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Altered behavioral and metabolic circadian rhythms in mice with disrupted NAD+oscillation

Authors :
Sahar, S
Nin, V
Barbosa, MT
Chini, EN
Sassone-Corsi, P
Source :
Sahar, S; Nin, V; Barbosa, MT; Chini, EN; & Sassone-Corsi, P. (2011). Altered behavioral and metabolic circadian rhythms in mice with disrupted NAD+oscillation. Aging, 3(8), 794-802. doi: 10.18632/aging.100368. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/8gm4c6wv
Publication Year :
2011
Publisher :
eScholarship, University of California, 2011.

Abstract

The Intracellular levels of nicotinamide adenine dinucleotide (NAD+) are rhythmic and controlled by the circadian clock. However, whether NAD+oscillation in turn contributes to circadian physiology is not fully understood. To address this question we analyzed mice mutated for the NAD+ hydrolase CD38. We found that rhythmicity of NAD+was altered in the CD38-deficient mice. The high, chronic levels of NAD+results in several anomalies in circadian behavior and metabolism. CD38-null mice display a shortened period length of locomotor activity and alteration in the rest-activity rhythm. Several clock genes and, interestingly, genes involved in amino acid metabolism were deregulated in CD38-null livers. Metabolomic analysis identified alterations in the circadian levels of several amino acids, specifically tryptophan levels were reduced in the CD38-null mice at a circadian time paralleling with elevated NAD+levels. Thus, CD38 contributes to behavioral and metabolic circadian rhythms and altered NAD+levels influence the circadian clock. © Sassone-Corsi et al.

Details

Language :
English
Database :
OpenAIRE
Journal :
Sahar, S; Nin, V; Barbosa, MT; Chini, EN; & Sassone-Corsi, P. (2011). Altered behavioral and metabolic circadian rhythms in mice with disrupted NAD+oscillation. Aging, 3(8), 794-802. doi: 10.18632/aging.100368. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/8gm4c6wv
Accession number :
edsair.od.......325..5a50fff05b53e18191d09ef6e25ca29e
Full Text :
https://doi.org/10.18632/aging.100368.