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Giant Centella asiatica , a novel cultivar rich in madecassoside and asiaticoside, suppresses α‑melanocyte‑stimulating hormone‑induced melanogenesis through MC1R binding.
- Source :
-
International journal of molecular medicine [Int J Mol Med] 2025 Jan; Vol. 55 (1). Date of Electronic Publication: 2024 Nov 08. - Publication Year :
- 2025
-
Abstract
- The present study investigated the anti‑melanogenesis effects of Giant Centella asiatica (GCA), a new cultivator of Centella asiatica (CA) cataloged by the Korea Forest Service in 2022, and compared its efficacy with that of traditional CA. GCA has a high yield per unit area and enhanced antioxidant properties. The anti‑melanogenic effects of GCA were investigated using B16F10 melanoma cells and a 3D human skin‑equivalent model. Key molecular mechanisms were elucidated through western blotting, cAMP assays and molecular docking studies. Focus was addressed on the effect of GCA on skin whitening by comparing the ability of a GCA extract to inhibit melanin production in B16F10 melanoma cells and a 3D human skin‑equivalent model to that of CA. The results showed that the GCA extracts more effectively reduced melanin production, which was attributed to their higher content of two active components, madecassoside and asiaticoside. Further investigation revealed that GCA primarily inhibited melanogenesis through the PKA‑cAMP response element‑binding (CREB)‑microphthalmia‑associated transcription factor (MITF) axis, a key regulatory pathway in melanin synthesis. Notably, the present study, to the best of our knowledge, is the first to demonstrate that madecassoside and asiaticoside, the two principal compounds in GCA, directly bound to MC1R, which contributed to the significant skin‑whitening effects. Moreover, GCA reduced melanin production in a 3D human skin‑equivalent model, showing efficacy within a complex skin environment. These results demonstrated the superior effectiveness of GCA to that of CA for skin anti‑melanogenesis, indicating its potential as a promising natural material for targeting pigmentation disorders.
- Subjects :
- Humans
Animals
Mice
Cell Line, Tumor
Molecular Docking Simulation
Melanoma, Experimental metabolism
Melanoma, Experimental pathology
Melanoma, Experimental drug therapy
Skin Pigmentation drug effects
Melanogenesis
Triterpenes pharmacology
Triterpenes chemistry
Centella chemistry
Melanins metabolism
Melanins biosynthesis
alpha-MSH metabolism
alpha-MSH pharmacology
Plant Extracts pharmacology
Plant Extracts chemistry
Receptor, Melanocortin, Type 1 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1791-244X
- Volume :
- 55
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- International journal of molecular medicine
- Publication Type :
- Academic Journal
- Accession number :
- 39513603
- Full Text :
- https://doi.org/10.3892/ijmm.2024.5454