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前额叶皮质代谢型谷氨酸受体 5 的上调介导了大鼠脊髓神经损伤后的神经病理性疼痛和负性情绪症状。

Upregulation of prefrontal metabotropic glutamate receptor 5 mediates neuropathic pain and negative mood symptoms after spinal nerve injury in rats.

机构信息

Department of Physiology, Seoul National University College of Medicine, Seoul, Korea.

Department of Brain and Cognitive Sciences, Seoul National University College of Natural Sciences, Seoul, Korea.

出版信息

Sci Rep. 2017 Aug 29;7(1):9743. doi: 10.1038/s41598-017-09991-8.

Abstract

Patients with chronic pain easily accompany the negative mood symptoms such as depression and anxiety, and these disturbances in turn affect the aversive perception of pain. However, the underlying mechanisms are largely unknown. We hypothesized that the alteration of metabotropic glutamate receptor 5 (mGluR5) in the brain region underlies such a comorbidity of aversive states. We scanned the brain of chronic neuropathic pain model rats using positron emission tomography (PET) technique with an mGluR5-selective radiotracer [11C] ABP688 and found various brain regions with higher or lower level of mGluR5 compared to control rats. Among the brain areas, a prominent upregulation of mGluR5 was shown in the prelimbic region (PrL) of the medial prefrontal cortex (mPFC) of chronic neuropathic pain animals. A pharmacological blockade of upregulated mGluR5 in the PrL ameliorated the negative symptoms including tactile hypersensitivity and depressive-like behavior, which relieved the subjects from the unpleasant state of chronic neuropathic pain condition. Conversely, lentiviral overexpression of the mGluR5 in the PrL of naïve rats successfully induced comorbid pain and negative moods. Our data provide deeper insight into the shared mechanism of pain perception and negative emotions, identifying a therapeutic target for the treatment of chronic pain and mood disorders.

摘要

患有慢性疼痛的患者容易伴随抑郁和焦虑等负面情绪症状,而这些干扰反过来又会影响对疼痛的厌恶感知。然而,其潜在机制在很大程度上尚不清楚。我们假设,大脑区域中代谢型谷氨酸受体 5(mGluR5)的改变是这种厌恶状态共病的基础。我们使用正电子发射断层扫描(PET)技术,通过 mGluR5 选择性放射性示踪剂 [11C] ABP688 对慢性神经性疼痛模型大鼠的大脑进行了扫描,与对照组大鼠相比,发现大脑中有多个区域的 mGluR5 水平较高或较低。在这些大脑区域中,慢性神经性疼痛动物的内侧前额叶皮质(mPFC)的额前皮质(PrL)中 mGluR5 的上调尤为明显。PrL 中上调的 mGluR5 的药理学阻断改善了包括触觉过敏和抑郁样行为在内的负面症状,使受试者摆脱了慢性神经性疼痛状态的不愉快状态。相反,在天真大鼠的 PrL 中过表达 mGluR5 可成功诱导共病性疼痛和负面情绪。我们的数据提供了对疼痛感知和负面情绪的共同机制的更深入了解,确定了治疗慢性疼痛和情绪障碍的治疗靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/890f/5575341/493de00e1ff6/41598_2017_9991_Fig1_HTML.jpg

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