Protective effects of H2S against H2O2-induced oxidative injury in RGC
	    		
		   		
		   			
		   		
	    	
    	 
    	10.13389/j.cnki.rao.2017.0130
   		
        
        	
        		- VernacularTitle:硫化氢对H2O2诱导的视网膜神经节细胞氧化损伤的保护作用
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Xin LUO
			        		
			        		;
		        		
		        		
		        		
			        		Taixiang LIU
			        		
			        		;
		        		
		        		
		        		
			        		Huixuan REN
			        		
			        		;
		        		
		        		
		        		
			        		Yan LUO
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		oxidative stress;
			        		
			        		
			        		
				        		retinal ganglion cell;
			        		
			        		
			        		
				        		hydrogen sulfide;
			        		
			        		
			        		
				        		optic atrophy 1
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Recent Advances in Ophthalmology
	            		
	            		 2017;37(6):515-518
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Objective To investigate the protective effects and possible mechanism of hydrogen sulfide (H2S) against oxidative stress injury induced by hydrogen peroxide (H2O2) in retinal ganglion cell-5 (RGC-5).Methods RGC-5 cells were divided into four groups:RGC-5 group (normal control group),RGC-5 + H2O2 (RGC-5 were cultured in 500 μmol · L-1 H2O2 for 24 hours) group,RGC-5 + NaHS (RGC-5 were cultured in 50 μmol · L-1 NaHS for 30 minutes) + H2O2 (RGC-5 were cultured in 500 μmol · L-1 H2 O2 for 24 hours) group,and RGC-5 + NaHS (RGC-5 were cultured in 50 μmol · L-1 NaHS for 30 minutes) group.Western blots were applied to measure the expression of cytochrome c (Cyt.c) and optic atrophy 1 (OPA1).The fluorescent dye JC-1 assay was chosen to detect the mitochondrial membrane potential (△Ψm).Furthermore,transmission electron microscope was used to observe the morphology of mitochondria.Results Compared with RGC-5 group,the expression of Cyt.c in RGC-5 + H2O2 group decreased in mitochondria,and increased in cytoplasm (all P < 0.05),but there was no statistical difference between RGC-5 group and RGC-5 + NarHS + H2O2 group (all P >0.05).Compared with RGC-5 group,the expression of Cyt.c in RGC-5 + NaHS group increased in mitochondria,and decreased in cytoplasm (all P < 0.05).Compared with RGC-5 group,the expression of OPA1 in RGC-5 + H2O2 group decreased in mitochondria,and increased in cytoplasm (all P < 0.05).In RGC-5 + NaHs + H2O2 group and RGC-5 + NaHS group,the expression of OPA1 within and outside the mitochondria had no significant difference compared with RGC-5 group (all P > 0.05).Compared with other three groups,the mitochondrial membrane potential in RGC-5 + H2O2 group obviously decreased,but there was no statistical difference among other three groups (P > 0.05).The mitochondria were globular swelled in RGC-5 group,but in other three groups,the mitochondria had slightly swelled.Conclusion H2S can protect the mitochondrial morphology and functions of RGC? 5 from H2O2-induced oxidative stress via preventing OPA1 release from mitochondria.