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      Changes in expression of proteasome in rats at different stages of atherosclerosis

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      https://www.riss.kr/link?id=A101958645

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      다국어 초록 (Multilingual Abstract)

      It has been suggested that proteasome system has a role in initiation, progression, and complication stages of
      atherosclerosis. Although there is still controversy, there has been no research that compares the expression of proteasome in tissue and serum at each of these stages. This study aimed to investigated the expression of proteasome at different stages of atherosclerosis using rat model. We measured the expression of aortic proteasome by immunohistochemical analyses and were then analyzed using ImageJ software for percentage of area and integrated density. We used Photoshop version 3.0 to analyze aortic proteasome expression as a comparison. We measured serum proteasome expression by enzyme linked immunosorbents assays. Kruskal-Wallis test was used to compare mean value of percentage of area and serum proteasome. Analysis of variance
      test was used to compare mean value of integrated density. Correlation test between vascular proteasome expression and serum proteasome expression was made using Spearman test. A P-value of 0.05 was considered statistically significant. Compared with normal, percentage of area was higher in initiation, progression, and complication. Compared with normal, integrated density was higher in initiation and further higher in progression and complication. Data from Image J is similar with data from Photoshop. Serum proteasome expression was higher in initiation compared with normal, and further higher in progression and complication. It was concluded that there were different vascular proteasome expression and serum proteasome expression at the stages of atherosclerosis. These results may be used in research into new marker and therapeutic target in atherosclerosis.
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      It has been suggested that proteasome system has a role in initiation, progression, and complication stages of atherosclerosis. Although there is still controversy, there has been no research that compares the expression of proteasome in tissue and s...

      It has been suggested that proteasome system has a role in initiation, progression, and complication stages of
      atherosclerosis. Although there is still controversy, there has been no research that compares the expression of proteasome in tissue and serum at each of these stages. This study aimed to investigated the expression of proteasome at different stages of atherosclerosis using rat model. We measured the expression of aortic proteasome by immunohistochemical analyses and were then analyzed using ImageJ software for percentage of area and integrated density. We used Photoshop version 3.0 to analyze aortic proteasome expression as a comparison. We measured serum proteasome expression by enzyme linked immunosorbents assays. Kruskal-Wallis test was used to compare mean value of percentage of area and serum proteasome. Analysis of variance
      test was used to compare mean value of integrated density. Correlation test between vascular proteasome expression and serum proteasome expression was made using Spearman test. A P-value of 0.05 was considered statistically significant. Compared with normal, percentage of area was higher in initiation, progression, and complication. Compared with normal, integrated density was higher in initiation and further higher in progression and complication. Data from Image J is similar with data from Photoshop. Serum proteasome expression was higher in initiation compared with normal, and further higher in progression and complication. It was concluded that there were different vascular proteasome expression and serum proteasome expression at the stages of atherosclerosis. These results may be used in research into new marker and therapeutic target in atherosclerosis.

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      참고문헌 (Reference)

      1 Herrmann J, "The ubiquitin-proteasome system in cardiovascular diseases : a hypothesis extended" 61 : 11-21, 2004

      2 Marfella R, "The possible role of the ubiquitin proteasome system in the development of atherosclerosis in diabetes" 6 : 35-, 2007

      3 Wilck N, "Targeting the ubiquitin-proteasome system in atherosclerosis: status quo, challenges, and perspectives" 21 : 2344-2363, 2014

      4 Bochmann I, "T lymphocytes export proteasomes by way of microparticles : a possible mechanism for generation of extracellular proteasomes" 18 : 59-68, 2014

      5 Wu M, "Sustained oxidative stress inhibits NF-kappaB activation partially via inactivating the proteasome" 46 : 62-69, 2009

      6 Russell JC, "Small animal models of cardiovascular disease: tools for the study of the roles of metabolic syndrome, dyslipidemia, and atherosclerosis" 15 : 318-330, 2006

      7 Dhanya SP, "Small animal models of atherosclerosis" 6 : e4-, 2008

      8 Stocker R, "Role of oxidative modifications in atherosclerosis" 84 : 1381-1478, 2004

      9 Van Herck JL, "Proteasome inhibitor bortezomib promotes a rupture-prone plaque phenotype in ApoE-deficient mice" 105 : 39-50, 2010

      10 Vieira O, "Oxidized LDLs alter the activity of the ubiquitin-proteasome pathway : potential role in oxidized LDL-induced apoptosis" 14 : 532-542, 2000

      1 Herrmann J, "The ubiquitin-proteasome system in cardiovascular diseases : a hypothesis extended" 61 : 11-21, 2004

      2 Marfella R, "The possible role of the ubiquitin proteasome system in the development of atherosclerosis in diabetes" 6 : 35-, 2007

      3 Wilck N, "Targeting the ubiquitin-proteasome system in atherosclerosis: status quo, challenges, and perspectives" 21 : 2344-2363, 2014

      4 Bochmann I, "T lymphocytes export proteasomes by way of microparticles : a possible mechanism for generation of extracellular proteasomes" 18 : 59-68, 2014

