Table of Contents
ISRN Neuroscience
Volume 2013 (2013), Article ID 253093, 9 pages
http://dx.doi.org/10.1155/2013/253093
Research Article

Xanthine Oxidase Does Not Contribute to Apoptosis after Brain Hypoxia-Ischemia in Immature Rabbits

1Division of Pediatric Critical Care Medicine, Department of Pediatrics, Harbor-UCLA Medical Center, Torrance, CA 90502, USA
2Division of Pediatric Critical Care Medicine, Department of Pediatrics, Los Angeles BioMedical Research Institute, Torrance, CA 90502, USA
3Division of Pediatric Critical Care Medicine, Department of Pediatrics, Harbor-UCLA Medical Center and Los Angeles BioMedical Research Institute, David Geffen School of Medicine at UCLA, Torrance, CA 90502, USA

Received 5 June 2013; Accepted 11 July 2013

Academic Editors: A. Unal and A. Witting

Copyright © 2013 Anthony Moretti et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background. The mechanisms involving the initiation of apoptosis after brain hypoxia-ischemia through caspase activation are not fully defined. Oxygen free radicals may be an important mediator of caspase initiation with reactive oxygen species generated by xanthine oxidase (XO) being one potential source. The purpose of this study was to examine the role of XO in apoptosis after global cerebral injury. Methods. Immature rabbits were subjected to 8 minutes hypoxia and 8 minutes ischemia and then 4 hours of reperfusion. In one group ( ), the XO substrate xanthine was infused to generate more oxygen free radicals to promote apoptosis while in another ( ), the XO inhibitor allopurinol was given to reduce apoptosis by preventing free radical production ( ). Control animals ( ) received the vehicles. Caspase 3, 8, and 9 enzyme activities were measured in the cerebral cortex, hippocampus, cerebellum, thalamus, and caudate. Results. Administration of xanthine increased ( ) caspase 3 activity but only in the hippocampus, and pretreatment with allopurinol did not reduce it. No differences ( ) were found in any other region nor were there any changes in caspases 8 or 9 activities. Conclusion. We conclude that XO is not a major factor in inducing apoptosis after hypoxic-ischemic brain injury.