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      小菟絲子丸이 ob/ob mouse의 혈당, 고지혈증, Polyol Pathway 및 항산화작용에 미치는 영향

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      https://www.riss.kr/link?id=A100312202

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Effects of Sotosaja hwan on Blood Glucose, Hyperlipidemia, Polyol Pathway and Antioxidative Mechanism in ob/ob Mouse Diabetes is a disease in which the body does not produce or properly use insulin. Etiological studies of diabetes and its complications showed that oxidative stress might play a major role. Therefore, many efforts have been tried to regulate free oxygen radicals for treating diabetes and its complications. Sotosaja-hwan has been known to be effective for the antiaging and composed of four crude herbs. In male ob/ob mouse in severe obesity, hyperinsulinemia and hyperlipidemia, which are features of NIDDM, the hyperglycemic activites and mechanisms of Sotosaja-hwan were examined. Mice were grouped and treated for 5 weeks as follows. Both the lean (C57/BL6J black mice) and diabetic (ob/ob mice) control groups received standard chow. The experimental groups were fed with a diet of chow supplemented with 30 and 90 mg Sotosaja-hwan per 1 kg of body weight for 14 days. The effects of Sotosaja-hwan extract on the ob/ob mice were observed by measuring the serum levels of glucose, insulin, lipid components, and the kidney levels of superoxide anion radical (·O₂⁻), MDA+HAE, GSH/GSSG ratio, and also the enzyme activities involved in polyol pathway. Sotosaja-hwan lowered the levels of serum glucose and insulin in a dose dependent manner. Total cholesterol, triglyceride and free fatty acid levels were decreased, while the HDL-cholesterol level was increased, in Sotosaja-hwan treated groups. Renal aldose reductase and sorbitol dehydrogenase activities were increased in the ob/ob mice, whereas those were inhibited in the Sotosaja-hwan-administered groups. Sotosaja-hwan inhibited the generation of ·O₂⁻ in the kidney. Finally, MDA+HAE levels was increased and GSH/GSSG ratio was decreased in the ob/ob mice, whereas those were improved in the Sotosaja-hwan-administered groups. Sotosaja-hwan showed the antidiabetic and antihyperlipidemic activities by regulating the activities of polyol pathway enzymes, scavenging reactive oxygen species and reducing the MDA+HAE levels in the ob/ob mice.
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      Effects of Sotosaja hwan on Blood Glucose, Hyperlipidemia, Polyol Pathway and Antioxidative Mechanism in ob/ob Mouse Diabetes is a disease in which the body does not produce or properly use insulin. Etiological studies of diabetes and its complication...

      Effects of Sotosaja hwan on Blood Glucose, Hyperlipidemia, Polyol Pathway and Antioxidative Mechanism in ob/ob Mouse Diabetes is a disease in which the body does not produce or properly use insulin. Etiological studies of diabetes and its complications showed that oxidative stress might play a major role. Therefore, many efforts have been tried to regulate free oxygen radicals for treating diabetes and its complications. Sotosaja-hwan has been known to be effective for the antiaging and composed of four crude herbs. In male ob/ob mouse in severe obesity, hyperinsulinemia and hyperlipidemia, which are features of NIDDM, the hyperglycemic activites and mechanisms of Sotosaja-hwan were examined. Mice were grouped and treated for 5 weeks as follows. Both the lean (C57/BL6J black mice) and diabetic (ob/ob mice) control groups received standard chow. The experimental groups were fed with a diet of chow supplemented with 30 and 90 mg Sotosaja-hwan per 1 kg of body weight for 14 days. The effects of Sotosaja-hwan extract on the ob/ob mice were observed by measuring the serum levels of glucose, insulin, lipid components, and the kidney levels of superoxide anion radical (·O₂⁻), MDA+HAE, GSH/GSSG ratio, and also the enzyme activities involved in polyol pathway. Sotosaja-hwan lowered the levels of serum glucose and insulin in a dose dependent manner. Total cholesterol, triglyceride and free fatty acid levels were decreased, while the HDL-cholesterol level was increased, in Sotosaja-hwan treated groups. Renal aldose reductase and sorbitol dehydrogenase activities were increased in the ob/ob mice, whereas those were inhibited in the Sotosaja-hwan-administered groups. Sotosaja-hwan inhibited the generation of ·O₂⁻ in the kidney. Finally, MDA+HAE levels was increased and GSH/GSSG ratio was decreased in the ob/ob mice, whereas those were improved in the Sotosaja-hwan-administered groups. Sotosaja-hwan showed the antidiabetic and antihyperlipidemic activities by regulating the activities of polyol pathway enzymes, scavenging reactive oxygen species and reducing the MDA+HAE levels in the ob/ob mice.

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      참고문헌 (Reference)

      1 "임상내분비학" 서울, 고려의학 394-414, 1999

      2 "고혈당 흰쥐에서 의 혈당 조절과 항산화작용에 관한 연구" 27 (27): 91-103, 2006

      3 "陳師文 등 編. 太平惠民和劑局方. 臺北" 旋風出版社 -10, 1985.

