香港六合彩-澳门六合彩-时时彩

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。

免佣百家乐规则| 大发888游戏场下载| 88娱乐城怎么样| 888娱乐城| 青浦区| 哪个百家乐官网网站信誉好| 百家乐投注法则| 百家乐稳赢投资法| 大发888娱乐场登陆| 百家乐官网佣金计算| 博彩交流| 菲彩百家乐官网的玩法技巧和规则| 赌场百家乐网站| 大连娱网棋牌官网| 百家乐官网免費游戏| 做生意门朝向什么方向| 威尼斯人娱乐城赌博网站| 五原县| G3百家乐官网的玩法技巧和规则| 大发在线德州扑克| 百家乐官网大小是什么| 百家乐娱乐城新澳博| 大发888娱乐下载| 百家乐官网实战路| 最佳场百家乐的玩法技巧和规则| 真钱现金斗地主| 百家乐官网是娱乐场最不公平的游戏| 澳门百家乐博| 百家乐官网合法| 澳门赌百家乐的玩法技巧和规则| 合水县| 百家乐桩闲落注点| 大发888屡败屡战| 博彩百家乐官网后一预测软件| 威尼斯人娱乐城信誉怎样| 迪威百家乐官网娱乐场| 网上百家乐官网游戏下载| 大发在线体育| 大发888黄金版娱乐场| 百家乐官网和21点| 百家乐官网斗牛稳赚|