Modeling Stroke in Mice: Permanent Coagulation of the Distal Middle Cerebral Artery

Stroke is the third most common cause of death and a main cause of acquired adult disability in developed countries. Only very limited therapeutical options are available for a small proportion of stroke patients in the acute phase. Current research is intensively searching for novel therapeutic strategies and is increasingly focusing on the sub-acute and chronic phase after stroke because more patients might be eligible for therapeutic interventions in a prolonged time window. These delayed mechanisms include important pathophysiological pathways such as post-stroke inflammation, angiogenesis, neuronal plasticity and regeneration. In order to analyze these mechanisms and to subsequently evaluate novel drug targets, experimental stroke models with clinical relevance, low mortality and high reproducibility are sought after. Moreover, mice are the smallest mammals in which a focal stroke lesion can be induced and for which a broad spectrum of transgenic models are available. Therefore, we describe here the mouse model of transcranial, permanent coagulation of the middle cerebral artery via electrocoagulation distal of the lenticulostriatal arteries, the so-called “coagulation model”. The resulting infarct in this model is located mainly in the cortex; the relative infarct volume in relation to brain size corresponds to the majority of human strokes. Moreover, the model fulfills the above-mentioned criteria of reproducibility and low mortality. In this video we demonstrate the surgical methods of stroke induction in the “coagulation model” and report histological and functional analysis tools.

[1]  Ninds,et al.  Effect of Intravenous Recombinant Tissue Plasminogen Activator on Ischemic Stroke Lesion Size Measured by Computed Tomography , 2000, Stroke.

[2]  M. Wintermark,et al.  Guidelines for the Early Management of Patients With Acute Ischemic Stroke: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association , 2013, Stroke.

[3]  David W Howells,et al.  Different Strokes for Different Folks: The Rich Diversity of Animal Models of Focal Cerebral Ischemia , 2010, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[4]  T. Schallert,et al.  CNS plasticity and assessment of forelimb sensorimotor outcome in unilateral rat models of stroke, cortical ablation, parkinsonism and spinal cord injury , 2000, Neuropharmacology.

[5]  Wei Zhou,et al.  Boosting Regulatory T Cells Limits Neuroinflammation in Permanent Cortical Stroke , 2013, The Journal of Neuroscience.

[6]  E. Hogan,et al.  A model of focal ischemic stroke in the rat: reproducible extensive cortical infarction. , 1986, Stroke.

[7]  A. Majid,et al.  Differences in Vulnerability to Permanent Focal Cerebral Ischemia Among 3 Common Mouse Strains , 2000, Stroke.

[8]  Suzanne E. Welcome,et al.  Mapping cortical change across the human life span , 2003, Nature Neuroscience.

[9]  P. Weinstein,et al.  Reversible middle cerebral artery occlusion without craniectomy in rats. , 1989, Stroke.

[10]  Robert J. Dempsey,et al.  Infarct volume quantification in mouse focal cerebral ischemia: a comparison of triphenyltetrazolium chloride and cresyl violet staining techniques , 2004, Journal of Neuroscience Methods.

[11]  A Hofman,et al.  Frequency of stroke in Europe: A collaborative study of population-based cohorts. ILSA Working Group and the Neurologic Diseases in the Elderly Research Group. Italian Longitudinal Study on Aging. , 2000, Neurology.

[12]  I. Whishaw,et al.  Quantitative and Qualitative Impairments in Skilled Reaching in the Mouse (Mus musculus) After a Focal Motor Cortex Stroke , 2002, Stroke.

[13]  C. Graffagnino,et al.  Nonocclusion and spontaneous recanalization rates in acute ischemic stroke: a review of cerebral angiography studies. , 2002, Archives of neurology.

[14]  U. Dirnagl,et al.  Modeling Stroke in Mice - Middle Cerebral Artery Occlusion with the Filament Model , 2011, Journal of visualized experiments : JoVE.

[15]  P. Hurn,et al.  Inhalational Anesthetics as Neuroprotectants or Chemical Preconditioning Agents in Ischemic Brain , 2007, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[16]  Y. H. Krikorian Life, Mechanism and Purpose , 1943, Philosophy of Science.

[17]  W. Hacke,et al.  'Malignant' middle cerebral artery territory infarction : Clinical course and prognostic signs , 1996 .

[18]  S. Thomas Carmichael,et al.  Rodent models of focal stroke: Size, mechanism, and purpose , 2005, NeuroRX.

[19]  K. N. Dollman,et al.  - 1 , 1743 .

[20]  D. Graham,et al.  Focal Cerebral Ischaemia in the Rat: 1. Description of Technique and Early Neuropathological Consequences following Middle Cerebral Artery Occlusion , 1981, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[21]  F. Veith,et al.  Letter by Paraskevas et al regarding article, "Guidelines for the prevention of stroke in patients with stroke or transient ischemic attack: a guideline for healthcare professionals from the American Heart Association/american Stroke Association". , 2011, Stroke.

[22]  D. Vivien,et al.  Mouse Model of In Situ Thromboembolic Stroke and Reperfusion , 2007, Stroke.

[23]  M. Kaste,et al.  Thrombolysis with alteplase 3 to 4.5 hours after acute ischemic stroke. , 2008, The New England journal of medicine.

[24]  T Brott,et al.  Measurements of acute cerebral infarction: lesion size by computed tomography. , 1989, Stroke.

[25]  A systems approach to immediate evaluation and management of hyperacute stroke. Experience at eight centers and implications for community practice and patient care. The National Institute of Neurological Disorders and Stroke (NINDS) rt-PA Stroke Study Group. , 1997, Stroke.

[26]  R A Swanson,et al.  A Semiautomated Method for Measuring Brain Infarct Volume , 1990, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[27]  M. Chopp,et al.  A New Rat Model of Thrombotic Focal Cerebral Ischemia , 1997, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[28]  Michel Boulouard,et al.  The adhesive removal test: a sensitive method to assess sensorimotor deficits in mice , 2009, Nature Protocols.

[29]  C. Sommer,et al.  Inhibition of lymphocyte trafficking shields the brain against deleterious neuroinflammation after stroke. , 2011, Brain : a journal of neurology.

[30]  Michael Chopp,et al.  A test for detecting long-term sensorimotor dysfunction in the mouse after focal cerebral ischemia , 2002, Journal of Neuroscience Methods.

[31]  S. Levine Effect of Intravenous Recombinant Tissue Plasminogen Activator on Ischemic Stroke Lesion Size Measured by Computed Tomography , 2000 .

[32]  D. Roberts,et al.  A rotarod suitable for quantitative measurements of motor incoordination in naive mice , 2004, Naunyn-Schmiedebergs Archiv für Pharmakologie und experimentelle Pathologie.