Neurovascular and neuronal protection by E64d after focal cerebral ischemia in rats
β Scribed by Tamiji Tsubokawa; Mitsuo Yamaguchi-Okada; John W. Calvert; Ihsan Solaroglu; Norihito Shimamura; Kenichiro Yata; John H. Zhang
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 855 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0360-4012
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
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 ΞΌβcalpain 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, bloodβbrain barrier permeability, histology, and immunohistochemistry. The E64dβtreated rats had significant brain protection against ischemic damage. We observed a reduction of infarction volume, brain edema, and improved neurological scores in E64dβtreated rats compared with the nontreated control. Furthermore, there was a remarkable reduction in both proteases and caspaseβ3 activation and apoptotic changes in both neurons and endothelial cells in E64dβtreated rats. These results suggest that E64d protects the brain against ischemic/reperfusion injury by attenuating neuronal and endothelial apoptosis. Β© 2006 WileyβLiss, Inc.
π SIMILAR VOLUMES
## Abstract Increasing age decreases the number of new neurons in the dentate gyrus and the subventricular zone (SVZ). Sildenafil, a phosphodiesterase type 5 (PDE5) inhibitor, enhances neurogenesis in young rats. The present study tested the hypothesis that sildenafil augments neurogenesis in aged