Influence of the nitric oxide-donor of sodium nitroprusside on the expression of hippocampal neurons gene cpp32 / 中国组织工程研究
Chinese Journal of Tissue Engineering Research
;
(53): 182-184,封三, 2006.
Article
Dans Chinois
| WPRIM
| ID: wpr-597649
ABSTRACT
BACKGROUND:
Alzheimer disease is a senile degenerative disease of nervous system. Neuron apoptosis is regarded as one of possible reasons,and neuron culture in vitro is a common method to research the mechanism of apoptosis.OBJECTIVE:
To observe the influences of nitric oxide-donor, sodium nitroprusside (SNP), on the expression of gene cpp32 in the cultured hippocarnpal neurons in vitro.DESIGN:
A randomized controlled animal experiment.SETTING:
Institute of Biochemistry and Molecular Biology in Guangdong Medical College.MATERIALS The experiment was carried out in the Institute of Biochemistry and Molecular Biology, Guangdong Medical College, and newborn (< 24 hours) Sprague-Dawley rats were used.METHODS:
The hippocampl neurons of rats were primarily cultured, and then treated with SNP of different terminal concentrations (0, 25, 50, 100,200, 400 μmol/L) for 24 hours, and the expressions of mRNA and protein were analyzed with RT-PCR and Western blot respectively. The hippocampl neurons of rats were treated with SNP of different terminal concentrations (0, 25, 50, 100, 200, 400 μmol/L) for 12 hours, and the activity of CPP32 enzyme was detected with CPP32 activity detected kit.MAIN OUTCOMEMEASURES:
The expressions cpp32 mRNA and CPP32 protein and activity of CPP32 were detected.RESULTS:
The cpp32 mRNA expression was unchanged as the increasing dose of SNP, but the pro-CPP32 was activated and the activity of CPP32 was increased significantly at 50 μmol/L SNP which was 3.02 times of that in the control group, and reached to the maximal value at 100 μmol/L which was 3.47 times of that in the control group.CONCLUSION:
SNP cannot increase the cpp32 mRNA expression, but can increase degradation of pro-CPP32 and activate CPP32.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Type d'étude:
Essai clinique contrôlé
langue:
Chinois
Texte intégral:
Chinese Journal of Tissue Engineering Research
Année:
2006
Type:
Article
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