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Bajijiasu Ameliorates ß-Amyloid-Triggered Endoplasmic Reticulum Stress and Related Pathologies in an Alzheimer's Disease Model.
Xu, Ting-Ting; Zhang, Yang; He, Jia-Yang; Luo, Dan; Luo, Yi; Wang, Yi-Jie; Liu, Wei; Wu, Jun; Zhao, Wei; Fang, Jiansong; Guan, Li; Huang, Shun; Wang, Hong; Lin, Li; Zhang, Shi-Jie; Wang, Qi.
Afiliação
  • Xu TT; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Zhang Y; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • He JY; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Luo D; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Luo Y; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Wang YJ; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Liu W; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Wu J; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Zhao W; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Fang J; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Guan L; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Huang S; Nanfang PET Center, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Wang H; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Lin L; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Zhang SJ; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Wang Q; Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China.
Cell Physiol Biochem ; 46(1): 107-117, 2018.
Article em En | MEDLINE | ID: mdl-29587274
ABSTRACT
BACKGROUND/

AIMS:

Alzheimer disease (AD) is a common neurodegenerative disease that is characterized by the deposition of beta-amyloid peptide and formation of intracellular neurofibrillary tangles. Due to the failure of various clinical trials of novel drugs for AD, effective drugs for AD treatment are urgently required.

METHODS:

In this study, we used the classic APP/PS1 mouse model to explore the neuroprotective effects of a new compound, bajijiasu, and the mechanisms involved. Behavioral tests and western blotting were performed to assess the beneficial effects of bajijiasu in APP/PS1 mice.

RESULTS:

Morris water maze and Y-maze test results showed that oral administration of bajijiasu (35 mg/kg/day and 70 mg/kg/day) improved learning and memory abilities in APP/PS1 mice. Bajijiasu reduced ROS and MDA levels in both the hippocampus and cortex. Moreover, western blotting results showed that bajijiasu protected neurons from apoptosis, elevated the expression levels of neurotrophic factors, and alleviated endoplasmic reticulum stress in both the hippocampus and cortex.

CONCLUSION:

These results indicate that the mechanisms underlying the effects of bajijiasu on AD might be related to beta-amyloid-downstream pathologies, particularly endoplasmic reticulum stress.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Precursor de Proteína beta-Amiloide / Fármacos Neuroprotetores / Dissacarídeos / Estresse do Retículo Endoplasmático Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Precursor de Proteína beta-Amiloide / Fármacos Neuroprotetores / Dissacarídeos / Estresse do Retículo Endoplasmático Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article