4.6 Review

Modeling subcortical ischemic white matter injury in rodents: unmet need for a breakthrough in translational research

期刊

NEURAL REGENERATION RESEARCH
卷 16, 期 4, 页码 638-642

出版社

WOLTERS KLUWER MEDKNOW PUBLICATIONS
DOI: 10.4103/1673-5374.295313

关键词

animal model; axonal degeneration; demyelination; hypertension; ischemia; oligodendrocytes; subcortical ischemic white matter injury; vascular cognitive impairment; white matter hyperintensities

资金

  1. National Research Foundation of Korea (NRF) - Korea government (MSIT
  2. Ministry of Science and ICT) [NRF-2018M3A9E8023853, NRF2018R1C1B6006145, NRF-2018R1A2A1A05020292, NRF-2019R1A5A2026045]
  3. National Research Foundation of Korea [2018M3A9E8023853] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Subcortical ischemic white matter injury (SIWMI) is a common cause of cognitive decline in the elderly, but the degeneration process of various white matter components in response to chronic ischemia is not fully understood. Different types of animal models exist, including chemically induced, vascular occlusive, and models with comorbid vascular risk factors.
Subcortical ischemic white matter injury (SIWMI), pathological correlate of white matter hyperintensities or leukoaraiosis on magnetic resonance imaging, is a common cause of cognitive decline in elderly. Despite its high prevalence, it remains unknown how various components of the white matter degenerate in response to chronic ischemia.This incomplete knowledge is in part due to a lack of adequate animal model. The current review introduces various SIWMI animal models and aims to scrutinize their advantages and disadvantages primarily in regard to the pathological manifestations of white matter components. The SIWMI animal models are categorized into 1) chemically induced SIWMI models, 2) vascular occlusive SIWMI models, and 3) SIWMI models with comorbid vascular risk factors. Chemically induced models display consistent lesions in predetermined areas of the white matter, but the abrupt evolution of lesions does not appropriately reflect the progressive pathological processes in human white matter hyperintensities. Vascular occlusive SIWMI models often do not exhibit white matter lesions that are sufficiently unequivocal to be quantified. When combined with comorbid vascular risk factors (specifically hypertension), however, they can produce progressive and definitive white matter lesions including diffuse rarefaction, demyelination, loss of oligodendrocytes, and glial activation, which are by far the closest to those found in human white matter hyperintensities lesions. However, considerable surgical mortality and unpredictable natural deaths during a follow-up period would necessitate further refinements in these models. In the meantime, in vitro SIWMI models that recapitulate myelinated white matter track may be utilized to study molecular mechanisms of the ischemic white matter injury. Appropriate in vivo and in vitro SIWMI models will contribute in a complementary manner to making a breakthrough in developing effective treatment to prevent progression of white matter hyperintensities.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据