1. Academic Validation
  2. Indirubin Derivative 7-Bromoindirubin-3-Oxime (7Bio) Attenuates Aβ Oligomer-Induced Cognitive Impairments in Mice

Indirubin Derivative 7-Bromoindirubin-3-Oxime (7Bio) Attenuates Aβ Oligomer-Induced Cognitive Impairments in Mice

  • Front Mol Neurosci. 2017 Nov 28;10:393. doi: 10.3389/fnmol.2017.00393.
Liping Chen 1 Chunhui Huang 1 2 Jieyi Shentu 1 2 Minjun Wang 1 2 Sicheng Yan 1 Fei Zhou 1 Zaijun Zhang 3 Chuang Wang 1 Yifan Han 4 Qinwen Wang 1 Wei Cui 1
Affiliations

Affiliations

  • 1 Ningbo Key Laboratory of Behavioral Neuroscience, Zhejiang Provincial Key Laboratory of Pathophysiology, School of Medicine, Ningbo University, Ningbo, China.
  • 2 Laboratory of Marine Natural Products, School of Marine Sciences, Ningbo University, Ningbo, China.
  • 3 Institute of New Drug Research, Guangdong Province Key Laboratory of Pharmacodynamic, Constituents of Traditional Chinese Medicine and New Drug Research, College of Pharmacy, Jinan University, Guangdong, China.
  • 4 Department of Applied Biology and Chemistry Technology, Institute of Modern Chinese Medicine, Hong Kong Polytechnic University, Hong Kong, China.
Abstract

Indirubins are natural occurring Alkaloids extracted from indigo dye-containing Plants. Indirubins could inhibit various kinases, and might be used to treat chronic myelocytic leukemia, Cancer and neurodegenerative disorders. 7-bromoindirubin-3-oxime (7Bio), an indirubin derivative derived from indirubin-3-oxime, possesses inhibitory effects against cyclin-dependent kinase-5 (CDK5) and glycogen synthase kinase-3β (GSK3β), two pharmacological targets of Alzheimer's disease (AD). In this study, we have discovered that 2.3-23.3 μg/kg 7Bio effectively prevented β-amyloid (Aβ) oligomer-induced impairments of spatial cognition and recognition without affecting bodyweight and motor functions in mice. Moreover, 7Bio potently inhibited Aβ oligomer-induced expression of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α). Furthermore, 7Bio significantly prevented the decreased expression of synapsin-1 and PSD-95, biomarkers of pre-synaptic and post-synaptic proteins in Aβ oligomer-treated mice. The mean optical density (OD) with hyper-phosphorylated tau (pTau), glial fibrillary acidic protein (GFAP) and CD45 positive staining in the hippocampus of 7Bio-treated mice were significantly decreased compared to those of Aβ oligomer-treated mice. In addition, Western blotting analysis showed that 7Bio attenuated Aβ oligomer-decreased expression of pSer9-GSK3β. Those results suggested that 7Bio could potently inhibit Aβ oligomer-induced neuroinflammation, synaptic impairments, tau hyper-phosphorylation, and activation of astrocytes and microglia, which may contribute to the neuroprotective effects of 7Bio. Based on these findings, we expected that 7Bio might be developed as a novel anti-AD lead compound.

Keywords

7-bromoindirubin-3-oxime; Alzheimer's disease; CDK5; GSK3β; β-amyloid.

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