Department of Physiology, Wakayama Medical University, Kimiidera 811-1, Wakayama City, 641-8509, Japan.
Department of Physiology, Wakayama Medical University, Kimiidera 811-1, Wakayama City, 641-8509, Japan.
Brain Res Bull. 2017 Sep;134:253-261. doi: 10.1016/j.brainresbull.2017.08.013. Epub 2017 Sep 1.
The perception and response to pain are severely impacted by exposure to stressors. In some animal models, stress increases pain sensitivity, which is termed stress-induced hyperalgesia (SIH). The insular cortex (IC) and anterior cingulate cortex (ACC), which are typically activated by noxious stimuli, affect pain perception through the descending pain modulatory system. In the present study, we examined the expression of phospho-cAMP response element-binding protein (pCREB) and early growth response 1 (Egr1) in the IC and ACC at 3h (the acute phase of peripheral tissue inflammation) after complete Freund's adjuvant (CFA) injection in naïve rats and rats preconditioned with forced swim stress (FS) to clarify the effect of FS, a stressor, on cortical cell activities in the rats showing SIH induced by FS. The CFA injection into the hindpaw induced mechanical hypersensitivity and increased the expression of the pCREB and Egr1 in the IC and ACC at 3h after the injection. FS (day 1, 10min; days 2-3, 20min) prior to the CFA injection enhanced the CFA-induced mechanical hypersensitivity and attenuated the increase in the expression of pCREB and Egr1 in the IC and ACC. These findings suggested that FS modulates the CFA injection-induced neuroplasticity in the IC and ACC to enhance the mechanical hypersensitivity. These findings are thought to signify stressor-induced dysfunction of the descending pain modulatory system.
应激暴露严重影响疼痛的感知和反应。在一些动物模型中,应激会增加疼痛敏感性,这被称为应激诱导性痛觉过敏(SIH)。岛叶皮层(IC)和前扣带皮层(ACC)通常对伤害性刺激激活,通过下行疼痛调制系统影响疼痛感知。在本研究中,我们在弗氏完全佐剂(CFA)注射后 3 小时(外周组织炎症的急性期)检查了未处理大鼠和强迫游泳应激(FS)预处理大鼠的 IC 和 ACC 中磷酸化 cAMP 反应元件结合蛋白(pCREB)和早期生长反应 1(Egr1)的表达,以阐明 FS(应激源)对 FS 诱导的 SIH 大鼠皮质细胞活性的影响。足底注射 CFA 会引起机械性痛觉过敏,并在注射后 3 小时增加 IC 和 ACC 中 pCREB 和 Egr1 的表达。在 CFA 注射之前进行 FS(第 1 天,10 分钟;第 2-3 天,20 分钟)会增强 CFA 诱导的机械性痛觉过敏,并减弱 IC 和 ACC 中 pCREB 和 Egr1 表达的增加。这些发现表明,FS 调节了 CFA 注射诱导的 IC 和 ACC 中的神经可塑性,以增强机械性痛觉过敏。这些发现被认为标志着下行疼痛调制系统的应激诱导功能障碍。