4.7 Article

Epimedium brevicornum Maxim. Extract exhibits pigmentation by melanin biosynthesis and melanosome biogenesis/transfer

期刊

FRONTIERS IN PHARMACOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2022.963160

关键词

Epimedium brevicornum Maxim; melanogenesis; melanosome biogenesis; tyrosinase activity; melanogenic ingredients

资金

  1. Open Project of National Major Science and Technology Infrastructure of Translational Medicine [TMSK-2021-404]
  2. Youth Innovation Research Foundation [A1-U21-205-01010109]
  3. National Natural Science Foundation of China [81972932]
  4. program of Shanghai E-research Institute of Bioactive Constituents in Traditional Chinese Medicine

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This study demonstrates the potential pigmentation effect of Epimedium brevicornum Maxim., and elucidates its related molecular mechanisms and melanogenesis basis. Epimedium Folium extract (EFE) has been shown to exhibit repigmentation effects by promoting melanin synthesis and melanosome biogenesis/transfer. Six main flavonoid ingredients were identified among EFE, with epimedin B (EB) being confirmed as a high-content, low-toxicity, and effective melanogenic compound. These findings provide valuable insights into the pharmacology of Epimedium herb and may offer a novel therapeutic approach for hypopigmentation disorders.
Epimedium brevicornum Maxim. (Epimedii Folium) is a traditional medicine widely utilized in China for sexual dysfunction and osteoporosis treatment. Recently, studies have reported that Epimedium flavonoid icariin displayed hair growth and melanogenic ability by targeting tyrosinase activity. Nevertheless, icariin hydrolysate icariside II and icaritin cause depigmentation due to their tyrosinase inhibition. These pigment functional discrepancies from Epimedium constituents arouse our great interest. Then, this study focused on the pigmentation effects of Epimedii Folium extract (EFE) on melanin synthesis and melanosome biogenesis/transfer, and further identified the bioactive constituents. First, in in vitro systemic studies, we discovered that the potent melanogenic and repigmented effects of EFE were dependent on concentration and amount of time in multi-melanocytes, normal human skin tissue, and vitiligo perilesional areas. In vivo, EFE exhibited repigmented effect on two kinds of depigmented models of N-phenylthiourea-induced zebrafish and hydroquinone-induced mice. Mechanistically, EFE strongly promoted tyrosinase activity and upregulated the protein expression of tyrosinase families which finally contribute to melanin biosynthesis by activating the MAPK/ERK1/2 signal pathway. In addition, EFE effectively increased melanosome number, accelerated melanosome maturity and cytoplasmic transport through the growth/extension of melanocyte dendrites, and induced melanosome transfer from melanocyte to keratinocyte for pigmentation. The six main flavonoid ingredients were identified among EFE. Compared to others, epimedin B (EB) was confirmed as a high-content, low-toxicity, and effective melanogenic compound in EFE. Taking all these together, this study systematically demonstrates the potential pigmentation effect of Epimedium brevicornum Maxim., and clarifies its related molecular mechanisms and melanogenesis basis. These results give additional insight into Epimedium herb pharmacology and may provide a novel therapy basis for hypopigmentation disorders.

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