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首页> 外文期刊>Molecular pain >The effect of deletion of the orphan G – protein coupled receptor (GPCR) gene MrgE on pain-like behaviours in mice
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The effect of deletion of the orphan G – protein coupled receptor (GPCR) gene MrgE on pain-like behaviours in mice

机译:孤儿G蛋白偶联受体(MPCR)基因MrgE的缺失对小鼠疼痛样行为的影响

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Background The orphan GPCR MrgE is one of an extended family of GPCRs that are expressed in dorsal root ganglia (DRG). Based on these expression patterns it has been suggested that GPCRs like MrgE may play a role in nociception however, to date, no direct supporting evidence has emerged. We generated mutant mice lacking MrgE and examined the effects of deletion of this gene in three pain behavioural models. The effect of MrgE gene deletion on expression of Mrgs and genes involved in sensory neurone function was also investigated. Results The absence of MrgE had no effect on the development of pain responses to a noxious chemical stimulus or an acute thermal stimulus. However, in contrast, the development but not the maintenance of neuropathic pain was affected by deletion of MrgE. The expression of Mrg genes was not significantly affected in the MrgE knockout (KO) mice with the sole exception of MrgF. In addition, the expression of 77 of 84 genes involved in sensory neuron development and function was also unaffected by deletion of MrgE. Of the 7 genes affected by MrgE deletion, 4 have previously been implicated in nociception. Conclusion The data suggests that MrgE may play a role in selective pain behavioural responses in mice.
机译:背景孤儿GPCR MrgE是在背根神经节(DRG)中表达的GPCR扩展家族之一。基于这些表达模式,已经提出了类似MrgE的GPCR可能在伤害感受中起作用,但是,迄今为止,还没有直接的支持证据出现。我们生成了缺少MrgE的突变小鼠,并在三种疼痛行为模型中研究了该基因缺失的影响。还研究了MrgE基因缺失对Mrgs表达和涉及感觉神经元功能的基因的影响。结果MrgE的缺乏对有害化学刺激或急性热刺激的疼痛反应的发展没有影响。然而,相反,MrgE的缺失影响神经性疼痛的发展而不是维持。除了MrgF以外,MrgE基因敲除(KO)小鼠中Mrg基因的表达没有受到显着影响。此外,MrgE的缺失也不会影响涉及感觉神经元发育和功能的84个基因中的77个基因的表达。在受MrgE缺失影响的7个基因中,先前有4个与伤害感受有关。结论数据表明MrgE可能在小鼠选择性疼痛行为反应中起作用。

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