Evaluation of Oxidative Stress Levels and Antioxidant Enzyme Activities in Burst Fractures.
Evaluation of Oxidative Stress Levels and Antioxidant Enzyme Activities in Burst Fractures.
复制标题
评估爆发骨折中氧化应激水平和抗氧化剂活性。
DOI:
10.12659/msm.908312
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发表时间:
2018-01-11
期刊:
影响因子:
--
通讯作者:
Aycan A
中科院分区:
文献类型:
--
作者:
Kuyumcu F;Aycan A
Spinal burst fractures are pathologies that occur in spinal injuries and cause significant mortality and morbidity as a result. Burst fractures in spinal cord injuries can result in rapid and significant oxidative stress. In addition to the primary injury in severe spinal cord injuries, subsequent secondary lesions are mainly due to inflammatory cascade activation and excessive production of free radicals. This study evaluated oxidative stress and antioxidant enzyme levels in burst fractures. Twenty patients with burst fractures were diagnosed and underwent surgery and 20 healthy control subjects were included in the study. Neurological status was evaluated using the American Spine Injury Association Impairment Scale (ASIA) before and after surgery. Neurological function was scored as ASIA A: complete deficits, ASIA B–D: incomplete deficits, and ASIA E: neurologically intact. Spectrophotometry was performed to measure malondialdehyde (MDA) and low glutathione (GSH), glutathione peroxidase (GPx) levels, which represent lipid peroxide content. Evaluations were performed within 2 days after injury in the patients. MDA levels were higher in the burst fracture group (p<0.001), whereas GSH and SOD activities were higher in the control group (both p<0.001). There was no statistically significant difference in GPx levels between the groups (p=0.482). Oxidative stress appears to be related to burst fractures. Considering the importance of burst fractures in spinal cord injuries, a better understanding of these mechanisms may help in defining the role of oxidative stress after burst fractures. Prospective, randomized, controlled trials may reveal new therapeutic approaches that include antioxidants for explosive fractures focusing on oxidative stress.
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影响因子:
3
作者:
Hu, R;Mustard, CA;Burns, C
通讯作者:
Burns, C
DOI:
10.1515/jbcpp-2013-0042
发表时间:
2014-02-01
影响因子:
--
作者:
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通讯作者:
Al-Jebreen, Abdulrahman M.
影响因子:
5.9
作者:
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通讯作者:
Koskinen, SK
影响因子:
7.4
作者:
Antunes, F;Han, D;Cadenas, E
通讯作者:
Cadenas, E
影响因子:
4.8
作者:
Kamencic, H;Griebel, RW;Juurlink, BHJ
通讯作者:
Juurlink, BHJ