Bassi Gabriel Shimizu, Dias Daniel Penteado Martins, Franchin Marcelo, Talbot Jhimmy, Reis Daniel Gustavo, Menezes Gustavo Batista, Castania Jaci Airton, Garcia-Cairasco Norberto, Resstel Leonardo Barbosa Moraes, Salgado Helio Cesar, Cunha Fernando Queiróz, Cunha Thiago Mattar, Ulloa Luis, Kanashiro Alexandre
Department of Immunology, Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, SP, Brazil.
Department of Physiology, Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, SP, Brazil.
Brain Behav Immun. 2017 Aug;64:330-343. doi: 10.1016/j.bbi.2017.04.003. Epub 2017 Apr 6.
Articular inflammation is a major clinical burden in multiple inflammatory diseases, especially in rheumatoid arthritis. Biological anti-rheumatic drug therapies are expensive and increase the risk of systemic immunosuppression, infections, and malignancies. Here, we report that vagus nerve stimulation controls arthritic joint inflammation by inducing local regulation of innate immune response. Most of the previous studies of neuromodulation focused on vagal regulation of inflammation via the efferent peripheral pathway toward the viscera. Here, we report that vagal stimulation modulates arthritic joint inflammation through a novel "afferent" pathway mediated by the locus coeruleus (LC) of the central nervous system. Afferent vagal stimulation activates two sympatho-excitatory brain areas: the paraventricular hypothalamic nucleus (PVN) and the LC. The integrity of the LC, but not that of the PVN, is critical for vagal control of arthritic joint inflammation. Afferent vagal stimulation suppresses articular inflammation in the ipsilateral, but not in the contralateral knee to the hemispheric LC lesion. Central stimulation is followed by subsequent activation of joint sympathetic nerve terminals inducing articular norepinephrine release. Selective adrenergic beta-blockers prevent the effects of articular norepinephrine and thereby abrogate vagal control of arthritic joint inflammation. These results reveals a novel neuro-immune brain map with afferent vagal signals controlling side-specific articular inflammation through specific inflammatory-processing brain centers and joint sympathetic innervations.
关节炎症是多种炎症性疾病的主要临床负担,尤其是在类风湿性关节炎中。生物抗风湿药物治疗昂贵,且会增加全身免疫抑制、感染和恶性肿瘤的风险。在此,我们报告迷走神经刺激通过诱导对先天免疫反应的局部调节来控制关节炎关节炎症。此前大多数神经调节研究集中于迷走神经通过传出外周通路对内脏炎症的调节。在此,我们报告迷走神经刺激通过由中枢神经系统蓝斑(LC)介导的一条新的“传入”通路调节关节炎关节炎症。传入性迷走神经刺激激活两个交感神经兴奋脑区:室旁下丘脑核(PVN)和蓝斑。蓝斑而非室旁下丘脑核的完整性对于迷走神经对关节炎关节炎症的控制至关重要。传入性迷走神经刺激抑制同侧而非对侧膝关节至半球蓝斑损伤处的关节炎症。中枢刺激随后会激活关节交感神经末梢,诱导关节去甲肾上腺素释放。选择性肾上腺素能β受体阻滞剂可阻止关节去甲肾上腺素的作用,从而消除迷走神经对关节炎关节炎症的控制。这些结果揭示了一种新的神经免疫脑图谱,其中传入性迷走神经信号通过特定的炎症处理脑中心和关节交感神经支配控制特定侧的关节炎症。