Kataoka Hiroharu, Yagi Takanobu, Ikedo Taichi, Imai Hirohiko, Kawamura Koichi, Yoshida Kazumichi, Nakamura Masanori, Aoki Tomohiro, Miyamoto Susumu
Department of Neurosurgery, Kyoto University, Graduate School of Medicine.
Center for Advanced Biomedical Science, Waseda University.
Neurol Med Chir (Tokyo). 2020 Jul 15;60(7):319-328. doi: 10.2176/nmc.st.2020-0072. Epub 2020 Jun 12.
Hemodynamic stress and chronic inflammation are closely associated with the pathogenesis of intracranial aneurysms (IAs). However, the hemodynamic and biological mechanisms triggering IA formation remain to be elucidated. To clarify them, computational fluid dynamics (CFD) and histopathological analyses in the early phase of IA development using an experimentally induced IA model in rats were conducted. Histological changes in the early phase of IA development were observed under a scanning electron microscope (SEM) and a transmission electron microscope (TEM). Using data from 7-T magnetic resonance angiography (7T-MRA), CFD analyses were performed to determine wall shear stress (WSS) and wall pressure (WP) at the prospective site of IA. A bump-like protrusion named an "intimal pad" was located in the anterior cerebral artery (ACA) immediately distal to the apex of the bifurcation. TEM showed the degeneration of the internal elastic lamina (IEL) and longitudinally elongated smooth muscle cells (SMCs) that switched from the contractile to the proliferative phenotype and penetrated between two divided layers of the degenerated IEL in the prospective site of the IA. However, no inflammatory cells were observed. CFD analyses showed no particular pattern of WSS and WP at the prospective IA site. IEL degeneration and the phenotypic change and longitudinal elongation of SMCs were identified as the early events in IA development. CFD analyses and TEM data suggest that these biological events may be derived from increased circumferential wall stress due to increased blood pressure and increased longitudinal wall strain due to the existence of the intimal pad.
血流动力学应激和慢性炎症与颅内动脉瘤(IA)的发病机制密切相关。然而,触发IA形成的血流动力学和生物学机制仍有待阐明。为了阐明这些机制,我们使用大鼠实验性诱导IA模型,对IA发展早期阶段进行了计算流体动力学(CFD)和组织病理学分析。在扫描电子显微镜(SEM)和透射电子显微镜(TEM)下观察了IA发展早期阶段的组织学变化。利用7-T磁共振血管造影(7T-MRA)数据,进行CFD分析以确定IA预期部位的壁面切应力(WSS)和壁面压力(WP)。在分叉顶端远端的大脑前动脉(ACA)中,发现了一个名为“内膜垫”的凸起样突出物。TEM显示,在IA预期部位,内弹性膜(IEL)退化,平滑肌细胞(SMC)纵向伸长,从收缩表型转变为增殖表型,并穿透退化的IEL的两个分开层之间。然而,未观察到炎性细胞。CFD分析显示,在IA预期部位没有特定的WSS和WP模式。IEL退化以及SMC的表型变化和纵向伸长被确定为IA发展的早期事件。CFD分析和TEM数据表明,这些生物学事件可能源于血压升高导致的周向壁应力增加以及内膜垫的存在导致的纵向壁应变增加。