Paeoniflorin found in Paeonia lactiflora root extract inhibits melanogenesis by regulating melanin-related signal transduction in B16F10 cells
- J Cosmet Dermatol. 2023 Jun 8. doi: 10.1111/jocd.15789.
- 1. Department of Dermatology, Taipei City Hospital, Taipei, Taiwan,ROC.
- 2. Center for General Education, Mackay Junior College of Medicine, Nursing, and Management, Taipei, Taiwan, ROC.
- 3. Department of Biological Science and Technology, College of Life Sciences, China Medical University, Taichung, Taiwan, ROC.
- 4. Ph.D. Program for Biotechnology Industry, China Medical University, Taichung, Taiwan, ROC.
- 5. Translational Research Laboratory, Department of Biotechnology, School of Biotechnology and Genetic Engineering, Bharathiar University, Coimbatore, India.
- 6. Cardiovascular and Mitochondrial Related Disease Research Center, Buddhist Tzu Chi Medical Foundation, Hualien Tzu Chi Hospital, Hualien, Taiwan, ROC.
- 7. Center of General Education, Buddhist Tzu Chi Medical Foundation, Tzu Chi University of Science and Technology, Hualien, Taiwan, ROC.
- 8. Department of Medical Research, China Medical University Hospital, China Medical University, Taiwan, ROC.
- 9. Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, ROC.
- 10. Department of Medical Laboratory Science and Biotechnology, Asia University, Taichung, Taiwan, ROC.
Background: Skin pigmentation is modulated by various processes, with melanogenesis playing a key role. Melanin is synthesized by the catalysis of melanogenesis-related Enzymes, such as Tyrosinase and tyrosine-related proteins TRP-1 and TRP-2. Paeoniflorin is the main bioactive component of Paeonia suffruticosa Andr., Paeonia lactiflora., or Paeonia veitchii Lynch and has been used for centuries for its anti-inflammatory, anti-oxidant, and anti-carcinogenic properties.
Aims & methods: In this study, melanin biosynthesis in mouse melanoma (B16F10) cells was induced using α-melanocyte-stimulating hormone (α-MSH), and then cells were co-treated with paeoniflorin to evaluate its potential anti-melanogenic effect.
Results: α-MSH stimulation increased melanin content, Tyrosinase activity, and melanogenesis-related markers in a dose-dependent manner. However, treatment with paeoniflorin reversed α-MSH-induced upregulation of melanin content and Tyrosinase activity. Furthermore, paeoniflorin inhibited cAMP response element-binding protein activation and TRP-1, TRP-2, and microphthalmia-associated transcription factor protein expression in α-MSH-stimulated B16F10 cells.
Conclusion: Overall, these findings show the potential of paeoniflorin as a depigmenting agent for cosmetic products.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: Melanocortin Receptor
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target: HSP