JP2001278769A - Skin cosmetic - Google Patents

Skin cosmetic

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Publication number
JP2001278769A
JP2001278769A JP2000091398A JP2000091398A JP2001278769A JP 2001278769 A JP2001278769 A JP 2001278769A JP 2000091398 A JP2000091398 A JP 2000091398A JP 2000091398 A JP2000091398 A JP 2000091398A JP 2001278769 A JP2001278769 A JP 2001278769A
Authority
JP
Japan
Prior art keywords
skin
actin
myosin
skin cosmetic
extract
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2000091398A
Other languages
Japanese (ja)
Inventor
Tsutomu Fujimura
努 藤村
Naoko Endo
菜穂子 遠藤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kao Corp
Original Assignee
Kao Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kao Corp filed Critical Kao Corp
Priority to JP2000091398A priority Critical patent/JP2001278769A/en
Publication of JP2001278769A publication Critical patent/JP2001278769A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a skin cosmetic which has a synergistically promoted skin- tightening effect and enhanced safety, improves the wrinkles and sagging of skins, and gives tensive and beautiful skins. SOLUTION: This skin cosmetic contains an integrin production-stimulating agent (one or more algae or plants selected from Fucus vesiclosus or Fucus evanescens, Laminaria japonika Areschoug, Hizikia fusiforme Okamura, Rosmarinus officinatis, Actinidia chinensis, Panax ginseng C. A. Meyer, Poria cocos Wolf, Prunus persica Batsch, and Arctium lappa L., or their extracts) and an actin-myosin-based activating agent (one or more plants selected from Scutellaria baicalensis Georgi, Phellodendron amurense Ruprecht, Gardenia jasminoides Ellis, Rehmannia glutinosa Liboschitz var. purpurea Makino, Zingiber officinale Roscoe and Astragalus sinicus, and their extracts).

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、皮膚の弾力性を改
善し、皮膚にハリを与える皮膚化粧料に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a skin cosmetic which improves skin elasticity and gives skin firmness.

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】皮膚の
老化等による肌のたるみは、皮膚の真皮結合組織の弾力
性の低下、皮下脂肪組織の支持力の低下、さらには皮膚
を支える筋力の低下等により生じると考えられており、
これを改善するために、これまでヒバマタ、カフェイ
ン、サイコサポニン等の肌の引き締め剤を含有する化粧
料が知られている(特開平5−124953号公報、特
開平10−72336号公報、特開平5−17332号
公報等)。
2. Description of the Related Art The sagging of the skin due to aging of the skin causes a decrease in the elasticity of the dermis connective tissue of the skin, a decrease in the supporting force of the subcutaneous adipose tissue, and a decrease in the muscle strength supporting the skin. It is thought to be caused by lowering etc.
In order to improve this, cosmetics containing skin tightening agents such as hibamata, caffeine, and saikosaponin have been known (JP-A-5-124953, JP-A-10-72336, and JP-A-10-72336). JP-A-5-17332, etc.).

【0003】しかし、斯かる肌の引き締め剤を単独で用
いた場合には、作用効果の点で必ずしも充分ではなく、
実際に肌内部に作用して肌を引き締め、たるみを有効に
改善するためには、引き締め剤を高濃度で配合して長期
間使用する必要があった。
[0003] However, when such a skin tightening agent is used alone, the effect is not always sufficient.
In order to actually act on the inside of the skin to tighten the skin and effectively improve the sagging, it was necessary to mix a tightening agent at a high concentration and use it for a long period of time.

【0004】本発明は、肌のたるみを有効に改善し、よ
り安全性の高い皮膚化粧料を提供することを目的とす
る。
[0004] It is an object of the present invention to effectively improve sagging of the skin and provide a safer skin cosmetic.

【0005】[0005]

【課題を解決するための手段】本発明者らは、皮膚のし
わ・たるみの発生メカニズム及び皮膚の弾力性を改善す
る成分について検討したところ、特定の植物成分にアク
チン−ミオシン系を活性化する作用があり、これらのア
クチン−ミオシン系活性化剤とインテグリン産生促進剤
とを併用した場合に、肌のたるみが有効に改善され、ハ
リのある美しい肌を実現できることを見出した。
Means for Solving the Problems The inventors of the present invention have examined the mechanism of generation of skin wrinkles and sagging and components that improve the elasticity of the skin, and found that the specific plant component activates the actin-myosin system. It has been found that, when these actin-myosin activators and integrin production promoters are used in combination, the sagging of the skin is effectively improved and firm and beautiful skin can be realized.

