标题:Effects of APP 5-mer peptide analogue P165 on the synaptic proteins and insulin signal transduction proteins
作者:Feng, Bo; Hu, Peng; Lu, Shu-Jun; Wang, Rong; Du, Yi-Feng
作者机构:[Feng, Bo; Du, Yi-Feng] Shandong Univ, Prov Hosp, Dept Neurol, Jinan 250021, Shandong, Peoples R China.; [Feng, Bo; Lu, Shu-Jun] Binzhou Med Univ, H 更多
通讯作者:Du, YF
通讯作者地址:[Du, YF]Shandong Univ, Prov Hosp, Dept Neurol, 324 Jingwu Rd, Jinan 250021, Shandong, Peoples R China.
来源:INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE
出版年:2014
卷:7
期:3
页码:549-557
关键词:Alzheimer's disease; APP 5-mer peptide analogue P165; diabetes mellitus;; insulin signal transduction; synapse
摘要:Diabetic encephalopathy (DE) is one of risk factors for Alzheimer's disease (AD). Our previous findings indicated that DE animals had impairment of learning and memory and degeneration of hippocampal neurons, which could be improved by neurotrophic peptide. APP 17-mer peptide is a synthesized peptide sequenced from soluble amyloid precursor protein. APP 17-mer peptide has neural protective effect, but is susceptible to enzyme degradation. Soluble APP 5-mer peptide is the active form of APP 17-mer peptide, and composed of arginine, glutamic acid, arginine, methionine and serine. P165, an APP 5-mer peptide analog reconstructed by our lab, is resistant to enzyme degradation, and can be orally used to protect neurons. In the present study, high glucose and A beta(25-35) were used to cause injury to human neuroblastoma cell line SH-SY5Y in vitro, and streptozotocin was used to induce diabetes in mice in vivo. The changes in synaptic proteins and proteins of insulin signal transduction which closely correlate with learning and memory were detected in these cells and the brain of mice. Results showed that P165 could up-regulate the expression of alpha-synuclein and insulin receptor (IR), down-regulate the expression of insulin receptor substrate-1 (IRS-1), PSD-95, Shank1 and MAPK expression. All these findings suggest that nicorandil might be a potential drug used for the treatment of AD.
收录类别:SCOPUS;SCIE
WOS核心被引频次:4
Scopus被引频次:6
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84897560963&partnerID=40&md5=ba31c89a2ab04be6edc1096e7a80b0c1
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