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Small interfering RNA targeting NF-κB attenuates lipopolysaccharide-induced acute lung injury in rats

机译:靶向NF-κB的小分子干扰RNA减轻脂多糖诱导的大鼠急性肺损伤

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Background To investigate the anti-inflammatory effects of specific small interfering RNA targeting NF-κB on lipopolysaccharide (LPS)-induced acute lung injury (ALI) in rats. Method Acute lung injury was induced in Sprague-Dawley rats by intraperitoneal injection with LPS (5?mg/kg), followed by immediate intratracheal instillation of siRNA targeting NF-κB p65 (40?μg/ml). Animals in each group were sacrificed at 1?h or 8?h after the instillation. Pulmonary histological changes were evaluated by hematoxylin-eosin staining. The levels of NF-κB and TNF-α were measured by qRT-PCR. Expressions of NF-κB in lung cells and TNF-α in bronchoalveolar lavage fluid (BALF) were determined by western blot analysis and enzyme-linked immunosorbent assay (ELISA) respectively. Results LPS administration reduced the rectal temperature and white blood cell counts at 1?h, increased lung wet/dry weight ratios, caused evident lung histopathological injury, and increased the detectable transcript and cytokine levels of TNF-α in lung tissue in BALF. siRNA targeting of NF-κB p65 effectively abrogated the expression of NF-κB p65 in lung cells and, aside from rectal temperatures, ameliorated all changes induced by LPS. Conclusions NF-κB knockdown exerts anti-inflammatory effects on LPS-induced ALI especially in the initial phase, which may be due in part to reduced levels of the proinflammatory cytokine TNF-α. NF-κB siRNA’s rapidity and effectiveness to abrogate ALI development may provide an effective therapeutic method with future clinical applications.
机译:背景研究靶向NF-κB的特定小干扰RNA对大鼠脂多糖(LPS)诱导的急性肺损伤(ALI)的抗炎作用。方法腹腔注射LPS(5?mg / kg),然后经气管内滴注靶向NF-κBp65(40?μg/ ml)的siRNA,诱发Sprague-Dawley大鼠急性肺损伤。滴注后1小时或8小时将每组动物处死。通过苏木精-伊红染色评价肺组织学变化。通过qRT-PCR测量NF-κB和TNF-α的水平。分别通过蛋白质印迹分析和酶联免疫吸附试验(ELISA)测定肺细胞中NF-κB的表达和支气管肺泡灌洗液(BALF)中的TNF-α的表达。结果LPS给药可降低1?h时的直肠温度和白细胞计数,增加肺干/湿重比,引起明显的肺组织病理学损伤,并增加BALF肺组织中可检测的转录本和细胞因子TNF-α的水平。靶向NF-κBp65的siRNA有效消除了肺细胞中NF-κBp65的表达,除直肠温度外,LPS诱导的所有变化均得到改善。结论NF-κB的抑制对LPS诱导的ALI具有抗炎作用,这可能部分是由于促炎性细胞因子TNF-α水平降低所致。 NF-κBsiRNA消除ALI发育的快速性和有效性可能为将来的临床应用提供有效的治疗方法。

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