Time course of the effects of the serotonin-selective reuptake inhibitor sertraline on central and peripheral serotonin neurochemistry in the rhesus monkey

被引:31
作者
Anderson, GM
Barr, CS
Lindell, S
Durham, AC
Shifrovich, I
Higley, JD
机构
[1] Yale Univ, Sch Med, Dept Child Psychiat, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Lab Med, New Haven, CT 06510 USA
[3] NIAAA, Lab Clin Studies Primate Unit, Poolesville, MD USA
关键词
serotonin; cerebrospinal fluid; CSF; rhesus monkey; cisternal; sertraline; selective serotonin reuptake inhibitor; SSRI; 5-hydroxyindoleacetic acid;
D O I
10.1007/s00213-004-2011-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale: Fundamental questions remain regarding the actions of the selectiveserotonin reuptake inhibitors (SSRIs). Objectives: To examine the time courseof central and peripheral neurochemical effects of sertraline (SER) in non-human primates. Methods: SER ( 20 mg/kg, p.o.) or placebo were administered daily for 4 weeks to two groups of six young adult male rhesus monkeys. Both groups received placebo during a 3-week baseline lead-in period and for 6 weeks after discontinuation. Blood and cisternal cerebrospinal fluid ( cCSF) samples were obtained on days -21, -14, -7, 0, +3, +7, +14, +21, +28, +35 and +70. Results: In animals receiving SER, mean (+/- SD) levels of cCSF serotonin (5-HT) increased from 38.6 +/- 9.0 pg/ml at baseline to 128 +/- 46.4 pg/ml during treatment (paired t= 4.17, P=0.014). Concentrations of cCSF 5-HT were 290% of baseline on day 0 (+ 3 h), ranged from 260% to 436% of baseline during treatment, and returned to baseline 7 days after discontinuation. Levels of cCSF 5-hydroxyindoleacetic acid declined to 51 +/- 2.0% of baseline by day + 3 and remained at similarly reduced levels during treatment. Plasma drug levels and decrements in platelet 5-HT were similar to those seen in patients. Conclusions: SER rapidly and substantially increases cCSF levels of 5-HT in primates, the extent of elevation is relatively constant during prolonged administration, and values return to baseline shortly after discontinuation. The results suggest that response latency for SSRIs in depression is not due to gradually increasing brain extracellular fluid 5-HT levels and tend not to support theories that positSSRI response latency as being due to autoreceptor desensitization, transporter downregulation, or drug accumulation.
引用
收藏
页码:339 / 346
页数:8
相关论文
共 58 条
[1]   DETERMINATION OF SEROTONIN IN WHOLE-BLOOD, PLATELET-RICH PLASMA, PLATELET-POOR PLASMA AND PLASMA ULTRAFILTRATE [J].
ANDERSON, GM ;
FEIBEL, FC ;
COHEN, DJ .
LIFE SCIENCES, 1987, 40 (11) :1063-1070
[2]   SEROTONIN IN HUMAN LUMBAR CEREBROSPINAL-FLUID - A REASSESSMENT [J].
ANDERSON, GM ;
MEFFORD, IN ;
TOLLIVER, TJ ;
RIDDLE, MA ;
OCAME, DM ;
LECKMAN, JF ;
COHEN, DJ .
LIFE SCIENCES, 1990, 46 (04) :247-255
[3]   SEROTONIN IN CISTERNAL CEREBROSPINAL-FLUID OF THE RAT - MEASUREMENT AND USE AS AN INDEX OF FUNCTIONALLY ACTIVE SEROTONIN [J].
ANDERSON, GM ;
TEFF, KL ;
YOUNG, SN .
LIFE SCIENCES, 1987, 40 (23) :2253-2260
[4]   Serotonin in cisternal cerebrospinal fluid of rhesus monkeys: basal levels and effects of sertraline administration [J].
Anderson, GM ;
Bennett, AJ ;
Weld, KP ;
Pushkas, JG ;
Ocame, DM ;
Higley, JD .
PSYCHOPHARMACOLOGY, 2002, 161 (01) :95-99
[5]   FLUOXETINE KINETICS AND PROTEIN-BINDING IN NORMAL AND IMPAIRED RENAL-FUNCTION [J].
ARONOFF, GR ;
BERGSTROM, RF ;
POTTRATZ, ST ;
SLOAN, RS ;
WOLEN, RL ;
LEMBERGER, L .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1984, 36 (01) :138-144
[6]   Rearing condition and rh5-HTTLPR interact to influence limbic-hypothalamic-pituitary-adrenal axis response to stress in infant macaques [J].
Barr, CS ;
Newman, TK ;
Shannon, C ;
Parker, C ;
Dvoskin, RL ;
Becker, ML ;
Schwandt, M ;
Champoux, M ;
Lesch, KP ;
Goldman, D ;
Suomi, SJ ;
Higley, JD .
BIOLOGICAL PSYCHIATRY, 2004, 55 (07) :733-738
[7]   CHRONIC TREATMENT WITH FLUVOXAMINE INCREASES EXTRACELLULAR SEROTONIN IN FRONTAL-CORTEX BUT NOT IN RAPHE NUCLEI [J].
BEL, N ;
ARTIGAS, F .
SYNAPSE, 1993, 15 (03) :243-245
[8]  
BEL N, 1992, EUR J PHARMACOL, V278, P1064
[9]  
Benmansour S, 2002, J NEUROSCI, V22, P6766
[10]  
Benmansour S, 1999, J NEUROSCI, V19, P10494