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热量限制对大脑衰老及相关病理状态的益处:理解其机制以设计新疗法。

Benefits of caloric restriction on brain aging and related pathological States: understanding mechanisms to devise novel therapies.

作者信息

Contestabile Antonio

机构信息

Department of Biology, University of Bologna, Italy.

出版信息

Curr Med Chem. 2009;16(3):350-61. doi: 10.2174/092986709787002637.

Abstract

Long term caloric restriction is known to counteract aging and extend lifespan in several organisms from yeasts to mammals. Recent research has provided solid ground to the concept that limiting calorie intake slows down brain aging and protects from age-related neurodegenerative diseases. The present review summarizes the most relevant among these data and highlights some genetic and molecular mechanisms responsible for caloric restriction-related neuroprotection. To understand these mechanisms is important because this information makes them potential targets for therapeutic intervention aimed at reproducing the metabolic, genetic and molecular features responsible for the beneficial effect of caloric restriction. Most promising among these targets are neurotrophins, such as BDNF, transcription factors, such as FoxO and PPAR, anti-aging proteins, such as sirtuins, and caloric restriction mimetics acting on oxidative stress and energy metabolism. Notwithstanding the complexity of any therapeutic strategy aimed at reproducing the beneficial effects of caloric restriction, due to multiplicity of the cellular pathways involved in the responses, a great expansion of medicinal chemistry research in this field is expected in the next future.

摘要

长期热量限制已知可对抗衰老并延长从酵母到哺乳动物等多种生物体的寿命。最近的研究为限制热量摄入可减缓大脑衰老并预防与年龄相关的神经退行性疾病这一概念提供了坚实基础。本综述总结了这些数据中最相关的内容,并强调了一些与热量限制相关的神经保护作用的遗传和分子机制。理解这些机制很重要,因为这些信息使它们成为旨在重现负责热量限制有益效果的代谢、遗传和分子特征的治疗干预的潜在靶点。这些靶点中最有前景的是神经营养因子,如脑源性神经营因子(BDNF)、转录因子,如叉头框蛋白O(FoxO)和过氧化物酶体增殖物激活受体(PPAR)、抗衰老蛋白,如沉默调节蛋白(sirtuins),以及作用于氧化应激和能量代谢的热量限制模拟物。尽管旨在重现热量限制有益效果的任何治疗策略都很复杂,由于参与反应的细胞途径多种多样,但预计在未来该领域的药物化学研究将有很大扩展。

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