دورية أكاديمية

Cypress tree (Chamaecyparis obtusa) Bark extract inhibits melanogenesis through repressing CREB and MITF signalling pathways in α-MSH-stimulated B16F10 cells

التفاصيل البيبلوغرافية
العنوان: Cypress tree (Chamaecyparis obtusa) Bark extract inhibits melanogenesis through repressing CREB and MITF signalling pathways in α-MSH-stimulated B16F10 cells
المؤلفون: Al Borhan Bayazid, Young Ah Jang, Soo Ah Jeong, Beong Ou Lim
المصدر: Food and Agricultural Immunology, Vol 33, Iss 1, Pp 498-510 (2022)
بيانات النشر: Taylor & Francis Group, 2022.
سنة النشر: 2022
المجموعة: LCC:Agriculture (General)
LCC:Immunologic diseases. Allergy
مصطلحات موضوعية: Cypress tree bark, B16F10 cells, melanogenesis, CREB/MITF: tyrosinase, Agriculture (General), S1-972, Immunologic diseases. Allergy, RC581-607
الوصف: Cypress tree (Chamaecyparis obtusa) bark is well-known for its bio-functional activities and high content of polyphenol and flavonoids. It has previously exhibited antioxidant, anti-pathogenic, and anti-inflammatory activities. Our study aimed to investigate the anti-melanogenic effect of Cypress Tree Bark extract (CBE). We evaluated cellular tyrosinase activity and melanin content in alpha-melanocyte-stimulating hormone (α-MSH) induced B16F10 murine melanoma cells. We analyzed microphthalmia-associated transcription factor (MITF), tyrosinase-related protein (TRP1 and TRP2), and cAMP response element-binding protein (CREB) activation via phosphorylation of AKT and ERK using western blot analysis. Tyrosinase, MITF, TRP1, and TRP2 mRNA expression were examined via real-time polymerase chain reaction. CBE restored melanin content and tyrosinase activity remarkably in α-MSH stimulated melanoma cells. It exhibited an anti-melanogenic effect through suppressing MITF, TRP1, TRP2, tyrosinase mRNA and protein expression in α-MSH-induced B16F10 cells. Furthermore, CBE has significantly inhibited CREB activation by suppressing AKT and extracellular signal-regulated kinase phosphorylation. Our data strongly suggest that CBE has potential effects against melanogenesis.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 09540105
1465-3443
0954-0105
Relation: https://doaj.org/toc/0954-0105; https://doaj.org/toc/1465-3443
DOI: 10.1080/09540105.2022.2095986
URL الوصول: https://doaj.org/article/e54f2e0835564606993abdbeda59f24e
رقم الأكسشن: edsdoj.54f2e0835564606993abdbeda59f24e
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:09540105
14653443
DOI:10.1080/09540105.2022.2095986