【0006】すなわち、本発明は、インテグリン産生促
進剤及びアクチン−ミオシン系活性化剤を含有する皮膚
化粧料を提供するものである。
That is, the present invention provides a skin cosmetic containing an integrin production promoter and an actin-myosin activator.

【0007】[0007]

【発明の実施の形態】本発明の化粧料は、インテグリン
産生促進剤及びアクチン−ミオシン系活性化剤を配合す
るものであるが、ここでインテグリンとは、細胞表面に
発現し、細胞接着に関与する受容体をいい、その構造は
αサブユニットとβサブユニットからなり、αサブユニ
ットは更にα1からα5、αL等が存在し、βサブユニ
ットはβ1、β2、β3等が存在することが知られてい
る。本発明者らは特定の天然成分にインテグリンの産生
を促進する作用があり、癌の転移抑制剤として有用であ
り(特開平11−246428号公報)、また皮膚のた
るみ改善や皮膚の引き締め効果があることを見出してい
る(特開平10−72336号公報)。
BEST MODE FOR CARRYING OUT THE INVENTION The cosmetic of the present invention contains an integrin production promoter and an actin-myosin activator. Here, integrin is expressed on the cell surface and is involved in cell adhesion. The structure is composed of α subunit and β subunit. It is known that α subunit has α1 to α5, αL, etc., and β subunit has β1, β2, β3, etc. Have been. The present inventors have found that a specific natural component has an action of promoting the production of integrin, which is useful as a cancer metastasis inhibitor (JP-A-11-246428), and which has an effect of improving sagging of skin and tightening of skin. It has been found that this is the case (Japanese Patent Laid-Open No. Hei 10-72336).

【0008】一方、近年皮膚のハリには、皮膚中の繊維
芽細胞に存在する張力繊維(アクチン−ミオシン束)が
関与し、Gタンパク質を介したアクチン−ミオシン系の
活性化(アクチン−ミオシン束の収縮)のメカニズムが
明らかにされ、アクチン−ミオシン系を活性化する物質
が皮膚のしわ・たるみの改善に有用であることが示唆さ
れている。しかし、インテグリンの産生を促進する成分
とアクチン−ミオシン系を活性化する成分とを併用する
ことにより、皮膚の弾力性が極めて良好に改善されるこ
とはこれまでに全く知られていない。
On the other hand, in recent years, tension of the skin (actin-myosin bundle) present in fibroblasts in the skin is involved in skin firmness, and activation of the actin-myosin system via G protein (actin-myosin bundle) is performed. The mechanism of actin-myosin system activation has been elucidated, suggesting that a substance that activates the actin-myosin system is useful for improving skin wrinkles and sagging. However, it has not been known at all heretofore that the elasticity of the skin is significantly improved by using a component that promotes integrin production in combination with a component that activates the actin-myosin system.

【0009】本発明におけるインテグリン産生促進剤と
しては、インテグリンの産生量を促進するものであり、
各種結合組織に存在するコラーゲン、ビトロネクチン、
フィブロネクチン、ラミニン等のマトリックスと線維芽
細胞等の結合組織に存在する細胞との相互作用を考える
と、α2サブユニット、α5サブユニット、β1サブユ
ニットの発現を促進するものが好ましく、更にα2サブ
ユニットの発現を促進し、同時にβ1サブユニットの発
現を促進するものがより望ましい。このようなインテグ
リン産生促進剤はほとんどなく、例えば単一化合物とし
てトランフォーミングファクター(TGFβ)が知られ
る他、ヒバマタ、マコンブ及びヒジキ等の海藻類、ロー
ズマリー、キウイ、ニンジン、ブクリョウ、トウニン及
びゴボウ等の植物が挙げられるが、インテグリンの産生
促進及び安全性の点から、ヒバマタ、マコンブ及びヒジ
キから選ばれる海藻類、ローズマリー、キウイ、ニンジ
ン、ブクリョウ、トウニン及びゴボウから選ばれる植物
又はそれらの抽出物が特に好ましい。
[0009] The integrin production promoter of the present invention promotes the production of integrin,
Collagen, vitronectin,
Considering the interaction between matrices such as fibronectin and laminin and cells present in connective tissues such as fibroblasts, those that promote the expression of α2 subunit, α5 subunit and β1 subunit are preferable, and α2 subunit is more preferable. What promotes the expression of β1 subunit at the same time is more desirable. There are almost no such integrin production promoters. For example, transforming factor (TGFβ) is known as a single compound, and seaweeds such as hibamata, makombu and hijiki, rosemary, kiwi, carrot, bukuro, tonin and burdock From the viewpoint of promotion of integrin production and safety, seaweeds selected from Hibamata, Macomb and Hijiki, plants selected from rosemary, kiwi, carrot, bukuro, Tonin and burdock, or extracts thereof. Is particularly preferred.

