A GREATER ROLE FOR THE NOREPINEPHRINE TRANSPORTER THAN THE SEROTONIN TRANSPORTER IN MURINE NOCICEPTION

被引:26
作者
Hall, F. S. [1 ]
Schwarzbaum, J. M. [1 ]
Perona, M. T. G. [1 ]
Templin, J. S. [1 ]
Caron, M. G. [2 ,3 ]
Lesch, K. -P. [4 ]
Murphy, D. L. [5 ]
Uhl, G. R. [1 ]
机构
[1] NIDA, Mol Neurobiol Branch, Intramural Res Program, Baltimore, MD 21224 USA
[2] Duke Univ, Dept Cell Biol, Durham, NC 27710 USA
[3] Duke Univ, Dept Med, Durham, NC 27710 USA
[4] Univ Wurzburg, Dept Psychiat, D-97080 Wurzburg, Germany
[5] NIMH, Clin Sci Lab, Intramural Res Program, Bethesda, MD 20892 USA
关键词
knockout mice; serotonin transporter; norepinephrine transporter; analgesia; nociception; amitriptyline; CENTRAL NERVOUS-SYSTEM; RAT FORMALIN TEST; MORPHINE-INDUCED ANTINOCICEPTION; MONOAMINE REUPTAKE INHIBITORS; TRICYCLIC ANTI-DEPRESSANTS; NUCLEUS RAPHE MAGNUS; SOLE ANALGESIC AGENT; PERIAQUEDUCTAL GRAY; NEUROPATHIC PAIN; INTRATHECAL CLONIDINE;
D O I
10.1016/j.neuroscience.2010.11.057
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Norepinephrine and serotonin involvement in nociceptive functions is supported by observations of analgesic effects of norepinephrine transporter (NET) and serotonin transporter (SERT) inhibitors such as amitriptyline. However, the relative contribution of NET and SERT to baseline nociception, as well as amitriptyline analgesia, is unclear. Amitriptyline and morphine analgesia in wild-type (WT) mice and littermates with gene knockout (KO) of SERT, NET or both transporters was conducted using the hotplate and tail-flick tests. Hypoalgesia was observed in NET KO mice, and to a lesser extent in SERT KO mice. The magnitude of this hypoalgesia in NET KO mice was so profound that it limited the assessment of drug-induced analgesia. Nonetheless, the necessary exclusion of these subjects because of profound baseline hypoalgesia strongly supports the role of norepinephrine and NET in basal nociceptive behavior while indicating a much smaller role for serotonin and SERT. To further clarify the role of NET and SERT in basal nociceptive sensitivity further experiments were conducted in SERT KO and NET KO mice across a range of temperatures. NET KO mice were again found to have pronounced thermal hypoalgesia compared to WT mice in both the hotplate and tail-flick tests, while only limited effects were observed in SERT KO mice. Furthermore, in the acetic acid writhing test of visceral nociception pronounced hypoalgesia was again found in NET KO mice, but no change in SERT KO mice. As some of these effects may have resulted from developmental consequences of NET KO, the effects of the selective NET blocker nisoxetine and the selective SERT blocker fluoxetine were also examined in WT mice: only nisoxetine produced analgesia in these mice. Collectively these data suggest that NET has a far greater role in determining baseline analgesia, and perhaps other analgesic effects, than SERT in mice. Published by Elsevier Ltd on behalf of IBRO.
引用
收藏
页码:315 / 327
页数:13
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