      5 Wu M, "Sustained oxidative stress inhibits NF-kappaB activation partially via inactivating the proteasome" 46 : 62-69, 2009

      6 Russell JC, "Small animal models of cardiovascular disease: tools for the study of the roles of metabolic syndrome, dyslipidemia, and atherosclerosis" 15 : 318-330, 2006

      7 Dhanya SP, "Small animal models of atherosclerosis" 6 : e4-, 2008

      8 Stocker R, "Role of oxidative modifications in atherosclerosis" 84 : 1381-1478, 2004

      9 Van Herck JL, "Proteasome inhibitor bortezomib promotes a rupture-prone plaque phenotype in ApoE-deficient mice" 105 : 39-50, 2010

      10 Vieira O, "Oxidized LDLs alter the activity of the ubiquitin-proteasome pathway : potential role in oxidized LDL-induced apoptosis" 14 : 532-542, 2000

      11 Hermann J, "Oxidative stress-related increase in ubiquitination in early coronary atherogenesis" 17 : 1730-1732, 2003

      12 Herrmann J, "On to the road to degradation : atherosclerosis and the proteasome" 85 : 291-302, 2010

      13 Dąbek J, "Nuclear factor kappa-lightchain-enhancer of activated B cells (NF-kappaB): a new potential therapeutic target in atherosclerosis?" 62 : 778-783, 2010

      14 Bennani-Kabchi N, "New model of atherosclerosis in insulin resistant sand rats : hypercholesterolemia combined with D2vitamin" 150 : 55-61, 2000

      15 Tan C, "Inhibition of the ubiquitinproteasome system : a new avenue for atherosclerosis" 44 : 1218-1225, 2006

      16 Kikuchi J, "Induction of ubiquitin-conjugating enzyme by aggregated low density lipoprotein in human macrophages and its implications for atherosclerosis" 20 : 128-134, 2000

      17 Marfella R, "Increased activity of the ubiquitin-proteasome system in patients with symptomatic carotid disease is associated with enhanced inflammation and may destabilize the atherosclerotic plaque : effects of rosiglitazone treatment" 47 : 2444-2455, 2006

      18 Pang J, "Hexarelin suppresses high lipid diet and vitamin D3-induced atherosclerosis in the rat" 31 : 630-638, 2010

      19 Lloyd-Jones D, "Heart disease and stroke statistics: 2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee" 119 : e21-e181, 2009

      20 Sixt SU, "Extracellular proteasome in the human alveolar space: a new housekeeping enzyme?" 292 : L1280-L1288, 2007

      21 Li J, "Effects of total glucosides from paeony(Paeonia lactiflora Pall)roots on experimental atherosclerosis in rats" 135 : 469-475, 2011

      22 Davis HR Jr, "Effects of ezetimibe on atherosclerosis in preclinical models" 215 : 266-278, 2011

      23 Vinitha R, "Effect of tamoxifen on lipids and lipid metabolising marker enzymes in experimental atherosclerosis in Wistar rats" 168 : 13-19, 1997

      24 Srivastava RA, "Dietary cholic acid lowers plasma levels of mouse and human apolipoprotein A-I primarily via a transcriptional mechanism" 267 : 4272-4280, 2000

      25 Murwani S, "Diet aterogenik pada tikus putih(Rattus novergicus strain Wistar)sebagai model hewan aterosklerosis" 22 : 6-12, 2006

      26 Bellavista E, "Current understanding on the role of standard and immunoproteasomes in inflammatory/immunological pathways of multiple sclerosis" 2014 : 739705-, 2014

      27 World Health Organization, "Cardiovascular diseases fact sheet" World Health Organization

      28 Pyle AL, "Atheromas feel the pressure : biomechanical stress and atherosclerosis" 177 : 4-9, 2010

      29 Fonarow GC, "Aggressive treatment of atherosclerosis: the time is now" 70 : 431-434, 2003

      30 Stary HC, "A definition of advanced types of atherosclerotic lesions and a histological classification of atherosclerosis. A report from the Committee on Vascular Lesions of the Council on Arteriosclerosis, American Heart Association" 92 : 1355-1374, 1995

      31 Doaa M. Abo El-Khair, "A comparative study on the effect of high cholesterol diet on the hippocampal CA1 area of adult and aged rats" 대한해부학회 47 (47): 117-126, 2014

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2022 평가예정 계속평가 신청대상 (계속평가)
      2020-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      2019-12-01 평가 등재후보 탈락 (계속평가)
      2018-12-01 평가 등재후보로 하락 (계속평가) KCI등재후보
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2010-02-02 학술지명변경 한글명 : 대한해부학회지 -> Anatomy and Cell Biology
      외국어명 : The Korean Journal of Anatomy -> Anatomy and Cell Biology
      KCI등재
      2008-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2007-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2006-01-01 평가 등재후보로 하락 (등재유지) KCI등재후보
      2004-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2001-07-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.15 0.15 0.1
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.1 0.09 0.223 0.03
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