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Review
. 2022 Sep 15;23(18):10750.
doi: 10.3390/ijms231810750.

Rodent Models of Post-Stroke Dementia

Affiliations
Review

Rodent Models of Post-Stroke Dementia

Hahn Young Kim et al. Int J Mol Sci. .

Abstract

Post-stroke cognitive impairment is one of the most common complications in stroke survivors. Concomitant vascular risk factors, including aging, diabetes mellitus, hypertension, dyslipidemia, or underlying pathologic conditions, such as chronic cerebral hypoperfusion, white matter hyperintensities, or Alzheimer's disease pathology, can predispose patients to develop post-stroke dementia (PSD). Given the various clinical conditions associated with PSD, a single animal model for PSD is not possible. Animal models of PSD that consider these diverse clinical situations have not been well-studied. In this literature review, diverse rodent models that simulate the various clinical conditions of PSD have been evaluated. Heterogeneous rodent models of PSD are classified into the following categories: surgical technique, special structure, and comorbid condition. The characteristics of individual models and their clinical significance are discussed in detail. Diverse rodent models mimicking the specific pathomechanisms of PSD could provide effective animal platforms for future studies investigating the characteristics and pathophysiology of PSD.

Keywords: amyloid deposits; chronic cerebral hypoperfusion; intracerebral hemorrhage; ischemic stroke; post-stroke dementia; rodent model; subarachnoid hemorrhage.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Diverse rodent animal models of post-stroke dementia. (Middle cerebral artery occlusion, MCAO; bilateral common carotid artery occlusion, BCCAo; Alzheimer’s disease, AD).

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References

    1. Murray C.J., Lopez A.D. Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study. Lancet. 1997;349:1436–1442. doi: 10.1016/S0140-6736(96)07495-8. - DOI - PubMed
    1. Ivan C.S., Seshadri S., Beiser A., Au R., Kase C.S., Kelly-Hayes M., Wolf P.A. Dementia after stroke: The Framingham Study. Stroke. 2004;35:1264–1268. doi: 10.1161/01.STR.0000127810.92616.78. - DOI - PubMed
    1. Pantoni L. Have Stroke Neurologists Entered the Arena of Stroke-Related Cognitive Dysfunctions? Not Yet, but They Should! Stroke. 2017;48:1441–1442. doi: 10.1161/STROKEAHA.117.016869. - DOI - PubMed
    1. Pendlebury S.T., Rothwell P.M. Prevalence, incidence, and factors associated with pre-stroke and post-stroke dementia: A systematic review and meta-analysis. Lancet Neurol. 2009;8:1006–1018. doi: 10.1016/S1474-4422(09)70236-4. - DOI - PubMed
    1. Weaver N.A., Kuijf H.J., Aben H.P., Abrigo J., Bae H.-J., Barbay M., Best J.G., Bordet R., Chappell F.M., Chen C.P.L.H., et al. Strategic infarct locations for post-stroke cognitive impairment: A pooled analysis of individual patient data from 12 acute ischaemic stroke cohorts. Lancet Neurol. 2021;20:448–459. doi: 10.1016/S1474-4422(21)00060-0. - DOI - PubMed