Simultaneous monitoring of inhibition of serotonin uptake by platelets and plasma drug concentrations following administration of duloxetine, a new antidepressant candidate, to healthy volunteers

被引:7
作者
Ishigooka, J
Nagata, E
Takahashi, A
Sugiyama, T
Uchiumi, M
Tsukahara, T
Murasaki, M
Miura, S
Oguma, T
Yano, Y
机构
[1] KITASATO UNIV,SCH MED,DIV BIOCHEM,SAGAMIHARA,KANAGAWA 228,JAPAN
[2] KITASATO UNIV,SCH ALLIED SCI,SAGAMIHARA,KANAGAWA 228,JAPAN
[3] SHIONOGI & CO LTD,SHIONOGI RES LABS,OSAKA 553,JAPAN
来源
CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL | 1997年 / 58卷 / 10期
关键词
5-hydroxytryptamine (serotonin); platelet; duloxetine; uptake inhibition; ex vivo;
D O I
10.1016/S0011-393X(97)80102-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Duloxetine is a new antidepressant candidate drug with inhibitory effects on norepinephrine and serotonin (5-HT) uptake. In the present study, simultaneous monitoring of the inhibition of 5-HT uptake by platelets and plasma drug concentrations was carried out in healthy volunteers during and after administration of 20 mg of duloxetine once daily for 1 week. Inhibition by duloxetine of 5-HT uptake by platelets and the appearance of the drug in plasma occurred simultaneously, and a strong inhibition greater than 80% to 90% was maintained during the experimental period. Until 2 days after the final administration, the observed values for 5-HT uptake inhibition rate were in good agreement with those simulated from total, but not final, plasma concentrations of duloxetine (r = .9846). Moreover, on the fourth day after the final administration, the observed values mere even higher than the simulated ones (observed mean value, 40.5 +/- 14.6; simulated value, 13.3). These results show that uptake of 5-HT is inhibited strongly and for a long period in the subjects taking duloxetine.
引用
收藏
页码:679 / 692
页数:14
相关论文
共 19 条
[1]   PHARMACOKINETIC OPTIMIZATION OF TRICYCLIC ANTIDEPRESSANT THERAPY [J].
FURLANUT, M ;
BENETELLO, P ;
SPINA, E .
CLINICAL PHARMACOKINETICS, 1993, 24 (04) :301-318
[2]  
HORNG JS, 1976, BIOCHEM PHARMACOL, V32, P1287
[3]   BIOCHEMICAL EFFECTS AND DRUG LEVELS IN RATS AFTER LONG-TERM TREATMENT WITH THE SPECIFIC 5-HT-UPTAKE INHIBITOR, CITALOPRAM [J].
HYTTEL, J ;
OVERO, KF ;
ARNT, J .
PSYCHOPHARMACOLOGY, 1984, 83 (01) :20-27
[4]  
ISHIGOOKA J, 1996, EUR NEUROPSYCHOPH S3, V6, P50
[5]  
LEWONARD BE, 1988, J CLIN PSYCHIAT, V49, P12
[6]   The determination of enzyme dissociation constants [J].
Lineweaver, H ;
Burk, D .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1934, 56 :658-666
[7]   BINDING OF SOME ANTIDEPRESSANTS TO THE 5-HYDROXYTRYPTAMINE TRANSPORTER IN BRAIN AND PLATELETS [J].
MARCUSSON, JO ;
ROSS, SB .
PSYCHOPHARMACOLOGY, 1990, 102 (02) :145-155
[8]   WHY SOME DEPRESSED-PATIENTS MAY HAVE LOW PLATELET H-3 IMIPRAMINE BINDING [J].
MELLERUP, ET ;
PLENGE, P .
ACTA PSYCHIATRICA SCANDINAVICA, 1990, 82 (04) :330-334
[9]   PLATELET H-3 IMIPRAMINE AND H-3 PAROXETINE BINDING DURING TREATMENT WITH PSYCHOACTIVE-DRUGS [J].
MELLERUP, ET ;
DAM, H ;
LAURITZEN, L ;
PLENGE, P .
BIOLOGICAL PSYCHIATRY, 1991, 30 (10) :1056-1058
[10]  
METZLER CM, 1974, BIOMETRICS, V30, P562