摘要来源: 前Med(Lausanne)。 2022; 9:1075465。 EPUB 2023 1月13日。PMID: 36714100 36714100
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摘要:
背景:背景: 急性肺损伤(Ali),而没有生命的疾病,有效地有效炎性疾病。巨噬细胞极化在肺部炎症的启动和分辨率中起关键作用。因此,调节巨噬细胞表型是急性LUN的潜在有效方法G受伤。加密酮(CTS)是一种亲脂性生物活性化合物,它是从多种药理作用的根部提取的,尤其是抗炎作用。 In this study, we investigated the therapeutic and immunomodulatory effects of CTS on ALI.
MATERIALS AND METHODS: The rat model of ALI was established by intratracheal instillation of LPS (5 mg/kg) to evaluate the lung protective effect of CTSand to explore the regulation of CTS在肺巨噬细胞极化的表型上。 LPS (1μg/mL) was used to stimulate RAW264.7 macrophagesto further explore the effect of CTS on the polarization and metabolic reprogramming of RAW264.7 macrophages and to clarify the potential mechanism of CTS anti-ALI.
RESULTS: CTS significantly improved lung功能,减少肺水肿,有效抑制肺部炎症性浸润,并减轻ALI。 bOthandresults表明,CTS抑制了巨噬细胞分化为M1表型,并在ALI期间促进了极化为M2表型。进一步表明,CTS显着抑制了LPS诱导的从有氧氧化到巨噬细胞糖酵解的代谢过渡。从机械上讲,CTS通过激活AMPK来阻止LPS诱导的巨噬细胞的代谢转化。