Where Dopaminergic and Cholinergic Systems Interact: A Gateway for Tuning Neurodegenerative Disorders

Historically, many investigations into neurodegenerative diseases have focused on alterations in specific neuronal populations such as, for example, the loss of midbrain dopaminergic neurons in Parkinson’s disease (PD) and loss of cholinergic transmission in Alzheimer’s disease (AD). However, it has...

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Main Authors: Marianne Amalric, Tommy Pattij, Ioannis Sotiropoulos, Joana M. Silva, Nuno Sousa, Samira Ztaou, Cristiano Chiamulera, Lars U. Wahlberg, Dwaine F. Emerich, Giovanna Paolone
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-07-01
Series:Frontiers in Behavioral Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnbeh.2021.661973/full
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author Marianne Amalric
Tommy Pattij
Ioannis Sotiropoulos
Ioannis Sotiropoulos
Joana M. Silva
Joana M. Silva
Nuno Sousa
Samira Ztaou
Samira Ztaou
Cristiano Chiamulera
Lars U. Wahlberg
Dwaine F. Emerich
Giovanna Paolone
author_facet Marianne Amalric
Tommy Pattij
Ioannis Sotiropoulos
Ioannis Sotiropoulos
Joana M. Silva
Joana M. Silva
Nuno Sousa
Samira Ztaou
Samira Ztaou
Cristiano Chiamulera
Lars U. Wahlberg
Dwaine F. Emerich
Giovanna Paolone
author_sort Marianne Amalric
collection DOAJ
description Historically, many investigations into neurodegenerative diseases have focused on alterations in specific neuronal populations such as, for example, the loss of midbrain dopaminergic neurons in Parkinson’s disease (PD) and loss of cholinergic transmission in Alzheimer’s disease (AD). However, it has become increasingly clear that mammalian brain activities, from executive and motor functioning to memory and emotional responses, are strictly regulated by the integrity of multiple interdependent neuronal circuits. Among subcortical structures, the dopaminergic nigrostriatal and mesolimbic pathways as well as cholinergic innervation from basal forebrain and brainstem, play pivotal roles in orchestrating cognitive and non-cognitive symptoms in PD and AD. Understanding the functional interactions of these circuits and the consequent neurological changes that occur during degeneration provides new opportunities to understand the fundamental inter-workings of the human brain as well as develop new potential treatments for patients with dysfunctional neuronal circuits. Here, excerpted from a session of the European Behavioral Pharmacology Society meeting (Braga, Portugal, August 2019), we provide an update on our recent work in behavioral and cellular neuroscience that primarily focuses on interactions between cholinergic and dopaminergic systems in PD models, as well as stress in AD. These brief discussions include descriptions of (1) striatal cholinergic interneurons (CINs) and PD, (2) dopaminergic and cholinergic modulation of impulse control, and (3) the use of an implantable cell-based system for drug delivery directly the into brain and (4) the mechanisms through which day life stress, a risk factor for AD, damage protein and RNA homeostasis leading to AD neuronal malfunction.
