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10.1155/2018/9524657

http://scihub22266oqcxt.onion/10.1155/2018/9524657
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suck abstract from ncbi


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pmid29643980
      Oxid+Med+Cell+Longev 2018 ; 2018 (ä): 9524657
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  • Perillaldehyde Inhibits AHR Signaling and Activates NRF2 Antioxidant Pathway in Human Keratinocytes #MMPMID29643980
  • Fuyuno Y ; Uchi H ; Yasumatsu M ; Morino-Koga S ; Tanaka Y ; Mitoma C ; Furue M
  • Oxid Med Cell Longev 2018[]; 2018 (ä): 9524657 PMID29643980 show ga
  • The skin covers the outer surface of the body, so the epidermal keratinocytes within it are susceptible to reactive oxygen species (ROS) generated by environmental pollutants such as benzo(a)pyrene (BaP), a potent activator of aryl hydrocarbon receptor (AHR). Antioxidant activity is generally mediated by the nuclear factor-erythroid 2-related factor-2 (NRF2) and heme oxygenase-1 (HO1) axis in human keratinocytes. Perillaldehyde is the main component of Perilla frutescens, which is a medicinal antioxidant herb traditionally consumed in East Asia. However, the effect of perillaldehyde on the AHR/ROS and/or NRF2/HO1 pathways remains unknown. In human keratinocytes, we found that perillaldehyde (1) inhibited BaP-induced AHR activation and ROS production, (2) inhibited BaP/AHR-mediated release of the CCL2 chemokine, and (3) activated the NRF2/HO1 antioxidant pathway. Perillaldehyde is thus potentially useful for managing inflammatory skin diseases or disorders related to oxidative stress.
  • |Antioxidants/metabolism [MESH]
  • |Basic Helix-Loop-Helix Transcription Factors/*antagonists & inhibitors/metabolism [MESH]
  • |Benzo(a)pyrene/pharmacology [MESH]
  • |Cell Line [MESH]
  • |Cell Nucleus/drug effects/metabolism [MESH]
  • |Cell Survival/drug effects [MESH]
  • |Chemokine CCL2/biosynthesis [MESH]
  • |Cytochrome P-450 CYP1A1/antagonists & inhibitors/biosynthesis [MESH]
  • |Heme Oxygenase-1/antagonists & inhibitors/metabolism [MESH]
  • |Humans [MESH]
  • |Keratinocytes/cytology/*drug effects/metabolism [MESH]
  • |Monoterpenes/*pharmacology [MESH]
  • |NF-E2-Related Factor 2/*metabolism [MESH]
  • |Reactive Oxygen Species/antagonists & inhibitors/metabolism [MESH]
  • |Receptors, Aryl Hydrocarbon/*antagonists & inhibitors/metabolism [MESH]


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