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Neuroprotective effect of atorvastatin in spinal cord ischemia-reperfusion injury

OBJECTIVES: Prevention of the development of paraplegia during the repair of the damage caused by descending thoracic and thoracoabdominal aneurysms remains an important issue. Therefore, we investigated the protective effect of atorvastatin on ischemia-induced spinal cord injury in a rabbit model....

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Autores principales: Nazli, Yunus, Colak, Necmettin, Alpay, Mehmet Fatih, Uysal, Sema, Uzunlar, Ali Kemal, Cakir, Omer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311118/
https://www.ncbi.nlm.nih.gov/pubmed/25672430
http://dx.doi.org/10.6061/clinics/2015(01)10
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author Nazli, Yunus
Colak, Necmettin
Alpay, Mehmet Fatih
Uysal, Sema
Uzunlar, Ali Kemal
Cakir, Omer
author_facet Nazli, Yunus
Colak, Necmettin
Alpay, Mehmet Fatih
Uysal, Sema
Uzunlar, Ali Kemal
Cakir, Omer
author_sort Nazli, Yunus
collection PubMed
description OBJECTIVES: Prevention of the development of paraplegia during the repair of the damage caused by descending thoracic and thoracoabdominal aneurysms remains an important issue. Therefore, we investigated the protective effect of atorvastatin on ischemia-induced spinal cord injury in a rabbit model. METHOD: Thirty-two rabbits were divided into the following four equally sized groups: group I (control), group II (ischemia-reperfusion), group III (atorvastatin treatment) and group IV (atorvastatin withdrawal). Spinal cord ischemia was induced by clamping the aorta both below the left renal artery and above the iliac bifurcation. Seventy-two hours postoperatively, the motor function of the lower limbs of each animal was evaluated according to the Tarlov score. Spinal cord and blood samples were obtained for histopathological and biochemical analyses. RESULTS: All of the rabbits in group II exhibited severe neurological deficits. Atorvastatin treatment (groups III and IV) significantly reduced the level of motor dysfunction. No significant differences were observed between the motor function scores of groups III and IV at the evaluated time points. Light microscopic examination of spinal cord tissue samples obtained at the 72(nd) hour of reperfusion indicated greater tissue preservation in groups III and IV than in group II. CONCLUSION: This study demonstrates the considerable neuroprotective effect of atorvastatin on the neurological, biochemical and histopathological status of rabbits with ischemia-induced spinal cord injury. Moreover, the acute withdrawal of atorvastatin therapy following the induction of spinal cord ischemia did not increase the neuronal damage in this rabbit model.
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spelling pubmed-43111182015-02-09 Neuroprotective effect of atorvastatin in spinal cord ischemia-reperfusion injury Nazli, Yunus Colak, Necmettin Alpay, Mehmet Fatih Uysal, Sema Uzunlar, Ali Kemal Cakir, Omer Clinics (Sao Paulo) Basic Research OBJECTIVES: Prevention of the development of paraplegia during the repair of the damage caused by descending thoracic and thoracoabdominal aneurysms remains an important issue. Therefore, we investigated the protective effect of atorvastatin on ischemia-induced spinal cord injury in a rabbit model. METHOD: Thirty-two rabbits were divided into the following four equally sized groups: group I (control), group II (ischemia-reperfusion), group III (atorvastatin treatment) and group IV (atorvastatin withdrawal). Spinal cord ischemia was induced by clamping the aorta both below the left renal artery and above the iliac bifurcation. Seventy-two hours postoperatively, the motor function of the lower limbs of each animal was evaluated according to the Tarlov score. Spinal cord and blood samples were obtained for histopathological and biochemical analyses. RESULTS: All of the rabbits in group II exhibited severe neurological deficits. Atorvastatin treatment (groups III and IV) significantly reduced the level of motor dysfunction. No significant differences were observed between the motor function scores of groups III and IV at the evaluated time points. Light microscopic examination of spinal cord tissue samples obtained at the 72(nd) hour of reperfusion indicated greater tissue preservation in groups III and IV than in group II. CONCLUSION: This study demonstrates the considerable neuroprotective effect of atorvastatin on the neurological, biochemical and histopathological status of rabbits with ischemia-induced spinal cord injury. Moreover, the acute withdrawal of atorvastatin therapy following the induction of spinal cord ischemia did not increase the neuronal damage in this rabbit model. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2015-01 /pmc/articles/PMC4311118/ /pubmed/25672430 http://dx.doi.org/10.6061/clinics/2015(01)10 Text en Copyright © 2015 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Research
Nazli, Yunus
Colak, Necmettin
Alpay, Mehmet Fatih
Uysal, Sema
Uzunlar, Ali Kemal
Cakir, Omer
Neuroprotective effect of atorvastatin in spinal cord ischemia-reperfusion injury
title Neuroprotective effect of atorvastatin in spinal cord ischemia-reperfusion injury
title_full Neuroprotective effect of atorvastatin in spinal cord ischemia-reperfusion injury
title_fullStr Neuroprotective effect of atorvastatin in spinal cord ischemia-reperfusion injury
title_full_unstemmed Neuroprotective effect of atorvastatin in spinal cord ischemia-reperfusion injury
title_short Neuroprotective effect of atorvastatin in spinal cord ischemia-reperfusion injury
title_sort neuroprotective effect of atorvastatin in spinal cord ischemia-reperfusion injury
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311118/
https://www.ncbi.nlm.nih.gov/pubmed/25672430
http://dx.doi.org/10.6061/clinics/2015(01)10
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