Neurovascular and neuronal protection by E64d after focal cerebral ischemia in rats

Calpains and cathepsins are two families of proteases that play an important role in ischemic cell death. In this study, we investigated the effect of E64d, a μ‐calpain and cathepsin B inhibitor, in the prevention of neuronal and endothelial apoptotic cell death after focal cerebral ischemia in rats. Rats underwent 2 hr of transient focal ischemia from middle cerebral artery occlusion (MCAO) and were sacrificed 24 hr later. E64d (5 mg/ kg intraperitoneally) was administered 30 min before MCAO. Assessment included neurological function, infarction volume, brain water content, blood–brain barrier permeability, histology, and immunohistochemistry. The E64d‐treated rats had significant brain protection against ischemic damage. We observed a reduction of infarction volume, brain edema, and improved neurological scores in E64d‐treated rats compared with the nontreated control. Furthermore, there was a remarkable reduction in both proteases and caspase‐3 activation and apoptotic changes in both neurons and endothelial cells in E64d‐treated rats. These results suggest that E64d protects the brain against ischemic/reperfusion injury by attenuating neuronal and endothelial apoptosis. © 2006 Wiley‐Liss, Inc.

[1]  J. Younger,et al.  Brain edema after intracerebral hemorrhage: the effects of systemic complement depletion. , 2002, Acta neurochirurgica. Supplement.

[2]  L. Ellerby,et al.  Lysosomal Protease Pathways to Apoptosis , 2001, The Journal of Biological Chemistry.

[3]  J. Garcìa,et al.  Neurological deficit and extent of neuronal necrosis attributable to middle cerebral artery occlusion in rats. Statistical validation. , 1995, Stroke.

[4]  John H. Zhang,et al.  Neurovascular Protection Reduces Early Brain Injury After Subarachnoid Hemorrhage , 2004, Stroke.

[5]  G. Kroemer,et al.  Lysosomal Membrane Permeabilization Induces Cell Death in a Mitochondrion-dependent Fashion , 2003, The Journal of experimental medicine.

[6]  M. Linnik,et al.  Six-hour window of opportunity for calpain inhibition in focal cerebral ischemia in rats. , 1998, Stroke.

[7]  N. Carragher Calpain inhibition: a therapeutic strategy targeting multiple disease states. , 2006, Current pharmaceutical design.

[8]  Y. Uchiyama,et al.  Delayed neuronal death in the CA1 pyramidal cell layer of the gerbil hippocampus following transient ischemia is apoptosis , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  John H. Zhang,et al.  Inhibition of Apoptosis by Hyperbaric Oxygen in a Rat Focal Cerebral Ischemic Model , 2003, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[10]  Junying Yuan,et al.  Cross-Talk between Two Cysteine Protease Families , 2000, The Journal of cell biology.

[11]  J. Pober,et al.  The cathepsin B death pathway contributes to TNF plus IFN-gamma-mediated human endothelial injury. , 2005, Journal of immunology.

[12]  G. D. del Zoppo,et al.  Cerebral Microvessel Responses to Focal Ischemia , 2003, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[13]  M Chopp,et al.  Cathepsin B and middle cerebral artery occlusion in the rat. , 1997, Journal of neurosurgery.

[14]  J. Gidday,et al.  Cerebral Endothelial Cell Apoptosis after Ischemia—Reperfusion: Role of PARP Activation and AIF Translocation , 2005, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[15]  M. Chopp,et al.  A selective cysteine protease inhibitor is non-toxic and cerebroprotective in rats undergoing transient middle cerebral artery ischemia , 2001, Brain Research.

[16]  R. Bartus,et al.  Calpain Inhibitor AK295 Protects Neurons From Focal Brain Ischemia: Effects of Postocdusion Intra-arterial Administration , 1994, Stroke.

[17]  G. Gores,et al.  Cathepsin B contributes to TNF-alpha-mediated hepatocyte apoptosis by promoting mitochondrial release of cytochrome c. , 2000, The Journal of clinical investigation.

[18]  T. Yamashima Implication of cysteine proteases calpain, cathepsin and caspase in ischemic neuronal death of primates , 2000, Progress in Neurobiology.

[19]  J. Braudeau,et al.  Activation of Proinflammatory Caspases by Cathepsin B in Focal Cerebral Ischemia , 2004, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[20]  Vijay P. Singh,et al.  Cathepsin B inhibition prevents trypsinogen activation and reduces pancreatitis severity. , 2002, American journal of physiology. Gastrointestinal and liver physiology.

[21]  J. Pober,et al.  The Cathepsin B Death Pathway Contributes to TNF Plus IFN-γ-Mediated Human Endothelial Injury1 , 2005, The Journal of Immunology.

[22]  A. Rami,et al.  μ-Calpain activation, DNA fragmentation, and synergistic effects of caspase and calpain inhibitors in protecting hippocampal neurons from ischemic damage , 2000, Brain Research.

[23]  A. Rami,et al.  Ischemic neuronal death in the rat hippocampus: the calpain–calpastatin–caspase hypothesis , 2003, Neurobiology of Disease.

[24]  John H. Zhang,et al.  Effect of hyperbaric oxygen on apoptosis in neonatal hypoxia-ischemia rat model. , 2003, Journal of applied physiology.