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Article Abstract

The dorsal striatum is a key node for many neurobiological processes such as motor activity, cognitive functions, and affective processes. The proper functioning of striatal neurons relies critically on metabotropic receptors. Specifically, the main adenosine and endocannabinoid receptors present in the striatum, ie, adenosine A receptor (AR) and cannabinoid CB receptor (CBR), are of pivotal importance in the control of neuronal excitability. Facilitatory and inhibitory functional interactions between striatal AR and CBR have been reported, and evidence supports that this cross-talk may rely, at least in part, on the formation of AR-CBR heteromeric complexes. However, the specific location and properties of these heteromers have remained largely unknown. Here, by using techniques that allowed a precise visualization of the heteromers in situ in combination with sophisticated genetically modified animal models, together with biochemical and pharmacological approaches, we provide a high-resolution expression map and a detailed functional characterization of AR-CBR heteromers in the dorsal striatum. Specifically, our data unveil that the AR-CBR heteromer (i) is essentially absent from corticostriatal projections and striatonigral neurons, and, instead, is largely present in striatopallidal neurons, (ii) displays a striking G protein-coupled signaling profile, where co-stimulation of both receptors leads to strongly reduced downstream signaling, and (iii) undergoes an unprecedented dysfunction in Huntington's disease, an archetypal disease that affects striatal neurons. Altogether, our findings may open a new conceptual framework to understand the role of coordinated adenosine-endocannabinoid signaling in the indirect striatal pathway, which may be relevant in motor function and neurodegenerative diseases.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854787PMC
http://dx.doi.org/10.1038/npp.2017.12DOI Listing

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