WASEDA'S REGIMEN
AMASHISO + ANALYSIS ON HAIR LOSS

 

WASEDA'S COMPREHENSIVE ANALYSIS ON HAIR LOSS 
&
INTRODUCTION TO AMASHISO
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the following is reprinted from a series of posts submitted by Waseda in forum # 22.

Footnote # 10

(10) Suppression of TGF-ß prevents apoptosis induction in the catagen hair follicle Y. Tsuji, T. Soma, L. Raftery, and T.

Hibino(http://www.ehrs.org/conferenceabstracts/
2001tokyo/researchabstracts)

Shiseido Life Science Research Center, Yokohama and MGH/Harvard Cutaneous Biology Research Center, Charlestown, MA, USA

Hair loss is the result of premature entry into catagen by various causes. In male pattern baldness, we have hypothesized the involvement of “catagen cascade”, in which a TGF-beta family member promotes caspase activation, resulting in the apoptosis of epithelial cells. In the previous study, we showed that TGF-beta2 was localized at the boundary area between germinative cells and DPC during the transition phase from late anagen to catagen. In the epithelial strand TGF-beta2 was detected in the regressing hair follicle. TUNEL-positive apoptotic cells and active caspase 3 and 9 were also observed in the area. In this study, we examined the role of TGF-beta2 in relation to apoptosis. Human hair follicles were cultured in the presence of TGF-beta2. Using active caspase-9 and –3 specific antibodies, we found that TGF-beta2 enhances the activation of these caspases in two regions, including the lower part of germinative matrix cells and outer most layer of outer root sheath cells. Dual staining for active caspase-9 and TUNEL demonstrated that active caspase-9 and TUNEL-staining mostly co-localized. Active caspase-3 positive cells were detected in the same region. We evaluated 400 plant extracts for activity in a TGF- beta suppression assay. An extract from Hydrangea macrophylla strongly inhibited TGF-beta induction in this assay and also promoted hair elongation in a hair follicle organ culture system. We tested the effect of the extract in vivo by applying it onto C57BL6 mouse for 10 days and scored the catagen stage of each hair follicle morphologically. Topical application of the extract remarkably delayed the progression of catagen. We isolated an active substance from the extract using a TGF-beta suppression assay. This substance showed a strong potential for hair elongation and also reduced caspase activation in cultured follicles. Collectively our results suggest that TGF-beta2 can enhance the induction of catagen via activation of caspases and that the suppressor of TGF-beta could be effective for the prevention of male pattern baldness. We are presently investigating the role of TGF-beta family members and their signal pathways in the endogenous mouse hair cycle.

 
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Footnotes to Waseda's Analysis


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