Yang Shao-Hua, Shetty Ritu A, Liu Ran, Sumien Nathalie, Heinrich Kevin R, Rutledge Margaret, Thangthaeng Nopporn, Brun-Zinkernagel Anne-Marie, Forster Michael J
Department of Pharmacology & Neuroscience, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107 USA.
Age (Dordr). 2006 Sep;28(3):297-307. doi: 10.1007/s11357-006-9026-4. Epub 2006 Dec 2.
Vascular dementia (VaD), incorporating cognitive dysfunction with vascular disease, ranks as the second leading cause of dementia in the United States, yet no effective treatment is currently available. The challenge of defining the pathological substrates of VaD is complicated by the heterogeneous nature of cerebrovascular disease and coexistence of other pathologies, including Alzheimer's disease (AD) types of lesion. The use of rodent models of ischemic stroke may help to elucidate the type of lesions that are responsible for cognitive impairment in humans. Endovascular middle cerebral artery (MCA) occlusion in rats is considered to be a convenient and reliable model of human cerebral ischemia. Both sensorimotor and cognitive dysfunction can be induced in the rat endovascular MCA occlusion model, yet sensorimotor deficits induced by endovascular MCA occlusion may improve with time, whereas data presented in this review suggest that in rats this model can result in a progressive course of cognitive impairment that is consistent with the clinical progression of VaD. Thus far, experimental studies using this model have demonstrated a direct interaction of cerebral ischemic damage and AD-type neuropathologies in the primary ischemic area. Further, coincident to the progressive decline of cognitive function, a delayed neurodegeneration in a remote area, distal to the primary ischemic area, the hippocampus, has been demonstrated in a rat endovascular MCA occlusion model. We argue that this model could be employed to study VaD and provide insight into some of the pathophysiological mechanisms of VaD.
血管性痴呆(VaD),即伴有血管疾病的认知功能障碍,是美国第二大痴呆病因,但目前尚无有效的治疗方法。脑血管疾病的异质性以及包括阿尔茨海默病(AD)类型病变在内的其他病理状况的共存,使得确定VaD的病理基础面临挑战。使用缺血性中风的啮齿动物模型可能有助于阐明导致人类认知障碍的病变类型。大鼠大脑中动脉(MCA)血管内闭塞被认为是一种方便且可靠的人类脑缺血模型。在大鼠大脑中动脉血管内闭塞模型中可诱导出感觉运动和认知功能障碍,然而,大脑中动脉血管内闭塞诱导的感觉运动缺陷可能会随时间改善,而本综述中的数据表明,在大鼠中该模型可导致与VaD临床进展一致的渐进性认知障碍病程。迄今为止,使用该模型的实验研究已证明原发性缺血区域脑缺血损伤与AD型神经病理学之间存在直接相互作用。此外,与认知功能的渐进性下降同时发生的是,在大鼠大脑中动脉血管内闭塞模型中已证明,在原发性缺血区域远端的海马等偏远区域存在延迟性神经变性。我们认为该模型可用于研究VaD,并深入了解VaD的一些病理生理机制。