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神经病理性疼痛模型中两个大鼠 mas 相关基因的调控

Regulation of two rat mas-related genes in a model of neuropathic pain.

作者信息

Gustafson Eric L, Maguire Maureen, Campanella Marilena, Tarozzo Glauco, Jia Yuping, Dong Xiao-Wei, Laverty Maureen, Murgolo Nicholas, Priestley Tony, Reggiani Angelo, Monsma Frederick, Beltramo Massimo

机构信息

Department of Discovery Technologies, Schering-Plough Research Institute, Kenilworth, NJ, USA.

出版信息

Brain Res Mol Brain Res. 2005 Dec 7;142(1):58-64. doi: 10.1016/j.molbrainres.2005.09.014. Epub 2005 Oct 24.

DOI:10.1016/j.molbrainres.2005.09.014
PMID:16246453
Abstract

The mas-related gene (Mrg) family is a large family of G-protein-coupled receptors which are variable in number depending on species. The so-called sensory-neuron-specific receptors (SNSRs) make up a subset of the Mrg family, and several of these have been implicated in nociceptive processes. To verify their specific localization in sensory ganglia, we have determined the expression patterns of two of them, rMrgA and rMrgC, in a panel of rat tissues. The quantitative PCR results in the rat tissue panel indicate that, while several non-neuronal tissues contain significant levels of mRNA for both receptors, these two receptors are most highly expressed in dorsal root ganglia and trigeminal ganglia. Given this, we have examined the effects of spinal nerve ligation (SNL) on the expression of these genes. Peripheral neuropathy induced by ligation of spinal nerves at L5 and L6 resulted in a pronounced mechanical allodynia. These behavioral changes in tactile sensitivity were accompanied by significant decreases (10- to 100-fold) in the mRNA expression of both rMrgA and rMrgC exclusively in the L5 and L6 dorsal root ganglia ipsilateral to the SNL. In situ hybridization studies demonstrated that this decrease did not result from neuronal loss but rather from a reduction in the hybridization signals for rMrgC over small-to-medium diameter L5 and L6 dorsal root ganglia neurons. While the functional implications of the altered regulation of rMrgA and rMrgC in neuropathic pain models remain unclear, the results suggest that therapeutics targeting these receptors may have limited utility.

摘要

Mas相关基因(Mrg)家族是一类G蛋白偶联受体大家族,其数量因物种而异。所谓的感觉神经元特异性受体(SNSR)构成了Mrg家族的一个亚群,其中一些与伤害感受过程有关。为了验证它们在感觉神经节中的特异性定位,我们确定了其中两个受体rMrgA和rMrgC在一组大鼠组织中的表达模式。大鼠组织组的定量PCR结果表明,虽然几种非神经组织中这两种受体的mRNA水平都很高,但这两种受体在背根神经节和三叉神经节中表达最高。鉴于此,我们研究了脊神经结扎(SNL)对这些基因表达的影响。L5和L6水平结扎脊神经诱导的周围神经病变导致明显的机械性异常性疼痛。触觉敏感性的这些行为变化伴随着仅在SNL同侧的L5和L6背根神经节中rMrgA和rMrgC的mRNA表达显著降低(10至100倍)。原位杂交研究表明,这种降低不是由于神经元丢失,而是由于rMrgC在L5和L6中小直径背根神经节神经元上的杂交信号减少。虽然在神经性疼痛模型中rMrgA和rMrgC调节改变的功能意义尚不清楚,但结果表明靶向这些受体的治疗方法可能效用有限。

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引用本文的文献

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Expression and distribution patterns of Mas-related gene receptor subtypes A-H in the mouse intestine: inflammation-induced changes.Mas 相关基因受体亚型 A-H 在小鼠肠道中的表达和分布模式:炎症诱导的变化。
Histochem Cell Biol. 2013 May;139(5):639-58. doi: 10.1007/s00418-013-1086-9. Epub 2013 Mar 17.
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The effect of inflammation on the expression and distribution of the MAS-related gene receptors MrgE and MrgF in the murine ileum.
炎症对小鼠回肠中 MAS 相关基因受体 MrgE 和 MrgF 的表达和分布的影响。
Histochem Cell Biol. 2011 Nov;136(5):569-85. doi: 10.1007/s00418-011-0862-7. Epub 2011 Sep 13.
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The effect of deletion of the orphan G - protein coupled receptor (GPCR) gene MrgE on pain-like behaviours in mice.孤儿G蛋白偶联受体(GPCR)基因MrgE缺失对小鼠疼痛样行为的影响。
Mol Pain. 2008 Jan 15;4:2. doi: 10.1186/1744-8069-4-2.