Le REVE HAIR SERUM


Wnt/β-Catenin SignalingDHTMechanotransductionNutrition

Ingredients to Activate Wnt/β-catenin signaling pathway

Morus Alba Root Extracts(MARE)

The MARE extract contained high concentrations of chlorogenic acid.

Activation of β-catenin in dermal papilla cells is crucial for inducing anagen state, growth factor secretion, and hair follicle formation.

The Chlorogenic acid is known for its antioxidant activity and the prevention of β-catenin phosphorylation, which induces β-catenin degradation. Thus, the β-catenin signaling pathway is activated. MARE increased, the mRNA and protein expression of several growth factors (KGF, VEGF, FGF2, and HGF) in the HFDPCs is significantly upregulated. MARE has great potential for promoting hair growth by inducing telogen-to-anagen transition in terms of enhanced angiogenic paracrine factor secretion from HFDPCs and following effect on enhanced tubular formation in endothelial cells and proliferation and maturation in keratinocytes.


Caffeine

1) Caffeine stimulated cell proliferation, inhibited apoptosis/necrosis, up-regulated IGF-1 gene expression and protein secretion, while TGF-β2 protein secretion was down-regulated.
2) Hair shaft elongation, prolonged anagen duration and stimulated hair matrix keratinocyte proliferation. (Optimal Concentration is 0.0005%~0.005%)

Stem Cell Culture Media

1) Conditioned media of ADSCs (ADSC-CM) increases the proliferation rate of human follicular cells.
2) ADSCs-derived proteins improve hair growth and protect human dermal papilla cells against cytotoxic injury caused by androgen and reactive oxygen species.
3) Moreover, ADSC-CM induces the anagen phase and promotes hair growth and enhances the elongation of hair shafts .

Cooper Tripeptide-1

Copper inhibit the formation of DHT by inhibiting the activity of the 5-a-reductase enzyme

In people who genetically have a lot of DHT receptors, which are the reducers of Testosterone, in hair follicle cells, DHT binds to these DHT receptors and Wnt/β-catenin (a key role in stimulating hair follicle stem cells and hair regeneration.) is inhibited, resulting in hair growth It strongly inhibits hypertonicity. To date, approved hair loss treatment agents (Pinasteride or Dutasteride) or Copper inhibit the formation of DHT by inhibiting the activity of the 5-a-reductase enzyme that causes Testosterone to be reduced to DHT (Dihydrotestosterone). And there is Minoxidil ( Vasodilator ), which improves nutrition by increasing blood flow to the hair follicles to increase blood flow to hair growth.

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0.5mm and 0.75mm mesoroller needle stimulates mechanotransduction signal on Hair follicle stem cell layer.

Mechanisms of mechanotransduction.

Graphical summary of the current knowledge on the transduction of mechanical signals into a cellular response.

A) Mechanical strain applied to the cell and (the resulting) fluid flow activate receptors and channels and their downstream signaling cascades. In a tissue context, strain is transmitted between cells via a series of adhesion molecules such as integrins, cadherins, and tight junctions. Transcription factors become nucleotropic and address DNA regulatory elements such as repressors, enhancers, and their specific DNA response elements. Adaptive transcription and translation are initiated and lead to changes in transcriptome, proteome, and especially the secretome to communicate with neighbors and distant tissues. The expression and secretion of extracellular matrix proteins as parts of the secretome are upregulated. As a consequence, the incoming forces and the resistive response to external forces are enhanced, and a new homeostasis situation is produced. Similarly, the production of proteins of the cytoskeleton is enhanced, the cytoskeleton is also becoming stiffer, and the contractile proteins generate even more active forces.

B) Fluid flow is sensed by the primary cilium. The relevant structural features of a primary cilium are schematically depicted on the right side, while the signaling cascades and tools for mechanotransduction are depicted on the left side. Deflection of the cilium generates signaling

Stretch-induced hair regeneration is dependent on strain and duration.  a Stretch for 7 days under different amounts of strain. Note hair regeneration occurred in response to 33 or 40% strain, but not in the control (without the device) or under 0 or 20% strain; n = 6 for each group. Day 0 represents the day on which strain was applied. *Anagen initiated in glue-fixed area due to hair plucking when removing the skin-stretching device.  b Stretch under 33% strain for different durations. Note hair regeneration occurred in the 7-day (total) and 10-day (only in peripheral area) duration groups, but not in the 5-day duration group; n = 6 for each group.

Zinc Palmitoyl Nonapeptide-14, Biotinoyl Tripeptide-1, Acetyl Hexapeptide-1, Acetyl Tetrapeptide-3,

Cystein,Serine, Glutamic Acid, Threonine, Glycine, Leucine, Valine, Arginine, Aspartic Acid,

Biotin, Dexpanthenol, Folic Acid, Vit B-6, Vit B-12

ADSC Culture Media, PDRN, Hyaluronic Acid, Caffeine, Copper Tripeptide-1, Chlorogenic Acids, Zinc Palmitoyl Nonapeptide-14, Biotinoyl Tripeptide-1, Acetyl Hexapeptide-1, Acetyl Tetrapeptide-3, Olipopeptide-1, Olipopeptide-2, Olipopeptide-4, Olipopeptide-127, Polypeptide-1, Polypeptide-2, Polypeptide-3, Polypeptide-4, Polypeptide-8, Polypeptide-9, Polypeptide-11, Polypeptide-13, Polypeptide-59, Polypeptide-62,Cystein, Serine, Glutamic Acid, Threonine, Glycine, Leucine, Valine, Arginine, Aspartic Acid, Biotin, Dexpanthenol, Folic Acid, Vit B-6, Vit B-12, NaCl (Sodium Chloride), HNa2PO4(H2O)2 (Disodium phosphate), Methylpropanediol, 1,2-Hexanediol, Water