PT  - JOURNAL ARTICLE
AU  - Liu, Xingrong
AU  - Vilenski, Olga
AU  - Kwan, Joyce
AU  - Apparsundaram, Subbu
AU  - Weikert, Robert
TI  - Unbound Brain Concentration Determines Receptor Occupancy: A Correlation of Drug Concentration and Brain Serotonin and Dopamine Reuptake Transporter Occupancy for Eighteen Compounds in Rats
AID  - 10.1124/dmd.109.026674
DP  - 2009 Jul 01
TA  - Drug Metabolism and Disposition
PG  - 1548--1556
VI  - 37
IP  - 7
4099  - http://dmd.aspetjournals.org/content/37/7/1548.short
4100  - http://dmd.aspetjournals.org/content/37/7/1548.full
SO  - Drug Metab Dispos2009 Jul 01; 37
AB  - It is a commonly accepted hypothesis that central nervous system (CNS) activity is determined by the unbound brain drug concentration. However, limited experimental data are available in the literature to support this hypothesis. The objective of this study was to test this hypothesis by examining the relationship between in vitro binding affinity (KI) and in vivo activity quantified as the drug concentration occupying 50% of the transporters (OC50) for 18 serotonin (SERT) and dopamine transporter (DAT) inhibitors. In vivo rat OC50 was determined by autoradiography using [3H]N,N-dimethyl-2,2-amino-4-cyanophenylthiobenzylamine and [3H](–)-2-β-carbomethoxy-3-β-(4-fluorophenyl)tropane-1,5-napthalenedisulfonate (WIN35,428) as the ligands to assess SERT and DAT occupancy, respectively. The unbound brain concentrations were calculated from total brain concentrations and the unbound brain fraction, which was determined by the brain homogenate method. The in vivo total brain SERT and DAT OC50 values (mean ± S.D.) were 408 ± 368- and 410 ± 395-fold greater than the KI values, respectively. In contrast, the in vivo unbound brain SERT and DAT OC50 values were only 3.3 ± 2.1- and 4.1 ± 4.0-fold different from the KI values. Therefore, prediction of the biophase drug concentration by using the unbound brain concentration rather than the total brain concentration results in an approximately 100-fold improvement for the accuracy. In the present study, a 10-fold improvement was also observed by using the unbound plasma concentration rather than the total plasma concentration to predict the biophase concentration in the brain. This study supports the hypothesis that CNS activity is more accurately determined by the unbound brain drug concentration and not by the total brain drug concentration.