Institut des Neurosciences Cellulaires et Intégratives, Centre National de la Recherche Scientifique, Strasbourg, France.
Biol Psychiatry. 2011 Nov 15;70(10):946-53. doi: 10.1016/j.biopsych.2011.07.017. Epub 2011 Sep 3.
Chronic pain is clinically associated with the development of affective disorders. However, studies in animal models of neuropathic pain are contradictory and the relationship with mood disorders remains unclear. In this study, we aimed to characterize the affective consequences of neuropathic pain over time and to study potential underlying mechanisms.
Neuropathic pain was induced by inserting a polyethylene cuff around the main branch of the right sciatic nerve in C57BL/6J mice. Anxiety- and depression-related behaviors were assessed over 2 months, using a battery of tests, such as elevated plus maze, marble burying, novelty suppressed feeding, splash test, and forced swimming test. Plasma corticosterone levels were assessed by radioimmunoassay. We also investigated changes in cyclic adenosine monophosphate response element (CRE) activity using CRE-LacZ transgenic mice.
Mice developed anxiety-related behavior 4 weeks after induction of the neuropathy, and depression-related behaviors were observed after 6 to 8 weeks. Control and neuropathic mice did not differ for basal or stress-induced levels of corticosterone or for hypothalamic-pituitary-adrenal axis negative feedback. After 8 weeks, the CRE-mediated activity decreased in the outer granule layer of dentate gyrus of neuropathic mice but not in the amygdala or in the anterior cingulate cortex.
Our results demonstrate that the affective consequences of neuropathic pain evolve over time, independently from the hypothalamic-pituitary-adrenal axis, which remains unaffected. CRE-mediated transcription within a limbic structure was altered at later time points of the neuropathy. These experiments provide a preclinical model to study time-dependent development of mood disorders and the underlying mechanism in a neuropathic pain context.
慢性疼痛与情感障碍的发展在临床上相关。然而,神经病理性疼痛动物模型的研究结果相互矛盾,与心境障碍的关系仍不清楚。在这项研究中,我们旨在随着时间的推移描述神经病理性疼痛的情感后果,并研究潜在的潜在机制。
通过将聚乙烯袖套插入 C57BL/6J 小鼠右侧坐骨神经主支周围,诱导神经病理性疼痛。使用高架十字迷宫、埋珠、新颖性抑制进食、飞溅试验和强迫游泳试验等一系列试验,在 2 个月内评估焦虑和抑郁相关行为。通过放射免疫测定评估血浆皮质酮水平。我们还使用 CRE-LacZ 转基因小鼠研究环磷酸腺苷反应元件 (CRE) 活性的变化。
在诱导神经病变后 4 周,小鼠出现焦虑相关行为,在 6 至 8 周后观察到抑郁相关行为。对照和神经病变小鼠在基础或应激诱导的皮质酮水平或下丘脑-垂体-肾上腺轴负反馈方面没有差异。8 周后,神经病变小鼠齿状回外颗粒层的 CRE 介导的活性降低,但杏仁核或前扣带皮层没有。
我们的研究结果表明,神经病理性疼痛的情感后果随着时间的推移而演变,与下丘脑-垂体-肾上腺轴无关,后者不受影响。在神经病变的后期时间点,边缘结构中的 CRE 介导的转录发生改变。这些实验提供了一种临床前模型,用于研究在神经病理性疼痛背景下心境障碍的时间依赖性发展及其潜在机制。