国际麻醉学与复苏杂志   2016, Issue (10): 5-5
    
急性肺损伤中过氧化物酶体增殖物激活受体γ通路参与的保护作用的阶段性研究
冯迪, 朱梦怡, 吕欣1()
1.上海市肺科医院
Research progress of PPAR pathway involved in protection against acute lung injury
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摘要:

摘要: 背景 急性肺损伤在临床上主要表现为严重的低氧血症、弥漫性肺浸润和肺微血管通透性增高所致的肺水肿。目前认为,急性肺损伤的主要发病机制为炎症反应失衡,促炎因子大量释放。过氧化物酶体增值物激活受体γ是调节目的基因表达的核内受体转录因子超家族成员,主要表达于脂肪组织以及巨噬细胞和其它脂肪贮存细胞。 目的 介绍过氧化物酶体增值物激活受体γ在急性肺损伤中的保护作用。 内容 过氧化物酶体增值物激活受体γ能降低凋亡抑制因子NF-κB的活性,具有广泛的抗炎作用,近年来的研究发现其在急性肺损伤的保护方面具有重要作用。 趋向 为预防和治疗急性肺损伤提供新思路。

关键词: 过氧化物酶体增殖物激活受体γ;急性肺损伤;炎症
Abstract:

Background ALI(acute lung injury,ALI) is characterized by severe hypoxemia, diffuse pulmonary infiltration and increased pulmonary microvascular permeability accompanied by pulmonary edema. Untill the present moment, the main pathogenesis underlying ALI is the imbalance of inflammation reaction and release of abundant proinflammatory factor. PPARγ(Peroxisome Proliferator Activated Receptor) is the superfamily member of nuclear receptor transcription factor. PPARγ(Peroxisome Proliferator Activated Receptor-gama) belong to a subfamily of the nuclear receptor superfamily, which regulate the expression of its target genes and are mainly expressed on adipose tissue,macrophages as well as other fat- storing cells. Objective Introduction PPAR pathway involved in protection against acute lung injury. Content PPARγ can downregulate the activity of apoptosis inhibitory factor NF-κB and possesses extensive anti-inflammatory action. Furthermore, recent researches have discoveried that PPARγtakes an important role in protection against ALI. Trend Provide new ideas for prevention and treatment of acute lung injury.

Key words: PPARγ, ALI, inflammation.