Frontiers in Physiology (May 2018)

Bushen Huoxue Attenuates Diabetes-Induced Cognitive Impairment by Improvement of Cerebral Microcirculation: Involvement of RhoA/ROCK/moesin and Src Signaling Pathways

  • Yuan Li,
  • Quan Li,
  • Quan Li,
  • Quan Li,
  • Chun-Shui Pan,
  • Chun-Shui Pan,
  • Chun-Shui Pan,
  • Li Yan,
  • Li Yan,
  • Li Yan,
  • Bai-He Hu,
  • Bai-He Hu,
  • Bai-He Hu,
  • Yu-Ying Liu,
  • Yu-Ying Liu,
  • Yu-Ying Liu,
  • Lei Yang,
  • Ping Huang,
  • Ping Huang,
  • Ping Huang,
  • Shao-Yang Zhao,
  • Chuan-She Wang,
  • Chuan-She Wang,
  • Chuan-She Wang,
  • Chuan-She Wang,
  • Jing-Yu Fan,
  • Jing-Yu Fan,
  • Jing-Yu Fan,
  • Xue-Mei Wang,
  • Jing-Yan Han,
  • Jing-Yan Han,
  • Jing-Yan Han,
  • Jing-Yan Han

DOI
https://doi.org/10.3389/fphys.2018.00527
Journal volume & issue
Vol. 9

Abstract

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Type 2 Diabetes mellitus (T2DM) is closely correlated with cognitive impairment and neurodegenerative disease. Bushen Huoxue (BSHX) is a compound Chinese medicine used clinically to treat diabetes-induced cognitive impairment. However, its underlying mechanisms remain unclear. In the present study, KKAy mice, a genetic model of type 2 diabetes with obesity and insulin resistant hyperglycemia, received a daily administration of BSHX for 12 weeks. Blood glucose was measured every 4 weeks. After 12 weeks, BSHX treatment significantly ameliorated the T2DM related insults, including the increased blood glucose, the impaired spatial memory, decreased cerebral blood flow (CBF), occurrence of albumin leakage, leukocyte adhesion and opening capillary rarefaction. Meanwhile, the downregulation of the tight junction proteins (TJ) claudin-5, occludin, zonula occluden-1 (ZO-1) and JAM-1 between endothelial cells, amyloid-β (Aβ) accumulation in hippocampus, increased AGEs and RAGE, and expression of RhoA/ROCK/moesin signaling pathway and phosphorylation of Src kinase in KKAy mice were significantly protected by BSHX treatment. These results indicate that the protective effect of BSHX on T2DM-induced cognitive impairment involves regulation of RhoA/ROCK1/moesin signaling pathway and phosphorylation of Src kinase.

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