      4 "竹瀝과 누에가루 배합약물이 db/db mouse의 혈당 강하에 미치는 영향" 17 (17): 759-764, 2003

      5 "珍糖元의 고혈당 조절 작용 및 기전에 관한 연구" 25 (25): 277-287, 2004

      6 "消渴의 傳變證과 당뇨병의 만성합병증에 대한 비교 고찰" 19 (19): 137-152, 1998

      7 "ob/ob mice에서 순기산의 항당뇨 활성 및 기전 연구" 2002

      8 "S.S. Use of an enzymatic method for cholesterol designed for continuous flow instrumention" 2335-2337, 1977.

      9 "S.P. The potential role of oxidative stress in diabetes and its complications Novel implication for theory and therapy in diabetic complications" 167-220, 1987.

      10 "S. In Hoppe-Seyler Thiefelder Handbuch der physiol. und path.-chem. Vol. VIa. Berlin-Heidelberg-New York" 1964.

      1 "임상내분비학" 서울, 고려의학 394-414, 1999

      2 "고혈당 흰쥐에서 의 혈당 조절과 항산화작용에 관한 연구" 27 (27): 91-103, 2006

      3 "陳師文 등 編. 太平惠民和劑局方. 臺北" 旋風出版社 -10, 1985.

      4 "竹瀝과 누에가루 배합약물이 db/db mouse의 혈당 강하에 미치는 영향" 17 (17): 759-764, 2003

      5 "珍糖元의 고혈당 조절 작용 및 기전에 관한 연구" 25 (25): 277-287, 2004

      6 "消渴의 傳變證과 당뇨병의 만성합병증에 대한 비교 고찰" 19 (19): 137-152, 1998

      7 "ob/ob mice에서 순기산의 항당뇨 활성 및 기전 연구" 2002

      8 "S.S. Use of an enzymatic method for cholesterol designed for continuous flow instrumention" 2335-2337, 1977.

      9 "S.P. The potential role of oxidative stress in diabetes and its complications Novel implication for theory and therapy in diabetic complications" 167-220, 1987.

      10 "S. In Hoppe-Seyler Thiefelder Handbuch der physiol. und path.-chem. Vol. VIa. Berlin-Heidelberg-New York" 1964.

      11 "R.J. Protein measurement with folin phenol reagent. J Biol Chem. 193" 265-275, 1951.

      12 "R.H. Colorimetric glucose oxidase method for blood glucose. Clin Chem Acta. 13" 133-135, 1966.

      13 "Pathophysiology of insulin resistance in human disease" 75 : 473-486, 1995

      14 "Pathogenesis of type 2 diabetes. Metabolic and molecular implications for identifying diabetes genes" 5 : 177-269, 1997

      15 "O. Increased plasma levels of glutathione and malondialdehyde after avute ethanol ingestion in humans. J hepatol. 9" grattaglia : 1989.

      16 "Non-insulin dependent diabetes mellitus. A genetically programmed failure of the β cell to compensate for insulin resistance" 334 : 777-783, 1998

      17 "M.K. A spectrophotometric method for the direct determination of cystein in the presense of other naturally occuring amino acid. Biochem J. 104" 1967.

      18 "M.J. A colorimetric method for estimation serum triglyceride. Clin Chem. 22" 1968.

      19 "M. Aminoguanidine treatment inhibit the development of experimental diabetic retinopathy. Proc Natl Acad Sci USA. 88" 11555-11558, 1991.

      20 "J.W. Role of oxidative stress in development of complications in diabetes. Diabetes. 40" 405-412, 1991.

      21 "J.R. Glucose-induced metabolic imbalance in the pathogenesis of diabetic vascular disease. Diabetes Metab Rev. 7" 35-59, 1991.

      22 "H. Chemistry and Biochemistry of 4-Hydroxynonenal" 81-128, 1991.

      23 "D.A. The linked roles of nitric oxide aldose reductase and Na-K-ATPase in the slowing of nerve conduction in the streptozotocin diabetic rat. J Clin Invest. 94" 853-859, 1994.

      24 "C.R. The molecular mechanism of insulin action. Ann Rev Med. 34" 145-160, 1985.

      25 "B.N. Detection of picomole levels of hydroperoxides using a fluorescent dichlorofluorescein fluorescent assay. Anal Biochem. 134" 111-116, 1983.

      26 "Acute onset of diabetic pathological changes in transgenic mice with human aldose reductase cDNA" 38 : 255-261, 1995

      27 "A.A. Animal models of diabetes mellitus. In Joslin's diabetes mellitus. pp 110-137" 1985.

      28 "179-208" 1992-, 3

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2026 평가예정 재인증평가 신청대상 (재인증)
      2020-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2017-01-01 평가 등재학술지 유지 (계속평가) KCI등재
      2016-03-10 학술지명변경 외국어명 : Korean Journal of Oriental Physiology & Pathology -> Journal of Physiology & Pathology in Korean Medicine KCI등재
      2016-02-24 학회명변경 한글명 : 대한동의병리학회 -> 한의병리학회
      영문명 : The Korean Society Of Oriental Pathology -> The Society of Pathology in Korean Medicine
      KCI등재
      2013-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-09-03 학술지명변경 외국어명 : Korean Journal of Oriental Medical Pathology -> Korean Journal of Oriental Physiology & Pathology KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2003-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2002-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2000-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.47 0.47 0.41
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.35 0.33 0.485 0.09
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