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5th EuropEan MolEcular IMagIng MEEtIng - ESMI

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<strong>5th</strong> <strong>EuropEan</strong> <strong>MolEcular</strong> <strong>IMagIng</strong> <strong>MEEtIng</strong> – EMIM2010<br />

Preclinical imaging of the type 1 cannabinoid receptor in neurodegenerative diseases<br />

Casteels C. (1) , Van Laere K. (1) .<br />

University Leuven, Division of Nuclear Medicine, Belgium<br />

cindy.casteels@med.kuleuven.be<br />

The endocannabinoid system (ECS) is an important<br />

modulatory system in the brain. It consists of a family<br />

of naturally occurring lipids, the endocannabinoids,<br />

of transport and degradation proteins, and of<br />

cannabinoid receptors. Type 1 cannabinoid (CB1)<br />

receptors are abundantly expressed in all brain areas,<br />

especially those involved in the control of motor<br />

function. CB1 receptor stimulation modulates<br />

GABA, glutamate and dopamine neurotransmitter<br />

release in a dynamic activity manner.1<br />

Dysregulation of cannabinoid-mediated control<br />

of basal ganglia function have been suggested to<br />

play a critical role in the pathogenesis and symptom<br />

development of Parkinson’s disease (PD) and<br />

Huntington’s disease (HD), providing rationale for<br />

potential ECS-targeted therapy in these diseases.2<br />

However, at present, limited clinical pilot trials have<br />

been inconclusive. As only in vitro, ex vivo and<br />

post mortem data on the ECS existed until recently,<br />

functional in vivo imaging may play an important<br />

role in the further evaluation of the neurobiological<br />

and clinical impact of the ECS in PD and HD.<br />

Here, we present the in vivo characterization of CB1<br />

receptor alterations in preclinical models of PD and<br />

HD using PET and [18F]MK-94703. Both genetic<br />

and toxin-based experimental models will be presented.<br />

Their relevance to mimic the human condition<br />

will be discussed as well.<br />

Acknowledgement: Financial support of the Research<br />

Council of the Katholieke Universiteit Leuven<br />

(OT/05/58), the Fund for Scientific Research,<br />

Flanders, Belgium (FWO/G.0548.06), and the Institute<br />

for the Promotion of Innovation by Science and<br />

Technology in Flanders (SBO50151) is gratefully<br />

acknowledged. This work is performed under European<br />

Commission FP6-project DiMI,LSHB-CT-<br />

2005-512146<br />

References:<br />

1. Katona et al., Nat. Med. 2008;<br />

2. Maccarrone et al., Prog. Neurobiol. 2007;<br />

3. Burns et al., Proc. Natl. Acad. Sci. U.S.A. 2007.<br />

<strong>EuropEan</strong> SocIEty for <strong>MolEcular</strong> <strong>IMagIng</strong> – <strong>ESMI</strong><br />

YIA applicant<br />

day1<br />

Parallel Session 2: NEUROSCIENCE I

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