Kaempferol Blocks the Skin Fibroblastic Interleukin 1β Expression and Cytotoxicity Induced by 12-O-tetradecanoylphorbol-13-acetate by Suppressing c-Jun N-terminal Kinase

• Published in: Nutrients Vol. 13; no. 9; p. 3079
• Main Authors: Park, Su-Ji, Kim, Do-Wan, Lim, Seong-Ryeong, Sung, Junghee, Kim, Tae Hoon, Min, In Sun, Choi, Chang-Hyung, Lee, Sei-Jung
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01-09-2021; MDPI
• Subjects: 12-O-Tetradecanoylphorbol-13-acetate; Acetic acid; Antioxidants; Apoptosis; c-Jun protein; Caspase-3; Cell death; Cytokines; Cytotoxicity; Fibroblasts; IL-1β; Inflammation; Inflammatory response; JNK protein; Kaempferol; mRNA; NF-κB protein; normal human dermal fibroblast; Oxidative stress; Phosphorylation; Proteins; reactive oxygen species; Skin; Software; Transcription factors; Variance analysis; United States > US; Switzerland; Japan
• ISSN: 2072-6643; 2072-6643
• DOI: 10.3390/nu13093079

Kaempferol, a bioflavonoid present in fruits and vegetables, has a variety of antioxidant and anti-inflammatory capacities, but the functional role of kaempferol in oxidative skin dermal damage has yet to be well studied. In this study, we examine the role of kaempferol during the inflammation and cell death caused by 12-O-tetradecanoylphorbol-13-acetate (TPA) in normal human dermal fibroblasts (NHDF). TPA (5 μM) significantly induced cytotoxicity of NHDF, where a robust increase in the interleukin (IL)-1β mRNA among the various pro-inflammatory cytokines. The skin fibroblastic cytotoxicity and IL-1β expression induced by TPA were significantly ameliorated by a treatment with 100 nM of kaempferol. Kaempferol blocked the production of the intracellular reactive oxygen species (ROS) responsible for the phosphorylation of c-Jun N-terminal kinase (JNK) induced by TPA. Interestingly, we found that kaempferol inhibited the phosphorylation of nuclear factor-kappa B (NF-κB) and the inhibitor NF-κB (IκBα), which are necessary for the expression of cleaved caspase-3 and the IL-1β secretion in TPA-treated NHDF. These results suggest that kaempferol is a functional agent that blocks the signaling cascade of the skin fibroblastic inflammatory response and cytotoxicity triggered by TPA.