Aveleira Célia A, Botelho Mariana, Cavadas Cláudia
a CNC - Center for Neuroscience and Cell Biology; University of Coimbra ; Coimbra , Portugal.
Autophagy. 2015;11(8):1431-3. doi: 10.1080/15548627.2015.1062202.
Aging was recently described as a life event programmed by the hypothalamus, a key brain region that is crucial for the neuroendocrine interaction between the central nervous system and the periphery. Autophagy impairment is a hallmark of aging, contributing to the aging phenotype and to the aggravation of age-related diseases. Since hypothalamic autophagy decreases with age, strategies to promote autophagy in the hypothalamus may be relevant for control of the aging process. NPY (neuropeptide Y) is an endogenous neuropeptide mainly produced by the hypothalamus. We recently reported, for the first time, that NPY stimulates autophagy in rodent hypothalamus and mediates caloric restriction-induced autophagy in hypothalamic neurons. Moreover, we observed that NPY acts through NPY1R (neuropeptide Y receptor Y1) or NPY5R activation involving a concerted action of different signaling pathways. Since both hypothalamic autophagy and NPY levels decrease with age, modulation of NPY levels could provide new putative therapeutic tools to ameliorate age-related deteriorations and extend longevity.
衰老最近被描述为一种由下丘脑编程的生命事件,下丘脑是大脑的一个关键区域,对中枢神经系统与外周之间的神经内分泌相互作用至关重要。自噬受损是衰老的一个标志,它导致衰老表型并加剧与年龄相关的疾病。由于下丘脑自噬随年龄增长而减少,促进下丘脑自噬的策略可能与控制衰老过程相关。神经肽Y(NPY)是一种主要由下丘脑产生的内源性神经肽。我们最近首次报道,NPY刺激啮齿动物下丘脑的自噬,并介导热量限制诱导的下丘脑神经元自噬。此外,我们观察到NPY通过NPY1R(神经肽Y受体Y1)或NPY5R激活发挥作用,涉及不同信号通路的协同作用。由于下丘脑自噬和NPY水平均随年龄增长而降低,调节NPY水平可能为改善与年龄相关的衰退和延长寿命提供新的潜在治疗工具。