JP6145106B2 - 精製したセコイリドイドグルコシド誘導体からなる発毛促進剤、IGF−1発現増加剤、VEGF発現増加剤、HGF発現増加剤、KGF発現増加剤、およびβ−カテニン発現増加剤 - Google Patents
精製したセコイリドイドグルコシド誘導体からなる発毛促進剤、IGF−1発現増加剤、VEGF発現増加剤、HGF発現増加剤、KGF発現増加剤、およびβ−カテニン発現増加剤 Download PDFInfo
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- JP6145106B2 JP6145106B2 JP2014542261A JP2014542261A JP6145106B2 JP 6145106 B2 JP6145106 B2 JP 6145106B2 JP 2014542261 A JP2014542261 A JP 2014542261A JP 2014542261 A JP2014542261 A JP 2014542261A JP 6145106 B2 JP6145106 B2 JP 6145106B2
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Description
(a)本発明は、セコイリドイドグルコシド(secoiridoid glucoside)誘導体(より具体的にはオレウロペイン)、またはこれの加水分解産物を有効成分として含む脱毛の予防または治療用の薬剤学的組成物、脱毛改善または発毛促進用の化粧料組成物及び機能性食品組成物を提供する。
(b)本発明は、慢性疾患である脱毛において長期投与時にも副作用がない天然化合物を有効成分としているだけでなく、育毛及び養毛に優れて安定的な効能を見せて、効率的な脱毛治療剤または発毛促進用の化粧料/機能性食品組成物として有用に用いられることができる。
実験動物の飼育及び発毛剤の皮下注射
(1)試料の準備
ビヒクル(Vehichle)として使用されたコーン油と対照薬であるミノキシジルはシグマアルドリッチ(株)から購入し、試験物質であるオレウロペインはExtrasynthese(株)から購入した。
生後6週齢の雄C57BL/6Nマウス12匹をオリエントバイオ(株)から購入し、2週間飼育室の環境に適応させた後、陰性対照群(Con群)、陽性対照群(MXD群)及びオレウロペイン群(Ole群)の計3つの群に分けて実験に使用した。動物飼育室は温度21±2.0℃、相対湿度50±5%で、12時間ずつ昼夜を維持した。一般の固形飼料(chow)を自由に水とともに供給した。
発毛効果を調べるために、背中の肌色がピンクを呈する休止期体毛の8週齢のマウスを使用した。マウス用クリッパーを使用してマウス背中の毛を除去した後、その部位に注射器を用いて毎日0.1mL分量の試料を皮下注射した。試験物質であるオレウロペイン(0.8mg/0.1mL)と対照薬として使用されたミノキシジル(0.003mg/0.1mL)は皮下注射を実施する直前にコーン油に溶解させて使用し、陰性対照群にはビヒクル(コーン油)のみを皮下注射した。試料の投与は毎日午後4時に1回ずつ6週間実施した。
発毛剤の皮下注射直前から皮下注射が終了する時点まで実験動物の体重を毎週測定した。陰性対照群であるCon群と試験群であるOle群、そして陽性対照群であるMXD群の初期体重は群同士でいずれも有意的な差がなかったし、皮下注射6週後に測定された体重も実験群同士で有意的な差がなかった。
(1)発毛の肉眼的特徴
マウスの背中部位に試料を6週間皮下注射しながら、毎週毛が伸びる様相を写真を撮って確認した。休止期(Telogen)に入っていったマウスは、除毛をしたとき、体表面の色がピンク色を呈した。試験を進行するにつれて体表面の色が黒色に変わって行く場合、毛周期が休止期から成長期(anagen)に戻ることを意味する。コーン油を皮下注射したマウスでは、6週後にもほとんど毛が伸びなかったが、Ole群では皮下注射3週目から毛が伸び始め、6週後には均一で旺盛に毛が伸びることを観察することができた。このようなオレウロペインの発毛促進効果は、対照薬であるミノキシジルよりもっと優れることが分かった(図1)。
