期刊
NEUROSCIENCE LETTERS
卷 453, 期 1, 页码 73-76出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2009.01.062
关键词
Atorvastatin; Rats; Spinal cord injury; Apoptosis; Locomotion
资金
- Centre de recherche, Hopital du Sacre-Coeur de Monteal and Fonds de la recherche en sante du Qebec (FRSQ).
The systemic administration of atorvastatin has been shown to be neuroprotective after spinal cord injury (SCI), by decreasing the inflammatory response at the lesion site and by reducing neuronal and oligodendrocyte apoptosis. The latter effect spares white matter at the injury site and improves locomotion. The aim of this study was to confirm the neuroprotective efficacy of atorvastatin as well as its early action in limiting apoptosis with its administration post-SCI. Female Sprague-Dawley rats received an intra peritoneal injection of: (1) statin/saline (5 mg/kg) at 2 h after the contusion injury; (2) physiological saline at 2 h post-SCI; or (3) physiological saline without injury. Statin-treated rats showed significant (p < 0.05) improvement in locomotion at week 4 post-SCI compared to vehicle-treated animals. Explaining this outcome, caspase-3 activity decreased by 50% (p<0.05), and the histological TUNEL method revealed a decrease of approximately 20% in apoptotic cells at the injury site (p < 0.01) at 4 h post-SCI in atorvastatin-treated rats in comparison to vehicle-treated controls. These data demonstrate that atorvastatin is effective after experimental spinal cord contusion injury in preventing early apoptosis at the injury site within 2 h post-administration. Crown Copyright (C) 2009 Published by Elsevier Ireland Ltd. All rights reserved.
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