• 제목/요약/키워드: $\beta$-type

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능실 추출물 및 그 분획물의 피부 광노화 억제 효능 (Inhibitory Effect of Fractionated Trapa Japonica Extracts on UVB-induced Skin Photoaging)

  • 남진주;이경은;박지은;문성준;염종경
    • 대한화장품학회지
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    • 제40권4호
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    • pp.321-330
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    • 2014
  • 자외선은 피부의 구조적, 생리학적 변화를 일으키는 대표적인 외부 환경 인자로서 광노화, 일광화상 및 피부암을 일으키는 원인이 된다. 이러한 자외선은 외부적인 스트레스 자극 인자로 작용하여 피부 세포 내에서 비활성 코르티손을 활성 코르티솔로 전환시키는 효소인 $11{\beta}$-hydroxysteroid dehydrogenase type 1 ($11{\beta}-HSD1$)의 발현 및 활성을 증가시킨다. 이에 본 연구에서는 UVB에 의해 증가된 $11{\beta}-HSD1$의 발현을 효과적으로 억제할 수 있는 천연 추출물을 발굴하고자 하였다. 사람 섬유아세포에 다양한 천연물을 스크리닝한 결과, 능실 추출물이 유의한 효과가 있음을 확인하고, 능실 추출물을 추가 분획하여 사람 섬유아세포와 3D skin model에서 피부 광노화 억제 소재로서의 가능성을 확인하였다. 능실 추출물 및 분획물은 섬유아세포에서 $11{\beta}-HSD1$의 발현을 억제함과 동시에 자외선에 의한 matrix metalloproteinase (MMP)-1, 3, 9 및 염증성 싸이토카인(IL-6, 8)의 발현 증가를 억제하였다. 또한, 3D skin model을 이용한 평가에서, 능실 추출물은 UVB에 의한 MMP-1 단백질 발현을 억제하였고, UVB에 의한 표피 두께 감소 및 각질형성세포의 증식 감소를 회복시켰다. 따라서, 본 연구 결과로부터 능실 추출물 및 분획물은 UVB에 의한 $11{\beta}-HSD1$의 발현 증가와 이에 수반하는 광노화를 효과적으로 예방함을 확인하였다.

TROGLITAZONE, A NOVEL ANTIDIABETIC DRUG -NEW AVENUE FOR TREATING INSULIN RESISTANCE-

  • Horikoshi, Hiroyoshi
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 1998년도 춘계학술대회
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    • pp.1-4
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    • 1998
  • Impaired insulin action in Type 2 diabetes is thought to lead to hyperglycemia, with both environmental and complex genetic factors playing key roles. Although the primary lesion in Type 2 diabetes is unknown, a number of studies suggest that metabolic defects in the liver, skeletal muscle and fat, and pancreatic ${\beta}$-cells contribute to the disease. These metabolic abnormalities are characterized by the overproduction of hepatic glucose, impaired insulin secretion, and peripheral insulin resistance. In current pharmacological treatment of Type 2 diabetes, sulfonylurea (SU) drugs have mainly been used as oral hypoglycemic drugs to stimulate endogenous insulin secretion from ${\beta}$ cells. SU drugs, however, sometimes aggravate the disease by causing fatigue of the pancreatic ${\beta}$ cells, which leads to reduced drug efficacy after long-term treatment. This class of drugs also leads to enhanced obesity arising from the stimulation of endogenous insulin secretion in obese Type 2 diabetic patients, plus an increased incidence of SU-induced hypoglycemia. Since 1980, a major challenge has been made by us to develop a potential pharmacological therapy for the treatment of insulin resistance in peripheral tissues and/or suppression of abnormal hepatic glucose production in Type 2 diabetic patients. Such a drug would be expected to have fewer side effects and retain long-term efficacy.

