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ALCO-ADO SIGNED

Unveiling the alcohol-dependent alterations in local dendritic translation of mRNAs in the prefrontal cortex during adolescence

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 ALCO-ADO project word cloud

Explore the words cloud of the ALCO-ADO project. It provides you a very rough idea of what is the project "ALCO-ADO" about.

neurocognitive    vulnerability    behavioral    impulsivity    form    immaturity    dependent    alcohol    adolescence    maladaptive    translatome    function    brain    usurps    prefrontal    shown    lasting    modifications    local    executive    analyze    populations    plasticity    cortex    male    uncover    synaptic    alpha    functions    males    multidisciplinary    consumption    females    eif2    addiction    differences    intense    connections    mrnas    modulates    sites    underlying    interneurons    defective    tests    adolescents    mesocorticolimbic    mice    impairs    strength    differential    frontal    composition    combining    mtorc1    regions    maturation    neurons    gabaergic    adolescent    modulating    mechanisms    during    profoundly    defects    imaging    regulators    learning    deleterious    memory    pfc    implicated    sensibility    excessive    female    neuronal    altered    drug    biochemistry    mainly    electrophysiology    involvement    modifies    translation    precise    proteins    alterations    heightened    drugs    psychological    behaviors    glutamatergic    poorly    undergoes    molecular   

Project "ALCO-ADO" data sheet

The following table provides information about the project.

Coordinator		 UNIVERSITE DE LIEGE 

Organization address
address: PLACE DU 20 AOUT 7
city: LIEGE
postcode: 4000
website: www.ulg.ac.be

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.
 Coordinator Country Belgium [BE]
 Total cost 178˙320 €
 EC max contribution 178˙320 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-RI
 Starting year 2019
 Duration (year-month-day) from 2019-04-01   to  2021-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITE DE LIEGE BE (LIEGE) coordinator 178˙320.00

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 Project objective

During adolescence, the brain undergoes intense maturation, particularly in the frontal areas. The prefrontal cortex (PFC) is implicated in executive functions, and its immaturity in adolescents is associated with increased impulsivity and heightened vulnerability to deleterious effects of drugs. Alcohol is the most consumed drug among adolescents, and its excessive consumption profoundly impairs PFC function, leading to long-lasting defective behaviors, psychological problems and neurocognitive defects. However, the precise mechanisms underlying alcohol-induced alterations in PFC maturation remain poorly understood. Alcohol addiction is considered being a maladaptive form of learning and memory, as alcohol usurps the molecular mechanisms underlying those processes, such as long-lasting synaptic plasticity. Long-lasting changes in the strength of synaptic connections mainly depend on the local translation of mRNAs at synaptic sites. It has been shown that alcohol modifies synaptic proteins composition by modulating the activity of key translation regulators, such as mTORC1 and eIF2α, in brain regions associated with the mesocorticolimbic pathway. Here, we propose to analyze the alcohol-dependent modifications of the synaptic translatome of specific neuronal populations (glutamatergic neurons and GABAergic interneurons) in the PFC of adolescent male and female mice, by using a multidisciplinary approach combining biochemistry, imaging, electrophysiology and behavioral tests. This project aims to uncover how alcohol modulates local translation of synaptic proteins in the PFC during adolescence, to identify the targeted synaptic mRNAs and analyze their involvement in altered synaptic plasticity underlying alcohol-dependent defective behaviors. In addition, this project aims at identifying the differential sensibility to alcohol’s effects between males and females as well as the differences in behavioral consequences.

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