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疼痛加剧慢性轻度应激诱导的大鼠去甲肾上腺素能传递变化。

Pain exacerbates chronic mild stress-induced changes in noradrenergic transmission in rats.

机构信息

Neuropsychopharmacology and Psychobiology Research Group, Department of Neuroscience, University of Cádiz, 11003 Cádiz, Spain; Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Instituto de Salud Carlos III, 28007 Madrid, Spain.

Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Instituto de Salud Carlos III, 28007 Madrid, Spain; Neuropsychopharmacology and Psychobiology Research Group, Psychobiology Area, Department of Psychology, University of Cadiz, Campus Universitario Rio San Pedro s/n, 11510 Cádiz, Spain.

出版信息

Eur Neuropsychopharmacol. 2014 Jun;24(6):996-1003. doi: 10.1016/j.euroneuro.2014.01.011. Epub 2014 Jan 18.

Abstract

Depression can influence pain and vice versa, yet the biological mechanisms underlying how one influences the pathophysiology of the other remains unclear. Dysregulation of locus coeruleus-noradrenergic transmission is implicated in both conditions, although it is not known whether this effect is exacerbated in cases of co-morbid depression and chronic pain. We studied locus coeruleus activity using immunofluorescence and electrophysiological approaches in rats subjected to unpredictable chronic mild stress (CMS, an experimental model of depression) and/or chronic constriction injury (CCI, a model of chronic neuropathic pain) for 2 weeks. CCI alone had no effect on any of the locus coeruleus parameters studied, while CMS led to a slight reduction in the electrophysiological activity of the locus coeruleus. Furthermore, CMS was associated with an increase in the number of tyrosine hydroxylase-positive cells in the locus coeruleus, although they were smaller in size. Interestingly, these effects of CMS were exacerbated when combined with CCI, even though no changes in the α2-adrenoreceptors or the noradrenaline transporter were observed in any group. Together, these findings suggest that CMS triggers several modifications in locus coeruleus-noradrenergic transmission that are exacerbated by co-morbid chronic pain.

摘要

抑郁症会影响疼痛,反之亦然,但目前尚不清楚其中一种疾病如何影响另一种疾病的病理生理学的生物学机制。蓝斑-去甲肾上腺素能传递的失调与这两种情况都有关,尽管尚不清楚这种影响是否在伴有抑郁和慢性疼痛的情况下加剧。我们使用免疫荧光和电生理方法研究了接受不可预测性慢性轻度应激(CMS,抑郁的实验模型)和/或慢性缩窄性损伤(CCI,慢性神经病理性疼痛模型)2 周的大鼠的蓝斑活动。CCI 单独对研究的任何蓝斑参数均无影响,而 CMS 导致蓝斑的电生理活性略有降低。此外,CMS 与蓝斑中酪氨酸羟化酶阳性细胞数量增加有关,尽管这些细胞的体积较小。有趣的是,尽管在任何组中都没有观察到 α2-肾上腺素能受体或去甲肾上腺素转运体的变化,但 CMS 的这些作用在与 CCI 合并时加剧。这些发现表明,CMS 引发了蓝斑-去甲肾上腺素能传递的几种改变,这些改变在合并慢性疼痛时加剧。

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