彩票网-捕鱼

學(xué)術(shù)預(yù)告 首頁(yè)  >  學(xué)術(shù)科研  >  學(xué)術(shù)預(yù)告  >  正文

學(xué)術(shù)預(yù)告-Modulating the Balance of Synaptic and Extrasynaptic NMDA Receptors as a strategy for Alzheimer's disease drug discovery
作者:     日期:2019-05-23     來(lái)源:    

講座主題:Modulating the Balance of Synaptic and Extrasynaptic NMDA Receptors as a strategy for Alzheimer's disease drug discovery

主講人:周文霞

工作單位:軍事醫(yī)學(xué)科學(xué)院

講座時(shí)間:2019年5月24日14:30

講座地點(diǎn):藥學(xué)院一樓報(bào)告廳

主辦單位:煙臺(tái)大學(xué)藥學(xué)院

內(nèi)容摘要:

The unbalance between synaptic (GluN2A, mediating the protective pathway) and extrasynaptic NMDA receptors (NMDARs) (GluN2B, mediating the excitotoxic pathway) has been found in Alzheimer’s disease (AD), indicating restoring the balance of GluN2A and GluN2B should be beneficial for AD therapy. In this study, the GluN2B-selective antagonist, ifenprodil, and the non-selective NMDAR agonist, NMDA, had little effects on amyloid-beta (Abeta)-induced long-term potentiation (LTP) deficits. Enhancing the activity of GluN2A had a protective effect against Abeta, and specific activation of GluN2A and inhibition of GluN2B showed a better protective effect. The combination of ifenprodil and D-cycloserine (a co-activator of NMDRs similar to D-serine) led to greater improvement in behavior tests than ifenprodil or D-cycloserine alone, meanwhile, the combination of ifenprodil and D-cycloserine reversed the signal pathway more significantly than ifenprodil or D-cycloserine alone. These results indicate that enhancing synaptic NMDARs and inhibiting extrasynaptic NMDARs concurrently showed protective effects against Abeta-induced neurotoxicity, suggesting that modulation of the balance between GluN2A and GluN2B might be a good strategy for drug discovery against AD.

主講人介紹:

周文霞,博士,研究員,博士生導(dǎo)師,軍事科學(xué)院軍事醫(yī)學(xué)研究院毒物藥物研究所中藥和神經(jīng)免疫藥理研究室主任。主要從事中藥藥理、神經(jīng)藥理、免疫藥理及網(wǎng)絡(luò)藥理學(xué)研究以及新藥研發(fā)。作為課題負(fù)責(zé)人曾先后承擔(dān)多項(xiàng)國(guó)家軍隊(duì)重點(diǎn)或重大課題,主要包括國(guó)家973項(xiàng)目課題、國(guó)家自然科學(xué)基金面上項(xiàng)目和重大研究計(jì)劃項(xiàng)目、國(guó)家重大新藥創(chuàng)制重大專項(xiàng)課題和國(guó)家科技支撐計(jì)劃課題等。獲北京市科學(xué)技術(shù)獎(jiǎng)一等獎(jiǎng)1項(xiàng)、軍隊(duì)及上海市科技進(jìn)步二等獎(jiǎng)3項(xiàng),發(fā)表學(xué)術(shù)論文180余篇(SCI收錄90余篇),主編(副主編)專著2部,參編3部,申請(qǐng)專利28項(xiàng),授權(quán)15項(xiàng) ,獲新藥臨床批件 2 項(xiàng),曾被評(píng)為全國(guó)優(yōu)秀科技工作者?,F(xiàn)任中國(guó)藥理學(xué)會(huì)副秘書長(zhǎng)、常務(wù)理事、網(wǎng)絡(luò)藥理專業(yè)委員會(huì)主任委員等職。

百家乐真钱在线| 百家乐官网佛牌| 博彩通评价| 百家乐官网路书| 星期八娱乐| 红树林百家乐的玩法技巧和规则| 哪个百家乐官网投注平台信誉好| 二八杠分析仪| 百家乐官网套路| 百家乐官网皇室百家乐官网| 娱乐城网| 至尊百家乐吕文婉| 哪里有百家乐赌博网站| 百家乐技巧心得| 百家乐官网在线赌场| 博彩通3333| 百家乐稳赢技法| 百家乐官网送现金200| 武陟县| 波克棋牌赢话费下载| 王牌百家乐官网的玩法技巧和规则| 998棋牌游戏| 678百家乐博彩娱乐网| 澳门百家乐官网论坛| 网站百家乐官网假| 百家乐官网技巧看路| 壹贰博娱乐城| 优博最新网址| 澳门顶级赌场百家乐的玩法技巧和规则 | 送58百家乐的玩法技巧和规则| 百家乐游戏发展| 百家乐官网翻天百度影音| 永利百家乐官网赌场娱乐网规则| 沙龙百家乐娱乐平台| 百家乐最新投注法| 3d棋牌游戏| 百家乐牌路分析仪| 澳门百家乐赌钱| 百家乐官网已破解的书籍| 洞口县| 真人百家乐官网蓝盾娱乐网|