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. 2012:2012:843569.
doi: 10.5402/2012/843569. Epub 2012 Oct 30.

Vitamins e and C alleviate the germ cell loss and oxidative stress in cryptorchidism when administered separately but not when combined in rats

Affiliations

Vitamins e and C alleviate the germ cell loss and oxidative stress in cryptorchidism when administered separately but not when combined in rats

Ayobami Oladele Afolabi et al. ISRN Pharmacol. 2012.

Abstract

The antioxidant effects of vitamins C and E on cryptorchidism-induced oxidative stress were investigated in male Sprague-Dawley rats. Forty rats (200-250 g) were randomly divided in a blinded fashion into five groups (n = 8). Group 1 was sham operated and treated with vehicle (corn-oil, 10 mL/kg). Groups 2, 3, 4, and 5 were rendered unilaterally cryptorchid and treated with vehicle (10 mL/kg), vitamin E solution (75 mg/kg), vitamin C solution (1.25 g/kg), and combination of vitamin E (75 mg/kg) and vitamin C (1.25 g/kg) solutions, respectively. Germ cell count, superoxide dismutase (SOD), total protein (TP), and testicular weight (TW) were lower, but malondialdhyde (MDA) was higher in the cryptorchid rats than the sham-operated rats. When administered separately, vitamins C and E increased germ cell count, SOD, TP, and TW but did not reduce MDA in the cryptorchid rats when compared to the vehicle-treated cryptorchid rats. However, there was no significant difference in these parameters between vehicle-treated and combined vitamins C- and E-treated rats. This suggests that vitamins E and C alleviate the germ cell loss and oxidative stress in cryptorchidism when administered separately but not when combined in rats.

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Figures

Figure 1
Figure 1
Germ cell count in noncryptorchid rats treated with vehicle (1), cryptorchid rats treated with vehicle (2), vitamin E (3), vitamin C (4), and combination of vitamins E and C (5). Values are expressed as mean ± SEM, (n = 8). ***P < 0.001 versus group 1; #P < 0.05 and ##P < 0.01 versus group 2.
Figure 2
Figure 2
Plasma SOD in noncryptorchid rats treated with vehicle (1), cryptorchid rats treated with vehicle (2), vitamin E (3), vitamin C (4), and combination of vitamins E and C (5). Values are expressed as Mean ± SEM, (n = 8). ***P < 0.001 versus group 1; ##P < 0.01 versus group 2.
Figure 3
Figure 3
Plasma MDA in noncryptorchid rats treated with vehicle (1), cryptorchid rats treated with vehicle (2), vitamin E (3), vitamin C (4), and combination of vitamins E and C (5). Values are expressed as Mean ± SEM, (n = 8). *P < 0.05 versus group 1; #P < 0.05 and ##P < 0.01 versus group 2.
Figure 4
Figure 4
Total plasma protein in noncryptorchid rats treated with vehicle (1), cryptorchid rats treated with vehicle (2), vitamin E (3), vitamin C (4), and combination of vitamins E and C (5). Values are expressed as Mean ± SEM, (n = 8). *P < 0.05, ***P < 0.001 versus group 1; ##P < 0.01 versus group 2.
Figure 5
Figure 5
Testicular weights in noncryptorchid rats treated with vehicle (1), cryptorchid rats treated with vehicle (2), vitamin E (3), vitamin C (4), and combination of vitamins E and C (5). Values are expressed as Mean ± SEM, (n = 8). ***P < 0.001 versus group 1; #P < 0.05 and ##P < 0.01 versus group 2.

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References

    1. Fairfield KM, Fletcher RH. Vitamins for chronic disease prevention in adults: scientific review. Journal of the American Medical Association. 2002;287(23):3116–3126. - PubMed
    1. Polidori MC, Mecocci P, Browne SE, Senin U, Beal MF. Oxidative damage to mitochondrial DNA in Huntington's disease parietal cortex. Neuroscience Letters. 1999;272(1):53–56. - PubMed
    1. Stampfer MJ, Hennekens CH, Manson JE, Colditz GA, Rosner B, Willett WC. Vitamin E consumption and the risk of coronary disease in women. New England Journal of Medicine. 1993;328(20):1444–1449. - PubMed
    1. Lee SH, Oe T, Blair IA. Vitamin C-induced decomposition of lipid hydroperoxides to endogenous genotoxins. Science. 2001;292(5524):2083–2086. - PubMed
    1. Halliwell B. Vitamin C: poison, prophylactic or panacea? Trends in Biochemical Sciences. 1999;24(7):255–259. - PubMed

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