Effects of dietary selenium and vitamin E concentrations on phospholipid hydroperoxide glutathione peroxidase expression in reproductive tissues of pubertal maturing male rats

• Published in: Biological trace element research Vol. 59; no. 1/3; pp. 195 - 206
• Main Authors: Lei, X.G, Ross, D.A, Parks, J.E, Combs, G.F. Jr
• Format: Journal Article
• Language: English
• Published: United States Springer Nature B.V 1997
• Subjects: ACTIVIDAD ENZIMATICA; ACTIVITE ENZYMATIQUE; Animals; APARATO GENITAL; BIOLOGICAL DEVELOPMENT; Body Weight; DESARROLLO BIOLOGICO; DEVELOPPEMENT BIOLOGIQUE; Diet; ENZYMIC ACTIVITY; Epididymis - enzymology; Epididymis - growth & development; Feeding Behavior; GENITAL SYSTEM; Glutathione Peroxidase - metabolism; Liver; Liver - enzymology; Male; NUTRITION; Organ Size; Rats; Rats, Sprague-Dawley; REPRODUCTIVE ORGANS; Rodents; Selenium; Selenium - administration & dosage; Selenium - blood; Seminal Vesicles - enzymology; Seminal Vesicles - growth & development; Sperm Count; Sperm Motility; SYSTEME GENITAL; Testis - enzymology; Testis - growth & development; Vitamin E; Vitamin E - administration & dosage; Vitamin E - blood; Yeasts
• ISSN: 0163-4984; 1559-0720
• DOI: 10.1007/BF02783245

Phospholipid hydroperoxide glutathione peroxidase (PHGPX) is the second intracellular selenium (Se)-dependent glutathione peroxidase (GSH-Px) identified in mammals. Our objectives were to determine the effect of dietary vitamin E and Se levels on PHGPX activity expression in testis, epididymis, and seminal vesicles of pubertal maturing rats, and the relationship of PHGPX expression with testicular development and sperm quality. Forty Sprague-Dawley male weanling rats (21-d old), were initially fed for 3 wk a torula yeast basal diet (containing 0.05 mg Se/kg) supplemented with marginal levels of Se (0.1 mg/kg as Na2SeO3) and vitamin E (25 IU/kg as all-rac-alpha-tocopheryl acetate). Then, rats were fed the basal diets supplemented with 0 or 0.2 mg Se/kg and 0 or 100 IU vitamin E/kg diet during the 3-wk period of pubertal maturing. Compared with the Se-supplemented rats, those fed the Se-deficient diets retained 31, 88, 67, and 50% of Se-dependent GSH-Px activities in liver, testis, epididymis, and seminal vesicles, respectively. Testes and seminal vesicles had substantially higher (5- to 20-fold) PHGPX activity than liver. Dietary Se deficiency did not affect PHGPX activities in the reproductive tissues, but reduced PHGPX activity in liver by 28% (P < 0.0001). Dietary vitamin E supplementation did not affect PHGPX activity in liver, whereas it raised PHGPX activity in seminal vesicles by 43% (P < 0.005). Neither dietary vitamin E nor Se levels affected body weight gains, reproductive organ weights, or sperm counts and morphology. In conclusion, expression of PHGPX activity in testis and seminal vesicles was high and regulated by dietary Se and vitamin E differently from that in liver.