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Using a novel animal model of the dopaminergic dysfunction of schizophrenia to trial an innovative treatment approach

Description du projet

Un nouveau traitement pour la schizophrénie

La schizophrénie est un trouble mental chronique associé à une altération de la capacité à interpréter la réalité. De plus en plus de preuves indiquent que les patients présentent une synthèse accrue de dopamine avant même l’apparition de la maladie. Les scientifiques du projet EDiPSPrevent, financé par l’UE, ont développé un modèle murin de schizophrénie qui récapitule le dysfonctionnement dopaminergique observé chez les patients. L’objectif du projet est d’étudier la neurotransmission chez ces animaux et de tester l’effet d’un médicament qui normalise l’augmentation de la dopamine. Les résultats fourniront des informations fondamentales sur la physiopathologie de la maladie et ouvriront de nouvelles possibilités de traitement des personnes à risque.

Objectif

Treatments for schizophrenia are inadequate, and intervening prior to disease onset is a novel approach to improve patient outcomes. Clinical studies using positron emission tomography (PET) have revealed that patients with chronic schizophrenia consistently show an increase in dopamine synthesis capacity in the striatum. This dysfunction is also evident in people at-risk of developing schizophrenia, specifically in those who are later diagnosed with this disorder. Normalizing this increase in pre-synaptic dopamine therefore reflects an extremely promising target for new treatments of schizophrenia. I developed a novel animal model of schizophrenia – Enhanced Dopamine in Prodromal Schizophrenia (EDiPS) – which replicates the pre-synaptic dopaminergic dysfunction seen so robustly in patients. In this project, I propose to firstly use state-of-art preclinical PET to examine pre-synaptic dopamine in EDiPS animals. This will confirm its translatability to the findings in the clinical population. Through a secondment, I will assess other key aspects of dopamine neurotransmission in these animals, focussing on the source of dopaminergic innervation to the striatum – the midbrain. As a complementary objective, I will assess any difference between male and female EDiPS animals for each of these outcomes. This is especially relevant to schizophrenia, which is a sexually dimorphic disorder. The second objective of this fellowship is to trial a novel approach to normalise the increase in pre-synaptic dopamine in EDiPS animals, through a Trace Amino Acid Receptor 1 (TAAR1) agonist. I will trial the TAAR1 agonist both acutely in adult EDiPS animals, and when given chronically during development, to simulate an intervention in the at-risk population. This will be the first study to examine the effects of a TAAR1 agonist in the developing brain. The scientific outcomes of this fellowship will have real-world implications for the treatment of patients with schizophrenia.

Champ scientifique (EuroSciVoc)

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Coordinateur

IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE
Contribution nette de l'UE
€ 212 933,76
Adresse
SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
SW7 2AZ LONDON
Royaume-Uni

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Type d’activité
Higher or Secondary Education Establishments
Liens
Coût total
€ 212 933,76