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남매에서 가족력을 가진 galactosialidosis 1례 (Galactosialidosis with a Family History in a Sibling)

  • 임선주;남상욱
    • 대한유전성대사질환학회지
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    • 제6권1호
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    • pp.32-39
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    • 2006
  • 저자들은 출생 후 정상적인 발달을 보이다가 생후 6개월부터 의식과 운동 발달의 퇴행을 보이던 13개월 환아에서 효소 검사를 시행하여 ${\beta}$-galactosidase의 결핍을 확인하고 $GM_1$-gangliosidosis type 1으로 진단하였지만, 후에 추가적으로 시행한 효소 검사에서 ${\alpha}$-neuraminidase의 결핍도 발견되어 galactosialidosis로 진단한 증례를 경험하였기에 문헌 고찰과 함께 보고하고자 한다.

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Immune-Enhancing Alkali-Soluble Glucans Produced by Wild-Type and Mutant Saccharomyces cerevisiae

  • Ha Chang-Hoon;Lim Ki-Hong;Jang Se-Hwan;Yun Cheol-Won;Paik Hyun-Dong;Kim Seung-Wook;Kang Chang-Won;Chang Hyo-Ihl
    • Journal of Microbiology and Biotechnology
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    • 제16권4호
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    • pp.576-583
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    • 2006
  • The alkali-soluble glucan of the yeast cell wall contains $\beta-(1,3)-$ and (1,6)-D-linkages and is known to systemically enhance the immune system. In the previous study [6], in order to isolate cell wall mutants, a wild-type strain was mutagenized by exposure to ultraviolet light, and the mutants were then selected via treatment with laminarinase $(endo-\beta-(1,3)-D-glucanase)$. The mass of alkali- and water-soluble glucans produced by the mutant was measured to be 33.8 mg/g of the dry mass of the yeast cell. Our results showed that the mutants generated the amount of alkali-soluble glucan 10-fold higher than that generated by the wild-type. Structural analysis showed that the alkali-soluble glucan from the mutants was associated with a higher degree of $\beta-(1,6)-D-linkage$ than was observed in conjunction with the wild-type. Yeast cell wall $\beta-glucan$ was shown to interact with macrophages via receptors, thereby inducing the release of tumor necrosis factor alpha $(TNF-\alpha)$ and nitric oxide. Alkali-soluble $\beta-glucans$, both from water-soluble and water-insoluble glucan, exhibited a higher degree of macrophage activity with regard to both the secretion of tumor necrosis factor alpha $(TNF-\alpha)$ and nitric oxide and direct phagocytosis, than did the positive control ($1{\mu}g$ of lipopolysaccharide).

사각채널내 와동발생기가 부착된 원형실린더 하류 유동 특성에 대한 실험적 연구 (Experimental Investigations of Flow Characteristics by Wing Type Vortex Generators Set up Behind a Circular Cylinder in a Rectangular Channel)

  • 이상민;하홍영;양장식;이기백
    • Journal of Advanced Marine Engineering and Technology
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    • 제25권5호
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    • pp.1076-1085
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    • 2001
  • Experimental investigations of the longitudinal vortices, which are produced by wing type vortex generators set up behind a circular cylinder in a rectangular channel, are presented. When the circular cylinder is set up in the rectangular channel, a horseshoe vortex is formed just upsteam of the circular cylinder. It generates a turbulent wake region behind the circular cylinder. Therefore, the region of the pressure loss behind the circular cylinder in increased and the size of the wake is small. These problems can be achieved by longitudinal vortices which are generated by wing-type vortex generator. In order to control the strength of longitudinal vortices, the angle of attack of the vortex generators is varied from 20 degree to 45, but the spacing between the vortex generators is fixed 6cm. The 3-dimensional mean velocity measurements are made using a five-hole probe. The vorticity field and streamwise velocity contour are obtained from the velocity field. The following results are obtained. Circulation strength is the maximum value when the angle of attack($\beta$) is $30^{\circ}$, and the vorticity field and streamwise velocity contour in case of $\beta$=$20^{\circ}$ show the trend similar to these in case of $\beta$=$30^{\circ}$, but do not in case of $\beta$=$45^{\circ}$.

