Abstract

Hair growth is regulated by the interaction between dermal papilla cells (DPC) and other cells inside the hair follicle. Here, we show the effect and action mechanism of mackerel-derived fermented fish oil (FFO) extract and its component docosahexaenoic acid (DHA) in the control of hair growth. The hair growth effect of FFO extract was evaluated by the culture method of vibrissa follicles and in vivo dotmatrix planimetry method. FFO extract increased the length of hair-fibers and enabled stimulated initiation into the anagen phase of the hair cycle. As expected, FFO extract significantly increased DPC proliferation. FFO extract induced the progression of the cell cycle and the activation of extracellular signal-regulated kinase (ERK), p38 and Akt. FFO extract induced nuclear translocation of β-catenin, a stimulator of anagen phase, through an increase of phospho-glycogen synthase kinase3β (GSK3β) level. Since various prostaglandins are known to promote hair growth in humans and mice, we examined the effect of DHA, a main omega-3 fatty acid of FFO, on DPC proliferation. DHA not only increased DPC proliferation but also upregulated levels of cell cycle-associated proteins such as cyclin D1 and cdc2 p34. These results show that FFO extract and DHA promote hair growth through the anagen-activating pathways in DPC.

Highlights

  • Hair loss is caused by various factors, including stress hormones, chemotherapy and insufficient nutrition, and is a serious problem for modern people regarding appearance [1,2,3,4]

  • The rat vibrissa follicles were cultured in medium supplemented with fermented fish oil (FFO) extract (12.5, 25, and 50 μg/mL) or minoxidil (10 μM) and were maintained for 14 days

  • On the 14th day after culture, FFO extract markedly increased the length of hair-fiber by 175.1% compared with the vehicle-treated control (100%) at a concentration of 12.5 μg/mL (Figure 1A,B)

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Summary

Introduction

Hair loss is caused by various factors, including stress hormones, chemotherapy and insufficient nutrition, and is a serious problem for modern people regarding appearance [1,2,3,4]. Minoxidil has been shown to induce proliferation through the activation of extracellular signal-regulated kinase (ERK) and Akt as well as the modulation of the level of cell cycle-associated proteins [19,20]. Other factors, such as adenosine and vascular endothelial growth factor (VEGF), increase the proliferation of DPC or hair growth by activation of ERK [21,22], whereas hepatocyte growth factor (HGF) induces the proliferation of melanoma cells by activation of p38 [23]. We investigated the effects and action mechanisms of FFO and DHA on hair growth

FFO Extract Increased the Hair-Fiber Length of Rat Vibrissa Follicles
Discussion
Reagents
Animals
Isolation and Culture of Rat Vibrissa Follicles
Hair Growth Activity In Vivo
Cell Viability Assay
Cell Cycle Analysis
Western Blot Analysis
Statistical Analysis

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