Outcome of experimental stroke in C57Bl/6 and Sv/129 mice assessed by multimodal ultra-high field MRI

Transgenic mice bred on C57Bl/6 or Sv/129 genetic background are frequently used in stroke research. It is well established that variations in cerebrovascular anatomy and hemodynamics can influence stroke outcome in different inbred mouse lines. We compared stroke development in C57Bl/6 and Sv/129 mice in the widely used model of transient middle cerebral artery occlusion (tMCAO) by multimodal ultra-high field magnetic resonance imaging (MRI)

Rat Model of Global Cerebral Ischemia: The Two-Vessel Occlusion (2VO) Model of Forebrain Ischemia

Animal models of brain ischemia can be divided into focal and global brain ischemia. Among global (often referred to as forebrain) ischemia animal models, the 2-vessel occlusion (2VO) and 4-vessel occlusion (4VO) models in rats are most frequently employed in the studies of molecular mechanisms of neuronal damage after brain ischemia followed by reperfusion. This chapter discusses the rat 2VO model. In this model, reversible forebrain ischemia is produced by bilateral common carotid artery (CCA) occlusion combined with systemic hypotension (50 mmHg) sufficient to induce brain ischemia. This ischemia-and-reperfusion model affects widespread areas of the forebrain. There are two chief histopatho-logical changes in this 2VO ischemia model: (1) selective neuronal vulnerability; typically CA1 pyramidal neurons of the hippocampus are most vulnerable, followed by dorsoventral striatal small- and medium-sized neurons, and pyramidal neurons in the layers 3–4 of the neocortex; and (2) delayed neuronal death, i.e., neuronal death does not occur immediately after transient ischemic episode, but takes place after 2–3 days of reperfusion. During the surgical procedure, this model requires artificial maintenance of (1) rectal and brain temperatures at 37°C, (2) the mean arterial blood pressure (MABP), and (3) blood gases. This 2VO ischemia model has the advantage of a one-step surgical procedure that produces high-grade forebrain ischemia. The reproducibility of the ischemic his-topathological damage of this model is more than 90%. This animal model is also suitable for molecular, biochemical, and physiological studies, as well as for evaluation of neuroprotective procedures and agents