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Graptopetalum paraguayense Extract Ameliorates Proteotoxicity in Aging and Age-Related Diseases in Model Systems
Authors:Yan-Xi Chen  Phuong Thu Nguyen Le  Tsai-Teng Tzeng  Thu-Ha Tran  Anh Thuc Nguyen  Irene Han-Juo Cheng  Chi-Ying F Huang  Young-Ji Shiao  Tsui-Ting Ching
Institution:1.Institute of Biopharmaceutical Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan; (Y.-X.C.); (T.-T.T.); (A.T.N.);2.Taiwan International Graduate Program in Molecular Medicine, National Yang Ming Chiao Tung University and Academia Sinica, Taipei 115, Taiwan; (P.T.N.L.); (T.-H.T.);3.Institute of Brain Science, National Yang Ming Chiao Tung University, Taipei 112, Taiwan;4.National Research Institute of Chinese Medicine, Ministry of Health and Welfare, Taipei 112, Taiwan
Abstract:Declines in physiological functions are the predominant risk factors for age-related diseases, such as cancers and neurodegenerative diseases. Therefore, delaying the aging process is believed to be beneficial in preventing the onset of age-related diseases. Previous studies have demonstrated that Graptopetalum paraguayense (GP) extract inhibits liver cancer cell growth and reduces the pathological phenotypes of Alzheimer’s disease (AD) in patient IPS-derived neurons. Here, we show that GP extract suppresses β-amyloid pathology in SH-SYS5Y-APP695 cells and APP/PS1 mice. Moreover, AMP-activated protein kinase (AMPK) activity is enhanced by GP extract in U87 cells and APP/PS1 mice. Intriguingly, GP extract enhances autophagy in SH-SYS5Y-APP695 cells, U87 cells, and the nematode Caenorhabditis elegans, suggesting a conserved molecular mechanism by which GP extract might regulate autophagy. In agreement with its role as an autophagy activator, GP extract markedly diminishes mobility decline in polyglutamine Q35 mutants and aged wild-type N2 animals in C. elegans. Furthermore, GP extract significantly extends lifespan in C. elegans.
Keywords:GP extract  neurodegenerative disease  Alzheimer’  s disease  amyloid-β    autophagy  longevity
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