首页> 美国卫生研究院文献>The Journal of Pharmacology and Experimental Therapeutics >Neuropeptides CRH SP HK-1 and Inflammatory Cytokines IL-6 and TNF Are Increased in Serum of Patients with Fibromyalgia Syndrome Implicating Mast Cells
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Neuropeptides CRH SP HK-1 and Inflammatory Cytokines IL-6 and TNF Are Increased in Serum of Patients with Fibromyalgia Syndrome Implicating Mast Cells

机译:纤维肌痛综合征患者的血清中神经肽CRHSPHK-1和炎性细胞因子IL-6和TNF升高提示肥大细胞

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摘要

Fibromyalgia syndrome (FMS) is a chronic, idiopathic condition of widespread musculoskeletal pain affecting more women than men. Even though clinical studies have provided evidence of altered central pain pathways, the lack of definitive pathogenesis or reliable objective markers has hampered development of effective treatments. Here we report that the neuropeptides corticotropin-releasing hormone (CRH), substance P (SP), and SP-structurally-related hemokinin-1 (HK-1) were significantly (P = 0.026, P < 0.0001, and P = 0.002, respectively) elevated (0.82 ± 0.57 ng/ml, 0.39 ± 0.18 ng/ml, and 7.98 ± 3.12 ng/ml, respectively) in the serum of patients with FMS compared with healthy controls (0.49 ± 0.26 ng/ml, 0.12 ± 0.1 ng/ml, and 5.71 ± 1.08 ng/ml, respectively). Moreover, SP and HK-1 levels were positively correlated (Pearson r = 0.45, P = 0.002) in FMS. The serum concentrations of the inflammatory cytokines interleukin (IL)-6 and tumor necrosis factor (TNF) were also significantly (P = 0.029 and P = 0.006, respectively) higher (2.97 ± 2.35 pg/ml and 0.92 ± 0.31 pg/ml, respectively) in the FMS group compared with healthy subjects (1.79 ± 0.62 pg/ml and 0.69 ± 0.16 pg/ml, respectively). In contrast, serum IL-31 and IL-33 levels were significantly lower (P = 0.0001 and P = 0.044, respectively) in the FMS patients (849.5 ± 1005 pg/ml and 923.2 ± 1284 pg/ml, respectively) in comparison with healthy controls (1281 ± 806.4 pg/ml and 3149 ± 4073 pg/ml, respectively). FMS serum levels of neurotensin were not different from controls. We had previously shown that CRH and SP stimulate IL-6 and TNF release from mast cells (MCs). Our current results indicate that neuropeptides could stimulate MCs to secrete inflammatory cytokines that contribute importantly to the symptoms of FMS. Treatment directed at preventing the secretion or antagonizing these elevated neuroimmune markers, both centrally and peripherally, may prove to be useful in the management of FMS.
机译:纤维肌痛综合征(FMS)是一种广泛存在的肌肉骨骼疼痛的慢性特发性疾病,受累的女性多于男性。即使临床研究提供了改变中枢性疼痛途径的证据,但缺乏确定的发病机制或可靠的客观标志物仍阻碍了有效治疗的发展。在这里,我们报道神经肽促肾上腺皮质激素释放激素(CRH),物质P(SP)和与SP结构相关的血红素1(HK-1)显着(P = 0.026,P <0.0001和P = 0.002,与健康对照组相比(分别为0.82±0.57 ng / ml,0.39±0.18 ng / ml和7.98±3.12 ng / ml),FMS患者的血清与健康对照组相比分别升高(0.49±0.26 ng / ml,0.12±0.1 ng / ml和5.71±1.08 ng / ml)。此外,FMS中SP和HK-1水平呈正相关(Pearson r = 0.45,P = 0.002)。炎性细胞因子白介素(IL)-6和肿瘤坏死因子(TNF)的血清浓度也显着较高(分别为P = 0.029和P = 0.006)(2.97±2.35 pg / ml和0.92±0.31 pg / ml, FMS组与健康受试者相比(分别为1.79±0.62 pg / ml和0.69±0.16 pg / ml)。相反,FMS患者的血清IL-31和IL-33水平显着降低(分别为P = 0.0001和P = 0.044)(分别为849.5±1005 pg / ml和923.2±1284 pg / ml)。健康对照(分别为1281±806.4 pg / ml和3149±4073 pg / ml)。 FMS血清神经降压素水平与对照组无差异。先前我们已经表明CRH和SP刺激肥大细胞(MC)释放IL-6和TNF。我们目前的结果表明,神经肽可以刺激MC分泌促成FMS症状的炎症细胞因子。旨在防止在中央和外周分泌或拮抗这些升高的神经免疫标志物的治疗可能被证明可用于FMS的管理。

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