【0010】本発明におけるヒバマタとはヒバマタ科
(Fucaceae)ヒバマタ属(Fucus)のFucus vesiclosus
又はFucus evanescensを、マコンブとはコンブ科(Lami
nariaceae)コンブ属(Laminaria)のL.japonika Aresc
hougを、ヒジキとはホンダワラ科(Sargassaceae)ヒジ
キ属(Hizikia)のH.fusiforme Okamuraを、ローズマリ
ーとはシソ科(Labiatae)のRosmarinus officinatis
を、キウイとはマタタビ属(Actinidia)のキウイ(Act
inidia chinensis)を、ニンジンとは、ウコギ科(Aral
iaceae)のオタネニンジン(Panax ginseng C. A. Meye
r(Panax schinsengNees))の細根を除いた根又はこれ
を軽く湯通ししたものを、ブクリョウとはサルノコシカ
ケ科(Polyporaceae)のマツホド(Poria cocos Wolf)
の外層をほとんど除いた菌核を、トウニンとはバラ科
(Rosaceae)のモモ(Prunus persicaBatschまたはPrun
us persica Batsch var. davidiana Maximowicz)の種
子を、ゴボウとはキク科(Compositae)のArctium lapp
a L.を示す。
In the present invention, “Hibamata” refers to Fucus vesiclosus of the genus Hucamata (Fucaceae).
Or Fucus evanescens, and the kelp is the family Laminariaceae (Lami
nariaceae) L.japonika Aresc of the genus Laminaria
houg, Hijiki means H. fusiforme Okamura of Sargassaceae, Hizikia, and Rosemary Rosmarinus officinatis of Labiatae.
The kiwi is a kiwi (Act) of the genus Actinidia
inidia chinensis, carrot and
iaceae) Panax ginseng CA Meye
r (Panax schinsengNees)) excluding the fine roots or those obtained by lightly blanching the roots. Bukryou is a pine beet (Poria cocos Wolf) of the family Polyporaceae.
The sclerotium excluding most of the outer layer of the peach is called tounin, peach (Prunus persicaBatsch or Prun
The seeds of us persica Batsch var. davidiana Maximowicz) and burdock are Arctium lapp of Compositae
a Indicates L.

【0011】一方、本発明のアクチン−ミオシン系活性
化剤とは、皮膚線維芽細胞に作用してその細胞張力を促
進するものをいうが、これまでに、牛乳から作られたホ
エイタンパクと加水分解カゼインに当該作用があること
が報告されている。本発明者らは、後記実施例2に示す
ように、新たにオウゴン、オウバク、クチナシ、ジオ
ウ、ショウキョウ及びレンゲソウの各植物抽出物に、皮
膚繊維芽細胞の張力を促進する作用があり、アクチン−
ミオシン系活性化物質であることを見出した。
On the other hand, the actin-myosin activator of the present invention refers to a substance which acts on skin fibroblasts to promote their cell tension, and has been used so far with whey protein made from milk and hydrolyzate. It has been reported that degraded casein has this effect. The present inventors, as shown in Example 2 described below, each of the plant extracts of Ogon, Obak, Gardenia, Jio, Ginger, and Astragalus have an effect of promoting the tension of dermal fibroblasts, −
It was found to be a myosin-based activator.

【0012】ここで、オウゴンとはシソ科(Labiatae)
のコガネバナ(Scutellaria baicalensis Georgi)の周
皮を除いた根を、オウバクとはミカン科(Rutaceae)の
キハダ(Phellodendron amurense Ruprecht)またはそ
の他同属植物の周皮を除いた樹を、クチナシとはアカネ
科(Rubiaceae)のGardenia jasminoides Ellisを、ジ
オウとはゴマノハグサ科(Scrophulariaceae)のアカヤ
ジオウ(Rehmannia glutinosa Liboschitz var. purpur
ea MakinoまたはRehmannia glutinosa Liboschitz)の
根またはそれを蒸したものを、ショウキョウとはショウ
ガ科(Zingiberaceae)のショウガ(Zingiber officina
le Roscoe)の根茎を、レンゲソウとはマメ科(Legumin
osae)のAstragalus sinicusをそれぞれ示す。
[0012] Here, "Ogon" refers to Labiatae
Scutellaria baicalensis Georgi (Scutellaria baicalensis Georgi) refers to the roots excluding the pericarp, oubak refers to the tree of Rutaceae (Rutaceae) without the pericarp, or to the gardenia (Rutaceae). Rubiaceae) Gardenia jasminoides Ellis, and Jio is a red croaker (Rehmannia glutinosa Liboschitz var. Purpur) of Scrophulariaceae.
ea Makino or Rehmannia glutinosa Liboschitz) or steamed roots, ginger is a ginger (Zingiber officina) of the Zingiberaceae family
le Roscoe) rhizome, and astragalus are legumes (Legumin)
osae) of Astragalus sinicus.