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Structure-Activity Relationship of Triterpenoids Isolated from Mitragyna stipulosa on Cytotoxicity

  • Tapondjou, Leon Azefack;Lontsi, David;Sondengam, Beiham Luc;Choudhary, Muhammad Iqbal;Park, Hee-Juhn;Choi, Jong-Won;Lee, Kyung-Tae
    • Archives of Pharmacal Research
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    • 제25권3호
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    • pp.270-274
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    • 2002
  • Chromatographic separation of the stem bark extract of Mitragyna stipulosa afforded triterpene derivatives ursolic acid (1), quinovic acid (2), quinivic acid $3-O-{\beta}-D-glucopyranoside$ (3, quinovin glycoside C), quinovic acid 3-O-[$(2-O-sulfo)-{\beta}-D-quinovopyranoside$] (4, zygophyloside D) and quinovic acid $3-O-{\beta}-D-quinovopyranosyl-27-O-{\beta}-D-glucopyranosyl$ ester (5, zygophyloside B). These five compounds were subjected to the cytotoxicity on MTT assay system. Compound 1 among tested showed the most potent cytotoxicity. Quinovic acid showed less potent cytotoxicity than ursolic acid and sugar linkages to 2 decreased the cytotoxicity. Compound 4 more potent than 3 with indicate that the sulfonyl group significantly enhances the activity. This indicates that the glycosidic linkage in ursane-type triterpenoids has mainly negative effect on cytotoxicity unlike in oleanane-type glycosides.

무청으로부터 분리된 이소람네틴 3-O-beta-D글루코피라노사이드의 항헤르페스 바이러스 1형(HSV-1) 효과 (Anti-Herpes Simplex Virus type I (HSV-1) Effect of Isorhamnetin 3-0-beta-D-Glucopyranoside Isolated from Brassica rapa)

  • 김호경;강봉주;박갑주;고병섭;황완균
    • 약학회지
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    • 제42권6호
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    • pp.607-612
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    • 1998
  • In the course of our search for anti-Herpes simplex virus type I (HSV 1) substances from natural sources, we screened crude drugs for their antiviral activity using SRB assay. T he methanol extract from herb of Brassica rapa (Cruciferae) was found to inhibit HSV-1. Though bioassay-directed fractionation of the extract, anti-HSV-1 agent was isolated by chromatographic separation using Amberlite XAD-4 and Sephadex LH-20. The structure of compound I was elucidated by spectral means including $^1H-^1H$ COSY, HMQC and HMBC to be isorhamnetin 3-O-${\beta}$-D-glucopyranoside (compound I). Compound I was active against HSV-1 with the 50% effective concentration of O.42mg/ml and the 50% cytotoxicity of 5.0mg/ml.

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산개성단 NGC 457 영역의 변광성 (VARIABLE STARS IN THE REGION OF THE OPEN CLUSTER NGC 457)

  • 전영범;박윤호;이상민
    • 천문학논총
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    • 제32권3호
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    • pp.421-438
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    • 2017
  • Through the short-period variability survey program, we obtained time-series BV CCD images for $1.5^{\circ}{\times}1.0^{\circ}$ region around the young open cluster NGC 457. As a result, we have detected 61 variable stars including 31 new ones after checking light curves of all stars by eyes. The 61 variable stars were included 14 ${\delta}$ Scuti variable stars, a ${\beta}$ Cephei variable star, 10 variable Be and slowly pulsating B stars, 13 eclipsing binary stars, 21 semi-long periodic or slow irregular variables and an RR Lyrae variable star, respectively. Many variable B-type stars were known through a well-defined zero-age main sequence to the ${\beta}$ Cepheid region of NGC 457. Most of the variable B-type stars found this paper were known variable stars. But, 11 out of 14 ${\delta}$ Scuti variable stars were newly discovered. The new variable stars except for ${\delta}$ Scuti stars were 4 variable B-type stars, 5 eclipsing binaries and 11 semi-long periodic or slow irregular variables. We have performed frequency analysis for all ${\delta}$ Scuti stars, a ${\beta}$ Cepheid star and an RR Lyrae star.