Imbe Hiroki, Kimura Akihisa
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. 2016 Oct;127:11-22. doi: 10.1016/j.brainresbull.2016.08.007. Epub 2016 Aug 12.
The rostral ventromedial medulla (RVM) and locus coeruleus (LC) play crucial roles in descending pain modulation system. In the present study we examined the expression of phospho-cAMP response element-binding protein (pCREB) and ΔFosB and the acetylation of histone H3 in the RVM and LC after forced swim stress (FS) and complete Freund's adjuvant (CFA) injection to clarify changes in descending pain modulatory system in a rat model of stress-induced hyperalgesia. FS (day 1, 10min; days 2-3, 20min) induced a significant increase in the expression of pCREB and ΔFosB and the acetylation of histone H3 in the RVM, whereas the FS induced a significant increase only in the acetylation of histone H3 in the LC. CFA injection into the hindpaw did not induce a significant change in those expression and acetylation. Quantitative image analysis demonstrated that the numbers of pCREB-, acetylated histone H3- and ΔFosB-IR cells in the RVM were significantly higher in the FS group than those in the naive group. The CFA injection after the FS did not affect the FS-induced increases in the expression of pCREB and ΔFosB and the acetylation of histone H3 in the RVM even though nullified the increase in the acetylation of histone H3 in the LC. These findings suggest different neuroplasticities between the RVM and LC after the FS, which may be involved in activity change of descending pain modulatory system after the CFA injection.
延髓头端腹内侧区(RVM)和蓝斑(LC)在下行性疼痛调制系统中发挥着关键作用。在本研究中,我们检测了强迫游泳应激(FS)和注射完全弗氏佐剂(CFA)后RVM和LC中磷酸化环磷酸腺苷反应元件结合蛋白(pCREB)、ΔFosB的表达以及组蛋白H3的乙酰化,以阐明应激诱导的痛觉过敏大鼠模型中下行性疼痛调制系统的变化。FS(第1天,10分钟;第2 - 3天,20分钟)诱导RVM中pCREB和ΔFosB的表达以及组蛋白H3的乙酰化显著增加,而FS仅诱导LC中组蛋白H3的乙酰化显著增加。后爪注射CFA并未诱导这些表达和乙酰化的显著变化。定量图像分析表明,FS组RVM中pCREB、乙酰化组蛋白H3和ΔFosB免疫反应阳性细胞的数量显著高于未处理组。FS后注射CFA尽管消除了LC中组蛋白H3乙酰化的增加,但并未影响FS诱导的RVM中pCREB和ΔFosB表达以及组蛋白H3乙酰化的增加。这些发现提示FS后RVM和LC之间存在不同的神经可塑性,这可能与CFA注射后下行性疼痛调制系统的活性变化有关。