• 제목/요약/키워드: Mouse skin

검색결과 714건 처리시간 0.027초

아토피성피부염유발제제(BMAC)를 이용한 Atopy dermatitis NC/Nga mouse model에서 아토피 크림과 자운고(紫雲膏)에 대한 피부발진 억제효과 (Topical Application of Atopy cream-Jawoongo ointment(A-J) of Ointment Inhibits Biostir mite antigen cream induced Atopy Dermatitis by Local Action in NC/Nga Mice)

  • 여의주;한재경;김윤희
    • 혜화의학회지
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    • 제17권2호
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    • pp.185-198
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    • 2008
  • Wished to examine closely effect that Atopy cream-Jawoongo ointment (A-J) used to atopy dermatitis disease patient get in atopy eruption control experimentally. In this research A-J ointment as treatment result to a NC/Nga mouse by BMAC ointment, clinical skin severity score decreased remarkably than control group. Thus, NC/Nga mice suffered from dermatitis very similar to human AD with IgE hyperproduction. Specially, result that measure IgE and IgG1 level in serum decreased remarkably than control group.

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피페리디노피리미딘계 유도체의 모발성장에 대한 효과 (Antialopecic Effect of Piperidinopyrimidine Derivative)

  • 신준수;김경순;강경환;문성준;이우영;김박광
    • 약학회지
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    • 제40권3호
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    • pp.340-342
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    • 1996
  • To investigate the antialopecic effect of N-4-salicylomide-2-amino-6-piperidinopyrimidine 3-oxide(SALMI) and its salt on the hair of black mouse (C57BL/6), this study was carrie d out. When salmi and its salt in ethanol solution were administered to the black mouse (C57BL/6) by route of skin, both of them promoted the growth of hair.

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음양곽 물추출물이 Bl6 Mouse Melanoma 세포의 멜라닌 생성에 미치는 영향 (Effect of the Aqueous Extract of Epimedium Koreanum Nakai on Melanin Formation in Bl6 Mouse Melanoma Cell Line)

  • 천현자;문연자;김정훈;김일광;전병훈;우원홍
    • 약학회지
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    • 제44권5호
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    • pp.455-462
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    • 2000
  • To investigate how the aqueous extracts of Epimedium koreanum Nakai (EK) affects pigmentation of skin, the aqueous extract of EK at various concentrations were incubated with 1 $\times$ 10$^{5}$ melanoma cells per well for 72 h. The morphology and number of cell line were not changed, but the aqueous extract of EK increased the tyrosinase activity and the content of melanin polymer in the cell line. These results indicate that the aqueous extract of EK promotes melanogenesis of Bl6 mouse melanoma cell line.

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The effects of some natural products on mouse melanoma cells in vitro

  • Cha, Eun-Jung;Kim, An-Keun
    • 대한약학회:학술대회논문집
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    • 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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    • pp.321.1-321.1
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    • 2002
  • To indentify inhibitors of melanogenesis. we compared the effect of some natural products on mushroom tyrosinase. human melanocytic tyrosinase activity and melanin content. The cytotoxicity of the component were also tested on cultured mouse melanoma cells, Each extract significantly inhibited tyrosinase activity and melanin synthesis in vitro and B 16 melanoma cell lines. In B 16 cell lines, watermelon's inner shell extract inhibited tyrosinase activity as strong as kojic acid at 150${\um}g$/${\mu}\ell$ concentration. And morning glory'seed extract inhibited melanin synthesis more than kojic acid at 150${\um}g$/${\mu}\ell$ concentration. Each extract were strong inhibitors of tyrosinase activity and total melanin synthesis in B 16 mouse melanoma cell lines at less than 100${\um}g$/${\mu}\ell$ concetration. These result show that extract of watermelon's inner shell. lettuce. morning glory's seed and licorice root could be developed as skin whitening component of cosmetics.