各試料を6週間皮下注射する間に、毎週毛の長さを測定した。Ole群の毛の長さは皮下注射3週目から陰性対照群に比べて有意的に(P<0.05)増加し、6週後には陰性対照群に比べて62%増加した。陽性対照群であるMXD群の毛の長さは4週目まで陰性対照群と全然差がなかったし、5週以後に増加する傾向を見せたが、陰性対照群と有意的な差を示すことはできなかった(図2)。したがって、オレウロペインは毛髪の成長を促進する効果があり、このような効果は発毛剤として商用化されているミノキシジルよりも優れることを確認した。
(1)組織学的分析法
皮下注射を実施してから6週後に、実験動物を剖検して皮下注射部位を中心に背中の肌組織試料をハサミと鉗子を用いて摘出した後、ホルマリンで固定した。段階別にアルコールとキシレンで脱水処理した後、パラフィンで包埋し、ミクロトームを用いて5μmの切片を作製し、さらにアルコールとキシレンでパラフィンを除去した。H&E(Hematoxylin & Eosin)染色を実施した後、光学顕微鏡で毛包組織の組織学的変化を観察した。病理検鏡担当者が検鏡して発毛周期を評価し、光学顕微鏡上で毛包(hair follicle)の数量及び直径を測定した。
各群の肌組織をH&E染色した後、顕微鏡検査をして発毛周期を観察した結果を下記の表1に示す。試験物質を投与する前(非処理)に測定された肌発毛周期は全部休止期と観察されたので、本試験に使用された8週齢の試験動物は発毛効能評価モデルとしての条件を揃えたものと判断された。皮下注射を6週間実施した後、組織病理学的に発毛周期を評価した結果、陰性対照群の場合、1例で成長期段階が観察され、MXD群の場合、1例、そしてOle群の場合、2例が成長期段階にあるものと観察された。
肌組織を対象とした免疫組織化学的検査
(1)免疫組織学的分析法
肌組織で毛髪成長に係るIGF1とβ−カテニンの発現量を観察するために、IGF1とβ−カテにンに対する一次抗体をそれぞれ1:50で希釈した後、組織切片に加えて室温で12時間反応させた。一次抗体の希釈は0.1Mリン酸緩衝液(PB)に1%正常ヤギ血清(Vector Laboratories Inc.)と0.3% Triton X−100(Sigma)混合液を使用した。組織切片を室温で15分間2回、0.1M PBで洗浄し、さらに1:200で希釈された二次抗体[ビオチン化抗ラビットIgG(Vector Laboratories Inc.)]と1時間室温で反応させた。さらに0.1M PBで15分間2回の水洗過程を経た後、パーオキシダーゼが標識されたABC溶液に浸漬して、室温で1時間反応させた。その後、さらに0.1M PBで15分間2回水洗して30mgの3,3’−ジアミノベンジジンを150mLの0.1M PBに溶かした溶液で5分間反応させた後、過酸化水素を0.005%濃度で添加して約5分間褐色発色反応を行った。反応の終わった組織はさらに0.1M PBで数回水洗してヘマトキシリンで20秒間対比染色した後、通常の方法によって脱水と透明化を経た後、封入して光学顕微鏡で観察した。
現在まで男性ホルモン及び成長ホルモン以外にもWnt/β−カテニンなどのような細胞内シグナル伝逹活性因子などが毛髪成長及び脱落に役割をすることが明らかになっており、脱毛抑制及び毛髪成長促進用の薬物の開発において、このようなWnt/β−カテニンシグナル伝達物質をターゲットとして効能をスクリーニングする研究が進行されて来ている。本発明では毛包の発生及び毛髪成長に中枢的な役割をするものとされているWnt/β−カテニンシグナル伝逹系を活性化させる物質を見出して、脱毛防止及び発毛促進用の製品の素材として応用しようとした。
(1)Trizol methodを用いたRNA分離方法
