Gene expression in uremic left ventricular hypertrophy: effects of hypertension andanemia.
	    		
		   		
	    	
    	
    	
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Robert H MAK
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Stella L CHANG
			        		
			        		;
		        		
		        		
		        		
			        		Aparna DRAKSHARAPU
			        		
			        		;
		        		
		        		
		        		
			        		Youngmi Kim PAK
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Division of Pediatric Nephrology, Department of Pediatrics, Oregon Health and Science University, Portland, OR 9720, USA.
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Original Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		anemia;
			        		
			        		
			        		
				        		cardiac hypertrophy;
			        		
			        		
			        		
				        		hypertension;
			        		
			        		
			        		
				        		left ventricular hypertrophy;
			        		
			        		
			        		
				        		uremia
			        		
			        		
	        			
        			
        		
 
        	
            
            	- MeSH:
            	
	        			
	        				
	        				
				        		
					        		Actins/genetics/metabolism;
				        		
			        		
				        		
					        		Anemia/*complications/drug therapy/metabolism;
				        		
			        		
				        		
					        		Animals;
				        		
			        		
				        		
					        		Atrial Natriuretic Factor/genetics/metabolism;
				        		
			        		
				        		
					        		Erythropoietin/pharmacology/therapeutic use;
				        		
			        		
				        		
					        		*Gene Expression;
				        		
			        		
				        		
					        		Heart Ventricles/chemistry/drug effects/pathology;
				        		
			        		
				        		
					        		Hydralazine/pharmacology/therapeutic use;
				        		
			        		
				        		
					        		Hypertension/*complications/drug therapy/metabolism;
				        		
			        		
				        		
					        		Hypertrophy, Left Ventricular/etiology/*genetics/metabolism;
				        		
			        		
				        		
					        		Male;
				        		
			        		
				        		
					        		Peptidyl-Dipeptidase A/genetics/metabolism;
				        		
			        		
				        		
					        		RNA, Messenger/analysis/metabolism;
				        		
			        		
				        		
					        		Rats;
				        		
			        		
				        		
					        		Rats, Sprague-Dawley;
				        		
			        		
				        		
					        		Transforming Growth Factor beta/genetics/metabolism;
				        		
			        		
				        		
					        		Uremia/etiology/*genetics/metabolism
				        		
			        		
	        			
	        			
            	
            	
 
            
            
            	- From:Experimental & Molecular Medicine
	            		
	            		 2004;36(3):251-258
	            	
            	
 
            
            
            	- CountryRepublic of Korea
 
            
            
            	- Language:English
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Hypertension and anemia may be causes of left ventricular hypertrophy (LVH) in uremia but the molecular mechanism is not known. Uremia was induced in male Spraugue Dawley rats by 5/6 nephrectomy. The following groups of rats were studied for 6 weeks; uremic rats (U) fed ad. lib., control rats (C) pair-fed with U, U rats given hydralazine (100 mg/kg/day) (UH), U rats given erythropoietin (48U/kg/week, i.p.) (UE). Both diastolic and mean arterial pressures are higher (P<0.01) in U and UE compared with C whereas both pressures in UH were normalized. Hemoglobin in U was lower than in C, and was normalized in UE. U, UH and UE had higher heart weight/body weight ratios (HW/BW) as well as left ventricular weight/body weight ratios (LV/BW) compared with C (P<0.01). Compared with U, UH has lower HW/BW and LV/BW (P <0.05) and UE has normal HW/BW but lower LV/BW than U (P<0.05). To see if the gene expression in uremic LVH is similar to that described in pressure overload LVH in which mRNA levels of angiotensin converting enzyme (ACE), transforming growth factor-beta1 (TGF-beta1), atrial natriuretic factors (ANF) and skeletal alpha-actin were increased, we measured these mRNA levels by Northern analysis. TGF-beta, ACE and alpha-actin mRNA levels were not changed in all 4 groups. ANF mRNA in U and UE was increased 3 fold over C, and normalized in UH. Treatment of anemia with erythropoietin improved uremic LVH but did not change ANF mRNA; whereas treatment of hypertension with hydralazine normalized ANF mRNA but did not completely correct uremic LVH. Thus, gene expression in uremic LVH is distinct from that in pressure- overload LVH, suggesting that other unidentified factor(s) might be involved in uremic LVH.