Herbal Extracts Induce Dermal Papilla Cell Proliferation of Human Hair Follicles.
- Author:
Hosein RASTEGAR
1
;
Hamidreza Ahmadi ASHTIANI
;
Mahmoud AGHAEI
;
Behrooz BARIKBIN
;
Amirohushang EHSANI
Author Information
- Publication Type:Original Article
- Keywords: Dermal papilla cell; Hair follicle; Herbal extracts; Proliferation
- MeSH: bcl-2-Associated X Protein; Blotting, Western; Bromodeoxyuridine; Cell Proliferation*; Cyclin D1; Cyclin-Dependent Kinase 4; Hair Follicle*; Hair*; Humans*; Lymphoma, B-Cell; Medicine, Traditional; Phosphotransferases; Polymerase Chain Reaction; Protein Isoforms; Reverse Transcription; RNA, Messenger
- From:Annals of Dermatology 2015;27(6):667-675
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND: The number of people suffering from balding or hair thinning is increasing, despite the advances in various medical therapies. Therefore, it is highly important to develop new therapies to inhibit balding and increase hair proliferation. OBJECTIVE: We investigated the effects of herbal extracts commonly used for improving balding in traditional medicine to identify potential agents for hair proliferation. METHODS: The expression levels of 5alpha-reductase isoforms (type I and II) were analyzed using quantitative real-time reverse transcription polymerase chain reaction in the human follicular dermal papilla cells (DPCs). The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenylteterazolium bromide and bromodeoxyuridine tests were used to evaluate the cell proliferation effect of herbal extracts in DPCs. The expression levels of extracellular signal-regulated kinase (ERK), Akt, cyclin D1, cyclin-dependent kinase 4 (Cdk4), B-cell lymphoma (Bcl-2) and Bcl-2-associated X protein (Bax) were measured using western blot analysis. RESULTS: The 5alpha-reductase isoform mRNAs and proteins were detected in the cultured DPCs, and the expression level of 5alpha-R2 in DPCs in the presence of the herbal extracts was gradually decreased. Herbal extracts were found to significantly increase the proliferation of human DPCs at concentrations ranging from 1.5% to 4.5%. These results show that the herbal extracts tested affected the protein expressions of ERK, Akt, cyclin D1, Cdk4, Bcl-2, and Bax in DPCs. CONCLUSION: These results suggest that herbal extracts exert positive effects on hair proliferation via ERK, Akt, cyclin D1, and Cdk4 signaling in DPCs; they also suggest that herbal extracts could be a great alternative therapy for increasing hair proliferation.
