Phan S H, Kunkel S L
Am J Pathol. 1986 Aug;124(2):343-52.
The role of alveolar macrophage activation and release of mediators remains unclear. In this study, this role is examined with respect to the effects of relatively selective inhibitors of arachidonate metabolism on the pathogenesis of pulmonary fibrosis. CBA/J mice were administered bleomycin (0.037 units) endotracheally to induce pulmonary fibrosis. Daily intraperitoneal injections of a lipoxygenase inhibitor, nordihydroguaiaretic acid (NDGA) inhibited pulmonary fibrosis in a dose-dependent manner (15-25 mg/kg body weight), as assessed by both lung collagen synthesis and total lung hydroxyproline content. The less specific inhibitor BW755c was also effective at a dose of 25 mg/kg. In contrast, the cyclooxygenase inhibitor, ibuprofen (15 mg/kg), was completely ineffective. Correlated with this antifibrogenic activity of NDGA was the inhibition of several other parameters of bleomycin-induced pulmonary fibrosis. Bleomycin treatment caused a greater than threefold increase in the percentage of alveolar macrophages expressing Ia antigen (from 7.7% +/- 1.07% to 29.9% +/- 4.16% of total recoverable alveolar macrophages). NDGA, but not ibuprofen, inhibited this increase in a dose-dependent manner. Associated with this indication of macrophage stimulation was an increase in spontaneous macrophage production of fibroblast growth factor (MDGF) activity as a result of bleomycin instillation. This increase was also inhibited by NDGA treatment. In contrast, bleomycin treatment caused a reduction in alveolar macrophage interleukin-1 (IL-1) production, and NDGA treatment did not alter this reduction, which suggests that MDGF is separate from IL-1 in this case, and that MDGF played a more dominant role, at least in this model of pulmonary fibrosis. This antifibrogenic activity of NDGA was accomplished without any reduction in spontaneous macrophage prostaglandin (PG)E2 production, which suggests the selectivity (versus cyclooxygenase pathway) of NDGA inhibition and the relative lack of importance of macrophage-derived PGE2 in modulating fibrogenesis in this model. The results of this study have thus demonstrated the importance of alveolar macrophage stimulation and increased production of MDGF in the pathogenesis of bleomycin-induced pulmonary fibrosis. The data also suggest that both macrophage parameters are subject to regulation by arachidonate metabolites.
肺泡巨噬细胞激活及介质释放的作用仍不清楚。在本研究中,通过花生四烯酸代谢相对选择性抑制剂对肺纤维化发病机制的影响来探究这一作用。对CBA/J小鼠经气管内给予博来霉素(0.037单位)以诱导肺纤维化。每日腹腔注射脂氧合酶抑制剂去甲二氢愈创木酸(NDGA)以剂量依赖性方式(15 - 25毫克/千克体重)抑制肺纤维化,这通过肺胶原合成和肺总羟脯氨酸含量来评估。特异性较低的抑制剂BW755c在25毫克/千克剂量时也有效。相比之下,环氧化酶抑制剂布洛芬(15毫克/千克)则完全无效。与NDGA的这种抗纤维化活性相关的是对博来霉素诱导的肺纤维化其他几个参数的抑制。博来霉素治疗使表达Ia抗原的肺泡巨噬细胞百分比增加了三倍多(从可回收肺泡巨噬细胞总数的7.7%±1.07%增至29.9%±4.16%)。NDGA而非布洛芬以剂量依赖性方式抑制了这种增加。与这种巨噬细胞刺激迹象相关的是,由于滴注博来霉素,巨噬细胞自发产生的成纤维细胞生长因子(MDGF)活性增加。这种增加也被NDGA治疗所抑制。相比之下,博来霉素治疗导致肺泡巨噬细胞白细胞介素 - 1(IL - 1)产生减少,而NDGA治疗并未改变这种减少,这表明在这种情况下MDGF与IL - 1是分开的,并且MDGF至少在这个肺纤维化模型中发挥了更主要的作用。NDGA的这种抗纤维化活性在巨噬细胞自发前列腺素(PG)E2产生未减少的情况下实现,这表明NDGA抑制的选择性(相对于环氧化酶途径)以及在该模型中巨噬细胞衍生的PGE2在调节纤维生成方面相对不太重要。本研究结果因此证明了肺泡巨噬细胞刺激和MDGF产生增加在博来霉素诱导的肺纤维化发病机制中的重要性。数据还表明这两个巨噬细胞参数都受花生四烯酸代谢产物调节。