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1.
Chinese Journal of Neuromedicine ; (12): 1101-1105, 2011.
Article in Chinese | WPRIM | ID: wpr-1033397

ABSTRACT

Objective To investigate the influence of rotenone neurotoxin on dopaminergic neurons from SD rats of different months and its mechanism.Methods Forty 3-month-old,4012-month-old and 40 20-month-old SD rats were chosen in our study and equally randomized into control group and rotenone treatment group,respectively(n=20); rotenone(1.0 mg/[kg·d])was given to the rats in the rotenone treatment group for 30 consecutive d(having drug withdrawal 1 d per week)to induce rotenone neurotoxin models.Tyrosine hydroxylase immunoreactivity in the substantia nigra pars compacta(SNpc)was observed.Levels of total superoxide dismutase(SOD)and catalase(CAT)were determined by colorimetric method and protein level of caspase-3 was determined by Western blotting.Results A significant decreased number of TH-positive cells in 3-,12-and 20-month-old rats of rotenone treatment group was noted as compared with that in the control group,respectively(P<0.05),and 20-month-old rats had the fewest number.SOD and CAT activities in 3 month-old rats of the control group enjoyed the highest level and decreased trend was noted in 20 month-old rats of the control group;as compared with those in the control group,the SOD and CAT activities in all the rats of rotenone treatment group increased significantly(P<0.05).Western blotting revealed that the expression of cleaved caspase-3 in all the rats of rotenone treatment group obviously increased as compared with those in the control group,and 20-month-old rats showed the highest level of active caspase-3.Conclusion Rotenone can induce the decrease of TH-positive cell level following the increase of rat age; increase levels ofcaspase-3 and oxidative stress may take part in the mechanism of high sensibility of old SD rats to rotenone.

2.
Journal of Forensic Medicine ; (6): 74-75, 2006.
Article in Chinese | WPRIM | ID: wpr-983137

ABSTRACT

OBJECTIVE@#To study the extracting and genotyping method of sweat latent fingerprint samples involved in cases.@*METHOD@#Chlex 100 extraction method was used to extract DNA. STR loci were typed after PCR amplification by Profiler Plus kit.@*RESULTS@#All the sweat latent fingerprint samples involved in cases obtained reliable results of STR genotyping.@*CONCLUSION@#It is very important to find and extract sweat latent fingerprint samples properly for STR genotyping.


Subject(s)
Humans , DNA/isolation & purification , DNA Fingerprinting/methods , Forensic Anthropology/methods , Genotype , Polymerase Chain Reaction/methods , Resins, Synthetic , Sweat , Tandem Repeat Sequences
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