英语科普小知识 减少热量摄入可延缓神经细胞损耗.docVIP

英语科普小知识 减少热量摄入可延缓神经细胞损耗.doc

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Activating an enzyme known to play a role in the anti-aging benefits of calorie restriction delays the loss of brain cells and preserves cognitive function in mice, according to a study published in the May 22 issue of The Journal of Neuroscience. The findings could one day guide researchers to discover drug alternatives that slow the progress of age-associated impairments in the brain. Previous studies have shown that reducing calorie consumption extends the lifespan of a variety of species and decreases the brain changes that often accompany aging and neurodegenerative diseases such as Alzheimers. There is also evidence that caloric restriction activates an enzyme called Sirtuin 1 (SIRT1), which studies suggest offers some protection against age-associated?impairments(损害)?in the brain. ? In the current study, Li-Huei Tsai, PhD, Johannes Gr?ff, PhD, and others at the Picower Institute For Learning and Memory, Massachusetts Institute of Technology, and Howard Hughes Medical Institute, tested whether reducing caloric intake would delay the onset of nerve cell loss that is common in neurodegenerative disease, and if so, whether SIRT1 activation was driving this effect. The group not only confirmed that caloric restriction delays nerve cell loss, but also found that a drug that activates SIRT1 produces the same effects. ? There has been great interest in finding compounds that mimic the benefits of caloric restriction that could be used to delay the onset of age-associated problems and/or diseases, said Luigi Puglielli, MD, PhD, who studies aging at the University of Wisconsin, Madison, and was not involved in this study. If proven safe for humans, this study suggests such a drug could be used as a preventive tool to delay the onset of neurodegeneration associated with several diseases that affect the aging brain, Puglielli added. ? In the study, Tsais team first decreased by 30 percent the normal diets of mice genetically engineered to rapidly undergo changes in th

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