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首页> 外文期刊>Molecular pain >Spinal cord stimulation modulates supraspinal centers of the descending antinociceptive system in rats with unilateral spinal nerve injury
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Spinal cord stimulation modulates supraspinal centers of the descending antinociceptive system in rats with unilateral spinal nerve injury

机译:脊髓刺激调节单侧脊髓神经损伤大鼠降神经痛感受系统的脊髓上中心

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摘要

Background The descending antinociceptive system (DAS) is thought to play crucial roles in the antinociceptive effect of spinal cord stimulation (SCS), especially through its serotonergic pathway. The nucleus raphe magnus (NRM) in the rostral ventromedial medulla is a major source of serotonin [5-hydroxytryptamine (5-HT)] to the DAS, but the role of the dorsal raphe nucleus (DRN) in the ventral periaqueductal gray matter is still unclear. Moreover, the influence of the noradrenergic pathway is largely unknown. In this study, we evaluated the involvement of these serotonergic and noradrenergic pathways in SCS-induced antinociception by behavioral analysis of spinal nerve-ligated (SNL) rats. We also investigated immunohistochemical changes in the DRN and locus coeruleus (LC), regarded as the adrenergic center of the DAS, and expression changes of synthetic enzymes of 5-HT [tryptophan hydroxylase (TPH)] and norepinephrine [dopamine β-hydroxylase (DβH)] in the spinal dorsal horn. Results Intrathecally administered methysergide, a 5-HT 1 - and 5-HT 2 -receptor antagonist, and idazoxan, an α 2 -adrenergic receptor antagonist, equally abolished the antinociceptive effect of SCS. The numbers of TPH-positive serotonergic and phosphorylated cyclic AMP response element binding protein (pCREB)-positive neurons and percentage of pCREB-positive serotonergic neurons in the DRN significantly increased after 3-h SCS. Further, the ipsilateral-to-contralateral immunoreactivity ratio of DβH increased in the LC of SNL rats and reached the level seen in na?ve rats, even though the number of pCREB-positive neurons in the LC was unchanged by SNL and SCS. Moreover, 3-h SCS did not increase the expression levels of TPH and DβH in the spinal dorsal horn. Conclusions The serotonergic and noradrenergic pathways of the DAS are involved in the antinociceptive effect of SCS, but activation of the DRN might primarily be responsible for this effect, and the LC may have a smaller contribution. SCS does not potentiate the synthetic enzymes of 5HT and norepinephrine in the neuropathic spinal cord.
机译:背景技术降级抗伤害感受系统(DAS)被认为在脊髓刺激(SCS)的抗伤害感受作用中起着至关重要的作用,尤其是通过其血清素能途径。延髓腹侧延髓中的核中缝大核(NRM)是5-羟色胺[5-羟色胺(5-HT)]进入DAS的主要来源,但是背侧中缝核(DRN)在腹腔导水管周围灰质中的作用是仍不清楚。此外,去甲肾上腺素途径的影响在很大程度上是未知的。在这项研究中,我们通过对脊髓神经结扎(SNL)大鼠的行为分析,评估了这些血清素能和去甲肾上腺素能途径在SCS诱导的抗伤害感受中的作用。我们还研究了DRN和肾小球蓝斑(LC)(被认为是DAS的肾上腺能中心)的免疫组织化学变化,以及5-HT [色氨酸羟化酶(TPH)]和去甲肾上腺素[多巴胺β-羟化酶(DβH)的合成酶的表达变化)]在脊髓背角。结果鞘内注射5-HT 1和5-HT 2受体拮抗剂美塞麦德和α2肾上腺素能受体拮抗剂艾达唑烷同样消除了SCS的镇痛作用。 3 h SCS后,DRN中TPH阳性的血清素能和磷酸化的环状AMP反应元件结合蛋白(pCREB)阳性神经元的数量以及pCREB阳性的血清素神经元的百分比显着增加。此外,即使SNL和SCS改变了LC中pCREB阳性神经元的数量,SNL大鼠LC中DβH的同侧对对侧免疫反应比也增加了,达到了幼稚大鼠中观察到的水平。此外,3 h SCS不会增加脊髓背角中TPH和DβH的表达水平。结论DAS的血清素能和去甲肾上腺素能途径参与了SCS的抗伤害感受作用,但DRN的激活可能是造成这种作用的主要原因,而LC的贡献可能较小。 SCS不能增强神经病性脊髓中5HT和去甲肾上腺素的合成酶。

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