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. 2022 Jan 28;23(3):1497. doi: 10.3390/ijms23031497

Table 3.

Experimental models of stroke modeling lacunar infarcts.

Mechanism Techniques Description Advantages Disadvantages References
Vasoconstriction of perforating arteries Endothelin-1, nitric oxide synthase inhibitor, and L-NAME Strong vasoconstrictive action that affects several microvessels Small subcortical infarcts Multiple vessels affected at once Horie, 2008 [119]
Capone, 2011 [120]
Cipolla, 2013 [135]
Cui, 2013 [122]
Embolism Microspheres, microthrombi injection, atheroemboli, black beads, preformed clots, and silicone rubber cylinders Injection of different materials in the carotid to produce micro-occlusions by lodging in brain vessels Multiple subcortical infarcts Mostly cortical infarcts, mechanism not related to SVD Rapp, 2003 [123]
Wang, 2012 [124]
Silasi, 2015 [125]
Spontaneous lesions High salt, spontaneous
in SHRSP, surgical narrowing of the aorta, and genetic mutations in the renin-angiotensin system
Mice breeds with an increased risk of stroke, genetically or surgically induced Mechanism consistent with hypertensive SVD Difficult to track lesion location and timing Hainsworth, 2008 [130]
Bailey, 2009 [6]
Mencl, 2013 [131]
Perforating artery occlusion Surgery (pial vessel disruption model), sodium laurate
thrombosis, and photothrombosis
Endothelium damage and thrombosis, using toxic substances or surgical models Accurate localization of the lesions Strokes larger than lacunar infarcts Walz, 2017 [126]
Wen, 2019 [127]
Transient large vessel occlusion Bilateral common carotid artery occlusion Repeated transient large vessel occlusion, followed by reperfusion Mechanism reflects the hypoperfusion in SVD Lesions are not related to small vessel pathology Choi, 2018 [128]
Kwon, 2015 [129]
Genetic models CADASIL mouse models, COL4A1/2 mouse models Studies in mice with rare genetic disorders which make them prone to SVD Mechanism related to genetic SVD etiology Not enough brain affection Ayata, 2010 [132]
Joutel, 2011 [133]
Ruchoux, 2003 [134]

CADASIL: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; COL4A1/2: collagen type 4 alpha 1 chain gene; L-NAME: N-nitro-L-arginine methylester; SHRSP: spontaneously hypertensive stroke-prone rats; SVD: small vessel disease.