The NAD+-dependent Family of Sirtuins in Cerebral Ischemia and Preconditioning.
Antioxid Redox Signal. 2017 Jul
Authors: Khoury N, Koronowski KB, Young JI, Perez-Pinzon MA
Abstract
Significance Sirtuins are an evolutionarily conserved family of NAD+-dependent lysine deacylases and ADP-ribosylases. Their requirement for NAD+ as a co-substrate allows them to act as metabolic sensors that couple changes in the energy status of the cell to changes in cellular physiological processes. NAD+ levels are affected by several NAD+-producing and -consuming pathways as well as by cellular respiration. Thus their intracellular levels are highly dynamic and become misregulated in a spectrum of metabolic disorders including cerebral ischemia. This, in turn, compromises several NAD+-dependent processes that can ultimately lead to cell death. Recent Advances A number of efforts have been made to replenish NAD+ in cerebral ischemic injuries as well as to understand the functions of one its important mediators, the sirtuin family of proteins through the use of pharmacological modulators or genetic manipulation approaches either before or after the insult. Critical Issues & Future Directions The results of these studies have regarded the sirtuin family of proteins as promising therapeutic targets for cerebral ischemic injuries. Yet, additional efforts are needed to understand the role of some of its less characterized members and to address the sex-specific effects observed with some members. Sirtuins also exhibit cell-type specific expression in the brain as well as distinct subcellular and regional localizations. As such, they are involved in diverse and sometimes opposing cellular processes that can either promote neuroprotection or further contribute to the injury which also stresses the need for the development and use of sirtuin-specific pharmacological agents.
PMID: 28683567 [PubMed - as supplied by publisher]
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