実験動物の肌組織で総RNAを分析定量するために、肌組織50〜100mgにTrizol溶液1mLを入れて均質化した後、4℃、12,000×gで10分間遠心分離した。上層液を新しいチューブに移した後、クロロホルム200μLを添加して、ボルテックスした。この過程を二回繰り返した後、上層液を新しいチューブに移した後、イソプロパノールと上層液を1:1の割合で添加した。10回強く振ってから室温で10分間放置した後、12,000×g、4℃で10分間遠心分離させた後、上層液を除去し、残りの沈殿物に70%エタノール 1mLを加えた後、7,500g、4℃で5分間遠心分離した。エタノールを除去した後、RNA沈殿物が入れられたチューブを室温で5分間乾燥させ、核酸加水分解酵素のない水(nuclease free water)を使用してRNA沈殿物を溶解させた。UV/VIS分光光度計(Beckman coulter, DU730)を用いて260nm及び280nm波長で抽出されたRNA試料の濃度を測定し、アガロースゲル電気泳動を行ってRNA試料の保全(integrity)を確認した。
RNAを分離した後、オリゴdTプライマーとSuperscript逆転写酵素(GIBCOBRL, Gaithersburg, MD,USA)を用いて逆転写を行うことにより、cDNAを合成した。逆転写を通じて得たcDNAを鋳型とし、増幅しようとする遺伝子のcDNAの5’と3’フランキング配列(flanking sequence)をプライマーとして使用してPCRを行った。このとき必要なプライマーは(株)バイオニアに合成を依頼して使用し、これらプライマー配列は下記の表2に示す。10×反応緩衝液[100mM KCl, 20mM Tris−HCl(pH8.0), 2.5mM MgCl2] 5μL、10mM dNTP 4μL、0.2μM センス及びアンチセンスプライマーをそれぞれ1μL入れた混合物に2μLのcDNAを反応させた反応混合液と2.5unitのTaqポリメラーゼ(Takara, Japan)を入れた後、蒸溜水で50μLに定容し、PCR機器を用いてPCRを行った。PCR条件は94℃(4分)、94℃(30秒)、30サイクルの[52℃(30秒)、72℃(45秒)]、そして72℃(10分)に設定した。増幅された産物1μLを1%アガロースゲルに電気泳動してDNAバンドを確認することで、遺伝子発現量を評価した。
6週間物質を皮下注射したマウスの背中の肌組織で発毛関連遺伝子の発現変化を評価するために、RT−PCRを行った。発毛促進メカニズムと知られているWnt/β−カテニンシグナル伝達物質の発現変化を調べた結果、Wnt10bとWnt10bの受容体であるFZDR(frizzled receptor 1)、そしてLRP5(low−density lipoprotein receptor−related protein 5)の発現がOle群で陰性対照群に比べて有意的に増加した。これによって、Wnt10bによって発現が抑制されるGSK3β(glycogen synthase kinase 3β)とAxinはOle群で陰性対照群に比べて有意的に減少した。Wnt/β−カテニンシグナル伝達体系の活性化によってβ−カテニンの発現がOle群で陰性対照群に比べて有意的に増加した。
Claims (2)
- 精製した下記式(2)で表されるセコイリドイドグルコシド(secoiridoid glucoside)誘導体からなることを特徴とする発毛促進剤。
- 精製した下記式(2)で表されるセコイリドイドグルコシド(secoiridoid glucoside)誘導体からなることを特徴とするIGF−1(Insulin−like growth factor 1)発現増加剤、VEGF(vascular endothelial growth factor)発現増加剤、HGF(hepatocyte growth factor)発現増加剤、KGF(keratocyte growth facfor)発現増加剤またはβ−カテニン発現増加剤。
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PCT/KR2013/006061 WO2014010900A1 (en) | 2012-07-09 | 2013-07-08 | Composition for preventing or treating hair loss or promoting hair growth comprising secoiridoid glucoside derivatives |
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