P.0830 LB-102 displays superior dopamine receptor occupancy compared to amisulpride in mouse and human PET studies

2021 ◽  
Vol 53 ◽  
pp. S606
Author(s):  
A. Vaino ◽  
A. Mintz ◽  
A. Eramo ◽  
N. Caito ◽  
G. Chand ◽  
...  
1990 ◽  
Vol 3 (1) ◽  
pp. 51-52
Author(s):  
L. Farde ◽  
A.-L. Nordstrom ◽  
F.-A. Wiesel ◽  
C. Halldin ◽  
G. Sedvall

1997 ◽  
Vol 42 (1) ◽  
pp. 15S
Author(s):  
G. Gründer ◽  
S. Schlegel ◽  
R. Schlösser ◽  
M. Müller ◽  
H. Wetzel ◽  
...  

2011 ◽  
Vol 32 (4) ◽  
pp. 759-768 ◽  
Author(s):  
Euitae Kim ◽  
Oliver D Howes ◽  
Bo-Hyung Kim ◽  
Jae Min Jeong ◽  
Jae Sung Lee ◽  
...  

Positron emission tomography (PET) studies of dopamine receptor occupancy can be used to assess dosing of antipsychotics. Typically, studies of antipsychotics have applied pharmacodynamic (PD) modeling alone to characterize the relationship between antipsychotic dose and its effect on the brain. However, a limitation of this approach is that it does not account for the discrepancy between the time courses of plasma concentration and receptor occupancy by antipsychotics. Combined pharmacokinetic—PD (PK—PD) modeling, by incorporating the time dependence of occupancy, is better suited for the reliable analysis of the concentration—occupancy relationship. To determine the effect of time on the concentration—occupancy relationship as a function of analysis approach, we measured dopamine receptor occupancy after the administration of aripiprazole using [11C]raclopride PET and obtained serial measurements of the plasma aripiprazole concentration in 18 volunteers. We then developed a PK—PD model for the relationship, and compared it with conventional approach (PD modeling alone). The hysteresis characteristics were observed in the competitor concentration—occupancy relationship and the value of EC50 was different according to the analysis approach ( EC50 derived from PD modeling alone = 11.1 ng/mL (95% confidence interval (CI) = 10.1 to 12.1); while that derived from combined PK—PD modeling = 8.63 ng/mL (95% CI = 7.75 to 9.51)). This finding suggests that PK—PD modeling is required to obtain reliable prediction of brain occupancy by antipsychotics.


NeuroImage ◽  
2003 ◽  
Vol 19 (3) ◽  
pp. 1205-1214 ◽  
Author(s):  
Kjell Erlandsson ◽  
Rodrigo A. Bressan ◽  
Rachel S. Mulligan ◽  
Peter J. Ell ◽  
Vincent J. Cunningham ◽  
...  

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.


1996 ◽  
Vol 11 ◽  
pp. 417s
Author(s):  
T. Mager ◽  
I. Dähne ◽  
S. Dresel ◽  
F. Pajonk ◽  
K.H.J. TatschMöller

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