Department of Anatomy and Cell Biology, University of Western Ontario, London, ON, N6A 5C1, Canada.
Centre for Functional and Metabolic Mapping, Robarts Research Institute, University of Western Ontario, London, ON, N6A 5K7, Canada.
Mol Neurobiol. 2018 Oct;55(10):8071-8083. doi: 10.1007/s12035-018-0904-4. Epub 2018 Mar 5.
Defect in brain microperfusion is increasingly recognized as an antecedent event to Alzheimer's disease (AD) and ischemia. Nevertheless, studies on the role of impaired microperfusion as a pathological trigger to neuroinflammation, Aβ deposition as well as blood-brain barrier (BBB) disruption, and the etiological link between AD and ischemia are lacking. In this study, we employ in vivo sequential magnetic resonance imaging (MRI) and computed tomography (CT) imaging in a co-morbid rat model of β-amyloid toxicity (Aβ) and ischemia (ET1) with subsequent histopathology of striatal lesion core and penumbra at 1, 7, and 28 days post injury. Within 24 h, cerebral injury resulted in increased BBB permeability due to the dissolution of β-dystroglycan (β-DG) and basement membrane laminin by active matrix metalloproteinase9 (MMP9). As a result, net flow of circulating IgG down a hydrostatic gradient into the parenchyma led to vasogenic edema and impaired perfusion, thus increasing the apparent hyperintensity in true fast imaging with steady-state free precession (true FISP) imaging and acute hypoperfusion in CT. This was followed by a slow recruitment of reactive astroglia to the affected brain and depolarization of aquaporin4 (AQP4) expression resulting in cytotoxic edema-in an attempt to resolve vasogenic edema. On d28, functional BBB was restored in ET1 rats as observed by astrocytic MMP9 release, β-DG stabilization, and new vessel formation. This was confirmed by reduced hyperintensity on true FISP imaging and normalized cerebral blood flow in CT. While, Aβ toxicity alone was not detrimental enough, Aβ+ET1 rats showed delayed differential expression of MMP9, late recruitment of astroglial cells, protracted loss of AQP4 depolarization, and thus delayed BBB restoration and cerebral perfusion.
脑微灌注缺陷越来越被认为是阿尔茨海默病(AD)和缺血的前期事件。然而,关于受损微灌注作为神经炎症、Aβ沉积以及血脑屏障(BBB)破坏的病理触发因素,以及 AD 和缺血之间的病因联系的研究尚缺乏。在这项研究中,我们在β淀粉样毒性(Aβ)和缺血(ET1)的合并大鼠模型中使用了体内连续磁共振成像(MRI)和计算机断层扫描(CT)成像,随后在损伤后 1、7 和 28 天对纹状体损伤核心和半影区进行了组织病理学检查。在 24 小时内,由于活性基质金属蛋白酶 9(MMP9)溶解β- 连接蛋白(β-DG)和基底膜层粘连蛋白,脑损伤导致 BBB 通透性增加。结果,循环 IgG 沿静水压力梯度净流入实质导致血管源性水肿和灌注受损,从而导致真实稳态自由进动(true FISP)成像中的表观高信号强度增加和 CT 中的急性低灌注。随后,反应性星形胶质细胞缓慢募集到受影响的大脑中,并导致水通道蛋白 4(AQP4)表达去极化,从而导致细胞毒性水肿,试图解决血管源性水肿。在 ET1 大鼠中,在 d28 时观察到星形胶质细胞 MMP9 释放、β-DG 稳定和新血管形成,功能性 BBB 得到恢复。这在 true FISP 成像上的高信号强度降低和 CT 中的脑血流正常化得到证实。虽然 Aβ 毒性本身还不够严重,但 Aβ+ET1 大鼠显示 MMP9 的差异表达延迟、星形胶质细胞的晚期募集、AQP4 去极化的持续丧失,以及 BBB 和脑灌注的延迟恢复。