Effects of Dietary Selenium Against Lead Toxicity on mRNA Levels of 25 Selenoprotein Genes in the Cartilage Tissue of Broiler Chicken

Biological Trace Element Research

Volumn 172, Issue 1, 2016, Pages 234-241

  Gao, H ^a   Liu, C P ^b   Song, S Q ^a   Fu, J ^b,c  

^a NANJING AGRICULTURAL UNIVERSITY   (China)

^b NORTHEAST AGRICULTURAL UNIVERSITY   (China)

^c Department of Obstetrics Gynecology   (United States)

Author keywords

Chicken cartilage; Lead; Selenium; Selenoprotein

Indexed keywords

LEAD; MESSENGER RNA; SELENIUM; SELENOPROTEIN;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BROILER; CARTILAGE; COMPARATIVE STUDY; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; CYTOTOXIC CONCENTRATION; DIO1 GENE; DIO2 GENE; DIO3 GENE; DOWN REGULATION; GENE; GENE EXPRESSION; GENETIC REGULATION; GPX1 GENE; GPX2 GENE; GPX3 GENE; GPX4 GENE; IN VITRO STUDY; LEAD POISONING; MALE; MENISCUS CARTILAGE; NONHUMAN; PROTEIN BLOOD LEVEL; PROTEIN EXPRESSION; SELENOPROTEIN GENE; SELH GENE; SELI GENE; SELK GENE; SELM GENE; SELO GENE; SELPB GENE; SELS GENE; SELT GENE; SELU GENE; SELW GENE; SEP15 GENE; SEPN1 GENE; SEPNN1 GENE; SEPX1 GENE; SPS2 GENE; SWORD CARTILAGE; TXNRD1 GENE; TXNRD2 GENE; TXNRD3 GENE; ANIMAL; ANIMAL MODEL; ARTICULAR CARTILAGE; BIOSYNTHESIS; CHICKEN; DIETARY SUPPLEMENT; DRUG EFFECTS; GENETICS; METABOLISM;

ANIMALS; CARTILAGE, ARTICULAR; CHICKENS; DIETARY SUPPLEMENTS; LEAD; LEAD POISONING; MALE; MODELS, ANIMAL; RNA, MESSENGER; SELENIUM; SELENOPROTEINS;

EID: 84949510032     PISSN: 01634984     EISSN: 15590720     Source Type: Journal    
DOI: 10.1007/s12011-015-0579-x     Document Type: Article

References (40)