【0013】本発明における藻類については、その全
藻、根、茎又は葉の1以上をそのまま又は粉砕して用い
ることができ、植物については、その植物の全草又は
葉、根、果実、種子、花のうちの1以上をそのまま又は
粉砕して用いることができる。
In the algae of the present invention, one or more of the whole algae, roots, stems and leaves can be used as they are or pulverized. For plants, the whole plant or leaves, roots, fruits and seeds of the plant can be used. , One or more of the flowers can be used as they are or crushed.

【0014】また、本発明における抽出物とは、更にこ
れを常温又は加温下にて抽出するか又はソックスレー抽
出器等の抽出器具を用いて抽出することにより得られる
各種溶剤抽出液、その希釈液、その濃縮液又はその乾燥
末を意味するものである。ここで抽出物は、1種の植物
からのものでも2種以上の植物から得られたものであっ
てもよい。
The extract in the present invention means various solvent extracts obtained by extracting the extract at room temperature or under heating or by using an extraction device such as a Soxhlet extractor, Liquid, its concentrated liquid or its dried powder. Here, the extract may be derived from one plant or from two or more plants.

【0015】本発明の藻類及び植物の抽出物を得るため
に用いられる抽出溶剤としては、極性溶剤、非極性溶剤
のいずれをも使用することができる。例えば、水;メタ
ノール、エタノール、プロパノール、ブタノール等のア
ルコール類;プロピレングリコール、ブチレングリコー
ル等の多価アルコール類;アセトン、メチルエチルケト
ン等のケトン類;酢酸メチル、酢酸エチル等のエステル
類;テトラヒドロフラン、ジエチルエーテル等の鎖状及
び環状エーテル類;ポリエチレングリコール等のポリエ
ーテル類;ジクロロメタン、クロロホルム、四塩化炭素
等のハロゲン化炭化水素類;ヘキサン、シクロヘキサ
ン、石油エーテル等の炭化水素類;ベンゼン、トルエン
等の芳香族炭化水素類;ピリジン類等が挙げられ、これ
らは2種以上を混合して用いることもできる。
As the extraction solvent used for obtaining the algae and plant extracts of the present invention, any of a polar solvent and a non-polar solvent can be used. For example, water; alcohols such as methanol, ethanol, propanol and butanol; polyhydric alcohols such as propylene glycol and butylene glycol; ketones such as acetone and methyl ethyl ketone; esters such as methyl acetate and ethyl acetate; tetrahydrofuran and diethyl ether Chain and cyclic ethers such as polyethylene glycol; polyethers such as polyethylene glycol; halogenated hydrocarbons such as dichloromethane, chloroform and carbon tetrachloride; hydrocarbons such as hexane, cyclohexane and petroleum ether; fragrances such as benzene and toluene. Group hydrocarbons; pyridines and the like, and these can be used as a mixture of two or more kinds.

【0016】上記抽出物は、そのまま用いることもでき
るが、当該抽出物を希釈、濃縮若しくは凍結乾燥した
後、粉末又はペースト状に調製して用いることもでき
る。
The above extract can be used as it is, but it can also be used after diluting, concentrating or freeze-drying the extract and then preparing it as a powder or paste.

【0017】また、液々分配等の技術により、上記抽出
物から不活性な夾雑物を除去して用いることもでき、本
発明においてはこのようなものを用いることが好まし
い。これらは、必要により公知の方法で脱臭、脱色等の
処理を施してから用いてもよい。
The extract may be used after removing inactive contaminants from the extract by a technique such as liquid-liquid distribution, and such an extract is preferably used in the present invention. These may be used after being subjected to a treatment such as deodorization and decoloration by a known method as necessary.

