Biomechanics Section, KU Leuven, Celestijnenlaan 300 box 2419, 3001, Leuven, Belgium.
Laboratory of Enteric Neuroscience (LENS), TARGID, KU Leuven, Leuven, Belgium.
Biomech Model Mechanobiol. 2020 Dec;19(6):2455-2489. doi: 10.1007/s10237-020-01349-w. Epub 2020 Jun 13.
Bridging veins (BVs) drain the blood from the cerebral cortex into dural sinuses. BVs have one end attached to the brain and the other to the superior sagittal sinus (SSS), which is attached to the skull. Relative movement between these two structures can cause BV to rupture producing acute subdural haematoma, a head injury with a mortality rate between 30 and 90%. A clear understanding of the BVs microstructure is required to increase the biofidelity of BV models when simulating head impacts. Twelve fresh BV samples draining in the superior sagittal sinus (SSS) from a single human cadaver were cut open along their length and placed on an inverted multiphoton microscope. To ensure that the BVs were aligned with the axial direction an in-house built, uniaxial tension set-up was used. Two scans were performed per sample. Before the first scan, a minor displacement was applied to align the tissue; then, a second scan was taken applying 50% strain. Each BV was scanned for a length of 5 mm starting from the drainage site into the SSS. Imaging was performed on a Zeiss LSM780 microscope with an 25[Formula: see text] water immersion objective (NA 0.8), coupled to a tunable MaiTai DS (Spectraphysics) pulsed laser with the wavelength set at 850 nm. Second harmonic and fluorescence signals were captured in forward and backward direction on binary GaAsP (BiG) detectors and stored as four colour Z-stacks. Prior to the calculation of the local orientations, acquired Z-stacks were denoised and enhanced to highlight fibrillar structures from the background. Then, for each Z-plane of the stack, the ImageJ plugin OrientationJ was used to extract the local 2D orientations of the fibres based on structure tensors. Two kinds of collagen architectures were seen. The most common (8[Formula: see text]12 samples) was single layered and had a uniform distribution of collagen. The less common (4[Formula: see text]12 samples) had 2 layers and 7 to 34 times thicker collagen bundles on the outer layer. Fibre angle analysis showed that collagen was oriented mainly along the axial direction of the vessel. The von Mises fittings showed that in order to describe the fibre distribution 3 components were needed with mean angles [Formula: see text] at [Formula: see text] 0.35, 0.21, [Formula: see text] 0.02 rad or [Formula: see text] 20.2[Formula: see text], 12.1[Formula: see text], [Formula: see text] 1.2[Formula: see text] relative to the vessel's axial direction which was also the horizontal scan direction.
桥静脉 (BVs) 将大脑皮层的血液引流到硬脑膜窦中。BVs 的一端附着在大脑上,另一端附着在矢状窦 (SSS) 上,而 SSS 又附着在颅骨上。这两个结构之间的相对运动可能会导致 BV 破裂,从而产生急性硬膜下血肿,这是一种死亡率在 30%至 90%之间的头部损伤。为了在模拟头部撞击时提高 BV 模型的生物逼真度,需要清楚地了解 BV 的微观结构。
从一个人体尸体的 SSS 中引流的 12 个新鲜 BV 样本沿其长度切开,并放置在倒置多光子显微镜上。为了确保 BV 与轴向对齐,使用了内部构建的单轴拉伸装置。每个样本进行两次扫描。在第一次扫描之前,施加一个小的位移来对齐组织;然后,施加 50%的应变进行第二次扫描。每个 BV 从引流部位到 SSS 扫描 5 毫米长。成像在 Zeiss LSM780 显微镜上进行,使用 25[Formula: see text] 水浸物镜 (NA 0.8),耦合到调谐 MaiTai DS (Spectraphysics) 脉冲激光器,波长设置为 850nm。二次谐波和荧光信号在正向和反向的二进制 GaAsP (BiG) 探测器上捕获,并存储为四个彩色 Z 堆叠。在计算局部取向之前,对采集的 Z 堆叠进行去噪和增强,以突出纤维状结构从背景中。然后,对于堆栈的每个 Z 平面,使用 ImageJ 插件 OrientationJ 根据结构张量提取纤维的局部 2D 取向。
观察到两种胶原结构。最常见的(8[Formula: see text]12 个样本)是单层的,胶原分布均匀。较少见的(4[Formula: see text]12 个样本)有 2 层,外层的胶原束厚 7 到 34 倍。纤维角度分析表明,胶原主要沿血管的轴向排列。冯·米塞斯拟合表明,为了描述纤维分布,需要 3 个分量,平均角度[Formula: see text]在[Formula: see text]0.35、0.21、[Formula: see text]0.02 弧度或[Formula: see text]20.2[Formula: see text]、12.1[Formula: see text]、[Formula: see text]1.2[Formula: see text]相对于血管的轴向,即水平扫描方向。