Hansen Michelle J, Chen Hui, Jones Jessica E, Langenbach Shenna Y, Vlahos Ross, Gualano Rosa C, Morris Margaret J, Anderson Gary P
Lung Health Research Centre, Department of Pharmacology and Therapeutics, The University of Melbourne, Victoria, Australia.
PLoS One. 2013 Nov 19;8(11):e80471. doi: 10.1371/journal.pone.0080471. eCollection 2013.
Obesity and cigarette smoking independently constitute major preventable causes of morbidity and mortality and obesity is known to worsen lung inflammation in asthma. Paradoxically, higher body mass index (BMI) is associated with reduced mortality in smoking induced COPD whereas low BMI increases mortality risk. To date, no study has investigated the effect of a dietary-induced obesity and cigarette smoke exposure on the lung inflammation and loss of skeletal muscle mass in mice. Male BALB/c mice were exposed to 4 cigarettes/day, 6 days/week for 7 weeks, or sham handled. Mice consumed either standard laboratory chow (3.5 kcal/g, 12% fat) or a high fat diet (HFD, 4.3 kcal/g, 32% fat). Mice exposed to cigarette smoke for 7 weeks had significantly more inflammatory cells in the BALF (P<0.05) and the mRNA expression of pro-inflammatory cytokines and chemokines was significantly increased (P<0.05); HFD had no effect on these parameters. Sham- and smoke-exposed mice consuming the HFD were significantly heavier than chow fed animals (12 and 13%, respectively; P<0.05). Conversely, chow and HFD fed mice exposed to cigarette smoke weighed 16 and 15% less, respectively, compared to sham animals (P<0.05). The skeletal muscles (soleus, tibialis anterior and gastrocnemius) of cigarette smoke-exposed mice weighed significantly less than sham-exposed mice (P<0.05) and the HFD had no protective effect. For the first time we report that cigarette smoke exposure significantly decreased insulin-like growth factor-1 (IGF-1) mRNA expression in the gastrocnemius and tibialis anterior and IGF-1 protein in the gastrocnemius (P<0.05). We have also shown that cigarette smoke exposure reduced circulating IGF-1 levels. IL-6 mRNA expression was significantly elevated in all three skeletal muscles of chow fed smoke-exposed mice (P<0.05). In conclusion, these findings suggest that a down-regulation in local IGF-1 may be responsible for the loss of skeletal muscle mass following cigarette smoke exposure in mice.
肥胖和吸烟各自都是发病率和死亡率的主要可预防原因,并且已知肥胖会加重哮喘中的肺部炎症。矛盾的是,较高的体重指数(BMI)与吸烟诱发的慢性阻塞性肺疾病(COPD)死亡率降低相关,而低BMI则增加死亡风险。迄今为止,尚无研究调查饮食诱导的肥胖和香烟烟雾暴露对小鼠肺部炎症和骨骼肌质量损失的影响。雄性BALB/c小鼠每天暴露于4支香烟,每周6天,持续7周,或进行假处理。小鼠食用标准实验室饲料(3.5千卡/克,12%脂肪)或高脂肪饮食(HFD,4.3千卡/克,32%脂肪)。暴露于香烟烟雾7周的小鼠支气管肺泡灌洗液(BALF)中的炎症细胞明显更多(P<0.05),促炎细胞因子和趋化因子的mRNA表达显著增加(P<0.05);HFD对这些参数没有影响。食用HFD的假处理和烟雾暴露小鼠比喂食饲料的动物明显更重(分别重12%和13%;P<0.05)。相反,与假处理动物相比,暴露于香烟烟雾的喂食饲料和HFD的小鼠体重分别减轻了16%和15%(P<0.05)。暴露于香烟烟雾的小鼠的骨骼肌(比目鱼肌、胫骨前肌和腓肠肌)重量明显低于假处理小鼠(P<0.05),HFD没有保护作用。我们首次报告,香烟烟雾暴露显著降低了腓肠肌和胫骨前肌中胰岛素样生长因子-1(IGF-1)的mRNA表达以及腓肠肌中IGF-1蛋白的表达(P<0.05)。我们还表明,香烟烟雾暴露降低了循环IGF-1水平。喂食饲料的烟雾暴露小鼠的所有三块骨骼肌中白细胞介素-6(IL-6)的mRNA表达均显著升高(P<0.05)。总之,这些发现表明,局部IGF-1的下调可能是小鼠香烟烟雾暴露后骨骼肌质量损失的原因。