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大鼠肠系膜完整弯曲微血管内血栓形成的机械机制。

Mechanical mechanisms of thrombosis in intact bent microvessels of rat mesentery.

作者信息

Liu Qin, Mirc David, Fu Bingmei M

机构信息

Department of Biomedical Engineering, The City College of the City University of New York, New York, NY 10031, USA.

出版信息

J Biomech. 2008 Aug 28;41(12):2726-34. doi: 10.1016/j.jbiomech.2008.06.013. Epub 2008 Jul 24.

Abstract

The hypothesis that thrombus can be induced by localized shear stresses/rates, such as in the bent/stretched microvessels, was tested both experimentally and computationally. Our newly designed in vivo experiments were performed on the microvessels (post-capillary venules, 20-50 microm diameter) of rat mesentery. These microvessels were bent/stretched with no/minimum injuries. In less than 60 min after the microvessels were bent/stretched, thrombi were formed in 19 out of 61 bent locations (31.1%). Interestingly, thrombi were found to be initiated at the inner wall of the curvature in these bent/stretched vessels. To investigate the mechanical mechanisms of thrombus induction, we performed a 3-D computational simulation using commercial software, FLUENT. To simulate the bending and stretching, we considered the vessels with different curvatures (0 degrees , 90 degrees and 180 degrees ) as well as different shaped cross-sections (circular and elliptic). Computational results demonstrated that the highest shear stress/rate and shear stress/rate gradient are located at the inner wall of the curved circular-shaped vessels. They are located at the two apexes of the wall with shorter axis for the 0 degrees (straight) elliptic-shaped vessel and towards the inner side when the vessels are bent. The differences of the shear stresses/rates and of the shear stress/rate gradients between the inner and outer walls become larger in more bent and elliptic-shaped microvessels. Comparison of our experimental and numerical simulation results suggests that the higher shear stress/rate and the higher shear stress/rate gradient at the inner wall are responsible for initiating the thrombosis in bent post-capillary venules.

摘要

血栓可由局部剪切应力/速率诱导形成,比如在弯曲/拉伸的微血管中,这一假说已通过实验和计算进行了验证。我们新设计的体内实验是在大鼠肠系膜的微血管(毛细血管后微静脉,直径20 - 50微米)上进行的。这些微血管在几乎没有/仅有最小程度损伤的情况下被弯曲/拉伸。在微血管被弯曲/拉伸后的不到60分钟内,61个弯曲部位中有19个(31.1%)形成了血栓。有趣的是,在这些弯曲/拉伸的血管中,血栓被发现是在弯曲处的内壁起始的。为了研究血栓形成的力学机制,我们使用商业软件FLUENT进行了三维计算模拟。为了模拟弯曲和拉伸,我们考虑了具有不同曲率(0度、90度和180度)以及不同形状横截面(圆形和椭圆形)的血管。计算结果表明,最高的剪切应力/速率和剪切应力/速率梯度位于弯曲圆形血管的内壁。对于0度(直的)椭圆形血管,它们位于短轴壁的两个顶点处,而当血管弯曲时则朝向内侧。在更弯曲和椭圆形的微血管中,内壁和外壁之间的剪切应力/速率以及剪切应力/速率梯度的差异变得更大。我们的实验结果与数值模拟结果的比较表明,内壁处较高的剪切应力/速率和较高的剪切应力/速率梯度是导致弯曲的毛细血管后微静脉中血栓形成的原因。

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