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Published on: August 16, 2018
A(2A) adenosine receptor binding parameters in platelets from patients affected by pathological gambling
Claudia Martini1, Simona Daniele, Michela Picchetti
1Department of Psychiatry, Neurobiology, Pharmacology and Biotechnology, University of Pisa, Pisa, Italy. cmartini@farm.unipi.it
Pathological gambling is linked to altered adenosine receptors. This study found higher A(2A) adenosine receptor binding affinity in patients with pathological gambling, suggesting adenosine system involvement in this impulse control disorder.
Area of Science:
- Neuroscience
- Pharmacology
- Psychiatry
Background:
- Impulse control disorders, such as pathological gambling (PG), are associated with interactions between adenosine A(2A) receptors and dopamine D(2) receptors.
- Understanding these interactions may provide insights into the neurobiology of PG.
Purpose of the Study:
- To investigate A(2A) adenosine receptor affinity and density in platelet membranes of individuals with pathological gambling compared to healthy controls.
- To explore the potential role of adenosine receptors as peripheral markers of dopamine dysfunction in PG.
Main Methods:
- Recruited 12 drug-free PG patients and 12 matched healthy controls.
- Diagnosed PG using standardized clinical interviews and screening tools.
- Assessed A(2A) adenosine receptor binding parameters, including affinity and density (Bmax), using [(3)H]ZM(241385) binding assays in platelet membranes.
Main Results:
- Significantly higher A(2A) adenosine receptor binding affinity was observed in PG patients compared to healthy controls.
- No significant differences in receptor density (Bmax) were found between the two groups.
Conclusions:
- The study demonstrates altered adenosine receptor parameters in pathological gambling for the first time, indicating the adenosine system's involvement.
- Elevated A(2A) adenosine receptor binding affinity may reflect dopamine system hyperactivity in PG, suggesting its utility as a peripheral marker for dopamine dysfunction.
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