【0018】斯かるインテグリン産生促進剤及びアクチ
ン−ミオシン系活性化剤を配合した組成物は、後記実施
例3及び4で示すように、極めて優れたコラーゲンゲル
収縮作用を有し、優れた皮膚の弾力性改善効果や引き締
め効果を示す。従って、当該組成物は、乾燥、紫外線等
の外界の刺激や、皮膚が老化することにより生ずる種々
の皮膚性状の変化、例えば皮膚のしわ、たるみ、はり及
び弾力の喪失等に対して有効な皮膚化粧料として、或い
は弾力性改善剤、たるみ改善剤等として用いることがで
きる。
The composition containing such an integrin production promoter and actin-myosin activator has an extremely excellent collagen gel shrinking action and an excellent skin effect as shown in Examples 3 and 4 described below. It shows an elasticity improving effect and a tightening effect. Accordingly, the composition is effective for external stimuli such as drying and ultraviolet rays, and various changes in skin properties caused by aging of the skin, for example, skin wrinkles, sagging, abrasion and loss of elasticity. It can be used as a cosmetic, or as an elasticity improver, a sag improver, or the like.

【0019】本発明の皮膚化粧料中、インテグリン産生
促進剤は、組成物中に0.001〜10重量%配合する
ことが好ましく、インテグリン産生促進剤として上記藻
類又は植物の抽出物を用いる場合には、固形分換算で
0.00001〜1重量%、特に0.0001〜0.1
重量%含有することが好ましい。
In the skin cosmetic of the present invention, the integrin production promoter is preferably incorporated in the composition in an amount of 0.001 to 10% by weight, and when the above algal or plant extract is used as the integrin production promoter. Is 0.00001 to 1% by weight in terms of solid content, particularly 0.0001 to 0.1
It is preferable that the content be contained by weight.

【0020】また、アクチン−ミオシン系活性化剤は、
組成物中に0.001〜10重量%含有することが好ま
しく、アクチン−ミオシン系活性化剤として上記植物抽
出物を用いる場合には、固形分換算で0.00001〜
1重量%、特に0.0001〜0.1重量%含有するこ
とが好ましい。
The actin-myosin activator comprises
The composition preferably contains 0.001 to 10% by weight, and when the above-mentioned plant extract is used as an actin-myosin activator, 0.00001 to
It is preferably contained in an amount of 1% by weight, particularly 0.0001 to 0.1% by weight.

【0021】本発明の皮膚化粧料には、インテグリン産
生促進剤及びアクチン−ミオシン系活性化剤の他、通常
使用される外用基材、他の薬効成分を配合できる。ここ
で用いられる外用基材としては、油性基剤をベースとす
るもの、油/水、水/油型の乳化系基剤をベースとする
もの、水をベースとするもののいずれであってもよい。
In addition to the integrin production promoter and actin-myosin activator, the skin cosmetic composition of the present invention may contain a commonly used external base material and other active ingredients. The external base material used herein may be any of those based on an oily base, those based on an oil / water or water / oil type emulsified base, and those based on water. .

【0022】油性基剤としては、例えば植物油、動物
油、合成油、シリコーン油、脂肪酸、天然または合成の
グリセリド等が挙げられる。また、保湿剤、紫外線吸収
剤、アルコール類、キレート類、pH調整剤、防腐剤、増
粘剤、色素、香料等を任意に組合わせて配合することが
できる。また、上記薬効成分としては特に制限はなく、
例えば鎮痛消炎剤、殺菌消毒剤、ビタミン類、皮膚柔軟
化剤等を必要に応じて適宜使用できる。また、皮膚化粧
料の形態としては、軟膏、クリーム、乳液、化粧水、ジ
ェル、パック剤、パップ剤、ファンデーション等が挙げ
られる。
The oleaginous base includes, for example, vegetable oils, animal oils, synthetic oils, silicone oils, fatty acids, natural and synthetic glycerides, and the like. Further, humectants, ultraviolet absorbers, alcohols, chelates, pH adjusters, preservatives, thickeners, pigments, fragrances, and the like can be arbitrarily combined and compounded. The medicinal component is not particularly limited,
For example, an analgesic antiphlogistic, a germicidal antiseptic, vitamins, emollients, etc. can be used as needed. Examples of the form of the skin cosmetic include ointments, creams, emulsions, lotions, gels, packs, cataplasms, foundations, and the like.

【0023】本発明の皮膚化粧料の使用量は、1日、1
回当たり100〜500mg、好ましくは200mgが
好ましい。
The amount of the skin cosmetic of the present invention is 1 day, 1 day
100 to 500 mg, preferably 200 mg per serving is preferred.

