Grape Seed Proanthocyanidin Extract Alleviates Arsenic-induced Oxidative Reproductive Toxicity in Male Mice.
	    		
		   		
		   			
		   		
	    	
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			        		Shu Gang LI
			        		
			        		
			        		
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			        		Yu Song DING
			        		
			        		
			        		
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			        		Qiang NIU
			        		
			        		
			        		
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			        		Shang Zhi XU
			        		
			        		
			        		
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			        		Li Juan PANG
			        		
			        		
			        		
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			        		Ru Lin MA
			        		
			        		
			        		
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			        		Ming Xia JING
			        		
			        		
			        		
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			        		Gang Ling FENG
			        		
			        		
			        		
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			        		Jia Ming LIU
			        		
			        		
			        		
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			        		Shu Xia GUO
			        		
			        		
			        		
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			        		Author Information
			        		
 - Publication Type:Journal Article
 - Keywords: Arsenic; Grape seed proanthocyanidin extract; Nrf2 signaling; Reproductive toxicity
 - MeSH: Animals; Antioxidants; metabolism; Arsenic; toxicity; Grape Seed Extract; pharmacology; Lipid Peroxidation; drug effects; Male; Mice; NF-E2-Related Factor 2; genetics; metabolism; Oxidative Stress; drug effects; Proanthocyanidins; pharmacology; Signal Transduction; drug effects; Sperm Count; Testis; cytology; drug effects; metabolism
 - From: Biomedical and Environmental Sciences 2015;28(4):272-280
 - CountryChina
 - Language:English
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		        	Abstract:
			       	
			       		
				        
				        	
OBJECTIVETo determine the ability of grape seed proanthocyanidin extract (GSPE) in alleviating arsenic-induced reproductive toxicity.
METHODSSixty male Kunming mice received the following treatments by gavage: normal saline solution (control); arsenic trioxide (ATO; 4 mg/kg); GSPE (400 mg/kg); ATO+GSPE (100 mg/kg); ATO+GSPE (200 mg/kg) and ATO+GSPE (400 mg/kg). Thereafter, the mice were sacrificed and weighed, and the testis was examined for pathological changes. Nuclear factor (erythroid-derived 2)-like 2 (Nrf2), heme oxygenase 1 (HO1), glutathione S-transferase (GST), NAD(P)H dehydrogenase, and quinone 1 (NQO1) expression in the testis was detected by real-time PCR. Superoxide dismutase (SOD), glutathione (GSH), total antioxidative capability (T-AOC), malondialdehyde (MDA), 8-hydroxydeoxyguanosine (8-OHdG), and reproductive indexes were analyzed.
RESULTSATO-treated mice showed a significantly decreased sperm count and testis somatic index and activity levels of SOD, GSH, and T-AOC than control group. Compared to the ATO-treated group, ATO +GSPE group showed recovery of the measured parameters. Mice treated with ATO+high-dose GSPE showed the highest level of mRNA expression of Nrf2, HO, NQO1, and GST.
CONCLUSIONGSPE alleviates oxidative stress damage in mouse testis by activating Nrf2 signaling, thus counteracting arsenic-induced reproductive toxicity.
 
            