1. Adonaylo VN, Oteiza PI (1999) Lead intoxication: antioxidant defenses and oxidative damage in rat brain. Toxicology 135:77–85
2. Flora SJ, Pande M, Mehta A (2003) Beneficial effect of combined administration of some naturally occurring antioxidants (vitamins) and thiol chelators in the treatment of chronic lead intoxication. Chem.-Biol. Interact. 145:267–280
3. Fisher IJ, Pain DJ, Thomas VG (2006) A review of lead poisoning from ammunition sources in terrestrial birds. Biol Conserv 131:421–432
4. Flora G, Gupta D, Tiwari A (2012) Toxicity of lead: a review with recent updates. Interdiscip Toxicol 5:47–58
5. Flora SJS (2002) Nutritional components modify metal absorption, toxic response and chelation therapy. J Nut Environ Med 12:53–67
6. Hartup BK (1996) Rehabilitation of native reptiles and amphibians in DuPage County, Illinois. J Wildl Dis 32:109–112
7. Gangoso L, Alvarez-Lloret P, Rodriguez-Navarro AA, et al. (2009) Long-term effects of lead poisoning on bone mineralization in vultures exposed to ammunition sources. Environ. Pollut. 157:569–574
8. Berglund M, Åkesson A, Bjellerup P, Vahter M (2000) Metal–bone interactions. Toxicol. Lett. 112–113:219–225
9. Nilsson U, Attewell R, Christoffersson JO, et al. (1991) Kinetics of lead in bone and blood after end of occupational exposure. Pharmacol. Toxicol. 68:477–484
10. Theppeang K, Glass TA, Bandeen-Roche K, et al. (2008) Associations of bone mineral density and lead levels in blood, tibia, and patella in urban-dwelling women. Environ. Health Perspect. 116:784–790
11. Chariot P, Bignani O (2003) Skeletal muscle disorders associated with selenium deficiency in humans. Muscle Nerve 27:662–668
12. Zhang JL, Zhang ZW, Shan AS, Xu SW (2014) Effects of dietary selenium deficiency or excess on gene expression of selenoprotein N in chicken muscle tissues. Biol. Trace Elem. Res. 157:234–241
13. Mariotti M, Ridge PG, Zhang Y, et al. (2012) Composition and evolution of the vertebrate and mammalian selenoproteomes. PLoS One 7:e33066
14. Liu CP, Fu J, Lin SL, Wang XS, Li S (2014) Effects of dietary selenium deficiency on mRNA levels of twenty-one selenoprotein genes in the liver of layer chicken. Biol. Trace Elem. Res. 159:192–198
15. Li JL, Ruan HF, Li HX, et al. (2011) Molecular cloning, characterization and mRNA expression analysis of a novel selenoprotein: avian selenoprotein W from chicken. Mol. Biol. Rep. 38:4015–4022
16. Yao H, Zhao W, Zhao X, et al. (2014) Selenium deficiency mainly influences the gene expressions of antioxidative selenoproteins in chicken muscles. Biol. Trace Elem. Res. 161:318–327
17. Huang JQ, Li DL, Zhao H, et al. (2011) The selenium deficiency disease exudative diathesis in chicks is associated with downregulation of seven common selenoprotein genes in liver and muscle. J Nutr 141:1605–1610
18. Cerklewski FL, Forbes RM (1976) Influence of dietary selenium on lead toxicity in the rat. J Nutr 106:778–783
19. Xu T, Gao X, Liu G (2015) The antagonistic effect of selenium on lead toxicity is related to the ion profile in chicken liver. Biol Trace Elem Res
20. Deng Z, Fu H, Xiao Y, et al. (2015) Effects of selenium on lead-induced alterations in abeta production and Bcl-2 family proteins. Environ. Toxicol. Pharmacol. 39:221–228
21. Vengris VE, Maré CJ (1974) Lead poisoning in chickens and the effect of lead on interferon and antibody production. Can J Comp Med 38(3):328–335
22. Liu C, Fu J, Liu C, Li S (2015) The role of nitric oxide and autophagy in liver injuries induced by selenium deficiency in chickens. RSC Adv. 5:50549–50556
23. Yao H, Liu W, Zhao W, et al. (2014) Different responses of selenoproteins to the altered expression of selenoprotein W in chicken myoblasts. RSC Adv. 4(109):64032–64042
24. Yao H-D, Wu Q, Zhang Z-W, et al. (2013) Selenoprotein W serves as an antioxidant in chicken myoblasts. BBA-General Subj 1830(4):3112–3120
25. Rayman MP (2000) The importance of selenium to human health. Lancet 356:233–241
26. Burk RF (1991) Molecular biology of selenium with implications for its metabolism. FASEB J 5:2274–2279
27. Berry MJ, Banu L, Larsen PR (1991) Type I iodothyronine deiodinase is a selenocysteine-containing enzyme. Nature 349:438–440
28. Xu XM, Carlson BA, Mix H, et al. (2007) Biosynthesis of selenocysteine on its tRNA in eukaryotes. PLoS Biol. 5:e4
29. Novoselov SV, Kryukov GV, Xu XM, et al. (2007) Selenoprotein H is a nucleolar thioredoxin-like protein with a unique expression pattern. J Biol Chem 282:11960–11968
30. Zhang JL, Li JL, Huang XD, et al. (2012) Dietary selenium regulation of transcript abundance of selenoprotein N and selenoprotein W in chicken muscle tissues. BioMetals 25:297–307
31. Guariniello S, Colonna G, Raucci R, et al. (2014) Structure-function relationship and evolutionary history of the human selenoprotein M (SelM) found over-expressed in hepatocellular carcinoma. Biochim. Biophys. Acta 1844:447–456
32. Malekirad AA, Oryan S, Fani A, et al. (2010) Study on clinical and biochemical toxicity biomarkers in a zinc-lead mine workers. Toxicol Ind Health 26:331–337
33. Kasperczyk S, Dobrakowski M, Kasperczyk A, Ostalowska A, Birkner E (2013) The administration of N-acetylcysteine reduces oxidative stress and regulates glutathione metabolism in the blood cells of workers exposed to lead. Clin Toxicol 51:480–486
34. Kasperczyk A, Machnik G, Dobrakowski M, et al. (2012) Gene expression and activity of antioxidant enzymes in the blood cells of workers who were occupationally exposed to lead. Toxicology 301:79–84
35. 2 in Se-deficient chicken liver. RSC Adv. 5:37896–37905
36. Tanekhy M (2015) Lead poisoning in Nile tilapia (Oreochromis niloticus): oxidant and antioxidant relationship. Environ. Monit. Assess. 187:154
37. Paton ND, Cantor AH, Pescatore AJ, Ford MJ, Smith CA (2002) The effect of dietary selenium source and level on the uptake of selenium by developing chick embryos. Poult. Sci. 81:1548–1554
38. Sun B, Wang R, Li J, Jiang Z, et al. (2011) Dietary selenium affects selenoprotein W gene expression in the liver of chicken. Biol. Trace Elem. Res. 143(3):1516–1523
39. Wang R, Sun B, Zhang Z, et al. (2011) Dietary selenium influences pancreatic tissue levels of selenoprotein W in chickens. J. Inorg. Biochem. 105(9):1156–1160
40. Pawlas N, Dobrakowski M, Kasperczyk A et al (2015) The level of selenium and oxidative stress in workers chronically exposed to lead. Biol Trace Elem Res