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Neuro-regeneration Therapeutic for Alzheimer's Dementia: Perspectives on Neurotrophic Activity

机译:Alzheimer痴呆的神经再生治疗:神经营养活性的透视

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Alzheimer's disease (AD), the leading disorder of memory impairment in our aging population, is increasing at an alarming rate. AD is currently identified by three 'gold standard criteria': (i) dementia in life, (ii) amyloid plaques at autopsy, and (iii) neurofibrillary tangles at autopsy. Several autopsy studies have indicated that dementia in life is a consequence of lost synaptic networks in the brain, while many clinical trials targeting neurotoxic amyloid beta (A beta) have consistently failed to produce therapeutic effects on memory function in AD patients. Restoring cognitive function(s) by activating endogenous repairing/regenerating mechanisms that are synaptogenic and antiapoptotic (preventing neuronal death), however, is emerging as a necessary disease-modifying therapeutic strategy against AD and possibly for other degenerative dementias, such as Parkinson's disease and multi-infarct dementia.
机译:Alzheimer的疾病(广告),我们老龄化人口中的内存障碍障碍症,正在以惊人的速度增加。 目前通过三个“黄金标准标准”:(i)痴呆的痴呆症,(ii)在尸检中的淀粉样蛋白斑块,(iii)尸检的神经纤维斑。 几项尸检研究表明,生活中的痴呆是丢失大脑中突触网络的结果,而靶向神经毒性淀粉样蛋白β(Aβ)的许多临床试验一致未能对AD患者的记忆功能产生治疗作用。 然而,通过激活具有突触和抗曝气剂(预防神经元死亡)的内源性修复/再生机制来恢复认知功能,作为对AD的必要疾病改性治疗策略,可能是帕金森病等其他退行性痴呆症 多梗塞痴呆症。

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