2. Academic Validation
  3. Rutin improves spatial memory in Alzheimer's disease transgenic mice by reducing Aβ oligomer level and attenuating oxidative stress and neuroinflammation

Rutin improves spatial memory in Alzheimer's disease transgenic mice by reducing Aβ oligomer level and attenuating oxidative stress and neuroinflammation

  • Behav Brain Res. 2014 May 1;264:173-80. doi: 10.1016/j.bbr.2014.02.002.
Peng-Xin Xu 1,  Shao-Wei Wang 2,  Xiao-Lin Yu 2,  Ya-Jing Su 1,  Teng Wang 2,  Wei-Wei Zhou 2,  He Zhang 2,  Yu-Jiong Wang 3,  Rui-Tian Liu 4
Affiliations

Affiliations

  • 1 National Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China; School of Life Science, Ningxia University, Yinchuan 750021, China.
  • 2 National Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
  • 3 School of Life Science, Ningxia University, Yinchuan 750021, China. Electronic address: wyj@nxu.edu.cn.
  • 4 National Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China. Electronic address: rtliu@home.ipe.ac.cn.
PMID: 24512768 DOI: 10.1016/j.bbr.2014.02.002
Abstract

Alzheimer's disease (AD) is a progressive, neurodegenerative disease characterized by extracellular β-amyloid (Aβ) plaques and intracellular neurofibrillary tangles in the brain. Aβ aggregation is closely associated with neurotoxicity, oxidative stress, and neuronal inflammation. The soluble Aβ oligomers are believed to be the most neurotoxic form among all forms of Aβ aggregates. We have previously reported a polyphenol compound rutin that could inhibit Aβ aggregation and cytotoxicity, attenuate oxidative stress, and decrease the production of nitric oxide and proinflammatory cytokines in vitro. In the current study, we investigated the effect of rutin on APPswe/PS1dE9 transgenic mice. Results demonstrated that orally administered rutin significantly attenuated memory deficits in AD transgenic mice, decreased oligomeric Aβ level, increased super oxide dismutase (SOD) activity and glutathione (GSH)/glutathione disulfide (GSSG) ratio, reduced GSSG and malondialdehyde (MDA) levels, downregulated microgliosis and astrocytosis, and decreased interleukin (IL)-1β and IL-6 levels in the brain. These results indicated that rutin is a promising agent for AD treatment because of its antioxidant, anti-inflammatory, and reducing Aβ oligomer activities.

Keywords

Alzheimer's disease; Neuroinflammation; Oligomer; Oxidative stress; Rutin; β-Amyloid.

Figures
Products