group. Furthermore, the activation of STAT3 in skin tissue was decreased in carnosol treated mice compared with control mice. In conclusion, these findings suggest that carnosol exhibited a potential anti-AD activity by inhibiting pro-inflammatory mediators through suppression of STAT3 activation via direct binding to DBD of STAT3.
鼠尾草酸是迷迭香中存在的一种酚类抗氧化剂。它以抗炎作用、镇痛活性和抗癌作用而闻名。然而,尚未有研究专门探讨其对特应性皮炎(AD)的影响。在此,我们表明鼠尾草酸可有效抑制RAW 264.7细胞中脂多糖(LPS)诱导的一氧化氮(NO)生成以及炎症标记蛋白(诱导型一氧化氮合酶和环氧化酶-2)的表达。此外,鼠尾草酸可有效抑制RAW 264.7细胞中信号转导和转录激活因子3(STAT3)的磷酸化及DNA结合活性。下拉实验和对接模型分析表明,鼠尾草酸直接与STAT3的DNA结合结构域(DBD)结合。接下来,我们使用5%邻苯二甲酸酐(PA)诱导的HR1小鼠AD模型,研究了鼠尾草酸(0.05 µg/cm)的抗特应活性。与对照小鼠相比,鼠尾草酸治疗显著减轻了5% PA诱导的皮肤组织中类似AD的皮肤炎症。此外,鼠尾草酸治疗可抑制皮肤组织中诱导型一氧化氮合酶和环氧化酶-2的表达。另外,与5% PA治疗组相比,鼠尾草酸治疗的小鼠血清中肿瘤坏死因子-α、白细胞介素-1β和免疫球蛋白E的水平显著降低。此外,与对照小鼠相比,鼠尾草酸治疗的小鼠皮肤组织中STAT3的激活减少。总之,这些发现表明,鼠尾草酸通过直接结合STAT3的DBD抑制STAT3激活,从而抑制促炎介质,表现出潜在的抗AD活性。