Details

Autor(en) / Beteiligte

• Chandra, Sonam
• Qureshi, Saba
• Chopra, Deepti
• Shukla, Saumya
• Patel, Sunil Kumar
• Singh, Jyoti
• Ray, Ratan Singh

Titel

UVR-induced phototoxicity mechanism of methyl N-methylanthranilate in human keratinocyte cell line

Ist Teil von

• Toxicology in vitro, 2022-04, Vol.80, p.105322-105322, Article 105322

Ort / Verlag

England: Elsevier Ltd

Erscheinungsjahr

2022

Link zum Volltext

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Fragrances are used in almost every cosmetic product. International Fragrance Association (IFRA) is the regulatory body that controls the use of fragrances in cosmetic products. Methyl-N-methylanthranilate (DMA) is a naturally derived fragrance, commonly used in cosmetic products such as fine perfumes, skin care products, etc. But there is a lack of detailed study in terms of its phototoxic and photogenotoxicity mechanisms under UVA/sunlight exposure. In this study, we have shown that DMA photodegrades in 4 h under UVA (1.5 mW/cm2) and sunlight. DMA (0.0001%–0.0025%) significantly reduced the cell viability as demonstrated by NRU and MTT assays in a dose-dependent manner under UVA (5.4 J/cm2) and sunlight (1 h) exposure in the HaCaT cell line. It generated excessive intracellular ROS (superoxide anion radical via type-I photodynamic reaction), resulting in lysosomal destabilization and mitochondrial membrane depolarization. Photo-activated DMA caused DNA fragmentation as observed by olive tail moment. DNA double-strand breaks was demonstrated by phosphorylation of H2AX-histone protein and formation of photo-micronuclei in skin keratinocytes. Additionally, photo-activated DMA upregulated the oxidative stress marker gene hemeoxygenase-1 and apoptotic marker genes (cytochrome-C, caspase-3, caspase-9). Activated caspase-cascade pathway established that photo-activated DMA can potentially trigger apoptosis in the human skin cells. •DMA showed maximum photodegradation in 4 h under UVA irradiation and sunlight.•DMA induced intracellular ROS followed type-I photodynamic reaction that upregulated oxidative stress marker HMOX-1.•DMA induced multiple cellular organelle (lysosome, miochondria) damage under UVA and sunlight exposure.•Photosensitized DMA induced DNA damage and apoptosis by activating caspase cascade in HaCaT cell line.