Rice bran mineral extract increases the expression of anagen-related molecules in human dermal papilla through wnt/catenin pathway.
Rice bran mineral extract increases the expression of anagen-related molecules in human dermal papilla through wnt/catenin pathway.
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DOI:
10.1080/16546628.2017.1412792
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发表时间:
2017
影响因子:
3.3
通讯作者:
Seo YK
中科院分区:
文献类型:
--
作者:
Kim YM;Kwon SJ;Jang HJ;Seo YK
The objective of this study is to evaluate of rice bran mineral extract (RBM) increases the expression of anagen-related molecules in human dermal papilla (DOCs). Four treatment groups were established to evaluate the efficacy of RBM, including a negative control, positive control (ascorbic acid), RBM and ortho-silicic acid (Si(OH)4) (OSA) group. Three days after the DPCs were administered the various treatments, western blot analysis showed that type I collagen expression was increased 2.5-fold in the OSA group and 4-fold in the RBM group, and ALP expression was increased 1.5-fold in the OSA and RBM group while the expression of fibronectin was increased ~3-fold in the OSA group and 2.5-fold in the RBM group. Also, the expression of Wnt-3α and β-catenin protein was increased in OSA and RBM group compared to control group. Furthermore, the expression of IL-1a was decreased by more than 50% in the OSA and RBM groups compared to the negative control. Analysis of mRNA expression by RT-qPCR showed that type I collagen increased 1.2-fold in the OSA- and RBM-treated DPCs, whereas type IV collagen increased 2.7-fold in the OSA group and 3.5-fold in the RBM group. However, TGF-β2 mRNA decreased about 80% in the OSA and RBM groups, respectively. Immunohistochemical staining of the DPCs for versican protein showed a significant increase in the OSA- and RBM-treated groups compared to the negative control. Thus, RBM have a potential to recover of DPCs activity and decreased inflammatory-related markers. It can be expected that hair loss prevention and hair growth enhancement can be expected when RBM is applied as a cosmetic product.
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影响因子:
3.7
作者:
Kim YE;Choi HC;Lee IC;Yuk DY;Lee H;Choi BY
通讯作者:
Choi BY
影响因子:
2.5
作者:
Iida, Machiko;Ihara, Setsunosuke;Matsuzaki, Takashi
通讯作者:
Matsuzaki, Takashi
影响因子:
3
作者:
Lobner, D
通讯作者:
Lobner, D
影响因子:
3.6
作者:
Boivin, Wendy A.;Jiang, Huijun;Hunt, David W. C.
通讯作者:
Hunt, David W. C.
影响因子:
2.7
作者:
COUCHMAN, JR;GIBSON, WT
通讯作者:
GIBSON, WT