CZ2HF mitigates -amyloid 25-35 fragment-induced learning and memory impairment through inhibition of neuroinflammation and apoptosis in rats

被引:6
作者
Zeng, Lingrong [1 ,2 ]
Gao, Jianmei [3 ]
Deng, Yuanyuan [1 ,2 ]
Shi, Jingshan [1 ,2 ]
Gong, Qihai [1 ,2 ]
机构
[1] Zunyi Med Univ, Dept Pharmacol, Minist Educ, Key Lab Basic Pharmacol, 6 Xuefu West Rd, Zunyi 563000, Guizhou, Peoples R China
[2] Zunyi Med Univ, Minist Educ, Joint Int Res Lab Ethnomed, Zunyi 563000, Guizhou, Peoples R China
[3] Zunyi Med Univ, Sch Pharm, Dept Clin Pharmacotherapeut, Zunyi 563000, Guizhou, Peoples R China
关键词
cu-zhi-2-hao-fang; -amyloid; 25-35; learning; memory; neuroinflammation; apoptosis; FACTOR-KAPPA-B; A-BETA; ACTIVATION; DEFICITS; CELL; METABOLISM; INJECTION; MECHANISM; TOXICITY; PROTECTS;
D O I
10.3892/ijmm.2018.3952
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cu-zhi-2-hao-fang (CZ2HF), a traditional Chinese medicine, has been used clinically for the treatment of amnesia. However, whether CZ2HF is capable of alleviating learning and memory impairment in Alzheimer's disease (AD) remains to be elucidated. The present study was designed to explore the effect and mechanism of CZ2HF on -amyloid 25-35 (A(25-35))-induced impairment in the learning and memory of rats. Morris water maze test was used to determine spatial learning and memory ability in A(25-35)-induced AD rats and hippocampal neuronal damage and apoptosis were observed using hematoxylin and eosin staining, Nissl staining and terminal deoxynucleotidyltransferase-mediated dUTP nick-end labeling (TUNEL) assays, respectively. The levels of -amyloid 1-42 (A(1-42)), pro-inflammatory factors, such as cyclooxygenase-2 (COX-2), tumor necrosis factor- (TNF-) and interleukin-1 (IL-1) and apoptosis-associated genes including B cell leukemia/lymphoma 2 (Bcl-2), Bcl-2-associated X, apoptosis regulator (Bax), pro-caspase-3, inhibitor of B (IB-) degradation and phosphorylated-nuclear factor-B p65 (p-NF-B p65) activation were analyzed using western blotting. The findings of the present study revealed that CZ2HF treatment significantly attenuated A(25-35)-induced cognitive impairments in rats. Subsequently, CZ2HF treatment markedly inhibited neuronal damage and deletions. Furthermore, CZ2HF reduced TNF-, IL-1, COX-2 protein expression levels, Bax/Bcl-2 ratio, and reduced A(1-42) and active-caspase-3 levels. In addition, IB- degradation and p-NF-B p65 activation were reduced by CZ2HF. These findings suggested that CZ2HF treatment improved A(25-35)-induced learning and memory impairment and hippocampal neuronal injury, and its underlying mechanism may be due to the inhibition of neuroinflammation and neuronal apoptosis. CZ2HF may be a potential agent for the treatment of AD.
引用
收藏
页码:557 / 566
页数:10
相关论文
共 34 条
[1]   Oligomers of beta-amyloid protein (Aβ1-42) induce the activation of cyclooxygenase-2 in astrocytes via an interaction with interleukin-1beta, tumour necrosis factor-alpha, and a nuclear factor kappa-B mechanism in the rat brain [J].
Carrero, I. ;
Gonzalo, M. R. ;
Martin, B. ;
Sanz-Anquela, J. M. ;
Arevalo-Serrano, J. ;
Gonzalo-Ruiz, A. .
EXPERIMENTAL NEUROLOGY, 2012, 236 (02) :215-227
[2]   Hataedock treatment has preventive therapeutic effects for atopic dermatitis through skin barrier protection in Dermatophagoides farinae-induced NC/Nga mice [J].
Cha, Ho-Yeol ;
Ahn, Sang-Hyun ;
Cheon, Jin-Hong ;
Park, Sun-Young ;
Kim, Kibong .
JOURNAL OF ETHNOPHARMACOLOGY, 2017, 206 :327-336
[3]  
Choi JH, 2017, FOOD FUNCT, V8, P2611, DOI [10.1039/c7fo00369b, 10.1039/C7FO00369B]
[4]   Atomic Resolution Structure of Monomorphic Aβ42 Amyloid Fibrils [J].
Colvin, Michael T. ;
Silvers, Robert ;
Ni, Qing Zhe ;
Can, Thach V. ;
Sergeyev, Ivan ;
Rosay, Melanie ;
Donovan, Kevin J. ;
Michael, Brian ;
Wall, Joseph ;
Linse, Sara ;
Griffin, Robert G. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (30) :9663-9674
[5]   Pharmacodynamics of Cholinesterase Inhibitors Suggests Add-on Therapy with a Low-Dose Carbamylating Inhibitor in Patients on Long-Term Treatment with Rapidly Reversible Inhibitors [J].
Darreh-Shori, Taher ;
Hosseini, Sharokh Makvand ;
Nordberg, Agneta .
JOURNAL OF ALZHEIMERS DISEASE, 2014, 39 (02) :423-440
[6]   Pharmacotherapeutic strategies in the treatment of severe Alzheimer's disease [J].
Deardorff, William James ;
Grossberg, George T. .
EXPERT OPINION ON PHARMACOTHERAPY, 2016, 17 (13) :1789-1800
[7]   Multi-Target Screening and Experimental Validation of Natural Products from Selaginella Plants against Alzheimer's Disease [J].
Deng, Yin-Hua ;
Wang, Ning-Ning ;
Zou, Zhen-Xing ;
Zhang, Lin ;
Xu, Kang-Ping ;
Chen, Alex F. ;
Cao, Dong-Sheng ;
Tan, Gui-Shan .
FRONTIERS IN PHARMACOLOGY, 2017, 8
[8]   Chloroquine attenuates lipopolysaccharide-induced inflammatory responses through upregulation of USP25 [J].
Ding, Changyu ;
Li, Fangfang ;
Long, Yupeng ;
Zheng, Jiang .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2017, 95 (05) :481-491
[9]   Icariside II, a novel phosphodiesterase 5 inhibitor, protects against H2O2-induced PC12 cells death by inhibiting mitochondria-mediated autophagy [J].
Gao, Jianmei ;
Deng, Yuanyuan ;
Yin, Caixia ;
Liu, Yuangui ;
Zhang, Wei ;
Shi, Jingshan ;
Gong, Qihai .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2017, 21 (02) :375-386
[10]   S-propargyl-cysteine (ZYZ-802), a sulphur-containing amino acid, attenuates beta-amyloid-induced cognitive deficits and pro-inflammatory response: involvement of ERK1/2 and NF-κB pathway in rats [J].
Gong, Qi-Hai ;
Pan, Li-Long ;
Liu, Xin-Hua ;
Wang, Qian ;
Huang, Hui ;
Zhu, Yi-Zhun .
AMINO ACIDS, 2011, 40 (02) :601-610