RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      KCI등재

      오령산의 피오글리타존 부작용 경감 효과 = Oryung-san Ameliorates Pioglitazone Side Effects

      한글로보기

      https://www.riss.kr/link?id=A103781312

      • 0

        상세조회
      • 0

        다운로드
      서지정보 열기
      • 내보내기
      • 내책장담기
      • 공유하기
      • 오류접수

      부가정보

      다국어 초록 (Multilingual Abstract)

      Thiazolidinediones (TZDs) induce insulin sensitization through the activation of PPAR${\gamma}$. However, the undesirable effect such as weight gain was observed. The purpose of this study was to find out an herbal drug that could reduce the side effe...

      Thiazolidinediones (TZDs) induce insulin sensitization through the activation of PPAR${\gamma}$. However, the undesirable effect such as weight gain was observed. The purpose of this study was to find out an herbal drug that could reduce the side effects of pioglitazone. Among herbal formula that we have searched, oryung-san (OR) inhibited the differentiation of preadipocytes and did not affect on glucose uptake in 3T3-L1 adipocytes. In vitro, glucose uptake assay and Oil Red-O staining in 3T3-L1 adipocytes were conducted. In vivo, pioglitazone (PIO, 30 mg/kg), oryung-san (OR, 300 mg/kg), or pioglitazone co-administered with oryung-san (PIO+OR) were administered orally for 7 weeks in high fat diet (HFD) fed ICR mice and measured the body weight and blood glucose level every week. PIO+OR group significantly reduced body weight gain, triglyceride, and total cholesterol compared to PIO group. In addition, PIO+OR group showed a significant reduction of plasma glucose level (72%) compared to HFD control group. Insulin levels in PIO+OR group was also markedly decreased by 85% and 41% compared to HFD control and PIO group, respectively. Diameter of white adipocytes was decreased in the PIO+OR group compared to that in PIO group. Moreover, PIO+OR group reduced expression of PPAR${\gamma}$ and SREBP1a compared to PIO group. Taken together, oryung-san can improve side effects of pioglitazone, such as weight gain and edema, and shows a synergistic effect in plasma insulin levels.

      더보기

      참고문헌 (Reference)

      1 "adipose-predominant exression and induction early in adipocyte differentiation. Endocrinology 135" 1994

      2 "Thiazolidinedions: a comparative review of approved uses" 2 : 429-, 2000

      3 "Therapeutic roles of peroxisome proliferator-activated receptor agonists" 54 : 2460-, 2005

      4 "The nuclear hormone receptor gene superfamily" 46 : 443-, 1995

      5 "Stimulation of adipogenesis in fibroblasts by PPAR g2" tonto (tonto): 1994

      6 P, "Single-step method of RNA isolation by acid guanidium thiocyanate-phenol chloroform extraction. Anal. Biochem. 162" 1987

      7 "Peroxisome proliferator-actovated receptor gene expression in human tissues" 99 : 2416-, 1997

      8 "PPARs: therapeutic targets for metabolic disease" 26 : 244-, 2005

      9 "PPAR-gand the control of adipogenesis" 79 : 111-, 1997

      10 Misra P, "PAT5A: a partial agonist of peroxisome proliferator-activated receptor g is a potent antidiabetic thiazolidinedione yet weakly adipogenic." 306 : 763-, 2003

      1 "adipose-predominant exression and induction early in adipocyte differentiation. Endocrinology 135" 1994

      2 "Thiazolidinedions: a comparative review of approved uses" 2 : 429-, 2000

      3 "Therapeutic roles of peroxisome proliferator-activated receptor agonists" 54 : 2460-, 2005

      4 "The nuclear hormone receptor gene superfamily" 46 : 443-, 1995

      5 "Stimulation of adipogenesis in fibroblasts by PPAR g2" tonto (tonto): 1994

      6 P, "Single-step method of RNA isolation by acid guanidium thiocyanate-phenol chloroform extraction. Anal. Biochem. 162" 1987

      7 "Peroxisome proliferator-actovated receptor gene expression in human tissues" 99 : 2416-, 1997

      8 "PPARs: therapeutic targets for metabolic disease" 26 : 244-, 2005

      9 "PPAR-gand the control of adipogenesis" 79 : 111-, 1997

      10 Misra P, "PAT5A: a partial agonist of peroxisome proliferator-activated receptor g is a potent antidiabetic thiazolidinedione yet weakly adipogenic." 306 : 763-, 2003

      11 "New approaches in the treatment of type 2 diabetes." 4 : 461-, 2000

      12 "Insulin resistance and antidiabetic drugs" 58 : 1511-, 1999

      13 Berger J. P, "Distinct properties and advantages of a novel peroxisome proliferator-activated protein [g] selective modulator" 17 : 662-, 2003

      14 "Dfferentiating members of th thiazoli- dinedione class: a focus on safety" 18 : 23-, 2002

      15 "Definition, diagnosis and classification of diabetes mellitus and its complications" 13 : 539-, 1998

      16 Huang C, "Berberine inhibits 3T3-L1 adipocyte differentiation through the PPAR-g pathway" 348 : 571-, 2006

      17 Chakrabrti R, "Antidiabetic and hypolipidemic potential of DRF 2519-a dual activator of PPAR-a and PPAR-g." 491 : 195-, 2004

      18 Rocchi S, "A unique PPAR-g ligand with potent insulin-sensitizing yet weak adipogenic activity" 8 : 737-, 2001

      19 Oberfield J. L, "A peroxisome proliferator-activated receptor ligand inhibits adipocyte differentiation" 96 : 6102-, 1999

      더보기

      분석정보

      View

      상세정보조회

      0

      Usage

      원문다운로드

      0

      대출신청

      0

      복사신청

      0

      EDDS신청

      0

      동일 주제 내 활용도 TOP

      더보기

      주제

      연도별 연구동향

      연도별 활용동향

      연관논문

      연구자 네트워크맵

      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

      인용정보 인용지수 설명보기

      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2003-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 유지 (등재후보1차) KCI등재후보
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      더보기

      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.2 0.2 0.22
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.23 0.18 0.403 0.02
      더보기

      이 자료와 함께 이용한 RISS 자료

      나만을 위한 추천자료

      해외이동버튼