SIRT1 in neurodevelopment and brain senescence

• Published in: Neuron (Cambridge, Mass.) Vol. 81; no. 3; pp. 471 - 483
• Main Authors: Herskovits, A Zara, Guarente, Leonard
• Format: Journal Article
• Language: English
• Published: United States Elsevier Limited 05-02-2014
• Subjects: Aging; Aging - metabolism; Animals; Behavior; Brain - cytology; Brain - physiology; Brain research; Cell culture; Cocaine; Disease; DNA damage; Humans; Learning - physiology; Mammals; Models, Biological; Neurodegenerative Diseases - genetics; Neurodegenerative Diseases - metabolism; Neurodegenerative Diseases - pathology; Neurons; Neurons - metabolism; Proteins; Rodents; Sirtuin 1 - genetics; Sirtuin 1 - metabolism
• ISSN: 0896-6273; 1097-4199
• DOI: 10.1016/j.neuron.2014.01.028

Sirtuins are nicotinamide adenine dinucleotide (NAD+)-dependent deacylases that have traditionally been linked with calorie restriction and aging in mammals. These proteins also play an important role in maintaining neuronal health during aging. During neuronal development, the SIR2 ortholog SIRT1 is structurally important, promoting axonal elongation, neurite outgrowth, and dendritic branching. This sirtuin also plays a role in memory formation by modulating synaptic plasticity. Hypothalamic functions that affect feeding behavior, endocrine function, and circadian rhythmicity are all regulated by SIRT1. Finally, SIRT1 plays protective roles in several neurodegenerative diseases including Alzheimer's, Parkinson's, and motor neuron diseases, which may relate to its functions in metabolism, stress resistance, and genomic stability. Drugs that activate SIRT1 may offer a promising approach to treat these disorders.