| Literature DB >> 26086271 |
Célia A Aveleira1, Mariana Botelho, Cláudia Cavadas.
Abstract
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.Entities:
Keywords: autophagy; caloric restriction; hypothalamus; neuropeptide Y
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Year: 2015 PMID: 26086271 PMCID: PMC4590601 DOI: 10.1080/15548627.2015.1062202
Source DB: PubMed Journal: Autophagy ISSN: 1554-8627 Impact factor: 16.016