Effect of clausenamide on hippocampal neuron apoptosis induced by sodium nitroprusside  被引量:1

Effect of clausenamide on hippocampal neuron apoptosis induced by sodium nitroprusside

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作  者:Yongjun Liu Qifeng Zhu 

机构地区:[1]Institute of Biochemistry and Molecular Biology, Guangdong Medical College, Zhanjiang 524023, Guangdong Province, China

出  处:《Neural Regeneration Research》2007年第1期33-37,共5页中国神经再生研究(英文版)

摘  要:BACKGROUND: Aggregation of β-amyloid peptide (A β ), excitatory intoxication, oxidation injury and inflammation reaction are generally regarded as the main pathogenesis for Alzheimer disease (AD). ( - ) clausenamide is characterized by promoting intelligent development, resisting oxidation, cleaning free radicals, resisting A β neurotoxicity and nerve cell apoptosis, inhibiting over phosphorylation of tau protein, and improving central cholinergic system. However, whether (-) clausenamide has an effect on hippocampal neuron apoptosis or not need further study. OBJECTIVE: To observe the effect of ( - ) clausenamide on survival rate of hippocampal neurons due to sodium nitroprusside (SNP) and analyze the possible pathways. DESIGN: Contrast observation. SETTING: Institute of Biochemistry and Molecular Biology, Guangdong Medical College. MATERIALS: A total of 12 male SD rats of 24 hours old were provided by the Experimental Animal Center of Guangdong Medical College. The primer was synthesized by Beijing Huada Genetic Engineering Company and (-) clausenamide (99.6%) was provided by Pharmacological Department of Chinese Academy of Medical Sciences. SNP was provided by Sigma Company. METHODS: Bilateral hippocampus was collected from newborn rats to establish single cell suspension. On the 12th day, hippocampal neurons were pretreated with 0.2, 0.4, 0.8 and 1.6 la mol/L ( - ) clausenamide for 6 hours; the culture medium was gotten rid of and neurons were washed with non-serum DMEM solution for three times. In addition, non-serum DMEM solution was added with the above mentioned volume of ( - ) clausenamide and 50 μ mol/L SNP to culture neurons for 24 hours and the collected cells were prepared for the experiment. Neurons were equally divided into control group (culture medium control), model group (SNP treatment) and experimental group [( - ) clausenamide + SNP]. Experiment of each group was done for three times at least. Survival rate of cells was meaBACKGROUND: Aggregation of β-amyloid peptide (A β ), excitatory intoxication, oxidation injury and inflammation reaction are generally regarded as the main pathogenesis for Alzheimer disease (AD). ( - ) clausenamide is characterized by promoting intelligent development, resisting oxidation, cleaning free radicals, resisting A β neurotoxicity and nerve cell apoptosis, inhibiting over phosphorylation of tau protein, and improving central cholinergic system. However, whether (-) clausenamide has an effect on hippocampal neuron apoptosis or not need further study. OBJECTIVE: To observe the effect of ( - ) clausenamide on survival rate of hippocampal neurons due to sodium nitroprusside (SNP) and analyze the possible pathways. DESIGN: Contrast observation. SETTING: Institute of Biochemistry and Molecular Biology, Guangdong Medical College. MATERIALS: A total of 12 male SD rats of 24 hours old were provided by the Experimental Animal Center of Guangdong Medical College. The primer was synthesized by Beijing Huada Genetic Engineering Company and (-) clausenamide (99.6%) was provided by Pharmacological Department of Chinese Academy of Medical Sciences. SNP was provided by Sigma Company. METHODS: Bilateral hippocampus was collected from newborn rats to establish single cell suspension. On the 12th day, hippocampal neurons were pretreated with 0.2, 0.4, 0.8 and 1.6 la mol/L ( - ) clausenamide for 6 hours; the culture medium was gotten rid of and neurons were washed with non-serum DMEM solution for three times. In addition, non-serum DMEM solution was added with the above mentioned volume of ( - ) clausenamide and 50 μ mol/L SNP to culture neurons for 24 hours and the collected cells were prepared for the experiment. Neurons were equally divided into control group (culture medium control), model group (SNP treatment) and experimental group [( - ) clausenamide + SNP]. Experiment of each group was done for three times at least. Survival rate of cells was mea

关 键 词:HIPPOCAMPUS NEURON APOPTOSIS CLAUSENA LANSIUM 

分 类 号:R742.02[医药卫生—神经病学与精神病学] R971[医药卫生—临床医学]

 

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