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VEGF-induced angiogenesis ameliorates the memory impairment in APP transgenic mouse model of Alzheimer's disease
Authors:Wang Ping  Xie Zhao-Hong  Guo Yu-Ji  Zhao Cui-Ping  Jiang Hao  Song Yan  Zhu Zheng-Yu  Lai Chao  Xu Shun-Liang  Bi Jian-Zhong
Affiliation:aDepartment of Neurology, The Second Hospital of Shandong University, 247#, Beiyuan Dajie, Jinan 250033, PR China;bKey Laboratory of the Ministry of Education for Experimental Teratology, Department of Histology and Embryology, Shandong University School of Medicine, 44#, Wenhua Xi Road, Jinan 250012, PR China
Abstract:Vascular endothelial growth factor (VEGF) was investigated in the present study to see whether it could provide a therapeutic opportunity for the treatment of Alzheimer’s disease (AD). PDGF-hAPPV717I transgenic mice were treated with VEGF or PBS by intraperitoneal injection for three consecutive days. The results showed that VEGF ameliorated the memory impairment of mice, accompanied by CD34+ cells increasing in peripheral blood, vWF+ vessels increasing in hippocampus, and CD34+/VEGFR2+, vWF+/VEGFR2+ and BrdU+/vWF+ cells expressing in hippocampus. Furthermore, the level of choline acetyltransferase (ChAT) was considerably enhanced and Aβ deposition was decreased in the brains of mice upon VEGF treatment. These observations suggest that VEGF should be pursued as a novel therapeutic agent for treatment of AD.
Keywords:Abbreviations: AD, Alzheimer&rsquo  s disease   Aβ, beta-amyloid   APP, beta-amyloid precursor protein   VEGF, vascular endothelial growth factor   EPCs, endothelial progenitor cells   vWF, von Willebrand factor   CD, cluster of differentiation   ChAT, choline acetyltransferase   PDGF, platelet-derived growth factor   NBM, nucleus basalis of Meynert   PBS, phosphate-buffered saline   BrdU, 5-bromo-2-deoxyuridine
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