Rhythmic Regulation of DNA Methylation Factors and Core-Clock Genes in Brain Structures Activated by Cocaine or Sucrose: Potential Role of Chromatin Remodeling

The circadian system interacts with the mesocorticolimbic reward system to modulate reward and memory in a time-of-day dependent manner. The circadian discrimination of reward, however, remains difficult to address between natural reinforcers and drugs of abuse. Circadian rhythms control cocaine sen...

Full description

Bibliographic Details
Main Authors: Lamis Saad, Andries Kalsbeek, Jean Zwiller, Patrick Anglard
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/12/8/1195
id doaj-14a698177dd243b280ab5c399e10c30b
record_format Article
spelling doaj-14a698177dd243b280ab5c399e10c30b2021-08-26T13:46:53ZengMDPI AGGenes2073-44252021-07-01121195119510.3390/genes12081195Rhythmic Regulation of DNA Methylation Factors and Core-Clock Genes in Brain Structures Activated by Cocaine or Sucrose: Potential Role of Chromatin RemodelingLamis Saad0Andries Kalsbeek1Jean Zwiller2Patrick Anglard3Laboratoire de Neurosciences Cognitives et Adaptatives (LNCA), UMR 7364 CNRS, Université de Strasbourg, Neuropôle de Strasbourg, 67000 Strasbourg, FranceThe Netherlands Institute for Neuroscience (NIN), Royal Netherlands Academy of Arts and Sciences (KNAW), 1105 BA Amsterdam, The NetherlandsLaboratoire de Neurosciences Cognitives et Adaptatives (LNCA), UMR 7364 CNRS, Université de Strasbourg, Neuropôle de Strasbourg, 67000 Strasbourg, FranceLaboratoire de Neurosciences Cognitives et Adaptatives (LNCA), UMR 7364 CNRS, Université de Strasbourg, Neuropôle de Strasbourg, 67000 Strasbourg, FranceThe circadian system interacts with the mesocorticolimbic reward system to modulate reward and memory in a time-of-day dependent manner. The circadian discrimination of reward, however, remains difficult to address between natural reinforcers and drugs of abuse. Circadian rhythms control cocaine sensitization and conversely cocaine causes long-term alteration in circadian periodicity in part through the serotonergic neurotransmission. Since neural circuits activated by cocaine and natural reinforcers do not completely overlap, we compared the effect of cocaine with that of sucrose, a strong reinforcer in rodents, by using passive chronic administration. The expression of fifteen genes playing a major role in DNA methylation (<i>Dnmts</i>, <i>Tets</i>), circadian rhythms (<i>Clock</i>, <i>Bmal1</i>, <i>Per1/2</i>, <i>Cry1/2</i>, <i>Rev-Erbβ</i>, <i>Dbp1)</i>, appetite, and satiety (<i>Orexin</i>, <i>Npy</i>) was analyzed in dopamine projection areas like the prefrontal cortex, the caudate putamen, and the hypothalamus interconnected with the reward system. The corresponding proteins of two genes (Orexin, Per2) were examined by IHC. For many factors controlling biological and cognitive functions, striking opposite responses were found between the two reinforcers, notably for genes controlling DNA methylation/demethylation processes and in global DNA methylation involved in chromatin remodeling. The data are consistent with a repression of critical core-clock genes by cocaine, suggesting that, consequently, both agents differentially modulate day/night cycles. Whether observed cocaine and sucrose-induced changes in DNA methylation in a time dependent manner are long lasting or contribute to the establishment of addiction requires further neuroepigenetic investigation. Understanding the mechanisms dissociating drugs of abuse from natural reinforcers remains a prerequisite for the design of selective therapeutic tools for compulsive behaviors.https://www.mdpi.com/2073-4425/12/8/1195cocainesucroseDNA methylationcircadian rhythmsappetite and satietyaddiction
collection DOAJ
language English
format Article
sources DOAJ
author Lamis Saad
Andries Kalsbeek
Jean Zwiller
Patrick Anglard
spellingShingle Lamis Saad
Andries Kalsbeek
Jean Zwiller
Patrick Anglard
Rhythmic Regulation of DNA Methylation Factors and Core-Clock Genes in Brain Structures Activated by Cocaine or Sucrose: Potential Role of Chromatin Remodeling