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spelling doaj.art-1a1cb78aa5534788b38d1b808aa46a712022-12-21T19:57:51ZengFrontiers Media S.A.Frontiers in Behavioral Neuroscience1662-51532021-07-011510.3389/fnbeh.2021.661973661973Where Dopaminergic and Cholinergic Systems Interact: A Gateway for Tuning Neurodegenerative DisordersMarianne Amalric0Tommy Pattij1Ioannis Sotiropoulos2Ioannis Sotiropoulos3Joana M. Silva4Joana M. Silva5Nuno Sousa6Samira Ztaou7Samira Ztaou8Cristiano Chiamulera9Lars U. Wahlberg10Dwaine F. Emerich11Giovanna Paolone12Centre National de la Recherche Scientifique (CNRS), UMR 7291, Laboratoire de Neurosciences Cognitives, Aix-Marseille University (AMU), Marseille, FranceAmsterdam Neuroscience, Department of Anatomy and Neurosciences, Amsterdam University Medical Centers, Amsterdam, NetherlandsLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, PortugalICVS/3B’s – PT Government Associate Laboratory, Braga, PortugalLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, PortugalICVS/3B’s – PT Government Associate Laboratory, Braga, PortugalICVS/3B’s – PT Government Associate Laboratory, Braga, PortugalCentre National de la Recherche Scientifique (CNRS), UMR 7291, Laboratoire de Neurosciences Cognitives, Aix-Marseille University (AMU), Marseille, FranceDepartment of Molecular Therapeutics, New York State Psychiatric Institute, Department of Psychiatry, Columbia University, New York, NY, United StatesDepartment of Diagnostic and Public Health, Section of Pharmacology, University of Verona, Verona, ItalyGloriana Therapeutics, Inc., Warren, RI, United StatesIndependent Researcher, Glocester, RI, United StatesDepartment of Diagnostic and Public Health, Section of Pharmacology, University of Verona, Verona, ItalyHistorically, many investigations into neurodegenerative diseases have focused on alterations in specific neuronal populations such as, for example, the loss of midbrain dopaminergic neurons in Parkinson’s disease (PD) and loss of cholinergic transmission in Alzheimer’s disease (AD). However, it has become increasingly clear that mammalian brain activities, from executive and motor functioning to memory and emotional responses, are strictly regulated by the integrity of multiple interdependent neuronal circuits. Among subcortical structures, the dopaminergic nigrostriatal and mesolimbic pathways as well as cholinergic innervation from basal forebrain and brainstem, play pivotal roles in orchestrating cognitive and non-cognitive symptoms in PD and AD. Understanding the functional interactions of these circuits and the consequent neurological changes that occur during degeneration provides new opportunities to understand the fundamental inter-workings of the human brain as well as develop new potential treatments for patients with dysfunctional neuronal circuits. Here, excerpted from a session of the European Behavioral Pharmacology Society meeting (Braga, Portugal, August 2019), we provide an update on our recent work in behavioral and cellular neuroscience that primarily focuses on interactions between cholinergic and dopaminergic systems in PD models, as well as stress in AD. These brief discussions include descriptions of (1) striatal cholinergic interneurons (CINs) and PD, (2) dopaminergic and cholinergic modulation of impulse control, and (3) the use of an implantable cell-based system for drug delivery directly the into brain and (4) the mechanisms through which day life stress, a risk factor for AD, damage protein and RNA homeostasis leading to AD neuronal malfunction.https://www.frontiersin.org/articles/10.3389/fnbeh.2021.661973/fullacetylcholinedopamineAlzheimer’s and Parkinson’s diseaseimpulse controlencapsulated cell-based system
spellingShingle Marianne Amalric
Tommy Pattij
Ioannis Sotiropoulos
Ioannis Sotiropoulos
Joana M. Silva
Joana M. Silva
Nuno Sousa
Samira Ztaou
Samira Ztaou
Cristiano Chiamulera
Lars U. Wahlberg
Dwaine F. Emerich
Giovanna Paolone
Where Dopaminergic and Cholinergic Systems Interact: A Gateway for Tuning Neurodegenerative Disorders
Frontiers in Behavioral Neuroscience
acetylcholine
dopamine
Alzheimer’s and Parkinson’s disease
impulse control
encapsulated cell-based system
title Where Dopaminergic and Cholinergic Systems Interact: A Gateway for Tuning Neurodegenerative Disorders
title_full Where Dopaminergic and Cholinergic Systems Interact: A Gateway for Tuning Neurodegenerative Disorders
title_fullStr Where Dopaminergic and Cholinergic Systems Interact: A Gateway for Tuning Neurodegenerative Disorders
title_full_unstemmed Where Dopaminergic and Cholinergic Systems Interact: A Gateway for Tuning Neurodegenerative Disorders
title_short Where Dopaminergic and Cholinergic Systems Interact: A Gateway for Tuning Neurodegenerative Disorders
title_sort where dopaminergic and cholinergic systems interact a gateway for tuning neurodegenerative disorders
topic acetylcholine
dopamine
Alzheimer’s and Parkinson’s disease
impulse control
encapsulated cell-based system
url https://www.frontiersin.org/articles/10.3389/fnbeh.2021.661973/full
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