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作 者:刘晓云[1] 卜晖[1] 李哲[1] 李彬[1] 孙萌萌[1] 李春岩[1]
机构地区:[1]河北医科大学第二医院神经内科
出 处:《细胞生物学杂志》2007年第1期135-139,共5页Chinese Journal of Cell Biology
基 金:河北省自然科学基金资助项目(No.303487)~~
摘 要:研究二相酶诱导剂3H-1,2-dithiole-3-thione(D3T)对体外培养的运动神经元的保护作用。选用生后7天的SD乳鼠脊髓腰段切成薄片进行体外培养,正常培养1周后分组干预,对照组只加入正常培养液,THA组于培养液中加入谷氨酸转运体抑制剂threo-hydroxyaspartate(THA),D3T48h+THA组于培养液中加入不同浓度的D3T,48h后同时给予THA和相应浓度的D3T。D3T+THA组于培养液中同时给予THA和不同浓度的D3T。培养4周后观察运动神经元数量和超微结构变化。另外对培养1周后的脊髓薄片给予不同浓度的D3T,观察D3T干预48h后运动神经元数量与相应对照组之间的差异。结果显示D3T对THA引起的运动神经元的丢失有保护作用,且能够减轻THA引起运动神经元超微结构损害。由此认为,二相酶诱导剂D3T有望成为肌萎缩侧索硬化治疗的新切入点。In this study, we want to investigate the role of phase Ⅱ enzyme inducer 3H-1,2-dithiole-3-thione (D3T) on motor neuron survival. The organotypic spinal cord cultures were prepared from 7 day old rat pup lumbar spinal cords. Lumbar spinal cords were collected under sterile conditions, sectioned transversely at 350 μm intervals. Slices were placed on the inserts. After 1 week in culture, the threo-hydroxyaspartate (THA) group, treated with THA alone to achieve a final concentration of 100 μmol/L. For the D3T48h+THA group, tissues were treated with D3T to achieve a final concentration of 15, 30 μmol/L, 48 hour later, the same concentration D3T and 100 μmol/L THA were added to the medium. For the D3T+THA group, tissues were treated with D3T to achieve a final concentration of 15, 30 μmol/L and 100 μmol/L THA were added simultaneously. 0.1%DMSO was added to the drug solubilizer control, no drugs added to the control group. After 4 weeks in culture, tissue were harvested, the number of motor neurons and the ultrastructure of motor neuron were observed by immunohistochemistry and electromicrography. We also compared D3T48h (add D3T 48 h after 7 day culture) group with control (no drug add after 7 day culture) by counting the number of motor neuron. The results showed that D3T can prevent THA-induced motor neuron death, increase motor neuron survival. It suggested that D3T have neuroprotective potential on THA-induced motor neuron death. Phase Ⅱ enzyme inducer may provide a novel neuroprotective strategy for the treatment of amyotrophic lateral sclerosis.
分 类 号:R744[医药卫生—神经病学与精神病学]
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