Chem. J. Chinese Universities

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Preliminary Study on Hippocampal Proteomics of Senescence-accelerated Mouse

DONG Lei1, JIANG Ning1, ZHOU Wen-Xia1, ZHANG Yong-Xiang1, GENG Miao1, ZHANG Xue-Min2, LIU Bing-Yu2, WANG Jie2   

    1. Beijing Institute of Pharmacology and Toxicology,
    2. National Center of Biomedical Analysis, Beijing 100850, China
  • Received:2006-02-27 Revised:1900-01-01 Online:2007-02-10 Published:2007-02-10
  • Contact: ZHOU Wen-Xia

Abstract: To investigate mechanisms of the deficits of learning and memory related with aging, the differentially expressed hippocampal proteins from 6- and 12-month-old SAM-prone/8(SAMP8)and age-matched SAM-resistance/1(SAMR1)were analyzed and compared. In comparison with the same age SAMR1, 15 proteins expressions in hippocampus of 6-month-old SAMP8 increased, 5 proteins expressions decreased significantly; 12 proteins expressions in hippocampus of 12-month-old SAMP8 increased, 2 proteins expressions decreased significantly and 2 proteins only expressed in SAMP8 hippocampus; and 22 proteins with significant changes were identified by MALDI-TOF-MS and the results were searched in MASCOT database. These identified proteins could be devided into four categories according to their functions: (1) energy metabolism; (2) mitochondrion function; (3) signal transduction; (4) other proteins. The results show that there were significant differences in hippocampus protein expressions between SAMP8 and SAMR1, and some differentially expressed proteins were correlated with the deficits of learning and memory in SAMP8 with aging, and these proteins could provide clues for the study and discovery of new protein targets for improving intelligence drugs.

Key words: Senescence-accelerated mouse, Hippocampus, Proteomics

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