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      Awake chronic mouse model of targeted pial vessel occlusion via photothrombosis

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          Abstract.

          Animal models of stroke are used extensively to study the mechanisms involved in the acute and chronic phases of recovery following stroke. A translatable animal model that closely mimics the mechanisms of a human stroke is essential in understanding recovery processes as well as developing therapies that improve functional outcomes. We describe a photothrombosis stroke model that is capable of targeting a single distal pial branch of the middle cerebral artery with minimal damage to the surrounding parenchyma in awake head-fixed mice. Mice are implanted with chronic cranial windows above one hemisphere of the brain that allow optical access to study recovery mechanisms for over a month following occlusion. Additionally, we study the effect of laser spot size used for occlusion and demonstrate that a spot size with small axial and lateral resolution has the advantage of minimizing unwanted photodamage while still monitoring macroscopic changes to cerebral blood flow during photothrombosis. We show that temporally guiding illumination using real-time feedback of blood flow dynamics also minimized unwanted photodamage to the vascular network. Finally, through quantifiable behavior deficits and chronic imaging we show that this model can be used to study recovery mechanisms or the effects of therapeutics longitudinally.

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          Most cited references39

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          CNS plasticity and assessment of forelimb sensorimotor outcome in unilateral rat models of stroke, cortical ablation, parkinsonism and spinal cord injury.

          We have reviewed a battery of useful tests for evaluating sensorimotor function and plasticity acutely and chronically in unilateral rat models of central nervous system injury. These tests include forelimb use for weight shifting during vertical exploration in a cylindrical enclosure, an adhesive removal test of sensory function, and forelimb placing. These tests monitor recovery of sensorimotor function independent of the extent of test experience. Data are presented for four models, including permanent focal ischemia, focal injury to the forelimb area of sensorimotor cortex, dopaminergic neurodegeneration of the nigrostriatal system, and cervical spinal cord injury. The effect of the dendrite growth promoting factor, Osteogenic Protein-1 (OP-1) on outcome following permanent middle cerebral artery (MCA) occlusion was used as an example to illustrate how the tests can be applied preclinically. OP-1 showed a beneficial effect on limb use asymmetry in the cylinder test.
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            Induction of reproducible brain infarction by photochemically initiated thrombosis.

            We have used a photochemical reaction in vivo to induce reproducible thrombosis leading to cerebral infarction in rats. After the intravenous injection of rose bengal, a potent photosensitizing dye, an ischemic lesion was formed by irradiating the left parietal convexity of the exposed skull for 20 minutes with green light (560 nm) from a filtered xenon arc lamp. Animals were allowed to survive from 30 minutes to 15 days after irradiation. Early microscopic alterations within the irradiated zone included the formation of thrombotic plugs and adjacent red blood cell stasis within pial and parenchymal vessels. Scanning electron microscopy revealed frequent platelet aggregates adhering to the vascular endothelium, often resulting in vascular occlusion. Carbon-black brain perfusion demonstrated that occlusion of vascular channels progressed after irradiation and was complete within 4 hours. Histopathological examination at 1, 5, and 15 days revealed that the associated infarct evolved reproducibly through several characteristic stages, including a phase of massive macrophage infiltration. Although cerebral infarction in this model is initiated by thrombosis of small blood vessels, the fact that the main pathological features of stroke are consistently reproduced should permit its use in assessing treatment regimens. Further, the capability of producing infarction in preselected cortical regions may facilitate the study of behavioral, functional, and structural consequences of acute and chronic stroke.
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              Neurorestorative therapies for stroke: underlying mechanisms and translation to the clinic.

              Restorative cell-based and pharmacological therapies for experimental stroke substantially improve functional outcome. These therapies target several types of parenchymal cells (including neural stem cells, cerebral endothelial cells, astrocytes, oligodendrocytes, and neurons), leading to enhancement of endogenous neurogenesis, angiogenesis, axonal sprouting, and synaptogenesis in the ischaemic brain. Interaction between these restorative events probably underpins the improvement in functional outcome. This Review provides examples of cell-based and pharmacological restorative treatments for stroke that stimulate brain plasticity and functional recovery. The molecular pathways activated by these therapies, which induce remodelling of the injured brain via angiogenesis, neurogenesis, and axonal and dendritic plasticity, are discussed. The ease of treating intact brain tissue to stimulate functional benefit in restorative therapy compared with treating injured brain tissue in neuroprotective therapy might more readily help with translation of restorative therapy from the laboratory to the clinic.
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                Author and article information

                Contributors
                Journal
                Neurophotonics
                Neurophotonics
                NEUROW
                NPh
                Neurophotonics
                Society of Photo-Optical Instrumentation Engineers
                2329-423X
                2329-4248
                30 January 2020
                January 2020
                30 January 2020
                : 7
                : 1
                : 015005
                Affiliations
                [a ]Boston University , Neurophotonics Center, Department of Biomedical Engineering, Boston, Massachusetts, United States
                [b ]Hacettepe University , Institute of Neurological Sciences and Psychiatry, Ankara, Turkey
                [c ]Copenhagen University , Department of Biomedical Sciences, Copenhagen, Denmark
                Author notes
                [* ]Address all correspondence to Smrithi Sunil, E-mail: ssunil@ 123456bu.edu
                Author information
                https://orcid.org/0000-0002-5141-7899
                https://orcid.org/0000-0001-6110-5285
                https://orcid.org/0000-0002-6709-7711
                https://orcid.org/0000-0001-7248-8728
                Article
                NPh-19074RR 19074RR
                10.1117/1.NPh.7.1.015005
                6992450
                32042854
                2413b356-e77b-4264-9648-8750a16281f2
                © The Authors. Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
                History
                : 15 July 2019
                : 2 January 2020
                Page count
                Figures: 7, Tables: 0, References: 50, Pages: 18
                Funding
                Funded by: National Institutes of Health https://doi.org/10.13039/100000002
                Award ID: R01-EB021018
                Award ID: R01 NS108472
                Award ID: R01-MH111359
                Funded by: Hacettepe Üniversitesi https://doi.org/10.13039/501100005378
                Award ID: TUI-2019-18106
                Categories
                Research Papers
                Paper
                Custom metadata
                Sunil et al.: Awake chronic mouse model of targeted pial vessel occlusion via photothrombosis

                stroke,photothrombosis,imaging,awake,chronic
                stroke, photothrombosis, imaging, awake, chronic

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