The protective mechanism of fructose-1,6-disphophate on the hypoxic-ischemic brain damage of neonatal rats
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3760/cma.j.issn.1673-4408.2009.05.002
   		
        
        	
        		- VernacularTitle:1,6-二磷酸果糖对新生鼠缺氧缺血性脑损伤的保护机制研究
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Weichao LI
			        		
			        		;
		        		
		        		
		        		
			        		Guilan CHU
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Fructose-1,6-disphophate;
			        		
			        		
			        		
				        		Brain ischemia;
			        		
			        		
			        		
				        		Brain hypoxic;
			        		
			        		
			        		
				        		Rat
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			International Journal of Pediatrics
	            		
	            		 2009;36(5):446-447
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Objective To explore the protective mechanism of fructose-1, 6-disphophate on the hypoxic-ischemic brain damage of neonatal rats.Methods Seven-day-old Wistar rats were randomly divided into HIBD control group,saline-treated group, FDP-treated group. FDP-treated group was redivided into groups of high, middle and low dose.The expression of caspase-3mRNA was detected at 24h after HIBD with RT-PCR. Results There were no sifnificant differences of the caspase-3 mRNA expression among the saline-treated group, HIBD group and low dose FDP-treated group(P >0.05).The expressions of caspase-3 mRNA in the middle and high dose FDP-treated groups decreased significantly as campared to the above three groups (P < 0.05), but there was no significant difference between the two groups (P > 0.05). Conclusion The neuronal protective mechanism of FDP might be related to dewnregulate the gene expression of caspase-3 in brain tissue,and decrease the apoptosis of neuron after HIBD.