Study on inhibitory effect of calycosin on hepatic stellate cell activation in rats by up-regulating peroxisome proliferator-activated receptor γ.
	    		
		   		
	    	
    	
    	
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Jian PING
			        		
			        		;
		        		
		        		
		        		
			        		Hong-yun CHEN
			        		
			        		;
		        		
		        		
		        		
			        		Yang ZHOU
			        		
			        		;
		        		
		        		
		        		
			        		Gao-feng CHEN
			        		
			        		;
		        		
		        		
		        		
			        		Lie-ming XU
			        		
			        		;
		        		
		        		
		        		
			        		Yang CHENG
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
            
            	- MeSH:
            	
	        			
	        				
	        				
				        		
					        		Animals;
				        		
			        		
				        		
					        		Cell Proliferation;
				        		
			        		
				        		
					        		drug effects;
				        		
			        		
				        		
					        		Cells, Cultured;
				        		
			        		
				        		
					        		Drugs, Chinese Herbal;
				        		
			        		
				        		
					        		pharmacology;
				        		
			        		
				        		
					        		Hepatic Stellate Cells;
				        		
			        		
				        		
					        		cytology;
				        		
			        		
				        		
					        		drug effects;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		Isoflavones;
				        		
			        		
				        		
					        		pharmacology;
				        		
			        		
				        		
					        		Male;
				        		
			        		
				        		
					        		PPAR gamma;
				        		
			        		
				        		
					        		genetics;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		Rats;
				        		
			        		
				        		
					        		Rats, Sprague-Dawley;
				        		
			        		
				        		
					        		Receptors, Cytoplasmic and Nuclear;
				        		
			        		
				        		
					        		genetics;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		Up-Regulation;
				        		
			        		
				        		
					        		drug effects
				        		
			        		
	        			
	        			
            	
            	
 
            
            
            	- From:
	            		
	            			China Journal of Chinese Materia Medica
	            		
	            		 2015;40(12):2383-2388
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	To observe the effect of calycosin on the proliferation and activation of primary hepatic stellate cells (HSCs) in rats, and prove calycosin shows the effects through peroxisome proliferator-activated receptor γ(PPARγ) and farnesoid X receptor (FXR). The results indicated that calycosin could inhibit HSC proliferation and expressions of activation marker smooth muscle actin-α and type I collagen. With the increase in HSC activation time, FXR expression reduced, but with no notable impact from calycosin. Calycosin could up-regulate PPARγ expression and its nuclear transition in a concentration-dependent manner. Its prohibitory effect on HSC activation could be blocked by PPARγ antagonist. In conclusion, calycosin could inhibit HSC activation and proliferation, which may be related with the up-regulation of PPARγ signal pathway.