【0024】[0024]

【実施例】製造例1〜22 表1に示す海草類及び植物の各部位の粉砕物1kgを抽出
溶剤5リットルに室温で1週間浸漬し、溶剤可溶成分を
抽出した。抽出液を分離した残渣について同様の操作を
繰り返し、合計10リットルの抽出液を得た。この抽出
液の溶剤を留去し、減圧乾固し、抽出物を得た。なお、
以下において、Wは水を、BGは1,3−ブチレングリ
コール、ETはエタノールを示す。
EXAMPLES Production Examples 1 to 22 1 kg of pulverized material of each part of seaweeds and plants shown in Table 1 was immersed in 5 liters of an extraction solvent at room temperature for one week to extract solvent-soluble components. The same operation was repeated for the residue from which the extract was separated to obtain a total of 10 liters of the extract. The solvent of this extract was distilled off and dried under reduced pressure to obtain an extract. In addition,
In the following, W represents water, BG represents 1,3-butylene glycol, and ET represents ethanol.

【0025】[0025]

【表1】 [Table 1]

【0026】実施例1 インテグリン産生促進の評価 線維芽細胞表面インテグリン量をFACScanにて測
定した。即ち、単層培養の線維芽細胞に表1に示す各種
サンプルを30〜100μMで作用させ、24時間後に
トリプシン/EDTAにより細胞を剥離し、FCSで中
和した後、細胞を0.01% FCS、0.02% N
aN3含有PBSにて洗浄し細胞を回収した。一次抗体
として抗ヒトインテグリンα2β1、抗ヒトインテグリ
ンα2、抗ヒトインテグリンβ1を100倍希釈で、二
次抗体としてFITCラベル抗マウスIgG1を100
倍希釈で用いた。ブランクは一次抗体にマウスIgG1
を用いた。結果を表2に示す。
Example 1 Evaluation of Promotion of Integrin Production The amount of fibroblast surface integrin was measured by FACScan. That is, various samples shown in Table 1 were allowed to act on fibroblasts in monolayer culture at 30 to 100 μM, and after 24 hours, the cells were detached with trypsin / EDTA, neutralized with FCS, and then cultured with 0.01% FCS. , 0.02% N
The cells were washed with PBS containing aN 3 and collected. Anti-human integrin α2β1, anti-human integrin α2, and anti-human integrin β1 were diluted 100-fold as the primary antibody, and FITC-labeled anti-mouse IgG1 was diluted 100 times as the secondary antibody.
Used in double dilution. Blank is mouse IgG1 as primary antibody
Was used. Table 2 shows the results.

【0027】[0027]

【表2】 [Table 2]

【0028】実施例2 アクチン−ミオシン系活性化に
よる細胞の張力発生の評価 Kolodneyらの方法(Kolodeney MSら、J. Cell Biol.,1
17,73‐82(1992))に準じて、線維芽細胞包埋コラー
ゲンゲルを作製し、得られたゲルを37℃に保温した無
血清培地中に固定し、50〜100mgの負荷をかけ安定
化させた後、無血清DMEMで最終濃度の50倍程度の
濃度に調整した表3に示すサンプルを1mL添加(濃度
0.001%、蒸発残分重量%)し、発生する力をIsoto
nic Transducerで計測し、BIOPACで記録した。得られた
データの試料添加前の比較的安定した5分間、添加後の
張力が最大となる5分間の平均の差を発生した張力とし
た。結果を表3に併せて示す。
Example 2 Evaluation of Cell Tension Generation by Activation of Actin-Myosin System Kolodney et al. (Kolodeney MS et al., J. Cell Biol., 1
17, 73-82 (1992)), a fibroblast-embedded collagen gel was prepared, and the obtained gel was fixed in a serum-free medium kept at 37 ° C., and a load of 50 to 100 mg was applied and stabilized. After that, 1 mL of a sample shown in Table 3 adjusted to about 50 times the final concentration with serum-free DMEM was added (concentration 0.001%, evaporation residue weight%), and the generated force was determined by Isoto.
Measured by nic Transducer and recorded by BIOPAC. The resulting tension was defined as the average difference between the relatively stable 5 minutes before addition of the sample and the 5 minutes after which the tension after addition was maximum. The results are shown in Table 3.

