Title of article :
CZYH Alleviates β-Amyloid-Induced Cognitive Impairment and Inflammation Response via Modulation of JNK and NF-κB Pathway in Rats
Author/Authors :
Deng, Yuanyuan Key Laboratory of Basic Pharmacology of Ministry of Education - Department of Pharmacology - Zunyi Medical University, Guizhou, China , Ye, Lianzhi Key Laboratory of Basic Pharmacology of Ministry of Education - Department of Pharmacology - Zunyi Medical University, Guizhou, China , Yu, Cheng Key Laboratory of Basic Pharmacology of Ministry of Education - Department of Pharmacology - Zunyi Medical University, Guizhou, China , Yin, Caixia Key Laboratory of Basic Pharmacology of Ministry of Education - Department of Pharmacology - Zunyi Medical University, Guizhou, China , Shi, Jingshan Key Laboratory of Basic Pharmacology of Ministry of Education - Department of Pharmacology - Zunyi Medical University, Guizhou, China , Gong, Qihai Key Laboratory of Basic Pharmacology of Ministry of Education - Department of Pharmacology - Zunyi Medical University, Guizhou, China
Pages :
10
From page :
1
To page :
10
Abstract :
Cu-Zhi-Yi-Hao (CZYH), an empirical formula of traditional Chinese medicine (TCM), has been used for amnesia treatment in clinical practice. However, its underlying pharmacological mechanism has not been fully illuminated. The current study was designed to investigate the neuroprotective effect of CZYH on a β-amyloid 25-35- (Aβ25-35-) induced learning and memory deficit rat model. CZYH (200, 400, or 800 mg/kg), donepezil (1.0 mg/kg), or distilled water was given to Aβ25-35-stimulated animals for 17 days consecutively. The Morris water maze test revealed that CZYH (400 or 800 mg/kg) administration improved the Aβ25-35-induced cognitive impairments in rats, and Nissl staining demonstrated that CZYH mitigated the Aβ-caused neuron loss. In addition, CZYH treatment markedly inhibited the activation of microglia as evidenced by a decreased level of IBA-1 and increased YM-1/2 protein expression. The protein expression levels of TNF-α, IL-1β, and COX-2 were also repressed by CZYH. Besides, CZYH treatment alleviated Aβ-induced IκB-α degradation and NF-κB p65 phosphorylation, as well as reduced the JNK phosphorylation level. In conclusion, the present study suggests that CZYH could improve learning and memory abilities and relieve neuron loss in Aβ25-35-induced rats, at least partly through inhibition of the neuroinflammatory response via inhibiting the JNK-dependent NF-κB activation, indicating that CZYH might be a promising formula for the treatment of AD.
Keywords :
CZYH Alleviates β-Amyloid-Induced , Cognitive Impairment , Inflammation Response , via Modulation , JNK , NF-κB Pathway
Journal title :
Behavioural Neurology
Serial Year :
2019
Full Text URL :
Record number :
2606262
Link To Document :
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