Effect of different challenge doses after repeated citalopram treatment on extracellular serotonin level in the medial prefrontal cortex:: In vivo microdialysis study

被引:4
作者
Muraki, Ihoko [1 ]
Inoue, Takeshi [1 ]
Hashimoto, Shinji [1 ]
Izumi, Takeshi [1 ]
Koyama, Tsukasa [1 ]
机构
[1] Hokkaido Univ, Grad Sch Med, Dept Psychiat, Sapporo, Hokkaido 0608638, Japan
关键词
citalopram; in vivo brain microdialysis; medial prefrontal cortex; serotonin; SSRI;
D O I
10.1111/j.1440-1819.2008.01851.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aims: In order to elucidate the relevance between the delayed onset of clinical efficacy of selective serotonin re-uptake inhibitors (SSRI) and extracellular 5-HT levels in the medial prefrontal cortex, the present study compared the ability of low-dose (3 mg/kg) and high-dose (30 mg/kg) citalopram to increase extracellular 5-HT levels in the medial prefrontal cortex following repeated citalopram treatment using in vivo microdialysis. Methods: An SSRI, citalopram, was given 10 mg/kg, s.c. twice daily for 6 days and once on the seventh day in rats. On the eighth day, rats received a single injection of citalopram (3 or 30 mg/kg s.c.), and extracellular 5-HT levels were assessed in the medial prefrontal cortex of rats using in vivo brain microdialysis. Results: There was no significant difference in basal extracellular 5-HT levels between the repeated citalopram group and the repeated saline group. The low-challenge dose of citalopram (3 mg/kg) produced significantly greater increases (170-200% at each time point) in the repeated citalopram group than in the repeated saline group (150%). The high-challenge dose of citalopram (30 mg/kg), however, increased extracellular 5-HT levels by 200-250% of basal levels in the repeated citalopram group, which was similar to the increases in the repeated saline group. Conclusions: Repeated SSRI treatment enhances the effect of low-dose SSRI on extracellular 5-HT levels but not that of high-dose SSRI.
引用
收藏
页码:568 / 574
页数:7
相关论文
共 34 条
[1]   The 5-HT1A receptor antagonist (S)-UH-301 augments the increase in extracellular concentrations of 5-HT in the frontal cortex produced by both acute and chronic treatment with citalopram [J].
Arborelius, L ;
Nomikos, GG ;
Hertel, P ;
Salmi, P ;
Grillner, P ;
Hook, BB ;
Hacksell, U ;
Svensson, TH .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1996, 353 (06) :630-640
[2]   Acceleration of the effect of selected antidepressant drugs in major depression by 5-HT1A antagonists [J].
Artigas, F ;
Romero, L ;
deMontigny, C ;
Blier, P .
TRENDS IN NEUROSCIENCES, 1996, 19 (09) :378-383
[3]  
ARTIGAS F, 1994, ARCH GEN PSYCHIAT, V51, P248
[4]   Citalopram dose-response revisited using an alternative psychometric approach to evaluate clinical effects of four fixed citalopram doses compared to placebo in patients with major depression [J].
Bech, P ;
Tanghoj, P ;
Andersen, HF ;
Overo, K .
PSYCHOPHARMACOLOGY, 2002, 163 (01) :20-25
[5]   Acute and chronic effects of citalopram on postsynaptic 5-hydroxytryptamine1A receptor-mediated feedback:: a microdialysis study in the amygdala [J].
Bosker, FJ ;
Cremers, TIFH ;
Jongsma, ME ;
Westerink, BHC ;
Wikström, VH ;
den Boer, JA .
JOURNAL OF NEUROCHEMISTRY, 2001, 76 (06) :1645-1653
[6]   Fluoxetine, but not other selective serotonin uptake inhibitors, increases norepinephrine and dopamine extracellular levels in prefrontal cortex [J].
Bymaster, FP ;
Zhang, W ;
Carter, PA ;
Shaw, J ;
Chernet, E ;
Phebus, L ;
Wong, DT ;
Perry, KW .
PSYCHOPHARMACOLOGY, 2002, 160 (04) :353-361
[7]   THE INHIBITORY EFFECT OF 8-OH-DPAT ON THE FIRING ACTIVITY OF DORSAL RAPHE SEROTONINERGIC NEURONS IN RATS IS ATTENUATED BY LESION OF THE FRONTAL-CORTEX [J].
CECI, A ;
BASCHIROTTO, A ;
BORSINI, F .
NEUROPHARMACOLOGY, 1994, 33 (05) :709-713
[8]   EFFECTS OF A SELECTIVE 5-HT REUPTAKE BLOCKER, CITALOPRAM, ON THE SENSITIVITY OF 5-HT AUTORECEPTORS - ELECTROPHYSIOLOGICAL STUDIES IN THE RAT-BRAIN [J].
CHAPUT, Y ;
DEMONTIGNY, C ;
BLIER, P .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1986, 333 (04) :342-348
[9]  
DELGADO PL, 1990, ARCH GEN PSYCHIAT, V47, P411