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Antioxidative and Neuroprotective Effects of Curcumin in an Alzheimer's Disease Rat Model Co-Treated with Intracerebroventricular Streptozotocin and Subcutaneous D-Galactose  ( SCI-EXPANDED收录)  

文献类型:期刊文献

英文题名:Antioxidative and Neuroprotective Effects of Curcumin in an Alzheimer's Disease Rat Model Co-Treated with Intracerebroventricular Streptozotocin and Subcutaneous D-Galactose

作者:Huang, Han-Chang[1,2];Zheng, Bo-Wen[1];Guo, Yu[1,2];Zhao, Jian[1,2];Zhao, Jiang-Yan[1,2];Ma, Xiao-Wei[2];Jiang, Zhao-Feng[1,2]

第一作者:黄汉昌

通讯作者:Huang, HC[1]

机构:[1]Beijing Union Univ, Beijing Key Lab Bioact Subst & Funct Foods, 197 Beitucheng West Rd, Beijing 100191, Peoples R China;[2]Beijing Union Univ, Coll Arts & Sci, Beijing, Peoples R China

第一机构:北京联合大学应用文理学院|北京联合大学生物化学工程学院

通讯机构:[1]corresponding author), Beijing Union Univ, Beijing Key Lab Bioact Subst & Funct Foods, 197 Beitucheng West Rd, Beijing 100191, Peoples R China.|[114172]北京联合大学应用文理学院;[11417]北京联合大学;[1141726]北京联合大学生物化学工程学院;

年份:2016

卷号:52

期号:3

起止页码:899-911

外文期刊名:JOURNAL OF ALZHEIMERS DISEASE

收录:;Scopus(收录号:2-s2.0-84971569664);WOS:【SCI-EXPANDED(收录号:WOS:000377137500012)】;

基金:This study was supported by the National Natural Science Foundation of China (31471587) and the Importation and Development of High-Caliber Talents Project of Beijing Municipal Institutions (CIT&TCD201504034).

语种:英文

外文关键词:Alzheimer's disease; animal model; curcumin; D-galactose; neurodegeneration; streptozotocin

摘要:Epidemiological data imply links between the increasing incidences of Alzheimer's disease (AD) and type 2 diabetes mellitus. In this study, an AD rat model was established by combining treatments with intracerebroventricular streptozotocin (icv-STZ) and subcutaneous D-galactose, and the effects of curcumin on depressing AD-like symptoms were investigated. In the AD model group, rats were treated with icv-STZ in each hippocampus with 3.0 mg/kg of bodyweight once and then were subcutaneously injected with D-galactose daily (125 mg/kg of bodyweight) for 7 weeks. In the curcumin-protective group, after icv-STZ treatment, rats were treated with D-galactose (the same as in the AD model group) and intraperitoneally injected with curcumin daily (10 mg/kg of bodyweight) for 7 weeks. Vehicle-treated rats were treated as control. Compared with the vehicle control, the amount of protein carbonylation and glutathione in liver, as well as malondialdehyde in serum, were upregulated but glutathione peroxidase activity in blood was downregulated in the AD model group. The shuttle index and locomotor activity of rats in the AD model group were decreased compared with the vehicle control group. Furthermore, AD model rats showed neuronal damage and neuron loss with formation of amyloid-like substances and neurofibrillary tangles, and the levels of both beta-cleavage of A beta PP and phosphorylation of tau (Ser396) were significantly increased compared with the vehicle control group. Notably, compared with the AD model group, oxidative stress was decreased and the abilities of active avoidance and locomotor activity were improved, as well as attenuated neurodegeneration, in the curcumin-protective group. These results imply the applications of this animal model for AD research and of curcumin in the treatment of AD.

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