12/15-Lipoxygenase Inhibition Reverses Cognitive Impairment, Brain Amyloidosis, and Tau Pathology by Stimulating Autophagy in Aged Triple Transgenic Mice

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• 作者：Antonio Di Meco^a ; Jian-Guo Li^a ; Benjamin E. Blass^b ; Magid Abou-Gharbia^b ; Elisabetta Lauretti^a ; Domenico Praticò ; ^a ; ^{praticod@temple.edu}
• 关键词：Alzheimer&rsquo ; s disease ; Amyloid beta ; Animal model ; Autophagy ; Tau protein ; 12/15-Lipoxygenase
• 刊名：Biological Psychiatry
• 出版年：2017
• 出版时间：15 January 2017
• 年：2017
• 卷：81
• 期：2
• 页码：92-100
• 全文大小：4389 K
• 卷排序：81

文摘

The 12/15-lipoxygenase (12/15-LO) enzyme is upregulated in the brains of patients with Alzheimer’s disease (AD), and its expression levels influence the onset of the AD-like phenotype in mouse models. However, whether targeting this pathway after the neuropathology and behavioral impairments have been established remains to be investigated.MethodsTriple transgenic (3xTg) mice received either PD146176—a selective and specific pharmacological inhibitor of 12/15-LO—or placebo starting at 12 months of age for 12 weeks. They were then assessed for the effect of the treatment on neuropathologies and behavioral impairments.ResultsAt the end of the study, mice in the control group showed a worsening of memory and learning abilities, whereas mice receiving PD146176 were undistinguishable from wild-type mice. The same group also had significantly lower amyloid beta levels and deposition, less tau neuropathology, increased synaptic integrity, and autophagy activation. Ex vivo and in vitro genetic and pharmacological studies found that the mechanism involved in these effects was the activation of neuronal autophagy.ConclusionsOur findings provide new insights into the disease-modifying action of 12/15-LO pharmacological inhibition and establish it as a viable therapeutic approach for patients with AD.