Effect of Panax Notoginseng Saponins on EMT of Rat Renal Proximal Tubular Epithelial Cells Induced by TGF-β1 
	    		
		   		
		   			
		   		
	    	
    	 
    	10.13422/j.cnki.syfjx.20190636
   		
        
        	
        		- VernacularTitle: 三七皂苷对TGF-β1诱导的大鼠肾小管上皮细胞EMT的影响 
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Jing PAN
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Yue-guang DU
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Yi GUO
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. College of Basic Medicine, Zhejiang Chinese Medical University, Hangzhou 310053, China
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Research Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		panax notoginseng saponins;
			        		
			        		
			        		
				        		transforming growth factor-β1(TGF-β1);
			        		
			        		
			        		
				        		silent information regulation 2 homolog 1(SIRT1)/TGF-β1/Smad pathway;
			        		
			        		
			        		
				        		epithelial-mesenchymal transition(EMT);
			        		
			        		
			        		
				        		diabetic nephropathy
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Experimental Traditional Medical Formulae
	            		
	            		 2019;25(6):89-94
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	 Objective:To investigate the intervention effect of panax notoginseng saponins (PNS) on epithelial-mesenchymal transition (EMT) of rat renal tubular epithelial cells (NRK-52E) induced by transforming growth factor-β1(TGF-β1), and analyze the mechanism based on the silent information regulation 2 homolog 1(SIRT1)/TGF-β1/Smad signaling pathway. Method:NRK-52E were cultured in DMEM medium with 10% fetal bovine serum, and divided into normal control group, TGF-β1 group (5 μg·L-1), resveratrol (RSV) group (50 mg·L-1), EX527 group (10 μmol·L-1), Panax notoginseng saponins (PNS) group (100 mg·L-1), and EX527+ PNS group (10 μmol·L-1+100 mg·L-1). Then cells were collected after drug intervention for 48 h. The expressions of α-SMA,E-cadherin,SIRT1,TGF-β1,Smad3,Smad4 mRNA in each group were detected by Real-time PCR. The protein expressions of α-SMA, E-cadherin,SIRT1 and TGF-β1 were detected by Western blot. Result:Compared with normal group, mRNA and protein expressions of α-SMA increased obviously(P<0.05), but E-cadherin decreased significantly(P<0.01)in TGF-β1 group. Compared with TGF-β1 group, mRNA and protein expressions of α-SMA decreased significantly(P<0.01), while E-cadherin increased(P<0.01)in resveratrol and PNS groups, and EMT was inhibited. Meanwhile, mRNA and protein expressions of SIRT1 increased significantly(P<0.01), while mRNA expressions of TGF-β1,Smad3,and Smad4 decreased(P<0.01). Under the intervention of SIRT1 blocker EX527, PNS could not play a significant inhibitory effect on the cells. Conclusion:PNS can prevent the occurrence of EMT of renal tubular epithelial cells induced by TGF-β1, and the mechanism may be related to active SIRT1 to inhibit TGF-β1/Smad pathway.