4.7 Article

Effects of Acanthus ebracteatus Vahl. extract and verbascoside on human dermal papilla and murine macrophage

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SCIENTIFIC REPORTS
卷 12, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41598-022-04966-w

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  1. Thailand Center of Excellence for Life Sciences (TCELS) [TC-A 6/61]
  2. National Research Council of Thailand (NRCT) [DBG6080005, IRN61W0005]
  3. Innovation in Chemistry (PERCH-CIC), Ministry of Higher Education, Science, Research and Innovation

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Androgenic alopecia is commonly caused by testosterone metabolism, leading to hair loss. Approved medications like Finasteride and Minoxidil may have side effects, but Acanthus ebracteatus Vahl extract and verbascoside could potentially promote dermal papilla cell growth and have anti-inflammatory effects.
Androgenic alopecia is a common type of hair loss, usually caused by testosterone metabolism generating dihydrotestosterone and hair follicular micro-inflammation. These processes induce dermal papilla cells to undergo apoptosis. Currently approved effective medications for alopecia are Finasteride, an oral 5 alpha-reductase inhibitor, Minoxidil, a topical hair growth promoter, and Diclofenac, an anti-inflammatory agent, all of which, however, have several adverse side effects. In our study, we showed the bioactivity of Acanthus ebracteatus Vahl. (AE) extract performed by 95% ethanol, and verbascoside (VB), a biomarker of AE extract. Both AE extract and VB were studied for their effects on dermal papilla cell viability and the cell cycle by using MTT assay and flow cytometry. The effect of an anti-inflammatory activity of AE extract and VB on IL-1 beta, NO, and TNF-alpha, released from LPS induced RAW 264.7 cells, and IL-1 alpha and IL-6 released from irradiated dermal papilla cells were detected using ELISA technique. The preventive effect on dermal papilla cell apoptosis induced by testosterone was determined by MTT assay. In controlled in vitro assays it was found that AE extract and VB at various concentrations induced dermal papilla cell proliferation which was indicated by an increase in the number of cells in the S and G2/M phases of the cell cycle. AE extract at 250 mu g/mL concentration or VB at 62.50 mu g/mL concentration prevented cell apoptosis induced by testosterone at a statistically significant level. In addition, both AE extract and VB greatly inhibited the release of pro-inflammatory cytokines from RAW 264.7 and dermal papilla cells. The release of IL-1 beta, TNF-alpha, and NO from RAW 264.7 cells, as well as IL-1 alpha and IL-6 from dermal papilla cells, was also diminished by AE extract 250 mu g/mL and VB 125 mu g/mL. Our results indicate that AE extract and VB are promising ingredients for anti-hair loss applications. However, further clinical study is necessary to evaluate the effectiveness of AE extract and VB as treatment for actual hair loss.

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