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1.
Asian Pacific Journal of Tropical Medicine ; (12): 982-985, 2013.
Article in English | WPRIM | ID: wpr-819745

ABSTRACT

OBJECTIVE@#To explore effect of 5-AZn-2 '-deoxycytidine on proliferation of human lung adenocarcinoma cell line A549 in vitro.@*METHODS@#Superoxide dismutase (SOD) activity was measured by hydroxylamine colorimetric method. Inhibition effect of 5-AZn-2' deoxycytidylic acid at different concentration and different time on growth of A549 cell was determined by MTT assay. Methylene dioxyamphetamine (MDA) was measured by thiobarbituric acid colorimetric method. Effect of 5-AZn-2' deoxycytidylic acid on apoptosis of A549 cell was determined by Hoechst 33258 dyeing detection.@*RESULTS@#5-AZn-2' deoxycytidylic acid had significant inhibition effect on proliferation of A549 cells in vitro, and the inhibition was notably dependent on time and dosage during 48-72 h; SOD level was significantly lower than those of control group (P<0.05, P<0.01), MDA level was significantly higher than those in the control group (P<0.05, P<0.01). A549 cells began to be in apoptosis after using 5-AZn-2'deoxycytidylic acid.@*CONCLUSIONS@#5- AZn-2' deoxycytidylic acid has significant inhibition effect on growth of A549 cell, and can lead the change of lipid peroxidation. It indicates that the mechanism has relationship with A549 cell cycle tissue and induction factor of apoptosis.


Subject(s)
Humans , Adenocarcinoma , Adenocarcinoma of Lung , Antimetabolites, Antineoplastic , Pharmacology , Apoptosis , Azacitidine , Pharmacology , Cell Line, Tumor , Cell Proliferation , Cell Shape , Decitabine , Lung Neoplasms , Malondialdehyde , Metabolism , Superoxide Dismutase , Metabolism
2.
Journal of Zhejiang University. Medical sciences ; (6): 402-409, 2012.
Article in Chinese | WPRIM | ID: wpr-336777

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of chronic lead exposure on expression of autophagy-associated proteins in rat hippocampus.</p><p><b>METHODS</b>SD rats were randomly divided into three groups: control group was given distilled water, lead-exposed groups were given 0.5 g/L (low-dose) or 2.0 g/L(high-dose) lead acetate solution in drinking water. The rat pups started to drink the lead content water until 60 d maturity. The lead contents in blood and brain samples were analyzed by graphite furnace atomic absorption spectrophotometry. The expressions of Beclin 1, LC3, LAMP2 and cathepsin B proteins were detected by Western blot and immunohistochemistry.</p><p><b>RESULTS</b>Compared with control group, the contents of lead were significantly higher in blood and hippocampus samples in chronic lead-exposed rats (P<0.01). Western blot showed that the expression of Beclin 1 and LC3-II/LC3-I increased significantly in high dose lead-exposed group compared with control group (P<0.05 or P<0.001). The confocal laser immunostaining results demonstrated that increased immunofluorescence staining of cathepsin B in hippocampal neurons compared with control animals.</p><p><b>CONCLUSION</b>The disturbance of autophagy-lysosome signaling molecules might be partially contribute to neurotoxicity of chronic lead exposure.</p>


Subject(s)
Animals , Female , Male , Rats , Apoptosis Regulatory Proteins , Metabolism , Autophagy , Physiology , Beclin-1 , Cathepsin B , Metabolism , Chronic Disease , Disease Models, Animal , Hippocampus , Metabolism , Pathology , Lead Poisoning , Metabolism , Pathology , Lysosomal-Associated Membrane Protein 2 , Metabolism , Microtubule-Associated Proteins , Metabolism , Rats, Sprague-Dawley , Signal Transduction
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