The lung inflammation and skeletal muscle wasting induced by subchronic cigarette smoke exposure are not altered by a high-fat diet in mice.

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 mo...

Full description

Bibliographic Details
Main Authors: Michelle J Hansen, Hui Chen, Jessica E Jones, Shenna Y Langenbach, Ross Vlahos, Rosa C Gualano, Margaret J Morris, Gary P Anderson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3834033?pdf=render
id doaj-c043a4d03f5c45baa8778eaf5c110389
record_format Article
spelling doaj-c043a4d03f5c45baa8778eaf5c1103892020-11-24T21:50:26ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01811e8047110.1371/journal.pone.0080471The lung inflammation and skeletal muscle wasting induced by subchronic cigarette smoke exposure are not altered by a high-fat diet in mice.Michelle J HansenHui ChenJessica E JonesShenna Y LangenbachRoss VlahosRosa C GualanoMargaret J MorrisGary P AndersonObesity 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.http://europepmc.org/articles/PMC3834033?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Michelle J Hansen
Hui Chen
Jessica E Jones
Shenna Y Langenbach
Ross Vlahos
Rosa C Gualano
Margaret J Morris
Gary P Anderson
spellingShingle Michelle J Hansen
Hui Chen
Jessica E Jones
Shenna Y Langenbach
Ross Vlahos
Rosa C Gualano
Margaret J Morris
Gary P Anderson
The lung inflammation and skeletal muscle wasting induced by subchronic cigarette smoke exposure are not altered by a high-fat diet in mice.
PLoS ONE
author_facet Michelle J Hansen
Hui Chen
Jessica E Jones
Shenna Y Langenbach
Ross Vlahos
Rosa C Gualano
Margaret J Morris
Gary P Anderson
author_sort Michelle J Hansen
title The lung inflammation and skeletal muscle wasting induced by subchronic cigarette smoke exposure are not altered by a high-fat diet in mice.
title_short The lung inflammation and skeletal muscle wasting induced by subchronic cigarette smoke exposure are not altered by a high-fat diet in mice.
title_full The lung inflammation and skeletal muscle wasting induced by subchronic cigarette smoke exposure are not altered by a high-fat diet in mice.
title_fullStr The lung inflammation and skeletal muscle wasting induced by subchronic cigarette smoke exposure are not altered by a high-fat diet in mice.
title_full_unstemmed The lung inflammation and skeletal muscle wasting induced by subchronic cigarette smoke exposure are not altered by a high-fat diet in mice.
title_sort lung inflammation and skeletal muscle wasting induced by subchronic cigarette smoke exposure are not altered by a high-fat diet in mice.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description 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.
url http://europepmc.org/articles/PMC3834033?pdf=render
work_keys_str_mv AT michellejhansen thelunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT huichen thelunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT jessicaejones thelunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT shennaylangenbach thelunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT rossvlahos thelunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT rosacgualano thelunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT margaretjmorris thelunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT garypanderson thelunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT michellejhansen lunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT huichen lunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT jessicaejones lunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT shennaylangenbach lunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT rossvlahos lunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT rosacgualano lunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT margaretjmorris lunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
AT garypanderson lunginflammationandskeletalmusclewastinginducedbysubchroniccigarettesmokeexposurearenotalteredbyahighfatdietinmice
_version_ 1725884034790195200