JP7519211B2 - 遺伝子発現促進用組成物 - Google Patents
遺伝子発現促進用組成物 Download PDFInfo
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- JP7519211B2 JP7519211B2 JP2020089375A JP2020089375A JP7519211B2 JP 7519211 B2 JP7519211 B2 JP 7519211B2 JP 2020089375 A JP2020089375 A JP 2020089375A JP 2020089375 A JP2020089375 A JP 2020089375A JP 7519211 B2 JP7519211 B2 JP 7519211B2
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Description
[1]ヤエヤマアオキの果実抽出物及び柑橘類の果皮抽出物を含む、美容用組成物。
[2]ヤエヤマアオキの果実抽出物及び柑橘類の果皮抽出物を含む、皮膚外用組成物。
[3]ヤエヤマアオキの果実抽出物及び柑橘類の果皮抽出物を含む、セリンパルミトイルトランスフェラーゼ、フィラグリン、ヒアルロン酸合成酵素3、インボルクリン、ロリクリン、トランスグルタミナーゼ-1、クローディン-1、オクルディン及びアクアポリン3からなる群から選ばれる少なくとも1種のタンパク質の遺伝子発現促進用組成物。
[4]前記タンパク質は、角化細胞内のタンパク質である、[3]に記載の組成物。
[5]ヤエヤマアオキの果実抽出物及び柑橘類の果皮抽出物を含む、コーニファイドエンベロープ形成促進用組成物。
[6]ヤエヤマアオキの果実抽出物及び柑橘類の果皮抽出物を含む、角層保湿機能改善用組成物。
[7]ヤエヤマアオキの果実抽出物及び柑橘類の果皮抽出物を含む、肌のキメ改善用組成物。
[8]前記柑橘類の果皮抽出物は、チンピエキスである、[1]~[7]のいずれか1項に記載の組成物。
「及び/又は」との用語は、列記した複数の関連項目のいずれか1つ、又は2つ以上の任意の組み合わせ若しくは全ての組み合わせを意味する。
「含有量」は、濃度と同義であり、組成物の全体量に対する成分の量の割合を意味する。ただし、成分の含有量の総量は、100%を超えることはない。本明細書では、別段の定めがない限り、含有量の単位は「質量%(wt%)」を意味する。
数値範囲の「~」は、本明細書において、その前後の数値を含む範囲であり、例えば、「0質量%~100質量%」は、0質量%以上であり、かつ、100質量%以下である範囲を意味する。
「遺伝子発現促進作用」は、遺伝子の発現量の増加を促進する作用、遺伝子産物(タンパク質)の翻訳量の増加を促進する作用、及び遺伝子産物の産生量の増加を促進する作用のうち少なくともいずれか1つの作用をいう。
「コーニファイドエンベロープ形成促進作用」は、コーニファイドエンベロープの形成を促進する作用、及び/又は形成されたコーニファイドエンベロープの維持が阻害されることを抑制する作用を意味する。
「角層保湿機能改善作用」は、角層の水分量及び/又は細胞面積が低下することを抑制する作用を意味する。
「肌のキメ改善作用」は、皮溝及び皮丘が鮮明に確認できる作用を意味する。
保湿機能因子の遺伝子発現促進作用、コーニファイドエンベロープ形成促進作用、角層保湿機能改善作用及び肌のキメ改善作用を総称して「有効作用」とよぶ。有効作用は、これらの作用のいずれか1種、2種、3種又は4種全ての作用をいう。
ヤエヤマアオキの果実抽出物及び柑橘類の果皮抽出物を含む組成物を適用した場合、角化細胞内における、保湿機能因子であるインボルクリン、ロリクリン、トランスグルタミナーゼ-1、セリンパルミトイルトランスフェラーゼ、フィラグリン、ヒアルロン酸合成酵素3、クローディン-1、オクルディン及びアクアポリン3をコードする9遺伝子の発現量は促進される。
(1-1)評価方法
正常ヒト新生児表皮角化細胞(NHEK;「KK-4009」;KURABO社製)を正常ヒト表皮角化細胞増殖培地(KGM;「HuMedia KG2 KK-2150S」;KURABO社製)を用いて培養した後、トリプシン処理により細胞を回収した。KGMを用いて35mmシャーレに30×104cells/2mLずつ播き、37℃、5%CO2下で一晩培養した。
mRNA発現促進率(%)=A/B×100
A:被験試料1-1~1-8添加時の補正値
B:被験試料無添加時(コントロール)の補正値
