KINETIC EFFECTS OF DESMETHYLIMIPRAMINE TREATMENT ON PLATELET SEROTONIN UPTAKE IN DEPRESSED-PATIENTS - A COMPARISON WITH IMIPRAMINE
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RAUSCH, JL
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UNIV TEXAS, DEPT VET AFFAIRS MED CTR, SW MED SCH, DEPT PSYCHIAT, DALLAS, TX 75230 USAUNIV TEXAS, DEPT VET AFFAIRS MED CTR, SW MED SCH, DEPT PSYCHIAT, DALLAS, TX 75230 USA
RAUSCH, JL
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MOELLER, FG
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UNIV TEXAS, DEPT VET AFFAIRS MED CTR, SW MED SCH, DEPT PSYCHIAT, DALLAS, TX 75230 USAUNIV TEXAS, DEPT VET AFFAIRS MED CTR, SW MED SCH, DEPT PSYCHIAT, DALLAS, TX 75230 USA
MOELLER, FG
[1
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[1] UNIV TEXAS, DEPT VET AFFAIRS MED CTR, SW MED SCH, DEPT PSYCHIAT, DALLAS, TX 75230 USA
The kinetic effects of desmethylimipramine (DMI) on platelet serotonin (5HT) uptake were compared to those of imipramine (IMI) in eight DMI-treated depressed patients and seven IMI-treated depressed patients, and compared to values after patients were off drug for 19 (+/- 8 SD) and 33 (+/- 15) days. As expected, IMI was a stronger inhibitor of 5HT uptake than DMI during treatment, with the mean apparent K(m) in treated patients being elevated nearly threefold over that of the drug-free condition. In DMI-treated patients, the mean K(m) was elevated nearly twofold over that of the drug-free condition. Although DMI is considered a preferential norepinephrine uptake inhibitor, the results suggest the following: (1) Significant decreases in the apparent platelet 5HT affinity are achieved with DMI; (2) the inhibition kinetics in depressed patients are competitive; (3) there was a significant relationship between K(m) change and depression outcome with DMI discontinuation; and (4) DMI, as a metabolite, appears to contribute to the 5HT uptake inhibition of IMI in vivo.