Long-Term Effects of Diesel Exhaust Particles on Airway Inflammation and Remodeling in a Mouse Model.
	    		
		   		
		   			
		   		
	    	
    	 
    	10.4168/aair.2016.8.3.246
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Byeong Gon KIM
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Pureun Haneul LEE
			        		
			        		;
		        		
		        		
		        		
			        		Shin Hwa LEE
			        		
			        		;
		        		
		        		
		        		
			        		Young En KIM
			        		
			        		;
		        		
		        		
		        		
			        		Mee Yong SHIN
			        		
			        		;
		        		
		        		
		        		
			        		Yena KANG
			        		
			        		;
		        		
		        		
		        		
			        		Seong Hwan BAE
			        		
			        		;
		        		
		        		
		        		
			        		Min Jung KIM
			        		
			        		;
		        		
		        		
		        		
			        		Taiyoun RHIM
			        		
			        		;
		        		
		        		
		        		
			        		Choon Sik PARK
			        		
			        		;
		        		
		        		
		        		
			        		An Soo JANG
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Korea. jas877@schmc.ac.kr
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Original Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Chronic;
			        		
			        		
			        		
				        		diesel exhaust particles;
			        		
			        		
			        		
				        		airway remodeling
			        		
			        		
	        			
        			
        		
 
        	
            
            	- MeSH:
            	
	        			
	        				
	        				
				        		
					        		Airway Remodeling;
				        		
			        		
				        		
					        		Animals;
				        		
			        		
				        		
					        		Bronchoalveolar Lavage;
				        		
			        		
				        		
					        		Collagen;
				        		
			        		
				        		
					        		Fibrosis;
				        		
			        		
				        		
					        		Goblet Cells;
				        		
			        		
				        		
					        		Hyperplasia;
				        		
			        		
				        		
					        		Inflammation*;
				        		
			        		
				        		
					        		Interferon-gamma;
				        		
			        		
				        		
					        		Interleukin-10;
				        		
			        		
				        		
					        		Interleukin-13;
				        		
			        		
				        		
					        		Interleukin-6;
				        		
			        		
				        		
					        		Interleukins;
				        		
			        		
				        		
					        		Lung;
				        		
			        		
				        		
					        		Lymphocytes;
				        		
			        		
				        		
					        		Mice*;
				        		
			        		
				        		
					        		Nebulizers and Vaporizers;
				        		
			        		
				        		
					        		Neutrophils;
				        		
			        		
				        		
					        		Plethysmography;
				        		
			        		
				        		
					        		Pneumonia;
				        		
			        		
				        		
					        		Ultrasonics;
				        		
			        		
				        		
					        		Vascular Endothelial Growth Factor A;
				        		
			        		
				        		
					        		Vehicle Emissions*
				        		
			        		
	        			
	        			
            	
            	
 
            
            
            	- From:Allergy, Asthma & Immunology Research
	            		
	            		 2016;8(3):246-256
	            	
            	
 
            
            
            	- CountryRepublic of Korea
 
            
            
            	- Language:English
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	PURPOSE: Diesel exhaust particles (DEPs) can induce and trigger airway hyperresponsiveness (AHR) and inflammation. The aim of this study was to investigate the effect of long-term DEP exposure on AHR, inflammation, lung fibrosis, and goblet cell hyperplasia in a mouse model. METHODS: BALB/c mice were exposed to DEPs 1 hour a day for 5 days a week for 3 months in a closed-system chamber attached to a ultrasonic nebulizer (low dose: 100 microg/m3 DEPs, high dose: 3 mg/m3 DEPs). The control group was exposed to saline. Enhanced pause was measured as an indicator of AHR. Animals were subjected to whole-body plethysmography and then sacrificed to determine the performance of bronchoalveolar lavage and histology. RESULTS: AHR was higher in the DEP group than in the control group, and higher in the high-dose DEP than in the low-dose DEP groups at 4, 8, and 12 weeks. The numbers of neutrophils and lymphocytes were higher in the high-dose DEP group than in the low-dose DEP group and control group at 4, 8, and 12 weeks. The levels of interleukin (IL)-5, IL-13, and interferon-gamma were higher in the low-dose DEP group than in the control group at 12 weeks. The level of IL-10 was higher in the high-dose DEP group than in the control group at 12 weeks. The level of vascular endothelial growth factor was higher in the low-dose and high-dose DEP groups than in the control group at 12 weeks. The level of IL-6 was higher in the low-dose DEP group than in the control group at 12 weeks. The level of transforming growth factor-beta was higher in the high-dose DEP group than in the control group at 4, 8, and 12 weeks. The collagen content and lung fibrosis in lung tissue was higher in the high-dose DEP group at 8 and 12 weeks. CONCLUSIONS: These results suggest that long-term DEP exposure may increase AHR, inflammation, lung fibrosis, and goblet cell hyperplasia in a mouse model.