各遺伝子のmRNA発現促進率の測定結果を表3に示す。また、表3の結果より、ノニ果汁、チンピエキス並びにノニ果汁及びチンピエキスについて、各遺伝子のmRNA発現促進効果の有無を評価してまとめたものを表4に示す。なお、表4において、「-」は発現抑制効果を、「+」は発現促進効果を、「++」は有意な発現促進効果を、「+-」は抑制及び促進のいずれの効果か判断がつかなかったことを示す。
(2-1)試料採取方法
普段よりスキンケアをしていない健全な成人男性の顔面頬部より角層をテープストリッピングにより採取した。採取後、大きさを揃えたテープ上の角層を、蒸留水でチンピエキス(75μg/ml)及びノニ果汁(25μg/ml)を溶解して調製した被験試料及びコントロール(蒸留水)に浸し、23℃、1日間の条件で処理した。チンピエキス及びノニ果汁は例1と同じものを用いた。処理後、角層を以下のコーニファイドエンベロープ(CE)成熟度評価法により、CEの成熟度を測定した。
図1に示すとおり、CEは、角層細胞の辺縁にある疎水性の膜状構造体である。CEは、インボルクリン、ロリクリンなどのタンパク質が架橋及び不溶化して形成され、細胞間脂質とともに皮膚のバリア機能に寄与する。
CE未成熟度(%)=A/B×100
A:緑色蛍光の面積
B:全CE(緑色発光及び赤色発光)の面積
チンピエキス及びノニ果汁を含む被験試料及びこれらを含まないコントロールのCE未成熟度の測定結果及び免疫染色撮影写真を図2に示す。図2に示すとおり、ノニ果汁及びチンピエキスを添加することにより、CEの未成熟度が有意に低下した。これらの結果より、ノニ果汁及びチンピエキスを含む組成物は、CEの成熟化を促進する、CE形成促進作用を有することがわかった。
(3-1)被験試料の適用方法
下記表5に示す成分を混合して、ローション状の被験試料及びコントロールを調製した。
測定部位について、皮膚計測器「Corneometer CM825」(COURAGE-KHAZAKA electronic GmbH社製)を用いて、製造業者の指示に従って角層水分量を測定した。1か所につき、5秒毎に範囲内を移動させながら4点にて測定し、その平均値を測定結果とした。測定結果について、対応のあるt検定にて統計解析を行った。ただし、被験者18名のうち、被験試料の適用量の少なかった1名を除き、17名について評価した。
測定部位よりテープストリッピングにて角層細胞を2層分採取した。2層目を採取したテープの一部を塩化ビニル製透明プレート「ユニサンデー(エンビシート)」(品番EB231-1、300mm×200mm、厚み1mmタイプ;Hikari社製)に貼付し、室温で一晩ヘキサン(特級グレード;関東化学社製)に浸して角層細胞をプレートに転写した。転写された角層細胞をデジタルマイクロスコープ「VHX-6000」(キーエンス社製)を用いて観察及び撮影した。ただし、被験者18名のうち、角層細胞をプレートに転写できなかった4名を除き、14名について評価した。
測定部位にマイクロスコープ「DG-3X」(スカラ社製)をあて、スコープが水平になり、かつスコープの面が皮膚にぴったりと接触するように被験者の頭の向きを調節し、1箇所につき2回撮影した。撮影した画像について、3名の事前に訓練を受けた社内評価者が目視で肌のキメのグレードを以下の基準(悪い:1←→良い:5)により評価した。
評価基準 5:皮溝と皮丘が鮮明に確認でき、均質である
4:皮溝と皮丘が鮮明に確認できるが、均質でない
3:皮溝と皮丘が確認できるが、鮮明でない
2:皮溝と皮丘がほぼ確認できない
1:皮溝と皮丘が全く確認できない
測定した角層水分量について、0Wの測定結果からの水分量の変化量(減少量)及び変化率をまとめたものを図3に示す。図3に示すとおり、ノニ果汁及びチンピエキスを含む被験試料を使用することにより、角層水分量の減少は抑制された。この結果より、ノニ果汁及びチンピエキスを含む組成物は、角層水分量の減少を抑制する作用を有することがわかった。
In vivo評価の被験者18名に対し、0W及び8Wにアンケート調査を行った。各項目について、0Wの肌状態を3とし、8Wの肌状態を5段階(悪い:1←→良い:5)で評価し、結果を集計して平均値を算出した。また、算出した平均値から、以下の基準により評価した。結果を表6に示す。
評価=(8Wの被験試料群の平均値)-(8Wのコントロール群の平均値)
「○」:評価≧0.05
「△」:-0.05<評価<0.05
「×」:評価≦-0.05
Claims (2)
- ヤエヤマアオキの果実抽出物及びマンダリンオレンジ果皮抽出物であるチンピエキスを含む、トランスグルタミナーゼ-1遺伝子発現促進用組成物。
- 前記トランスグルタミナーゼ-1は、角化細胞のトランスグルタミナーゼ-1である、請求項1に記載の組成物。
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