Choi Sun-Il, Lee Jin-Ha, Kim Jae-Min, Jung Tae-Dong, Cho Bong-Yeon, Choi Seung-Hyun, Lee Dae-Won, Kim Jinkyung, Kim Jong-Yea, Lee Ok-Hawn
Department of Food Science and Biotechnology, Kangwon National University, Chuncheon 24341, Korea.
Jeongseon Yaccho Co., Ltd., Jeongseon 26125, Korea.
Int J Mol Sci. 2017 Jun 5;18(6):1200. doi: 10.3390/ijms18061200.
To protect from reactive oxygen species (ROS) damages, skin cells have evolved to have antioxidant enzymes, such as copper and zinc-dependent superoxide dismutase (SOD1), mitochondrial manganese-dependent superoxide dismutase (SOD2), catalase (CAT), glutathione peroxidase (GPX), and glutathione reductase (GR), and suppressed the expression of matrix metalloproteinases (MMPs) through the mitogen-activated protein kinase (MAPK) signaling pathways, such as c-Jun N-terminal kinase (JNK) and p38. Bioactive compounds analyses were performed using a high-performance liquid chromatography-photodiode array detector (HPLC-PDA) system. The antioxidant activity of Hance (UMH) extracts was estimated in vitro. The anti-aging activity of UMH extracts was estimated in vivo using the SKH-1 hairless mice. The UMH extracts reduced the H₂O₂-induced intracellular ROS production and the cell damages in human dermal fibroblasts (HDFs). Moreover, the H₂O₂-induced phosphorylation of JNK and p38 was detected in HDF and UMH extracts blocked the phosphorylation. These results suggest that UMH extracts can reduce the expression of MMPs and the reduced MMPs lead to the inhibition of collagen degradation. In addition, oral administration of the UMH extracts decreased the depth, thickness, and length of wrinkles on UVB exposed hairless mice. Therefore, UMH extracts play an advantage of the functional materials in antioxidant and anti-aging of skin.
为了抵御活性氧(ROS)的损伤,皮肤细胞已进化出具有抗氧化酶,如铜锌依赖性超氧化物歧化酶(SOD1)、线粒体锰依赖性超氧化物歧化酶(SOD2)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPX)和谷胱甘肽还原酶(GR),并通过丝裂原活化蛋白激酶(MAPK)信号通路,如c-Jun氨基末端激酶(JNK)和p38,抑制基质金属蛋白酶(MMPs)的表达。使用高效液相色谱-光电二极管阵列检测器(HPLC-PDA)系统进行生物活性化合物分析。体外评估了光叶海桐(UMH)提取物的抗氧化活性。使用SKH-1无毛小鼠在体内评估了UMH提取物的抗衰老活性。UMH提取物减少了H₂O₂诱导的人皮肤成纤维细胞(HDFs)内的ROS产生和细胞损伤。此外,在HDF中检测到H₂O₂诱导的JNK和p38磷酸化,而UMH提取物可阻断这种磷酸化。这些结果表明,UMH提取物可降低MMPs的表达,而MMPs的减少会导致胶原蛋白降解受到抑制。此外,口服UMH提取物可减少紫外线B照射的无毛小鼠皱纹的深度、厚度和长度。因此,UMH提取物在皮肤抗氧化和抗衰老方面具有作为功能性材料的优势。