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大鼠脊髓横断后 5-羟色胺 2A 受体表达的时程:一项免疫组织化学研究。

The time course of serotonin 2A receptor expression after spinal transection of rats: an immunohistochemical study.

机构信息

Department of Neuroscience and Pharmacology, University of Copenhagen, Blegdamsvej 3, DK-2200, Copenhagen, Denmark.

出版信息

Neuroscience. 2011 Mar 17;177:114-26. doi: 10.1016/j.neuroscience.2010.12.062. Epub 2011 Jan 4.

DOI:10.1016/j.neuroscience.2010.12.062
PMID:21211552
Abstract

Hyperexcitability of motoneurons is one of the key mechanism that has been demonstrated to underlie the pathogenesis of spasticity after spinal injury. Serotonin (5-HT) denervation supersensitivity is one of the mechanisms underlying this increased motoneuron excitability. In this study, to examine whether the supersensitivity is caused by 5-HT receptor upregulation we investigated changes in levels of 5-HT2A receptor immunoreactivity (5-HT2AR-IR) following a spinal transection in the sacral spinal cord of rats at seven different time points post injury: 2, 8, 16 h, and 1, 2, 7 and 28 days, respectively. 5-HT2AR-IR density was analyzed in motoneurons (regions containing their somata and dendrites) in the spinal segments below the lesion. The results showed no significant changes in 5-HT2AR-IR in the motoneurons up to 16 h following the transection. After 1-day, however the levels of 5-HT2AR-IR increased in the motoneurons and their dendrites, with the density level being 3.4-fold higher in spinalized rats than in sham-operated rats. The upregulation increased progressively until a maximal level was reached at 28 days post-injury. We also investigated 5-HT and 5-HT transporter expressions at five different post injury time points: 1, 2, 7, 21 and 60 days and they showed concurrent down-regulation changes after 2 days. These results suggest that the upregulation of 5-HT2ARs may at least partly underlie the development of 5-HT denervation supersensitivity in spinal motoneurons following spinal injury and thereby implicates their involvement in the pathogenesis of the subsequent development of spasticity.

摘要

运动神经元的过度兴奋是脊髓损伤后痉挛发病机制的关键机制之一。5-羟色胺(5-HT)去神经超敏是这种运动神经元兴奋性增加的机制之一。在这项研究中,为了研究这种超敏反应是否是由 5-HT 受体上调引起的,我们在脊髓损伤后七个不同时间点(分别为损伤后 2、8、16 小时和 1、2、7 和 28 天),在大鼠的骶髓脊髓横断后,分别研究了 5-HT2A 受体免疫反应性(5-HT2AR-IR)水平的变化。5-HT2AR-IR 密度在损伤以下脊髓节段的运动神经元(包含其体和树突的区域)中进行分析。结果显示,在横断后 16 小时内,运动神经元中的 5-HT2AR-IR 没有明显变化。然而,在 1 天后,运动神经元及其树突中的 5-HT2AR-IR 水平增加,脊髓切断大鼠的密度水平比假手术大鼠高 3.4 倍。这种上调逐渐增加,直到在损伤后 28 天达到最大值。我们还在五个不同的损伤后时间点(1、2、7、21 和 60 天)研究了 5-HT 和 5-HT 转运体的表达,结果显示它们在 2 天后同时发生下调变化。这些结果表明,5-HT2AR 的上调可能至少部分解释了脊髓损伤后脊髓运动神经元中 5-HT 去神经超敏的发展,从而暗示它们参与了随后痉挛发展的发病机制。

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