Sun Guanghui, Dang Yongkang, Lin Yanke, Zeng Wanying, Wu Zongjian, Zhang Xingwang, Dong Dong, Wu Baojian
College of Pharmacy, Jinan University, Guangzhou, China.
Institute of Molecular Rhythm and Metabolism, Guangzhou University of Chinese Medicine, Guangzhou, China.
Front Pharmacol. 2022 Sep 30;13:991917. doi: 10.3389/fphar.2022.991917. eCollection 2022.
Georgi (SBG) is a traditional Chinese medicine widely used to treat disorders such as hypertension, dysentery and hemorrhaging. Here, we aimed to assess the pharmacological effects of SBG on skin aging and to investigate the underlying mechanisms. Mice with skin aging were established by treatment with D-galactose and ultraviolet-B. SBG (topical application) showed a protective effect on skin aging in mice, as evidenced by less formation of skin wrinkles, higher levels of SOD (superoxide dismutase) and HYP (hydroxyproline) as well as a lower level of MDA (malondialdehyde). In the meantime, skin MMP-1 and p53 expression were lower, epidermis was thinner and collagen amount was higher in SBG-treated mice. Anti-skin aging effects of SBG were also confirmed in NIH3T3 and HaCaT cells, as well as in mouse primary dermal fibroblasts and human primary epidermal keratinocytes. Furthermore, we found that loss of (a known repressor of Bmal1) up-regulated skin BMAL1 (a clock component and a known anti-aging factor) and ameliorated skin aging in mice. Moreover, SBG dose-dependently increased the expression of BMAL1 in the skin of aged mice and in senescent NIT3H3 cells. In addition, based on a combination of Gal4 chimeric, luciferase reporter and expression assays, SBG was identified as an antagonist of REV-ERBα and thus an inducer of BMAL1 expression. In conclusion, SBG antagonizes REV-ERBα to up-regulate BMAL1 and to protect against skin aging in mice.
葛根(SBG)是一种广泛用于治疗高血压、痢疾和出血等病症的传统中药。在此,我们旨在评估葛根对皮肤衰老的药理作用并探究其潜在机制。通过用D-半乳糖和紫外线-B处理建立皮肤衰老小鼠模型。葛根(局部应用)对小鼠皮肤衰老具有保护作用,表现为皮肤皱纹形成减少、超氧化物歧化酶(SOD)和羟脯氨酸(HYP)水平升高以及丙二醛(MDA)水平降低。同时,在葛根处理的小鼠中,皮肤基质金属蛋白酶-1(MMP-1)和p53表达较低,表皮更薄且胶原蛋白含量更高。葛根的抗皮肤衰老作用在NIH3T3细胞、HaCaT细胞、小鼠原代真皮成纤维细胞和人原代表皮角质形成细胞中也得到了证实。此外,我们发现缺失(一种已知的Bmal1阻遏物)上调了皮肤中的BMAL1(一种生物钟成分和已知的抗衰老因子)并改善了小鼠的皮肤衰老。而且,葛根剂量依赖性地增加了老年小鼠皮肤和衰老NIT3H3细胞中BMAL1的表达。此外,基于Gal4嵌合体、荧光素酶报告基因和表达分析的组合,葛根被鉴定为REV-ERBα的拮抗剂,因此是BMAL1表达的诱导剂。总之,葛根拮抗REV-ERBα以上调BMAL1并保护小鼠免受皮肤衰老。