Brain-derived neurotrophic factor in Alzheimer’s disease and its pharmaceutical potential

被引:0
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作者
Lina Gao
Yun Zhang
Keenan Sterling
Weihong Song
机构
[1] Jining Medical University,Shandong Collaborative Innovation Center for Diagnosis, Treatment and Behavioral Interventions of Mental Disorders, Institute of Mental Health, College of Pharmacy
[2] The University of British Columbia,Townsend Family Laboratories, Department of Psychiatry
[3] Xuanwu Hospital,National Clinical Research Center for Geriatric Disorders
[4] Capital Medical University,Institute of Aging, Key Laboratory of Alzheimer’s Disease of Zhejiang Province, School of Mental Health and The Affiliated Kangning Hospital
[5] Wenzhou Medical University,undefined
[6] Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine,undefined
[7] Vision and Brain Health),undefined
关键词
Brain-derived neurotrophic factor; Alzheimer’s disease; Amyloid β protein; Tau protein; Neuroinflammation; Neuronal apoptosis;
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摘要
Synaptic abnormalities are a cardinal feature of Alzheimer’s disease (AD) that are known to arise as the disease progresses. A growing body of evidence suggests that pathological alterations to neuronal circuits and synapses may provide a mechanistic link between amyloid β (Aβ) and tau pathology and thus may serve as an obligatory relay of the cognitive impairment in AD. Brain-derived neurotrophic factors (BDNFs) play an important role in maintaining synaptic plasticity in learning and memory. Considering AD as a synaptic disorder, BDNF has attracted increasing attention as a potential diagnostic biomarker and a therapeutical molecule for AD. Although depletion of BDNF has been linked with Aβ accumulation, tau phosphorylation, neuroinflammation and neuronal apoptosis, the exact mechanisms underlying the effect of impaired BDNF signaling on AD are still unknown. Here, we present an overview of how BDNF genomic structure is connected to factors that regulate BDNF signaling. We then discuss the role of BDNF in AD and the potential of BDNF-targeting therapeutics for AD.
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