Tashiro Hiroki, Takahashi Koichiro, Sadamatsu Hironori, Kato Go, Kurata Keigo, Kimura Shinya, Sueoka-Aragane Naoko
Division of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga, 849-8501, Japan.
Institute of Tokyo Environmental Allergy, Tokyo, Japan.
Inflammation. 2017 Jun;40(3):1072-1086. doi: 10.1007/s10753-017-0550-4.
Obesity is one of the phenotypes of severe asthma, which is considered to be a heterogeneous syndrome; however, its interaction with airway inflammation is not fully understood. The aim of this study was to clarify the role of saturated fatty acids in augmenting airway inflammation induced by house dust mite (HDM) in obesity. Subjects were Balb/c mice fed a high-fat diet (HFD) for 10 weeks, followed by sensitization and exposure to HDM. Subjects were also administered palmitic acid (PA) for 4 weeks with concurrent sensitization and exposure to HDM. Airway inflammation was assessed by quantifying the amount of inflammatory cells in bronchoalveolar lavage (BAL) and airway resistance was measured. In vitro, lipopolysaccharide (LPS)-primed macrophages were stimulated by PA. The amount of monocyte chemoattractant protein-1 (MCP-1), interleukin-1β (IL-1β), and tumor necrosis factor α (TNF-α) was examined in the supernatant. Compared to normal chow mice, HFD mice underwent significant increases in body weight; increases in number of lung macrophages, including circulating monocytes and alveolar macrophages; and increases in bronchoalveolar lavage fluid (BALF) total cell count, including neutrophils but not eosinophils, after HDM sensitization and exposure. In vitro, PA induced MCP-1 and augmented LPS-primed production of IL-1β and TNF-α in macrophages. Among HDM mice that were administered PA, there was an increase BALF total cell count, including neutrophils but not eosinophils, compared to vehicle mice. In conclusion, saturated fatty acid increased the number of lung macrophages and augmented HDM-induced neutrophilic airway inflammation in a HFD mouse model.
肥胖是重度哮喘的表型之一,重度哮喘被认为是一种异质性综合征;然而,其与气道炎症的相互作用尚未完全明确。本研究的目的是阐明饱和脂肪酸在肥胖状态下增强屋尘螨(HDM)诱导的气道炎症中的作用。将Balb/c小鼠喂食高脂饮食(HFD)10周,随后进行HDM致敏和暴露。同时,给予小鼠棕榈酸(PA)4周,并同时进行HDM致敏和暴露。通过定量支气管肺泡灌洗(BAL)中的炎症细胞数量评估气道炎症,并测量气道阻力。在体外,用PA刺激脂多糖(LPS)预处理的巨噬细胞。检测上清液中单核细胞趋化蛋白-1(MCP-1)、白细胞介素-1β(IL-1β)和肿瘤坏死因子α(TNF-α)的含量。与正常饮食小鼠相比,HFD小鼠在HDM致敏和暴露后体重显著增加;肺巨噬细胞数量增加,包括循环单核细胞和肺泡巨噬细胞;支气管肺泡灌洗液(BALF)总细胞计数增加(包括中性粒细胞但不包括嗜酸性粒细胞)。在体外,PA诱导巨噬细胞产生MCP-1,并增强LPS预处理的IL-1β和TNF-α的产生。在给予PA的HDM小鼠中,与给予赋形剂的小鼠相比,BALF总细胞计数增加(包括中性粒细胞但不包括嗜酸性粒细胞)。总之,在HFD小鼠模型中,饱和脂肪酸增加了肺巨噬细胞数量,并增强了HDM诱导的嗜中性气道炎症。