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热量限制通过激活神经肽Y和胃饥饿素受体刺激大鼠皮质神经元中的自噬。

Caloric restriction stimulates autophagy in rat cortical neurons through neuropeptide Y and ghrelin receptors activation.

作者信息

Ferreira-Marques Marisa, Aveleira Célia A, Carmo-Silva Sara, Botelho Mariana, Pereira de Almeida Luís, Cavadas Cláudia

机构信息

CNC - Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.

Faculty of Pharmacy, University of Coimbra, Coimbra, Portugal.

出版信息

Aging (Albany NY). 2016 Jul;8(7):1470-84. doi: 10.18632/aging.100996.

Abstract

Caloric restriction is an anti-aging intervention known to extend lifespan in several experimental models, at least in part, by stimulating autophagy. Caloric restriction increases neuropeptide Y (NPY) in the hypothalamus and plasma ghrelin, a peripheral gut hormone that acts in hypothalamus to modulate energy homeostasis. NPY and ghrelin have been shown to be neuroprotective in different brain areas and to induce several physiological modifications similar to those induced by caloric restriction. However, the effect of NPY and ghrelin in autophagy in cortical neurons is currently not known. Using a cell culture of rat cortical neurons we investigate the involvement of NPY and ghrelin in caloric restriction-induced autophagy. We observed that a caloric restriction mimetic cell culture medium stimulates autophagy in rat cortical neurons and NPY or ghrelin receptor antagonists blocked this effect. On the other hand, exogenous NPY or ghrelin stimulate autophagy in rat cortical neurons. Moreover, NPY mediates the stimulatory effect of ghrelin on autophagy in rat cortical neurons. Since autophagy impairment occurs in aging and age-related neurodegenerative diseases, NPY and ghrelin synergistic effect on autophagy stimulation may suggest a new strategy to delay aging process.

摘要

热量限制是一种抗衰老干预措施,已知在多种实验模型中至少部分通过刺激自噬来延长寿命。热量限制会增加下丘脑的神经肽Y(NPY)和血浆胃饥饿素,胃饥饿素是一种外周肠激素,作用于下丘脑以调节能量平衡。已证明NPY和胃饥饿素在不同脑区具有神经保护作用,并能诱导一些与热量限制所诱导的生理变化相似的变化。然而,目前尚不清楚NPY和胃饥饿素对皮质神经元自噬的影响。我们使用大鼠皮质神经元细胞培养物来研究NPY和胃饥饿素在热量限制诱导的自噬中的作用。我们观察到,一种模拟热量限制的细胞培养基能刺激大鼠皮质神经元的自噬,而NPY或胃饥饿素受体拮抗剂可阻断这种作用。另一方面,外源性NPY或胃饥饿素能刺激大鼠皮质神经元的自噬。此外,NPY介导了胃饥饿素对大鼠皮质神经元自噬的刺激作用。由于自噬功能障碍发生在衰老和与年龄相关的神经退行性疾病中,NPY和胃饥饿素对自噬刺激的协同作用可能提示了一种延缓衰老过程的新策略。

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