Short title:REM sleep deprivation differentially affects the genes of liver and brain in rats.
Highlights of the study: Microarray analysis compared the expression pattern of genes related to many biological, molecular and physiological processes in brain and liver. Analysis revealed about the basic genetic tool-kit involved with REM sleep deprivation and its loss in brain and liver. Many of the genes involved in critical physiological processes like apoptosis and circadian rhythms are found differentially expresses in brain and liver.
AbstractFundamental questions about sleep and its universal existence remain elusive. The common presence of sleep across phyla suggests that it must serve some indispensable cellular and/or molecular function needed for survival. Microarray studies, performed in several model systems, have identified classes of genes that are believed to regulate "sleep-state" or viceversa. This has led to the following concepts: first, a function of sleep is to maintain synaptic homeostasis; second, sleep is a stage of macromolecule biosynthesis which is needed during the waking period; third, extending wakefulness leads to the downregulation of several important metabolic pathways which needs to be balanced for extended survival; and, fourth, extending wakefulness leads to endoplasmic reticulum stress. In human sleep studies, microarrays are being pragmatic to the identification of biomarkers for sleepiness and for the common sleep disorders. This study tries to find out the correlative processes which happen across different tissue system in the maintenance of sleep. We compared the gene expression profile in brain and liver due to REM sleep deprivation. Our result suggests that sleep deprivation affects a different set of genes in the brain and liver.