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BACKGROUND: The neuroprotective effects of (-)-epigallocatechin-3-gallate (EGCG), the main polyphenolic constituent of green tea, have been widely reported. However, the action mechanisms,in particular in D-galactose-induced aging mice, remain poorly understood.OBJECTIVE: The present study investigated the protective effects of EGCG on D-galactose-induced hippocampus neuronal apoptosis in aging mice, as well as the relationship with expression of p75ICD, JNK2, and p53 proteins.DESIGN, TIME AND SETTING: A randomized, controlled, molecular biological, animal experiment was performed at the Laboratory of Pharmacology, Pharmaceutical College of China Medical University, China, from September 2006 to July 2008.MATERIALS: D-galactose and EGCG (Sigma, USA), as well as terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick-end labeling (TUNEL) In Situ Cell Apoptosis Detection Kit (Promega, USA), were used in this study.METHODS: A total of 64 mice were equally and randomly divided into D-galactose model, low-dose EGCG, high-dose EGCG, and control groups. Mice in the D-galactose model, low-dose EGCG,and high-dose EGCG groups were subcutaneously injected with 3% D-galactose (150 mg/kg),daily for 6 weeks, to establish a mouse model of aging. Mice in the control group were treated with saline (5 mL/kg). At 3 weeks following injection, mice in the low-dose EGCG and high-dose EGCG groups were orally administered EGCG at a dose of 2 mg/kg and 6 mg/kg, respectively, once a day,for 4 consecutive days. Mice in the control and D-galactose model groups received distilled water (5 mL/kg).MAIN OUTCOME MEASURES: Memory function was evaluated using a step-through passive avoidance test. Neuronal apoptosis in the mouse hippocampus was detected using TUNEL staining.Expression levels of the intracellular domain of the p75 neurotrophin receptor (p75NTR)-p75ICD,JNK2, and p53 proteins in the hippocampus were determined using Western blot analysis.RESULTS: The aging mouse model was induced by subcutaneous injection of D-galactose, which resulted in obvious memory impairment, increased apoptotic index, and increased protein expression levels of p75ICD, JNK2, and p53 in the hippocampus, compared with control mice (P