【0029】[0029]

【表3】 [Table 3]

【0030】実施例3 線維芽細胞包埋コラーゲンゲル
の収縮に与える影響 コラーゲンゲルは文献「J.Cell Science,102,315(19
92)」または「J.Invest.Dermatol,93,792(1989)」に準じた
方法で作製した。すなわち、氷冷下コラーゲンゲル溶液
(新田ゼラチン社製、tapel−A(3.0mg/ml,pH=3))
にHEPES(250mM)の0.05Nの水酸化ナトリウム溶
液、DMEM(GIBCO DMEM,low glucose)5倍濃縮溶液、
FCS(2%、Fatal Calf Serum)、精製水を加え、十
分に攪拌中和した後、最終濃度0.01〜0.001重
量%(蒸発残分重量%)の表4及び5に示す被験物質
(製造例1〜23で得た海藻類若しくは植物抽出物、及
びコントロールとしてエタノール又は1,3−ブチレン
グリコール)を加え、最後にヒ卜皮膚線維芽細胞(ヒト
包皮由来)の懸濁液を加え十分に攪拌し、気泡を取り除
いた後、24穴プレートに各穴1mlずつ注入し、直ちに
37℃でゲル化させた。この際のコラーゲン濃度は1.
5mg/mLに調製した。24時間後ゲルの周囲を剥離し、
培地を加え培養した。ゲル体積測定は、文献(J.Cell
Science,102,315(1992))に準じ重量測定方法で行っ
た。すなわち10%ホルマリン固定(4℃,24時間)
後、水の表面張力をTriton XlOO(和光純薬社製)(1
%)を加えることで減じた後、重量を測定した。結果を
表4及び5に併せて示す。
Example 3 Influence on Collagen of Fibroblast-Embedded Collagen Gel Collagen gel is described in J. Cell Science, 102, 315 (19).
92) "or" J. Invest. Dermatol, 93, 792 (1989) ". That is, a collagen gel solution (tapel-A (3.0 mg / ml, pH = 3) manufactured by Nitta Gelatin Co., Ltd.) under ice cooling.
HEPES (250 mM) in 0.05 N sodium hydroxide solution, DMEM (GIBCO DMEM, low glucose) 5-fold concentrated solution,
FCS (2%, Fatal Calf Serum) and purified water were added, and the mixture was thoroughly stirred and neutralized, and then the test substances having a final concentration of 0.01 to 0.001% by weight (evaporation residue weight%) shown in Tables 4 and 5 (The seaweed or plant extract obtained in Production Examples 1 to 23 and ethanol or 1,3-butylene glycol as a control) were added, and finally, a suspension of human skin fibroblasts (derived from human foreskin) was added. After sufficiently stirring to remove air bubbles, 1 ml of each well was poured into a 24-well plate, and immediately gelled at 37 ° C. The collagen concentration at this time was 1.
It was adjusted to 5 mg / mL. After 24 hours, peel around the gel,
The medium was added and cultured. Gel volume measurement is described in the literature (J. Cell
Science, 102, 315 (1992)). That is, 10% formalin fixation (4 ° C, 24 hours)
Then, the surface tension of the water was adjusted to Triton XlOO (manufactured by Wako Pure Chemical Industries, Ltd.) (1
%) And then weighed. The results are shown in Tables 4 and 5.

【0031】[0031]

【表4】 [Table 4]

【0032】[0032]

【表5】 [Table 5]

【0033】インテグリン産生促進剤とアクチン−ミオ
シン系活性化剤の併用により、線維芽細胞包埋コラーゲ
ンゲルの直径および体積が小さくなり、ゲルの収縮が相
乗的に促進されることが示された。
It was shown that the combined use of an integrin production promoter and an actin-myosin activator reduced the diameter and volume of a fibroblast-embedded collagen gel and synergistically promoted gel shrinkage.

【0034】実施例4 表6に示したサンプルを用いて、パネラーにより皮膚た
るみ(頬)改善度を評価した。ヒバマタエキス単独、あ
るいはヒバマタエキスにショウキョウ又はオウバクを配
合したジェルを用い、各サンプルにつき10名ずつパネ
ラーによる評価を行った。各エキス配合ジェルを一日朝
夜1回ずつ2週間、顔面頬から顎にかけての部分に塗布
した。以下のスコアにより評価した。結果を表6に併せ
て示す。
Example 4 Using the samples shown in Table 6, the degree of improvement in skin sagging (cheek) was evaluated by panelists. Each sample was evaluated by a panel of 10 panelists using a gel of HIBAMATA extract alone or a mixture of HIBAMATA extract and Ginger or Oba. Each extract-containing gel was applied once a day, in the morning and at night, to the area from the cheek to the chin for 2 weeks. The following scores were used for evaluation. The results are shown in Table 6.

【0035】−1:悪化した 0:変わらない、わからない 1:微かにたるみが改善した 2:ややたるみが改善した 3:たるみが改善した 4:非常にたるみが改善した-1: Deteriorated 0: No change, I do not know 1: Slightly improved slack 2: Slightly improved slack 3: Improved slack 4: Very improved slack

【0036】[0036]

【表6】 [Table 6]

【0037】表6より本発明の試料C及びDについて
は、引き締め効果が実感された。
From Table 6, the tightening effect was felt for the samples C and D of the present invention.