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Compound K improves skin barrier function by increasing SPINK5 expression

  • Park, No-June;Bong, Sim-Kyu;Lee, Sullim;Jung, Yujung;Jegal, Hyun;Kim, Jinchul;Kim, Si-Kwan;Kim, Yong Kee;Kim, Su-Nam
    • Journal of Ginseng Research
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    • 제44권6호
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    • pp.799-807
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    • 2020
  • Background: The skin acts as a barrier to protect organisms against harmful exogenous agents. Compound K (CK) is an active metabolite of ginsenoside Rb1, Rb2 and Rc, and researchers have focused on its skin protective efficacy. In this study, we hypothesized that increased expression of the serine protease inhibitor Kazal type-5 (SPINK5) may improve skin barrier function. Methods: We screened several ginsenosides to increase SPINK5 gene promoter activity using a transactivation assay and found that CK can increase SPINK5 expression. To investigate the protective effect of CK on the skin barrier, RT-PCR and Western blotting were performed to investigate the expression levels of SPINK5, kallikrein 5 (KLK5), KLK7 and PAR2 in UVB-irradiated HaCaT cells. Measurement of transepidermal water loss (TEWL) and histological changes associated with the skin barrier were performed in a UVB-irradiated mouse model and a 1-chloro-2,4-dinitrobenzene (DNCB)-induced atopic dermatitis-like model. Results: CK treatment increased the expression of SPINK5 and decreased the expression of its downstream genes, such as KLKs and PAR2. In the UVB-irradiated mouse model and the DNCB-induced atopic dermatitis model, CK restored increased TEWL and decreased hydration and epidermal hyperplasia. In addition, CK normalized the reduced SPINK5 expression caused by UVB or DNCB, thereby restoring the expression of the proteins involved in desquamation to a level similar to normal. Conclusions: Our data showed that CK contributes to improving skin-barrier function in UVB-irradiated and DNCB-induced atopic dermatitis-like models through SPINK5. These results suggest that therapeutic attempts with CK might be useful in treating barrier-disrupted diseases.

Red ginseng oil promotes hair growth and protects skin against UVC radiation

  • Truong, Van-Long;Keum, Young-Sam;Jeong, Woo-Sik
    • Journal of Ginseng Research
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    • 제45권4호
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    • pp.498-509
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    • 2021
  • Background: A wide range of environmental factors, such as diseases, nutritional deficiencies, ageing, hormonal imbalances, stress, and ultraviolet (UV) radiation, may affect the structure and function of the skin that covers the entire surface of the human body. In this study, we investigated roles of red ginseng oil (RGO) in enhancing skin functions, including hair growth and skin protection, using mouse models. Methods: For hair growth experiment, shaved dorsal skins of C57BL/6 mice were topically applied with vehicle, RGO, RGO's major compounds, or minoxidil for consecutive 21 days and skin tissues were examined the hair growth promoting capacity. For skin protection experiment, SKH-1 hairless mice were topically applied with vehicle or RGO twice a day for three days prior to exposure to UVC radiation at 20 kJ/cm2. Skin tissues were collected to evaluate skin protective effects of RGO. Results: Topical application of RGO to C57BL/6 mice effectively promoted hair regeneration by inducing early telogen-to-anagen transition and significantly increasing the density and bulb diameter of hair follicles. Major compounds, including linoleic acids and β-sitosterol, contributed to RGO-promoted hair growth. Treatment with RGO as well as its major components upregulated expression of hair growth-related proteins. Furthermore, in SKH-1 hairless mice, RGO had a protective effect against UVC-induced skin damage by inhibiting inflammation and apoptosis, as well as inducing cytoprotective systems. Conclusion: These data suggest that RGO may be a potent agent for improving skin health and thereby preventing and/or treating hair loss and protecting skin against UV radiation.