Genes
cocaine
sucrose
DNA methylation
circadian rhythms
appetite and satiety
addiction
author_facet Lamis Saad
Andries Kalsbeek
Jean Zwiller
Patrick Anglard
author_sort Lamis Saad
title Rhythmic Regulation of DNA Methylation Factors and Core-Clock Genes in Brain Structures Activated by Cocaine or Sucrose: Potential Role of Chromatin Remodeling
title_short Rhythmic Regulation of DNA Methylation Factors and Core-Clock Genes in Brain Structures Activated by Cocaine or Sucrose: Potential Role of Chromatin Remodeling
title_full Rhythmic Regulation of DNA Methylation Factors and Core-Clock Genes in Brain Structures Activated by Cocaine or Sucrose: Potential Role of Chromatin Remodeling
title_fullStr Rhythmic Regulation of DNA Methylation Factors and Core-Clock Genes in Brain Structures Activated by Cocaine or Sucrose: Potential Role of Chromatin Remodeling
title_full_unstemmed Rhythmic Regulation of DNA Methylation Factors and Core-Clock Genes in Brain Structures Activated by Cocaine or Sucrose: Potential Role of Chromatin Remodeling
title_sort rhythmic regulation of dna methylation factors and core-clock genes in brain structures activated by cocaine or sucrose: potential role of chromatin remodeling
publisher MDPI AG
series Genes
issn 2073-4425
publishDate 2021-07-01
description The circadian system interacts with the mesocorticolimbic reward system to modulate reward and memory in a time-of-day dependent manner. The circadian discrimination of reward, however, remains difficult to address between natural reinforcers and drugs of abuse. Circadian rhythms control cocaine sensitization and conversely cocaine causes long-term alteration in circadian periodicity in part through the serotonergic neurotransmission. Since neural circuits activated by cocaine and natural reinforcers do not completely overlap, we compared the effect of cocaine with that of sucrose, a strong reinforcer in rodents, by using passive chronic administration. The expression of fifteen genes playing a major role in DNA methylation (<i>Dnmts</i>, <i>Tets</i>), circadian rhythms (<i>Clock</i>, <i>Bmal1</i>, <i>Per1/2</i>, <i>Cry1/2</i>, <i>Rev-Erbβ</i>, <i>Dbp1)</i>, appetite, and satiety (<i>Orexin</i>, <i>Npy</i>) was analyzed in dopamine projection areas like the prefrontal cortex, the caudate putamen, and the hypothalamus interconnected with the reward system. The corresponding proteins of two genes (Orexin, Per2) were examined by IHC. For many factors controlling biological and cognitive functions, striking opposite responses were found between the two reinforcers, notably for genes controlling DNA methylation/demethylation processes and in global DNA methylation involved in chromatin remodeling. The data are consistent with a repression of critical core-clock genes by cocaine, suggesting that, consequently, both agents differentially modulate day/night cycles. Whether observed cocaine and sucrose-induced changes in DNA methylation in a time dependent manner are long lasting or contribute to the establishment of addiction requires further neuroepigenetic investigation. Understanding the mechanisms dissociating drugs of abuse from natural reinforcers remains a prerequisite for the design of selective therapeutic tools for compulsive behaviors.
topic cocaine
sucrose
DNA methylation
circadian rhythms
appetite and satiety
addiction
url https://www.mdpi.com/2073-4425/12/8/1195
work_keys_str_mv AT lamissaad rhythmicregulationofdnamethylationfactorsandcoreclockgenesinbrainstructuresactivatedbycocaineorsucrosepotentialroleofchromatinremodeling
AT andrieskalsbeek rhythmicregulationofdnamethylationfactorsandcoreclockgenesinbrainstructuresactivatedbycocaineorsucrosepotentialroleofchromatinremodeling
AT jeanzwiller rhythmicregulationofdnamethylationfactorsandcoreclockgenesinbrainstructuresactivatedbycocaineorsucrosepotentialroleofchromatinremodeling
AT patrickanglard rhythmicregulationofdnamethylationfactorsandcoreclockgenesinbrainstructuresactivatedbycocaineorsucrosepotentialroleofchromatinremodeling
_version_ 1721193114632192000