Expression of HMG-CoA reductase in human coronary atherosclerotic plaques and relationship to plaque destabilisation

被引:8
|
作者
Lee, Cheol Whan
Park, Chan-Sik [2 ]
Hwang, Ilseon [3 ]
Kim, Youngji [4 ]
Park, Duk-Woo
Kang, Soo-Jin
Lee, Seung-Hwan
Kim, Young-Hak
Park, Seong-Wook
Park, Seung-Jung [1 ]
机构
[1] Univ Ulsan, Div Cardiol, Asan Med Ctr, Dept Med, Seoul 138736, South Korea
[2] Univ Ulsan, Dept Pathol, Seoul 138736, South Korea
[3] Keimyung Univ, Dept Pathol, Sch Med, Taegu, South Korea
[4] Univ Ulsan, Asan Insitute Life Sci, Seoul 138736, South Korea
关键词
INTRAVASCULAR ULTRASOUND; RANDOMIZED-TRIAL; IN-VITRO; ATORVASTATIN; INTERVENTION; STATINS; INHIBITOR; THERAPY; RUPTURE;
D O I
10.1136/hrt.2009.190934
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Little is known about hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase expression in human coronary atherosclerotic plaques. Objective To investigate the expression of HMG-CoA reductase in coronary atherectomy tissues obtained from patients with unstable and stable angina and examine the relationship of HMG-CoA with plaque instability. Methods Atherectomy specimens were obtained from 43 patients with unstable (n=22) or stable (n=21) angina who underwent directional coronary atherectomy for de novo coronary artery lesions. The specimens were stained with haematoxylin-eosin and incubated with antibodies specific to HMG-CoA reductase, macrophages, smooth muscle cells and endothelial cells. Histology and immunohistochemistry data were morphometrically evaluated using an image-analysing system. Results Baseline characteristics were similar between the two groups. Immunopositive areas of HMG-CoA reductase, macrophages, endothelial cells and thrombi were significantly greater in patients with unstable angina than those in patients with stable angina. However, the immunopositive area of smooth muscle cells was not different between the two groups. Macrophage-positive areas correlated well with areas of HMG-CoA reductase in patients with unstable angina (r=0.72, p < 0.001), but not in patients with stable angina (r=0.02, p=0.937). Conclusion HMG-CoA reductase was present in coronary atherosclerotic plaques and was more commonly expressed in unstable plaques than in stable plaques. Local HMG-CoA reductase in coronary artery lesions may contribute to plaque instability.
引用
收藏
页码:715 / 720
页数:6
相关论文
共 50 条
  • [1] Transcriptional Regulation of HMG-CoA Synthase and HMG-CoA Reductase Genes by Human ACBP
    Vock, Christina
    Doering, Frank
    Nitz, Inke
    CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2008, 22 (5-6) : 515 - 524
  • [2] Regulation of HMG-CoA reductase expression by hypoxia
    Pallottini, Valentina
    Guantario, Barbara
    Martini, Chiara
    Totta, Pierangela
    Filippi, Irene
    Carraro, Fabio
    Trentalance, Anna
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2008, 104 (03) : 701 - 709
  • [3] HMG-COA REDUCTASE INHIBITORS
    ENDO, A
    ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY, 1985, 183 : 295 - 310
  • [4] HMG-COA REDUCTASE INHIBITORS
    ENDO, A
    HASUMI, K
    NATURAL PRODUCT REPORTS, 1993, 10 (06) : 541 - 550
  • [5] HMG-CoA reductase inhibitors
    Illingworth, DR
    Tobert, JA
    ADVANCES IN PROTEIN CHEMISTRY, VOL 56: DRUG DISCOVERY AND DESIGN, 2001, 56 : 77 - 114
  • [6] HMG-COA REDUCTASE INHIBITORS
    不详
    BRITISH JOURNAL OF HOSPITAL MEDICINE, 1988, 40 (06): : 477 - 477
  • [7] HMG-COA REDUCTASE INHIBITORS
    GRUNDY, SM
    JOURNAL OF INTERNAL MEDICINE, 1990, 228 (03) : 201 - 205
  • [8] Effect of HMG-CoA reductase inhibitors on regression of coronary plaque: A volumetric intravascular ultrasound analysis
    Nishioka, H
    Hirose, M
    Kataoka, T
    Sakamoto, T
    Kamimori, K
    Kobayashi, Y
    Shimada, K
    Yoshimura, T
    AMERICAN JOURNAL OF CARDIOLOGY, 2003, 92 (6A): : 196L - 196L
  • [9] HMG-CoA reductase inhibitors
    不详
    EXPERT OPINION ON THERAPEUTIC PATENTS, 1996, 6 (01) : 77 - 78
  • [10] A QM/MM Evaluation of the Missing Step in the Reduction Mechanism of HMG-CoA by Human HMG-CoA Reductase
    Mihaljevic-Juric, Paula
    Sousa, Sergio F.
    PROCESSES, 2021, 9 (07)