Kang Minseo, Lee Sanghyun, Jang Dae Sik, Lee Sullim, Kim Daeyoung
Department of Life Science, College of Bio-Nano Technology, Gachon University, Seongnam 13120, Republic of Korea.
Department of Plant Science and Technology, Chung-Ang University, Anseong 17546, Republic of Korea.
Curr Issues Mol Biol. 2025 Aug 7;47(8):631. doi: 10.3390/cimb47080631.
With increasing interest in natural therapeutic strategies for skin aging, plant-derived compounds have gained attention for their potential to protect against oxidative stress and inflammation. In this study, we investigated the anti-aging and anti-inflammatory effects of flavonoids isolated from using a tumor necrosis factor-alpha (TNF-α)-stimulated normal human dermal fibroblast (NHDF) model. The aerial parts of were extracted and analyzed by high-performance liquid chromatography (HPLC), leading to the identification of four major compounds: maltol, chlorogenic acid, ellagic acid, and quercitrin. Each compound was evaluated for its antioxidant and anti-aging activities in TNF-α-stimulated NHDFs. Among them, ellagic acid exhibited the most potent biological activity and was selected for further mechanistic analysis. Ellagic acid significantly suppressed intracellular reactive oxygen species (ROS) generation and matrix metalloproteinase-1 (MMP-1) secretion (both < 0.001), while markedly increasing type I procollagen production ( < 0.01). Mechanistic studies demonstrated that ellagic acid inhibited TNF-α-induced phosphorylation of mitogen-activated protein kinases (MAPKs), downregulated cyclooxygenase-2 (COX-2), and upregulated heme oxygenase-1 (HO-1), a key antioxidant enzyme. Additionally, ellagic acid attenuated the mRNA expression of inflammatory cytokines, including interleukin-6 (IL-6) and interleukin-8 (IL-8), indicating its broad modulatory effects on oxidative and inflammatory pathways. Collectively, these findings suggest that ellagic acid is a promising plant-derived bioactive compound with strong antioxidant and anti-inflammatory properties, offering potential as a therapeutic agent for the prevention and treatment of skin aging.
随着人们对皮肤衰老自然治疗策略的兴趣日益增加,植物源化合物因其具有抵御氧化应激和炎症的潜力而受到关注。在本研究中,我们使用肿瘤坏死因子-α(TNF-α)刺激的正常人皮肤成纤维细胞(NHDF)模型,研究了从[植物名称未给出]中分离出的黄酮类化合物的抗老化和抗炎作用。对[植物名称未给出]的地上部分进行提取并通过高效液相色谱(HPLC)分析,鉴定出四种主要化合物:麦芽酚、绿原酸、鞣花酸和槲皮苷。评估了每种化合物在TNF-α刺激的NHDF中的抗氧化和抗老化活性。其中,鞣花酸表现出最强大的生物活性,并被选用于进一步的机制分析。鞣花酸显著抑制细胞内活性氧(ROS)的产生和基质金属蛋白酶-1(MMP-1)的分泌(两者均P<0.001),同时显著增加I型前胶原的产生(P<0.01)。机制研究表明,鞣花酸抑制TNF-α诱导的丝裂原活化蛋白激酶(MAPK)磷酸化,下调环氧合酶-2(COX-2),并上调关键抗氧化酶血红素加氧酶-1(HO-1)。此外,鞣花酸减弱了包括白细胞介素-6(IL-6)和白细胞介素-8(IL-8)在内的炎性细胞因子的mRNA表达,表明其对氧化和炎症途径具有广泛的调节作用。总体而言,这些发现表明鞣花酸是一种有前景的植物源生物活性化合物,具有强大的抗氧化和抗炎特性,有望作为预防和治疗皮肤衰老的治疗剂。