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Ganoderic Acid A To Alleviate Neuroinflammation of Alzheimer's Disease in Mice by Regulating the Imbalance of the Th17/Tregs Axis.
Zhang, Yan; Wang, Xinyan; Yang, Xiaomei; Yang, Xiudong; Xue, Jianfei; Yang, Yanjun.
Affiliation
  • Zhang Y; School of Chemical and Pharmaceutical Engineering, Jilin Institute of Chemical Technology, Jilin 132022, P. R. China.
  • Wang X; Graduate School, Jilin Institute of Chemical Technology, Jilin 132022, P. R. China.
  • Yang X; Nutritional Department, Jilin Medical University Affiliated Hospital, Jilin 132013, P. R. China.
  • Yang X; School of Chemical and Pharmaceutical Engineering, Jilin Institute of Chemical Technology, Jilin 132022, P. R. China.
  • Xue J; School of Chemical and Pharmaceutical Engineering, Jilin Institute of Chemical Technology, Jilin 132022, P. R. China.
  • Yang Y; School of Chemical and Pharmaceutical Engineering, Jilin Institute of Chemical Technology, Jilin 132022, P. R. China.
J Agric Food Chem ; 69(47): 14204-14214, 2021 Dec 01.
Article in En | MEDLINE | ID: mdl-34798773
ABSTRACT
Ganoderic acid A (GAA) is a kind of lanostane-type triterpenoid isolated from Ganoderma lucidum. Imbalance of the Th17/Tregs axis exists in the progress of neuroinflammation of Alzheimer's disease (AD). In this study, the alleviating neuroinflammatory effect of GAA on d-galactose mice was studied from the aspect of regulating the imbalance of the Th17/Tregs axis. The Morris water maze test was used to evaluate the cognitive ability of AD mice. Flow cytometry was used to detect the percentages of IL-17A, IL-17F, IL-21, IL-22, and CD4+CD25+Foxp3+ in peripheral blood. Transmission electron microscopy was used to assess the cerebral mitochondrial ultrastructure. Metabolomic analysis based on gas chromatography-mass spectrometry was used to evaluate the mitochondrial dysfunction metabolism. Western blot analysis was used to detect the protein expressions of cytokines secreted by Th17 cells and Treg cells in the brain. As the results show, GAA has an alleviating neuroinflammatory effect on AD mice via regulating the imbalance of the Th17/Tregs axis. The potential mechanism was related to inhibition of the JAK/STAT signaling pathway induced by Th17 cells and enhancement of the mitochondrial oxidative phosphorylation by regulating Treg cells, thereby improving mitochondrial dysfunction of AD mice.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Th17 Cells / Alzheimer Disease Limits: Animals Language: En Journal: J Agric Food Chem Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Th17 Cells / Alzheimer Disease Limits: Animals Language: En Journal: J Agric Food Chem Year: 2021 Document type: Article
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