Hair Growth Effect of DN106212 in C57BL/6 Mouse and Its Network Pharmacological Mechanism of Action.
Ji Yun BaekByoung Ha KimDong-Wook KimWon-Yung LeeChang-Eop KimHyun-Young KimJae Sung PyoEun-Seok ParkKi Sung KangPublished in: Current issues in molecular biology (2023)
Centipeda minima (CMX) has been widely investigated using network pharmacology and clinical studies for its effects on hair growth via the JAK/STAT signaling pathway. Human hair follicle papilla cells exhibit hair regrowth through the expression of Wnt signaling-related proteins. However, the mechanism of action of CMX in animals has not been elucidated fully. This study examined the effect of induced hair loss and its side-effects on the skin, and observed the mechanism of action of an alcoholic extract of CMX (DN106212) on C57BL/6 mice. Our results showed that DN106212 was more effective in promoting hair growth than dimethyl sulfoxide in the negative control and tofacitinib (TF) in the positive control when mice were treated with DN106212 for 16 days. We confirmed that DN106212 promotes the formation of mature hair follicles through hematoxylin and eosin staining. We also found that the expression of vascular endothelial growth factor ( Vegfa ), insulin-like growth factor 1 ( Igf1 ), and transforming growth factor beta 1 ( Tgfb1 ) is related to hair growth using PCR. DN106212-treated mice had significantly higher expression of Vegfa and Igf1 than TF-treated ones, and inhibiting the expression of Tgfb1 had similar effects as TF treatment. In conclusion, we propose that DN106212 increases the expression of hair growth factors, promotes the development of hair follicles, and promotes hair growth. Although additional experiments are needed, DN106212 may serve as an experimental basis for research on natural hair growth-promoting agents.
Keyphrases
- poor prognosis
- signaling pathway
- vascular endothelial growth factor
- binding protein
- transforming growth factor
- epithelial mesenchymal transition
- endothelial cells
- rheumatoid arthritis
- type diabetes
- metabolic syndrome
- cell death
- high resolution
- adipose tissue
- newly diagnosed
- high glucose
- diabetic rats
- single molecule
- high speed