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  • Book
    Ning Chen, editor.
    Summary: This book establishes a bridge between exercise-mediated functional status of autophagy and non-communicable chronic diseases for elucidating and clarifying the corresponding signal pathways and underlying mechanisms. The book consists of 13 chapters focusing on the in-depth discussion on signal pathways for regulating the functional status of autophagy for the prevention, treatment and rehabilitation of chronic diseases, the optimization of exercise intervention strategies for common and frequently-occurring chronic diseases, and the development of exercise mimetic pills for the persons with disability for exercise performance, or the persons without willing to exercise. This book is interesting and will be useful to a wide readership in the various fields of exercise science, exercise fitness, sports medicine, preventive medicine, and functional foods.

    Contents:
    Chapter 1. Molecular processes and regulation of autophagy
    Chapter 2. Acute and chronic exercise on autophagy
    Chapter 3. The beneficial roles of exercise-mediated autophagy in T2DM
    Chapter 4. Exercise-induced autophagy and obesity
    5. Exercise-mediated autophagy and non-alcoholic fatty liver disease
    Chapter 6. Exercise-mediated autophagy and brain aging
    Chapter 7. Exercise-mediated autophagy and Alzheimers disease
    Chapter 8. Exercise-induced autophagy and Parkinsons disease
    Chapter 9.Exercise-mediated autophagy in cardiovascular diseases
    Chapter 10. Exercise-induced autophagy in the prevention and treatment of sarcopenia
    Chapter 11. Prospective advances in exercise-induced autophagy on health
    Chapter 12. Exercise mimetic pills for chronic diseases based on autophagy
    Chapter 13. Exercise-mediated functional status of autophagy is beneficial to health.
    Digital Access Springer 2021
  • Article
    Pearson JR.
    Clin Chem. 1978 Oct;24(10):1823-5.
    The methods for barbiturate, opiate, methadone, and amphetamine have been modified for use with the American Monitor KDA. The modification, which incorporates automatic correction for endogenous lysozyme activity, was evaluated by comparing results obtained with the KDA for human urine samples containing known amounts of drug(s) with results obtained with the procedure recommended by Syva for the Gilford 3500. There was 98% agreement bewteen the two systems. Six calibrators and 40 samples can be assayed for all four drugs in about 2.5 h. The procedure has proven to be reliable for screening urine samples obtained from clients at a methadone treatment center.
    Digital Access Access Options