Effect of Colchicine on Platelet-Platelet and Platelet-Leukocyte Interactions: a Pilot Study in Healthy Subjects
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  • 作者:Binita Shah ; Nicole Allen ; Bhisham Harchandani ; Michael Pillinger…
  • 关键词:colchicine ; platelet aggregation ; neutrophil ; monocyte ; tissue adhesion
  • 刊名:Inflammation
  • 出版年:2016
  • 出版时间:February 2016
  • 年:2016
  • 卷:39
  • 期:1
  • 页码:182-189
  • 全文大小:2,007 KB
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  • 作者单位:Binita Shah (1) (2)
    Nicole Allen (1)
    Bhisham Harchandani (1)
    Michael Pillinger (3)
    Stuart Katz (1)
    Steven P. Sedlis (1) (2)
    Christina Echagarruga (1)
    Svetlana Krasnokutsky Samuels (3)
    Pajazit Morina (1)
    Prabhjot Singh (1)
    Liza Karotkin (1)
    Jeffrey S. Berger (4)

    1. Department of Medicine, Division of Cardiology, New York University School of Medicine, 227 E 30th Street, Office 835, New York, NY, 10016, USA
    2. Department of Medicine, Section of Cardiology, Veterans Affairs New York Harbor Health Care System, New York, NY, USA
    3. Department of Medicine, Division of Rheumatology, New York University School of Medicine, New York, NY, USA
    4. Department of Medicine, Divisions of Cardiology and Hematology, New York University School of Medicine, New York, NY, USA
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Rheumatology
    Internal Medicine
    Pharmacology and Toxicology
    Pathology
  • 出版者:Springer Netherlands
  • ISSN:1573-2576
文摘
The cardioprotective mechanisms of colchicine in patients with stable ischemic heart disease remain uncertain. We tested varying concentrations of colchicine on platelet activity in vitro and a clinically relevant 1.8-mg oral loading dose administered over 1 h in 10 healthy subjects. Data are shown as median [interquartile range]. Colchicine addition in vitro decreased light transmission platelet aggregation only at supratherapeutic concentrations but decreased monocyte- (MPA) and neutrophil-platelet aggregation (NPA) at therapeutic concentrations. Administration of 1.8 mg colchicine to healthy subjects had no significant effect on light transmission platelet aggregation but decreased the extent of MPA (28 % [22–57] to 22 % [19–31], p = 0.05) and NPA (19 % [16–59] to 15 % [11–30], p = 0.01), platelet surface expression of PAC-1 (370 mean fluorescence intensity (MFI) [328–555] to 333 MFI [232–407], p = 0.02) and P-selectin (351 MFI [269–492] to 279 [226–364], p = 0.03), and platelet adhesion to collagen (10.2 % [2.5–32.6] to 2.0 % [0.2–9.5], p = 0.09) 2 h post-administration. Thus, in clinically relevant concentrations, colchicine decreases expression of surface markers of platelet activity and inhibits leukocyte-platelet aggregation but does not inhibit homotypic platelet aggregation. KEY WORDS colchicine platelet aggregation neutrophil monocyte tissue adhesion

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