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Intraperitoneal Alpha-Lipoic Acid to prevent neural damage after crush injury to the rat sciatic nerve

OBJECTIVE: Crush injury to the sciatic nerve causes oxidative stress. Alfa Lipoic acid (a-LA) is a neuroprotective metabolic antioxidant. This study was designed to investigate the antioxidant effects of pretreatment with a-LA on the crush injury of rat sciatic nerve. METHODS: Forty rats were random...

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Autores principales: Senoglu, Mehmet, Nacitarhan, Vedat, Kurutas, Ergul Belge, Senoglu, Nimet, Altun, Idris, Atli, Yalcin, Ozbag, Davut
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2789059/
https://www.ncbi.nlm.nih.gov/pubmed/19939272
http://dx.doi.org/10.1186/1749-7221-4-22
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author Senoglu, Mehmet
Nacitarhan, Vedat
Kurutas, Ergul Belge
Senoglu, Nimet
Altun, Idris
Atli, Yalcin
Ozbag, Davut
author_facet Senoglu, Mehmet
Nacitarhan, Vedat
Kurutas, Ergul Belge
Senoglu, Nimet
Altun, Idris
Atli, Yalcin
Ozbag, Davut
author_sort Senoglu, Mehmet
collection PubMed
description OBJECTIVE: Crush injury to the sciatic nerve causes oxidative stress. Alfa Lipoic acid (a-LA) is a neuroprotective metabolic antioxidant. This study was designed to investigate the antioxidant effects of pretreatment with a-LA on the crush injury of rat sciatic nerve. METHODS: Forty rats were randomized into four groups. Group I and Group II received saline (2 ml, intraperitoneally) and a-LA (100 mg/kg, 2 ml, intraperitoneally) in the groups III and IV at the 24 and 1 hour prior to the crush injury. In groups II, III and IV, the left sciatic nerve was exposed and compressed for 60 seconds with a jeweler's forceps. In Group I (n = 10), the sciatic nerve was explored but not crushed. In all groups of rats, superoxide dismutase (SOD) and catalase (CAT) activities, as well as malondialdehyde (MDA) levels were measured in samples of sciatic nerve tissue. RESULTS: Compared to Group I, Group II had significantly decreased tissue SOD and CAT activities and elevated MDA levels indicating crush injury (p < 0.05). In the a-LA treatment groups (groups III and IV), tissue CAT and SOD activities were significantly increased and MDA levels significantly decreased at the first hour (p < 0.05) and on the 3(rd )day (p < 0.05). There was no significant difference between a-LA treatment groups (p > 0.05). CONCLUSION: A-LA administered before crush injury of the sciatic nerve showed significant protective effects against crush injury by decreasing the oxidative stress. A-LA should be considered in the treatment of peripheral nerve injuries, but further studies are needed to explain the mechanism of its neuroprotective effects.
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spelling pubmed-27890592009-12-05 Intraperitoneal Alpha-Lipoic Acid to prevent neural damage after crush injury to the rat sciatic nerve Senoglu, Mehmet Nacitarhan, Vedat Kurutas, Ergul Belge Senoglu, Nimet Altun, Idris Atli, Yalcin Ozbag, Davut J Brachial Plex Peripher Nerve Inj Research Article OBJECTIVE: Crush injury to the sciatic nerve causes oxidative stress. Alfa Lipoic acid (a-LA) is a neuroprotective metabolic antioxidant. This study was designed to investigate the antioxidant effects of pretreatment with a-LA on the crush injury of rat sciatic nerve. METHODS: Forty rats were randomized into four groups. Group I and Group II received saline (2 ml, intraperitoneally) and a-LA (100 mg/kg, 2 ml, intraperitoneally) in the groups III and IV at the 24 and 1 hour prior to the crush injury. In groups II, III and IV, the left sciatic nerve was exposed and compressed for 60 seconds with a jeweler's forceps. In Group I (n = 10), the sciatic nerve was explored but not crushed. In all groups of rats, superoxide dismutase (SOD) and catalase (CAT) activities, as well as malondialdehyde (MDA) levels were measured in samples of sciatic nerve tissue. RESULTS: Compared to Group I, Group II had significantly decreased tissue SOD and CAT activities and elevated MDA levels indicating crush injury (p < 0.05). In the a-LA treatment groups (groups III and IV), tissue CAT and SOD activities were significantly increased and MDA levels significantly decreased at the first hour (p < 0.05) and on the 3(rd )day (p < 0.05). There was no significant difference between a-LA treatment groups (p > 0.05). CONCLUSION: A-LA administered before crush injury of the sciatic nerve showed significant protective effects against crush injury by decreasing the oxidative stress. A-LA should be considered in the treatment of peripheral nerve injuries, but further studies are needed to explain the mechanism of its neuroprotective effects. BioMed Central 2009-11-25 /pmc/articles/PMC2789059/ /pubmed/19939272 http://dx.doi.org/10.1186/1749-7221-4-22 Text en Copyright © 2009 Senoglu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Senoglu, Mehmet
Nacitarhan, Vedat
Kurutas, Ergul Belge
Senoglu, Nimet
Altun, Idris
Atli, Yalcin
Ozbag, Davut
Intraperitoneal Alpha-Lipoic Acid to prevent neural damage after crush injury to the rat sciatic nerve
title Intraperitoneal Alpha-Lipoic Acid to prevent neural damage after crush injury to the rat sciatic nerve
title_full Intraperitoneal Alpha-Lipoic Acid to prevent neural damage after crush injury to the rat sciatic nerve
title_fullStr Intraperitoneal Alpha-Lipoic Acid to prevent neural damage after crush injury to the rat sciatic nerve
title_full_unstemmed Intraperitoneal Alpha-Lipoic Acid to prevent neural damage after crush injury to the rat sciatic nerve
title_short Intraperitoneal Alpha-Lipoic Acid to prevent neural damage after crush injury to the rat sciatic nerve
title_sort intraperitoneal alpha-lipoic acid to prevent neural damage after crush injury to the rat sciatic nerve
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2789059/
https://www.ncbi.nlm.nih.gov/pubmed/19939272
http://dx.doi.org/10.1186/1749-7221-4-22
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