Permanent Middle Cerebral Artery Occlusion in Sheep: A Novel Large Animal Model of Focal Cerebral Ischemia

As effective stroke treatment by thrombolysis is bound to a narrow time window excluding most patients, numerous experimental treatment strategies have been developed to gain new options for stroke treatment. However, all approaches using neuroprotective agents that have been successfully evaluated in rodents have subsequently failed in clinical trials. Existing large animal models are of significant scientific value, but sometimes limited by ethical drawbacks and mostly do not allow for long-term observation. In this study, we are introducing a simple, but reliable stroke model using permanent middle cerebral artery occlusion in sheep. This model allows for control of ischemic lesion size and subsequent neurofunctional impact, and it is monitored by behavioral phenotyping, magnetic resonance imaging, and positron emission tomography. Neuropathologic and (immuno)-histologic investigations showed typical ischemic lesion patterns whereas commercially available antibodies against vascular, neuronal, astroglial, and microglial antigens were feasible for ovine brain specimens. Based on absent mortality in this study and uncomplicated species-appropriate housing, long-term studies can be realized with comparatively low expenditures. This model could be used as an alternative to existing large animal models, especially for longitudinal analyses of the safety and therapeutic impact of novel therapies in the field of translational stroke research.

[1]  Bernhard Neundörfer,et al.  Lifetime Cost of Ischemic Stroke in Germany: Results and National Projections From a Population-Based Stroke Registry: The Erlangen Stroke Project , 2006, Stroke.

[2]  W. Mali,et al.  Diffusion-weighted magnetic resonance imaging in acute stroke. , 1998, Stroke.

[3]  Yaoquan Liu,et al.  A reversible middle cerebral artery occlusion model using intraluminal balloon technique in monkeys. , 2006, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

[4]  J. Kornegay,et al.  Handbook of Veterinary Neurology , 1993 .

[5]  R. Ridley,et al.  Functional and histological evidence for the protective effect of NXY-059 in a primate model of stroke when given 4 hours after occlusion. , 2003, Stroke.

[6]  P. Lapchak,et al.  Advances in ischemic stroke treatment: neuroprotective and combination therapies , 2007, Expert opinion on emerging drugs.

[7]  P. Sanberg,et al.  Timing of Cord Blood Treatment after Experimental Stroke Determines Therapeutic Efficacy , 2006, Cell transplantation.

[8]  A. Green Why do neuroprotective drugs that are so promising in animals fail in the clinic? An industry perspective , 2002, Clinical and experimental pharmacology & physiology.

[9]  Anne-Lise D. Maag,et al.  Adherent Self-Renewable Human Embryonic Stem Cell-Derived Neural Stem Cell Line: Functional Engraftment in Experimental Stroke Model , 2008, PloS one.

[10]  G Marchal,et al.  Early Postischemic Hyperperfusion: Pathophysiologic Insights from Positron Emission Tomography , 1999, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[11]  Gereon R Fink,et al.  Development of brain infarct volume as assessed by magnetic resonance imaging (MRI): Follow‐up of diffusion‐weighted MRI lesions , 2004, Journal of magnetic resonance imaging : JMRI.

[12]  G. Zoppo Why do all drugs work in animals but none in stroke patients ? 1 Drugs promoting cerebral blood flow , 1995 .

[13]  Hans-Christoph Diener,et al.  NXY-059 for the treatment of acute ischemic stroke. , 2007, The New England journal of medicine.

[14]  J. Garcìa,et al.  CEREBRAL INFARCTION: EVOLUTION OF HISTOPATHOLOGICAL CHANGES AFTER OCCLUSION OF A MIDDLE CEREBRAL ARTERY IN PRIMATES , 1974 .

[15]  J. Sleigh,et al.  Cerebral cortical effects of desflurane in sheep: comparison with isoflurane, sevoflurane and enflurane , 2006, Acta anaesthesiologica Scandinavica.

[16]  M. Luby,et al.  Magnetic resonance imaging and computed tomography in emergency assessment of patients with suspected acute stroke: a prospective comparison , 2007, The Lancet.

[17]  W. Heiss,et al.  Stroke--acute interventions. , 2002, Journal of neural transmission. Supplementum.

[18]  P. Wouters,et al.  Spinal somatosensory evoked potentials after epidural isoproterenol in awake sheep , 1997, Canadian journal of anaesthesia = Journal canadien d'anesthesie.

[19]  A. Förschler,et al.  [MRI of experimental focal cerebral ischemia in sheep]. , 2007, RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin.

[20]  M. Fisher,et al.  Perspectives on neuroprotective stroke therapy. , 2006, Biochemical Society transactions.

[21]  Jeffrey J. Kelly,et al.  Spatial Heterogeneity in Oligodendrocyte Lineage Maturation and Not Cerebral Blood Flow Predicts Fetal Ovine Periventricular White Matter Injury , 2006, The Journal of Neuroscience.

[22]  H. Nguyen,et al.  Near infrared spectroscopy (NIRS) measurements during global cerebral ischemia in sheep. , 2003, Advances in experimental medicine and biology.

[23]  R. Higashida,et al.  Trial Design and Reporting Standards for Intra-Arterial Cerebral Thrombolysis for Acute Ischemic Stroke , 2003, Stroke.

[24]  T. Back,et al.  Lesion evolution in cerebral ischemia , 2004, Journal of Neurology.

[25]  Stroke Therapy Academic Industry Roundtable Recommendations for standards regarding preclinical neuroprotective and restorative drug development. , 1999, Stroke.

[26]  R. Traystman Animal models of focal and global cerebral ischemia. , 2003, ILAR journal.