首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Antibody array analysis of peripheral and blood cytokine levels in rats after masseter inflammation.
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Antibody array analysis of peripheral and blood cytokine levels in rats after masseter inflammation.

机译:咬肌炎症后大鼠外周血和血液细胞因子水平的抗体阵列分析。

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This study was undertaken to evaluate the changes in cytokine levels in response to orofacial deep tissue inflammation. Inflammation was induced by injecting complete Freund's adjuvant (CFA, 0.05 ml 1:1 oil/saline suspension) into the masseter of the male Sprague-Dawley rat under brief halothane anesthesia. At 30 min, 5 h and 24 h after CFA injection (n = 3-4/time point), tissues were dissected from masseter and total proteins isolated. Rat Cytokine Antibody Array 1.1 (RayBiotech) coated with 19 specific cytokine antibodies were probed with protein samples and the relative cytokine levels were compared. Compared to saline-injected rats, there were significant increases (p < 0.05-0.01) in the levels of seven cytokines in the masseter tissue after CFA, including interleukin (IL)-1beta (5 h), IL-6 (5 h), tumor necrosis factor-alpha (5 h), monocyte chemoattractant protein-1 (5 h, 24 h), cytokine-induced neutrophil chemoattractant-2 and -3 (5 h, 24 h), and tissue inhibitor of metalloproteinase-1 (5 h, 24 h). All 19 cytokines were detected in the blood samples, but they did not show significant changes after inflammation. Masseter hyperalgesia and allodynia occurred at 30 min and persisted at 5-24 h after inflammation, as assessed by probing the skin above the masseter with von Frey filaments. The present results indicate selective localized cytokine responses to masseter inflammation. Although different cytokines exist in the blood, their levels did not mirror, nor did not appear to depend on, the local cytokine levels. The findings provide specific targets for further studying the involvement of cytokines in orofacial inflammation and hyperalgesia.
机译:进行该研究以评估响应于口腔深部组织炎症的细胞因子水平的变化。在短暂的氟烷麻醉下,将完全的弗氏佐剂(CFA,0.05 ml 1:1油/盐水悬浮液)注入雄性Sprague-Dawley大鼠的咬肌中,引起炎症。注射CFA后30分钟,5小时和24小时(n = 3-4 /时间点),从咬肌切开组织并分离总蛋白。用蛋白质样品探测包被有19种特异性细胞因子抗体的大鼠细胞因子抗体阵列1.1(RayBiotech),并比较相对细胞因子水平。与注射盐水的大鼠相比,CFA后咬肌组织中的七种细胞因子的水平显着增加(p <0.05-0.01),包括白介素(IL)-1β(5 h),IL-6(5 h) ,肿瘤坏死因子-α(5 h),单核细胞趋化蛋白1(5 h,24 h),细胞因子诱导的中性粒细胞趋化因子2和-3(5 h,24 h)和金属蛋白酶1( 5小时,24小时)。在血样中检测到所有19种细胞因子,但在炎症后它们并未显示出明显变化。咬肌痛觉过敏和异常性疼痛在发炎后30分钟发生,并在炎症后5-24小时持续,这是通过用von Frey细丝探查咬肌上方的皮肤评估的。本结果表明对咬肌炎症的选择性局部细胞因子反应。尽管血液中存在不同的细胞因子,但是它们的水平并未反映出局部细胞因子水平,也似乎没有依赖于局部细胞因子水平。这些发现为进一步研究细胞因子在口面部炎症和痛觉过敏中的参与提供了具体的目标。

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