Department of Medicine, Division of Pulmonary, Allergy and Critical Care Medicine, Emory University and Atlanta VA Medical Center, Atlanta, GA 30033, USA.
PPAR Res. 2012;2012:617063. doi: 10.1155/2012/617063. Epub 2012 Jul 26.
Acute lung injury (ALI) is an inflammatory condition culminating in respiratory failure. There is currently no effective pharmacological treatment. Nitrated fatty acids (NFAs) have been shown to exert anti-inflammatory effects. We therefore hypothesized that delivery of NFAs directly to the site of inflammation would reduce the severity of ALI. Pulmonary delivery of 10-nitro-oleate following endotoxin-induced ALI in mice reduced markers of lung inflammation and injury, including capillary leakage, lung edema, infiltration of neutrophils into the lung, and oxidant stress, as well as plasma levels of proinflammatory cytokines. Nitro-oleate delivery likewise downregulated expression of proinflammatory genes by alveolar macrophages, key cells in regulation of lung inflammation. These effects may be accounted for by the observed increases in the activity of PPAR-γ and the PPAR-γ-induced antioxidant transcription factor Nrf2, together with the decreased activity of NF-κB. Our results demonstrate that pulmonary delivery of NFAs reduces severity of acute lung injury and suggest potential utility of these molecules in other inflammatory lung diseases.
急性肺损伤(ALI)是一种炎症性疾病,最终导致呼吸衰竭。目前尚无有效的药物治疗方法。硝酰基脂肪酸(NFAs)已被证明具有抗炎作用。因此,我们假设将 NFAs 直接输送到炎症部位会减轻 ALI 的严重程度。在小鼠内毒素诱导的 ALI 后,通过肺部输送 10-硝基-油酸可降低肺炎症和损伤的标志物,包括毛细血管渗漏、肺水肿、中性粒细胞浸润到肺部和氧化应激,以及促炎细胞因子的血浆水平。同样,硝酰基油酸的输送也下调了肺泡巨噬细胞中促炎基因的表达,肺泡巨噬细胞是调节肺炎症的关键细胞。这些作用可能归因于观察到的 PPAR-γ 活性增加和 PPAR-γ 诱导的抗氧化转录因子 Nrf2 以及 NF-κB 活性降低。我们的研究结果表明,通过肺部输送 NFAs 可减轻急性肺损伤的严重程度,并提示这些分子在其他炎症性肺病中的潜在应用价值。