Li Yuan, Li Quan, Pan Chun-Shui, Yan Li, Hu Bai-He, Liu Yu-Ying, Yang Lei, Huang Ping, Zhao Shao-Yang, Wang Chuan-She, Fan Jing-Yu, Wang Xue-Mei, Han Jing-Yan
Integrated Laboratory of Traditional Chinese Medicine and Western Medicine, Peking University First Hospital, Beijing, China.
Tasly Microcirculation Research Center, Peking University Health Science Center, Beijing, China.
Front Physiol. 2018 May 15;9:527. doi: 10.3389/fphys.2018.00527. eCollection 2018.
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.
2型糖尿病(T2DM)与认知障碍和神经退行性疾病密切相关。补肾活血(BSHX)是一种临床上用于治疗糖尿病所致认知障碍的复方中药。然而,其潜在机制尚不清楚。在本研究中,KKAy小鼠是一种伴有肥胖和胰岛素抵抗性高血糖的2型糖尿病遗传模型,每天给予BSHX治疗12周。每4周测量一次血糖。12周后,BSHX治疗显著改善了与T2DM相关的损伤,包括血糖升高、空间记忆受损、脑血流量(CBF)降低、白蛋白渗漏、白细胞粘附的发生以及毛细血管稀疏的出现。同时,BSHX治疗显著保护了KKAy小鼠内皮细胞间紧密连接蛋白(TJ)claudin-5、occludin、小带闭合蛋白-1(ZO-1)和连接粘附分子-1(JAM-1)的下调、海马中淀粉样β蛋白(Aβ)的积累、晚期糖基化终末产物(AGEs)和晚期糖基化终末产物受体(RAGE)的增加以及RhoA/ROCK/埃兹蛋白信号通路的表达和Src激酶的磷酸化。这些结果表明,BSHX对T2DM诱导的认知障碍的保护作用涉及RhoA/ROCK1/埃兹蛋白信号通路的调节和Src激酶的磷酸化。