Ab'/> Involvement of glucose related energy crisis and endoplasmic reticulum stress: Insinuation of streptozotocin induced Alzheimer's like pathology
首页> 外文期刊>Cellular Signalling >Involvement of glucose related energy crisis and endoplasmic reticulum stress: Insinuation of streptozotocin induced Alzheimer's like pathology
【24h】

Involvement of glucose related energy crisis and endoplasmic reticulum stress: Insinuation of streptozotocin induced Alzheimer's like pathology

机译:葡萄糖相关能源危机和内质网的参与:链脲佐菌素的暗示诱导阿尔茨海默氏症等病理学

获取原文
获取原文并翻译 | 示例
       

摘要

AbstractThe present study was conducted to correlate the cellular and molecular alterations in Alzheimer's pathology employing streptozotocin (STZ) induced experimental rat model. The STZ was administered in rat brain bilaterally by intracerebroventricular route using stereotaxic surgery followed by donepezil dosing. The Alzheimer's related pathological marker like acetylcholinesterase (AChE) activity, tau phosphorylation and amyloid aggregation were observed after STZ administration. STZ treatment showed decreased glucose and glucose transporters (GLUT) level along with augmented level of calcium in both cortical and hippocampal regions of rat brain. Increased calcium level may correlate with endoplasmic reticulum (ER) stress and significantly increased expression of ER stress markers like GRP78, GADD and caspase-12 were observed in STZ treated rat brain. Cellular communication was also affected by STZ administration as observed by increased expression connexin 43. With this view the activation of astrocytes and microglia was also assessed and observed by augmented GFAP and cd11b expression which were partially inhibited with donepezil treatment. The significantly increased level of degenerating neurons, caspase-3 and DNA fragmentation was also observed in rat brain regions which were not inhibited with donepezil treatment and validating the clinical observations. In conclusion, study indicated the STZ induced occurrence of Alzheimer's pathology. Further, STZ administration also caused depleted glucose level, inhibited mitochondrial activity, augmented calcium levels, ER stress, altered cellular communication and neuronal death which were partially attenuated with donepezil t
机译:<![cdata [ 抽象 目前的研究是为了与使用链脲佐菌素(STZ)诱导的实验大鼠的阿尔茨海默病病病理学的细胞和分子改变相关模型。使用立体岩手术,随后用立体外科,在大鼠脑内施用STZ在大鼠脑中施用。在STZ给药后观察到阿尔茨海默氏植物的相关病理标志物,如乙酰胆碱酯酶(ACHE)活性,TAU磷酸化和淀粉样蛋白聚集。 STZ治疗表现出葡萄糖和葡萄糖转运蛋白(葡萄糖转运蛋白(葡萄糖)水平随着大鼠皮质和海马区域的增强水平。增加的钙水平可以与内质网(ER)胁迫相关,并且在STZ处理的大鼠大脑中观察到GRP78,GADD和Caspase-12等ER应激标记物的表达显着增加。通过增加表达Connexin 43观察到的STZ施用的细胞通信也受到STZ给药的影响。通过这种观点,还通过增强GFAP和CD11b表达来评估和观察半胶质细胞和微胶质细胞的激活,所述CD11b表达与多奈哌齐治疗部分抑制。在大鼠脑区中也观察到退化神经元,Caspase-3和DNA碎片水平显着增加,所述大鼠脑区不抑制多奈哌齐治疗并验证临床观察。总之,研究表明了STZ诱导的阿尔茨海默病病症发生。此外,STZ施用还引起葡萄糖水平,抑制线粒体活性,增强钙水平,ER应激,改变的细胞通信和神经元死亡,其部分地衰减与Denpezil T.

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号