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The impact of factor Xa inhibition on axial dependent arterial thrombus formation triggered by a tissue factor rich surface
被引:4
|作者:
Pugh, Nicholas
[1
]
Jarvis, Gavin E.
[2
]
Koch, Annelize
[3
]
Sakariassen, Kjell S.
[4
]
Davis, Bill
[3
]
Farndale, Richard W.
[1
]
机构:
[1] Univ Cambridge, Dept Biochem, Cambridge CB1 2QW, England
[2] Queens Univ Belfast, Sch Pharm, Belfast BT9 7BL, Antrim, North Ireland
[3] Cambridge Univ Hosp NHS Fdn Trust, Addenbrookes Ctr Clin Invest, Addenbrookes Hosp, Cambridge CB2 2GG, England
[4] KellSa Sas, I-13900 Biella, BI, Italy
基金:
英国医学研究理事会;
关键词:
Factor Xa inhibition;
Thrombus formation;
Tissue factor;
Axial dependence;
Flow conditions;
PLATELET-ADHESION;
COMBINED ASPIRIN;
FLOWING BLOOD;
COLLAGEN;
THROMBOGENESIS;
SHEAR;
CLOPIDOGREL;
THERAPY;
DISEASE;
HUMANS;
D O I:
10.1007/s11239-011-0658-6
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
This study was designed to assess the effect of Factor Xa antagonists on thrombus formation at various axial positions on a tissue factor rich surface under arterial blood flow conditions. Non-anticoagulated, flowing human blood, drawn directly from an antecubital vein, was perfused over a tissue factor coated cover slip in a parallel-plate perfusion chamber. Thrombus surface coverage, thrombus mean height and fibrin surface coverage were measured at six different axial positions by confocal microscopy. Both thrombus surface coverage and mean height decreased along the cover slip axis whereas the fibrin surface coverage increased. Pre-chamber treatment of blood with the direct Factor Xa inhibitors Razaxaban and 813893 resulted in significantly reduced thrombus and fibrin formation at all axial positions investigated (P < 0.05). Thrombus and fibrin deposition in a laminar flow chamber changed with axial position with surface coverage measurements being more reproducible than thrombus mean height. Data were more reproducible towards the centre of the flow chamber than at the extremities. Razaxaban and 813893 inhibited thrombus and fibrin formation at the highest concentrations tested. No difference in drug effect was apparent at different axial positions. In conclusion, axial position influences the degree of thrombus and fibrin deposition with measurements being less reproducible at the extremities of the flow chamber. This technique may prove useful for analysing anti-thrombotic drug effects before progression to clinical trials.
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页码:6 / 15
页数:10
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