자외선 조사 무모쥐 피부조직에 도포한 애엽(Mugwort) 추출물의 주름개선 효과 (Antiwrinkle Effects of Mugwort (Artemisia vulgaris) Extracts on UVB-Irradiated Hairless Mouse Skin)

  • 박시향;홍유미;최영준;최진호;김병관
    • 한국식품영양과학회지
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    • 제37권9호
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    • pp.1136-1141
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    • 2008
  • 무모쥐의 등에 애엽 추출물과 아스코르브산 함유 스킨로션을 도포하고 자외선을 조사하여 애엽 추출물과 아스코르브산의 주름 개선 효과를 알아보았다. 애엽 추출물 도포군의 피부조직 두께는 대조군에 비해 $12.5{\sim}21.4%$의 유의적인 감소 효과를 보였다. 표면 거칠기 측정기에 의한 피부 주름의 형성 정도를 측정하는 지표인 Ra값은 ME-1.0, ME-2.0과 ME-5.0 도포군에서 $23.7{\sim}31.1%$로 유의적으로 감소하였고 (p<0.01), Rq치는 ME-1.0, ME-2.0와 ME-5.0에서 $11.2{\sim}21.2%$, Rz의 측정치에서는 ME-1.0(19.8%), ME-2.0(22.1%), ME-5.0(24.5%) 그룹에서 대조군에 비해 크게 감소하였다. Rt치는 ME-1.0, ME-2.0와 ME-5.0 그룹에서 농도 증가에 따라 14.2%에서 22.7%의 유의적인 감소효과가 있었다. 아스코르브산 도포그룹은 애엽과 비슷한 감소효과를 보여주었지만, 애엽의 주름 개선효과에는 미치지 못하였다. MMP-1 활성은 애엽 메탄올 추출물 그룹에서 $19.3%{\sim}22.6%$까지 감소하였고, 콜라겐의 생성은 ME-2.0과 ME-5.0그룹에서 10% 정도의 유의적인 증가 효과가 있었다. 이처럼 애엽 메탄올 추출물은 피부의 광손상에 대한 피부 보호 및 피부의 주름 개선효과가 탁월하고, 또한 강력한 항산화제인 아스코르브산보다 그 효과가 우수하여 피부노화 현상과 주름 개선을 위한 기능성 화장품 소재로 이용가치가 있을 것으로 여겨진다.

음파영동 경피약물수송에 의한 Piroxicam Gel의 경피투과 (Skin Permeability of piroxicam Gel by Phonophoretic Transdermal Drug Delivery)

  • 최석주;오명화;김태열
    • The Journal of Korean Physical Therapy
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    • 제14권4호
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    • pp.147-162
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    • 2002
  • Transdermal permeation enhancer has been used to increased skin absorption. External control of drug release and skin absorption can also be achieved by iontophoresis or phonophoresis. However, because several problems with iontophoresis are that it has a risk to skin damage because of the change of pH and the increase of current density in applying it and that it can be applied only in the form of water solution, This study is to enhance drug permeation via skin following application of ultrasound. For this goal, in gel containing piroxicam, the degree of skin permeation in vitro and anti-inflammatory effect in in vivo were investigated. Permeation study using hairless mouse skin was performed at 37 $^{\circ}C$ using buffer saline as the receptor solution. The amount of piroxicam were quantified using a HPLC system consisting of solvent delivery system. Following adoption of ultrasound 1 MHZ, it showed relatively high permeation rate where it was compared with non treated by ultrasound. The influence of duty cycle having an effect on skin permeation rate was slight higher in the case of using pulsed mode. Skin permeation increase attended by intensity of ultrasound, the permeation of trice was accelerated at 2.0 W/$cm^{2}$ than 1.0 W/$cm^{2}$. The skin permeation of piroxicam was substantially influenced by ultrasound. Anti-inflammatory effects were determined using carrageenan-induced paw swelling method in SD rat. Paw swelling tests showed that pulsed phonophoresis group was more effective than control group and only gel application group. The conclusion of phonophoresis was found to improve significantly the skin permeation in vitro and the anti-inflammatory effect in vivo.

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