Gene dose-dependent alterations in extraneuronal serotonin but not dopamine in mice with reduced serotonin transporter expression

被引:206
作者
Mathews, TA
Fedele, DE
Coppelli, FM
Avila, AM
Murphy, DL
Andrews, AM
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[2] Penn State Univ, Huck Inst Life Sci, University Pk, PA 16802 USA
[3] NIMH, Clin Sci Lab, NIH, Bethesda, MD 20892 USA
关键词
serotonin transporter; knockout; microdialysis; zero net flux; serotonin; 5-hydroxyindoteacetic acid; dopamine; 3-4-dihydroxyphenylacetic acid; monoamine oxidase;
D O I
10.1016/j.jneumeth.2004.05.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Serotonin (5-HT) plays an integral regulatory role in mood, anxiety, cognition. appetite and aggressive behavior. Many therapeutic and illicit drugs that modulate these functions act at the serotonin transporter (SERT), thus a mouse model with reduced transporter expression was created to further investigate the effects of differential serotonin reuptake. In the present study. in vivo microdialysis was used to determine homeostatic alterations in extracellular 5-HT levels in unanesthetized SERT knockout mice. SERT-/- mice had significantly higher levels of basal dialysate 5-HT than SERT+/+ mice in striatum and frontal cortex. In addition. although gene-specific increases in 5-HT were evident. neuroadaptive alterations in dialysate dopamine levels were not detected in striatum. Zero net flux microdialysis was utilized to further investigate alterations in extracellular 5-HT. Using this method, a gene dose-dependent increase in extraneuronal 5-HT was observed in striatum (2.8 +/- 1.9.4 +/- 1 and 18 +/- 3 nM) and frontal cortex (1.4 +/- 0.4, 3.5 +/- 0.9 and 14 +/- 1 nM) in SERT+/+, SERT+/- and SERT-/- mice. respectively. Potassium stimulation revealed greater depolarization-induced increases in striatal 5-HT but not dopamine in SERT-/- mice. Furthermore, dialysate 5-hydroxyindoleacetic acid (5-HIAA) levels were reduced in striatum in a gene dose-dependent manner. while DOPAC was unchanged in SERT knockout mice. Finally. determination of monoamine oxidase (MAO) activity revealed no significant differences in K-M or V-max of type-A or type-B isozymes indicating that alterations in SERT expression do not cause adaptive changes in the activities of these key catabolic enzymes. Overall, these results demonstrate that constitutive reductions in SERT are associated with increase's in 5-HT in the extracellular signaling space in the absence of changes in dopamine neurochemistry. Furthermore. use of zero net flux microdialysis appears warranted in investigations of serotonergic synaptic function where modest changes in extracellular 5-HT are. thought to occur in response to altered uptake. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 181
页数:13
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