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Neuroprotective effects of low-concentration alpha-tocopherol Confocal laser microscopy observations

Neuroprotective effects of low-concentration alpha-tocopherol Confocal laser microscopy observations
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摘要 BACKGROUND:Alpha-tocopherol(α-tocopherol) can effectively relieve neuronal damage induced by oxygen-centered free radicals.However,the effective dose remains controversial. OBJECTIVE:To evaluate the protective effects of low-concentrationα-tocopherol on neuronal membranes. DESIGN,TIME AND SETTING:Contrast observation and in vitro study,performed at Laboratory of Neurosurgery,Tianjin Huanhu Hospital between April and September 2006. MATERIALS:Fetal cortical neurons were derived from two 14-day pregnant SD rats,andα-tocopherol was provided by Sigma,USA. METHODS:The neurons were randomly assigned to six groups:(1) normal:neurons were cultured under normal conditions;(2) oxidative damage:oxidative free radicals was damaged using the Fenton reaction;(3)α-tocopherol:neurons were cultured in different concentrations ofα-tocopherol 10,20,40,and 80 mg/L for 2 hours,respectively. MAIN OUTCOME MEASURES:Neuronal membrane damage was observed using a confocal laser microscope,and malonaldehyde production was detected using the thiobarbituric acid method. RESULTS:At normal,biological concentrations(10 mg/L),α-tocopherol induced no change in the damaged neurons(P>0.05).However,at a concentration of 80 mg/L,the number of damaged neurons was significantly reduced,compared with the damage group(P<0.05). Malonaldehyde levels following 80 mg/Lα-tocopherol treatment were less than the oxygen free radical damage group(P<0.05),but greater than the control group(P<0.01). CONCLUSION:A concentration of 80 mg/Lα-tocopherol can effectively protect the neuronal Gel membrane from oxidative damage. BACKGROUND: Alpha-tocopherol ( α-tocopherol) can effectively relieve neuronal damage induced by oxygen-centered free radicals. However, the effective dose remains controversial. OBJECTIVE: To evaluate the protective effects of low-concentration α-tocopherol on neuronal membranes. DESIGN, TIME AND SETTING: Contrast observation and in vitro study, performed at Laboratory of Neurosurgery, Tianjin Huanhu Hospital between April and September 2006. MATERIALS: Fetal cortical neurons were derived from two 14-day pregnant SD rats, and α-tocopherol was provided by Sigma, USA. METHODS: The neurons were randomly assigned to six groups: (1) normal: neurons were cultured under normal conditions; (2) oxidative damage: oxidative free radicals was damaged using the Fenton reaction; (3) α-tocopherol: neurons were cultured in different concentrations of -tocopherol 10, 20, 40, and 80 mg/L for 2 hours, respectively. MAIN OUTCOME MEASURES: Neuronal membrane damage was observed using a confocal laser microscope, and malonaldehyde production was detected using the thiobarbituric acid method. RESULTS: At normal, biological concentrations (10 mg/L), α-tocopherol induced no change in the damaged neurons (P 〉 0.05). However, at a concentration of 80 mg/L, the number of damaged neurons was significantly reduced, compared with the damage group (P 〈 0.05). Malonaldehyde levels following 80 mg/L α-tocopherol treatment were less than the oxygen free radical damage group (P 〈 0.05), but greater than the control group (P 〈 0.01). CONCLUSION: A concentration of 80 mg/L α-tocopherol can effectively protect the neuronal cell membrane from oxidative damage
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2009年第2期135-138,共4页 中国神经再生研究(英文版)
基金 Supported by:the 211 Key Subject Construction Foundation of Tianjin,No. 05YFGD5F02500
关键词 激光共聚焦显微镜 神经保护作用 低浓度 微镜观察 氧自由基损伤 神经元损伤 FENTON反应 大脑皮层神经元 α-tocopherol confocal laser microscopy cell membrane low-concentration
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