Dopamine receptor density and white mater integrity: 18F-fallypride positron emission tomography and diffusion tensor imaging study in healthy and schizophrenia subjects

2018 ◽  
Vol 14 (3) ◽  
pp. 736-752 ◽  
Author(s):  
Serge A. Mitelman ◽  
Monte S. Buchsbaum ◽  
Bradley T. Christian ◽  
Brian M. Merrill ◽  
Bradley R. Buchsbaum ◽  
...  
2020 ◽  
Vol 13 (2) ◽  
pp. 457-463 ◽  
Author(s):  
Tim Vanbellingen ◽  
Manuela Pastore-Wapp ◽  
Stefanie Kübel ◽  
Thomas Nyffeler ◽  
Anne-Catherine Schüpfer ◽  
...  

1990 ◽  
Vol 5 (4) ◽  
pp. 231-240 ◽  
Author(s):  
JL Martinot ◽  
ML Paillère-Martinot ◽  
C Loc'h ◽  
P Péron Magnan ◽  
B Mazoyer ◽  
...  

SummaryThe striatal D2 receptor density/affinity index was assessed using positron emission tomography and 76Br-Bromolisuride in 15 schizophrenics, first untreated, and afterwards receiving neuroleptics, and in 14 control subjects. The patients received low or conventional doses of neuroleptics. The schizophrenics receiving low doses (n = 6) had preponderant negative symptoms. Mean D2 receptor occupancy was 24 ± 20%. Despite this weak central D2 receptor blockade, a significant decrease in negative symptoms was observed, a result consistent with the hypothesis of a disinhibitory action of some neuroleptics administered in low doses. The patients treated with conventional doses (n = 9) had mixed positive and negative symptoms, and the mean D2 receptor occupancy was 54 ± 13%. Significant decreases in positive symptoms, but also in negative symptoms, were obtained with this treatment. Before treatment, there was no significant difference in the striatal D2 receptor density/affinity index between: 1) patients and controls, 2) negative and mixed schizophrenics, and 3) the subsequent responder and non-responder patients. In addition, the D2 dopamine receptor occupancy by neuroleptics did not significantly differ in responder or nonresponder patients, suggesting that the central D2 dopamine receptor blockade is a necessary, but insufficient condition to account for the antipsychotic effect of neuroleptics.


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