【0038】実施例5 処方例 表7〜12に示す各成分を常法に従い、攪拌、混合する
ことにより本発明の各種皮膚化粧料を調製した。
Example 5 Formulation Examples Various components of the present invention were prepared by stirring and mixing the components shown in Tables 7 to 12 in a conventional manner.

【0039】[0039]

【表7】 [Table 7]

【0040】[0040]

【表8】 [Table 8]

【0041】[0041]

【表9】 [Table 9]

【0042】[0042]

【表10】 [Table 10]

【0043】[0043]

【表11】 [Table 11]

【0044】[0044]

【表12】 [Table 12]

【0045】[0045]

【発明の効果】インテグリン産生促進剤及びアクチン−
ミオシン系活性化剤を配合した本発明の皮膚化粧料は、
インテグリン産生促進剤又はアクチン−ミオシン系活性
化剤を単独で用いた場合に比べ、相乗的に皮膚引き締め
効果が促進され、より安全性の高いものであることか
ら、肌のしわ・たるみを改善し、ハリのある美しい肌に
整える化粧料として有用である。
EFFECT OF THE INVENTION Integrin production promoter and actin
The skin cosmetic of the present invention containing a myosin-based activator,
Compared with the case where the integrin production promoter or actin-myosin activator is used alone, the skin tightening effect is synergistically promoted, and since it is safer, wrinkles and sagging of the skin are improved. It is useful as a cosmetic that prepares firm and beautiful skin.

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4C083 AA111 AA112 AA122 AB032 AB332 AB352 AB442 AC022 AC072 AC122 AC132 AC242 AC292 AC342 AC402 AC712 AC852 AC902 AD092 AD352 AD512 BB60 CC02 CC04 CC05 DD23 DD27 DD31 DD41 EE11  ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4C083 AA111 AA112 AA122 AB032 AB332 AB352 AB442 AC022 AC072 AC122 AC132 AC242 AC292 AC342 AC402 AC712 AC852 AC902 AD092 AD352 AD512 BB60 CC02 CC04 CC05 DD23 DD27 DD31 DD41 EE11

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 インテグリン産生促進剤及びアクチン−
ミオシン系活性化剤を含有する皮膚化粧料。
1. An integrin production promoter and actin-
Skin cosmetics containing a myosin-based activator.
【請求項2】 インテグリン産生促進剤が、ヒバマタ、
マコンブ、ヒジキ、ローズマリー、キウイ、ニンジン、
ブクリョウ、トウニン及びゴボウから選ばれる1種以上
の海藻類若しくは植物又はそれらの抽出物である請求項
1記載の皮膚化粧料。
2. The integrin production promoter is Hibamata,
Macomb, Hijiki, Rosemary, Kiwi, Carrot,
2. The skin cosmetic according to claim 1, which is at least one kind of seaweed or plant selected from bukuro, tonin and burdock, or an extract thereof.
【請求項3】 アクチン−ミオシン系活性化剤が、オウ
ゴン、オウバク、クチナシ、ジオウ、ショウキョウ及び
レンゲソウから選ばれる1種以上の植物又はそれらの抽
出物である請求項1又は2記載の皮膚化粧料。
3. The skin cosmetic composition according to claim 1, wherein the actin-myosin activator is at least one plant selected from Japanese gourd, oak, gardenia, zio, ginger, and astragalus or an extract thereof. Fees.
【請求項4】 皮膚化粧料が、皮膚の弾力性を改善する
ものである請求項1〜3のいずれか1項記載の皮膚化粧
料。
4. The skin cosmetic according to claim 1, wherein the skin cosmetic improves skin elasticity.
JP2000091398A 2000-03-29 2000-03-29 Skin cosmetic Pending JP2001278769A (en)

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Cited By (20)

* Cited by examiner, † Cited by third party
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JP2003183171A (en) * 2001-12-21 2003-07-03 Ichimaru Pharcos Co Ltd Elastase activity inhibitor
WO2003099244A1 (en) * 2002-05-27 2003-12-04 Beiersdorf Ag Cosmetic and/or dermatological preparation comprising 2,3-dibenzylbutyrolactones
DE10223486A1 (en) * 2002-05-27 2003-12-11 Beiersdorf Ag Cosmetic and / or dermatological preparation with 2,3-dibenzylbutyrolactones
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JP2009067701A (en) * 2007-09-11 2009-04-02 Maruzen Pharmaceut Co Ltd Growth promoter of keratinized cell of epidermis and transglutaminase-1 production promoter
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